333 results on '"Aye T"'
Search Results
52. RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processes
- Author
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Bennett, Alexis H., primary, O’Donohue, Marie-Francoise, additional, Gundry, Stacey R., additional, Chan, Aye T., additional, Widrick, Jeffrey, additional, Draper, Isabelle, additional, Chakraborty, Anirban, additional, Zhou, Yi, additional, Zon, Leonard I., additional, Gleizes, Pierre-Emmanuel, additional, Beggs, Alan H., additional, and Gupta, Vandana A., additional
- Published
- 2018
- Full Text
- View/download PDF
53. Utility of chloroquine diphosphate in the blood bank laboratory
- Author
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Aye, T., primary and Arndt, P.A., additional
- Published
- 2018
- Full Text
- View/download PDF
54. Age-Related Male Reproductive Investment in Courtship Display and Nuptial Gifts in a Moth,Ostrinia scapulalis
- Author
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Aye T. Win, Wataru Kojima, and Yukio Ishikawa
- Subjects
Courtship display ,Ecology ,media_common.quotation_subject ,Longevity ,Zoology ,Biology ,Fecundity ,Courtship ,Spermatophore ,Animal Science and Zoology ,Mating ,Reproduction ,Nuptial gift ,Ecology, Evolution, Behavior and Systematics ,media_common - Abstract
Due to a trade-off between current and future reproduction, costly reproductive investments should be increased towards the end of a lifespan when the probability of reproduction becomes low (terminal investment hypothesis). We investigated age-related changes in male reproductive investment towards courtship display and the spermatophore in three age classes (young, middle-aged and old) of a monandrous moth, Ostrinia scapulalis. As predicted, old males had higher mating success than young and middle-aged males in no-choice tests. Moreover, two-choice tests revealed that middle-aged males had a higher success rate than young males because of their higher courtship frequency rather than any female preference for them. It was found that old males produced a larger spermatophore than young and middle-aged males, suggesting greater reproductive effort. The protein content of spermatophores also tended to increase with male age. Despite the age-related variation in spermatophore size and protein content, age did not affect female fecundity or longevity. A decrease in the number of sperm in the older males might counteract the nutritional benefit of larger spermatophores. Alternatively, fitness components other than longevity and fecundity may be influenced by male age.
- Published
- 2013
55. Implications of differentiated care for successful ART scale-up in a concentrated HIV epidemic in Yangon, Myanmar
- Author
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Mesic, A, Fontaine, J, Aye, T, Greig, J, Thwe, TT, Moretó-Planas, L, Kliesckova, J, Khin, K, Zarkua, N, Gonzalez, L, Guillergan, EL, O'Brien, Daniel, Mesic, A, Fontaine, J, Aye, T, Greig, J, Thwe, TT, Moretó-Planas, L, Kliesckova, J, Khin, K, Zarkua, N, Gonzalez, L, Guillergan, EL, and O'Brien, Daniel
- Published
- 2017
56. Design and Construction of Compressive Force Measuring Device for Engineering and Biomaterials
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Isiguzo E. Ahaneku and Aye T. Ajiboye
- Subjects
Compressive strength ,Materials science ,business.industry ,Mechanical engineering ,Ranging ,Structural engineering ,business - Abstract
This paper presents the design and construction of a device for measuring compressive force of engineering and biomaterials. The device was calibrated and tested. The results obtained show that the device is adequate for measuring compressive force, ranging from 0-100kN in a situation where a percentage error of up to 0.4% is permissible.
- Published
- 2012
57. The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies
- Author
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Stacey R. Gundry, Vandana Gupta, Alan H. Beggs, Aye T. Chen, Louis M. Kunkel, Yi Zhou, Wayne I. Lencer, Leonard I. Zon, and Genri Kawahara
- Subjects
Male ,musculoskeletal diseases ,animal structures ,Molecular Sequence Data ,Mutant ,Mutation, Missense ,Motor Activity ,Muscular Dystrophies ,Dystroglycans ,Genetic model ,Genetics ,medicine ,Dystroglycan ,Animals ,Humans ,Point Mutation ,Muscle, Skeletal ,Terminal cisternae ,Molecular Biology ,Zebrafish ,Genetics (clinical) ,Base Sequence ,biology ,Skeletal muscle ,Articles ,General Medicine ,Zebrafish Proteins ,biology.organism_classification ,Molecular biology ,Dystroglycan complex ,Disease Models, Animal ,medicine.anatomical_structure ,biology.protein ,Female - Abstract
In a forward genetic approach to identify novel genes for congenital muscle diseases, a zebrafish mutant, designated patchytail, was identified that exhibits degenerating muscle fibers with impaired motility behavior. Genetic mapping identified a genomic locus containing the zebrafish ortholog of the dystroglycan gene (DAG1). Patchytail fish contain a point mutation (c.1700T>A) in dag1, resulting in a missense change p.V567D. This change is associated with reduced transcripts and a complete absence of protein. The absence of α-dystroglycan and β-dystroglycan caused destabilization of dystroglycan complex, resulting in membrane damages. Membrane damage was localized on the extracellular matrix at myosepta as well as basement membrane between adjacent myofibers. These studies also identified structural abnormalities in triads at 3 days post fertilization (dpf) of dystroglycan-deficient muscles, significantly preceding sarcolemmal damage that becomes evident at 7 dpf. Immunofluorescence studies identified a subpopulation of dystroglycan that is expressed at t-tubules in normal skeletal muscles. In dag1-mutated fish, smaller and irregular-shaped t-tubule vesicles, as well as highly disorganized terminal cisternae of sarcoplasmic reticulum, were common. In addition to skeletal muscle defects, dag1-mutated fish have brain abnormalities and ocular defects in posterior as well as anterior chambers. These phenotypes of dystroglycan-deficient fish are highly reminiscent of the phenotypes observed in the human conditions muscle–eye–brain disease and Walker–Warburg syndrome. This animal model will provide unique opportunities in the understanding of biological functions of dystroglycan in a wide range of dystroglycanopathies, as disruption of this gene in higher vertebrates results in early embryonic lethality.
- Published
- 2011
58. Efficacy and safety of anticoagulation in thyrotoxic atrial fibrillation: a systematic review and meta-analysis
- Author
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Eng-Loon Tng, Yee Sian Tiong, Aye Thida Aung, Nicole Ya Yuan Chong, and Zhemin Wang
- Subjects
thyrotoxicosis ,atrial fibrillation ,stroke ,thromboembolism ,anticoagulation ,direct oral anticoagulants ,Diseases of the endocrine glands. Clinical endocrinology ,RC648-665 - Abstract
Background: Evidence on the efficacy and safety of anticoagulation in preven ting stroke and thromboembolic events in people with thyrotoxic atrial fibri llation is scarce. Objective: We evaluated the efficacy and safety of anticoagulation in peopl e with thyrotoxic atrial fibrillation. Methods: Our study protocol was published in the International Prospect ive Register of Systematic Reviews (registration no. CRD42020222782). Four d atabases and two systematic review registers were searched through 25 November 2 020 for interventional and observational studies comparing anticoagulation therapy with active comparators, placebo, or no treatment in people with thyrotoxic atrial fibril lation. Random-effects meta-analysis and sensitivity analysis were performed. Quality of evidence was described using the GRADE framework. Results: In the study, 23,145 records were retrieved. One randomized co ntrolled trial and eight cohort studies were ultimately included. Effect estima tes on the efficacy and safety of anticoagulation were extracted. Meta-analysis using t he inverse variance and random-effects methods was conducted on four cohort studies with 3443 participants and 277 events. Anticoagulation in people with thyrotoxic atria l fibrillation reduced the risk of ischemic stroke and systemic thromboembolism by 3% (95% CI: 1–6%). Warfarin may prevent ischemic stroke in people with thyrotoxic atrial fib rillation if the CHA2DS2- VASc score exceeds 1 and when atrial fibrillation persists beyon d 7 days. Direct oral anticoagulants may be associated with fewer bleeding events tha n warfarin. Conclusions: Anticoagulation prevents ischemic stroke and systemic thromboe mbolism in people with thyrotoxic atrial fibrillation. Direct oral anticoag ulants may be associated with fewer bleeding events.
- Published
- 2022
- Full Text
- View/download PDF
59. The role of the C-domain of bacteriophage T4 gene 32 protein in ssDNA binding and dsDNA helix-destabilization: Kinetic, single-molecule, and cross-linking studies
- Author
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Aye T. Win, Mark C. Williams, Brian J. Anderson, Hendrik Perdana, Matthew A. Malinowski, Kiran Pant, Richard L. Karpel, and Christopher Pabst
- Subjects
0301 basic medicine ,Conformational change ,DNA Repair ,lcsh:Medicine ,Biochemistry ,Physical Chemistry ,law.invention ,chemistry.chemical_compound ,law ,Cross-Linking ,Bacteriophage T4 ,lcsh:Science ,Recombination, Genetic ,Multidisciplinary ,Physics ,Melting ,Condensed Matter Physics ,Nucleic acids ,Chemistry ,Cross-Linking Reagents ,Physical Sciences ,Recombinant DNA ,Thermodynamics ,Phase Transitions ,Protein Binding ,Research Article ,DNA Replication ,DNA recombination ,DNA repair ,Protein domain ,DNA, Single-Stranded ,Viral Proteins ,03 medical and health sciences ,Protein Domains ,DNA-binding proteins ,Escherichia coli ,Genetics ,Binding site ,Protein Interactions ,Relaxation (Physics) ,Binding Sites ,Biology and life sciences ,Chemical Bonding ,Oligonucleotide ,lcsh:R ,DNA replication ,Proteins ,DNA ,Kinetics ,030104 developmental biology ,chemistry ,Mutation ,Linear Models ,Biophysics ,lcsh:Q - Abstract
The model single-stranded DNA binding protein of bacteriophage T4, gene 32 protein (gp32) has well-established roles in DNA replication, recombination, and repair. gp32 is a single-chain polypeptide consisting of three domains. Based on thermodynamics and kinetics measurements, we have proposed that gp32 can undergo a conformational change where the acidic C-terminal domain binds internally to or near the single-stranded (ss) DNA binding surface in the core (central) domain, blocking ssDNA interaction. To test this model, we have employed a variety of experimental approaches and gp32 variants to characterize this conformational change. Utilizing stopped-flow methods, the association kinetics of wild type and truncated forms of gp32 with ssDNA were measured. When the C-domain is present, the log-log plot of k vs. [NaCl] shows a positive slope, whereas when it is absent (*I protein), there is little rate change with salt concentration, as expected for this model.A gp32 variant lacking residues 292-296 within the C-domain, ΔPR201, displays kinetic properties intermediate between gp32 and *I. The single molecule force-induced DNA helix-destabilizing activitiesas well as the single- and double-stranded DNA affinities of ΔPR201 and gp32 truncated at residue 295 also fall between full-length protein and *I. Finally, chemical cross-linking of recombinant C-domain and gp32 lacking both N- and C-terminal domains is inhibited by increasing concentrations of a short single-stranded oligonucleotide, and the salt dependence of cross-linking mirrors that expected for the model. Taken together, these results provide the first evidence in support of this model that have been obtained through structural probes.
- Published
- 2018
60. RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processes
- Author
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Bennett, Alexis H, primary, O’Donohue, Marie-Francoise, additional, Gundry, Stacey R., additional, Chan, Aye T., additional, Widrick, Jeffery, additional, Draper, Isabelle, additional, Chakraborty, Anirban, additional, Zhou, Yi, additional, Zon, Leonard I., additional, Gleizes, Pierre-Emmanuel, additional, Beggs, Alan H., additional, and Gupta, Vandana A, additional
- Published
- 2017
- Full Text
- View/download PDF
61. Risk stratification in stable coronary artery disease
- Author
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Aye, T., primary and Graham, R., additional
- Published
- 2017
- Full Text
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62. ‘Low-grade’ astroblastoma with rapid recurrence: a case report
- Author
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Teresa M. M. Thomas, Patrick P. L. Lau, Philip C.W. Lui, and Aye T. Khin
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Pathology ,medicine.medical_specialty ,medicine.anatomical_structure ,Tanycyte ,business.industry ,Astroblastoma ,medicine ,Histogenesis ,medicine.disease ,business ,Pathology and Forensic Medicine - Abstract
Sir,Astroblastoma is a rare and controversial brain tumour of uncertain histogenesis. The tanycyte has been suggested as a possible cell origin. The tumour usually affects children and young adults...
- Published
- 2006
63. Myocardial strain in a health and disease: CMR feature tracking analysis in cardiac hypertrophy
- Author
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James C. Moon, Andrea Barison, Vanessa Cobb, Aye T Hline, Thomas A. Treibel, Steven K White, Andrew S. Flett, Daniel Sado, Sanjay M Banypersad, and Anna S Herrey
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Medicine(all) ,medicine.medical_specialty ,lcsh:Diseases of the circulatory (Cardiovascular) system ,Radiological and Ultrasound Technology ,Intraclass correlation ,business.industry ,Hypertrophic cardiomyopathy ,Disease ,medicine.disease ,Stenosis ,Aortic valve replacement ,lcsh:RC666-701 ,Internal medicine ,Poster Presentation ,Myocardial strain ,cardiovascular system ,medicine ,Cardiology ,Feature tracking ,Radiology, Nuclear Medicine and imaging ,Cardiology and Cardiovascular Medicine ,business ,Angiology - Abstract
Methods Ninety-five healthy volunteers, 45 patients with AndersonFabry disease (AFD), 48 with hypertension (HT), 65 with hypertrophic cardiomyopathy (HCM), 62 with severe aortic stenosis (AS), 85 with systemic amyloidosis (AMY) were enrolled. Longitudinal and transversal strain was calculated from 3 long-axis cine views, circumferential and radial strain from 3 short-axis cine images using a dedicated software (Tomtec Feature Tracking). Fourteen healthy volunteers were scanned twice, and inter-study, inter-observer, intra-observer intraclass correlation coefficients ranged between 0.36 and 0.77. Forty AS patients underwent a second scan six months after aortic valve replacement.
- Published
- 2013
64. The presence of an alternative food source changes the tending behavior of the big-headed ant, <italic>Pheidole megacephala</italic> (Hymenoptera: Formicidae) on <italic>Dysmicoccus brevipes</italic> (Homoptera: Pseudococcidae).
- Author
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Win, Aye T., Kinoshita, Tetsu, and Tsuji, Kazuki
- Abstract
The mutualistic association between ants and hemipterans is often facultative and can be affected by the availability of other food sources. In the present study we tested whether the tending behavior of the big-headed ant,
Pheidole megacephala (Fabricius), had a negative impact on the pink pineapple mealybug,Dysmicoccus brevipes (Cockerell), when alternative food sources: (1) sugar solution, (2) purified water + mealworms and (3) sugar solution + mealworms versus with purified water (control) were provided to the ant colonies. We found that the frequency of ant tending onD. brevipes decreased when ants were provided with alternative food sources. However, we did not see any aggressive behaviors and predation of ants onD. brevipes. Also, the survival ofD. brevipes was not different among food condition treatments. These results suggest that the decreased tending frequency of ants can lead to the decline in ant protection service to mealybugs. [ABSTRACT FROM AUTHOR]- Published
- 2018
- Full Text
- View/download PDF
65. The Impact of Action Planning after Causation-and-Effectuation-Based Entrepreneurship Education
- Author
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Khin Sandar Thein, Yoshi Takahashi, and Aye Thanda Soe
- Subjects
action planning ,entrepreneurial self-efficacy ,entrepreneurial intention ,opportunity recognition ,entrepreneurship education ,Psychology ,BF1-990 - Abstract
The entrepreneurship literature shows inconsistent results in outcome effectiveness, such as entrepreneurial self-efficacy (ESE), entrepreneurial intention (EI), and entrepreneurial behavior. This could be due to the sole focus on the motivational aspects of behavioral change. Action planning, a volitional intervention used to modify health behavior, could resolve the inconsistent results mentioned above. Therefore, this study aims to evaluate the direct impacts of action planning intervention (API) following entrepreneurship education (EE) on ESE, EI, and opportunity recognition and to examine the behavioral change process from motivational and volitional perspectives. In this randomized controlled trial (RCT), we considered action planning to enhance entrepreneurial behavior after EE. The sample included 83 participants from a university in Myanmar. We randomly assigned the students to the API and control groups. We collected data on ESE and EI before and after training. We used objective measures for opportunity recognition through an opportunity evaluation framework. Serial mediation analysis revealed that the volitional impact on opportunity recognition was positively significant. From a motivational standpoint, ESE improved significantly, but we found no significant impact on EI; ESE and EI were serial mediators, with no specific mediation solely by ESE or EI. The findings contribute to the EE literature by presenting a brief and cost-effective API for EE.
- Published
- 2023
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66. A quark model for baryon residues
- Author
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Aye, T. M.
- Published
- 1973
- Full Text
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67. Prevalence and risk factors of anxiety and depression among the community-dwelling elderly in Nay Pyi Taw Union Territory, Myanmar
- Author
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Su Myat Cho, Yu Mon Saw, Thu Nandar Saw, Thet Mon Than, Moe Khaing, Aye Thazin Khine, Tetsuyoshi Kariya, Pa Pa Soe, San Oo, and Nobuyuki Hamajima
- Subjects
Medicine ,Science - Abstract
Abstract Providing elderly mental healthcare in Myanmar is challenging due to the growing elderly population and limited health resources. To understand common mental health problems among Myanmar elderly, this study explored the prevalence and risk factors of anxiety and depression among the elderly in the Nay Pyi Taw Union Territory, Myanmar. A cross-sectional study was conducted among 655 elderly by face-to-face interviews with a pretested questionnaire. Descriptive analysis and multiple logistic regression analyses were performed. The prevalence of anxiety and depression were 39.4% (33.5% for males and 42.4% for females) and 35.6% (33.0% for males and 36.9% for females), respectively. The adjusted odds ratio of having anxiety was significant for having low education level, having comorbidity, having BMI
- Published
- 2021
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68. A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish
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Leonard I. Zon, Louis M. Kunkel, Chiara Manzini, Alan H. Beggs, Jennifer Myers, Vandana Gupta, Genri Kawahara, Thomas E. Hall, Peter D. Currie, Yi Zhou, and Aye T. Chen
- Subjects
Pathology ,Anatomy and Physiology ,Muscle Fibers, Skeletal ,lcsh:Medicine ,Muscular Dystrophies ,0302 clinical medicine ,Muscular dystrophy ,lcsh:Science ,Zebrafish ,Musculoskeletal System ,Musculoskeletal Anatomy ,0303 health sciences ,Multidisciplinary ,Splice site mutation ,Muscle Biochemistry ,Animal Models ,Cell biology ,Extracellular Matrix ,Congenital muscular dystrophy ,Medicine ,Muscle ,medicine.symptom ,ITGA7 ,Research Article ,medicine.medical_specialty ,Nonsense mutation ,Biology ,Muscle disorder ,03 medical and health sciences ,Model Organisms ,Genetic Mutation ,medicine ,Genetics ,Animals ,Humans ,030304 developmental biology ,Base Sequence ,lcsh:R ,Muscle weakness ,Human Genetics ,Molecular Development ,Zebrafish Proteins ,medicine.disease ,biology.organism_classification ,Genetics of Disease ,Mutation ,lcsh:Q ,Laminin ,RNA Splice Sites ,030217 neurology & neurosurgery ,Developmental Biology - Abstract
Congenital muscular dystrophy (CMD) is a clinically and genetically heterogeneous group of inherited muscle disorders. In patients, muscle weakness is usually present at or shortly after birth and is progressive in nature. Merosin deficient congenital muscular dystrophy (MDC1A) is a form of CMD caused by a defect in the laminin-α2 gene (LAMA2). Laminin-α2 is an extracellular matrix protein that interacts with the dystrophin-dystroglycan (DGC) complex in membranes providing stability to muscle fibers. In an N-ethyl-N-nitrosourea mutagenesis screen to develop zebrafish models of neuromuscular diseases, we identified a mutant fish that exhibits severe muscular dystrophy early in development. Genetic mapping identified a splice site mutation in the lama2 gene. This splice site is highly conserved in humans and this mutation results in mis-splicing of RNA and a loss of protein function. Homozygous lama2 mutant zebrafish, designated lama2(cl501/cl501), exhibited reduced motor function and progressive degeneration of skeletal muscles and died at 8-15 days post fertilization. The skeletal muscles exhibited damaged myosepta and detachment of myofibers in the affected fish. Laminin-α2 deficiency also resulted in growth defects in the brain and eye of the mutant fish. This laminin-α2 deficient mutant fish represents a novel disease model to develop therapies for modulating splicing defects in congenital muscular dystrophies and to restore the muscle function in human patients with CMD.
- Published
- 2012
69. Characterization of immune-matched hematopoietic transplantation in zebrafish
- Author
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Alexandra C. H. Smith, Jill L. O. de Jong, Aye T. Chen, Leonard I. Zon, Yi Zhou, Emily K. Pugach, Elizabeth A. Mayhall, Henry A. Feldman, and Caroline E. Burns
- Subjects
medicine.medical_specialty ,Transplantation Conditioning ,Hematopoiesis and Stem Cells ,Immunology ,Major histocompatibility complex ,Biochemistry ,Chimerism ,Major Histocompatibility Complex ,Immune system ,Internal medicine ,medicine ,Animals ,Zebrafish ,Hematology ,biology ,Hematopoietic Stem Cell Transplantation ,Hematopoietic stem cell ,Cell Biology ,biology.organism_classification ,Histocompatibility ,Transplantation ,Haematopoiesis ,medicine.anatomical_structure ,Models, Animal ,biology.protein - Abstract
Evaluating hematopoietic stem cell (HSC) function in vivo requires a long-term transplantation assay. Although zebrafish are a powerful model for discovering the genetics of hematopoiesis, hematopoietic transplantation approaches have been underdeveloped. Here we established a long-term reconstitution assay in adult zebrafish. Primary and secondary recipients showed multilineage engraftment at 3 months after transplantation. Limiting dilution data suggest that at least 1 in 65 000 zebrafish marrow cells contain repopulating activity, consistent with mammalian HSC frequencies. We defined zebrafish haplotypes at the proposed major histocompatibility complex locus on chromosome 19 and tested functional significance through hematopoietic transplantation. Matching donors and recipients dramatically increased engraftment and percentage donor chimerism compared with unmatched fish. These data constitute the first functional test of zebrafish histocompatibility genes, enabling the development of matched hematopoietic transplantations. This lays the foundation for competitive transplantation experiments with mutant zebrafish HSCs and chemicals to test for effects on engraftment, thereby providing a model for human hematopoietic diseases and treatments not previously available.
- Published
- 2011
70. cpsf1 is required for definitive HSC survival in zebrafish
- Author
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Yi Zhou, Niccolo Bolli, John P. Kanki, Jeong-Soo Lee, Jennifer Rhodes, Elspeth Payne, Leonard I. Zon, Adam Johnston, Feng Guo, Aye T. Chen, Evisa Gjini, A. Thomas Look, and Rodney A. Stewart
- Subjects
Male ,Myeloid ,Cell Survival ,Hematopoiesis and Stem Cells ,Cellular differentiation ,Immunology ,Cleavage and polyadenylation specificity factor ,Biology ,Biochemistry ,Blood cell ,medicine ,Animals ,Zebrafish ,Regulation of gene expression ,Hematopoietic Tissue ,Cleavage And Polyadenylation Specificity Factor ,Gene Expression Regulation, Developmental ,Cell Differentiation ,Cell Biology ,Hematology ,biology.organism_classification ,Hematopoietic Stem Cells ,Hematopoiesis ,Haematopoiesis ,medicine.anatomical_structure ,Phenotype ,Mutagenesis ,Cancer research - Abstract
A comprehensive understanding of the genes and pathways regulating hematopoiesis is needed to identify genes causally related to bone marrow failure syndromes, myelodysplastic syndromes, and hematopoietic neoplasms. To identify novel genes involved in hematopoiesis, we performed an ethyl-nitrosourea mutagenesis screen in zebrafish (Danio rerio) to search for mutants with defective definitive hematopoiesis. We report the recovery and analysis of the grechetto mutant, which harbors an inactivating mutation in cleavage and polyadenylation specificity factor 1 (cpsf1), a gene ubiquitously expressed and required for 3′ untranslated region processing of a subset of pre-mRNAs. grechetto mutants undergo normal primitive hematopoiesis and specify appropriate numbers of definitive HSCs at 36 hours postfertilization. However, when HSCs migrate to the caudal hematopoietic tissue at 3 days postfertilization, their numbers start decreasing as a result of apoptotic cell death. Consistent with Cpsf1 function, c-myb:EGFP+ cells in grechetto mutants also show defective polyadenylation of snrnp70, a gene required for HSC development. By 5 days postfertilization, definitive hematopoiesis is compromised and severely decreased blood cell numbers are observed across the myeloid, erythroid, and lymphoid cell lineages. These studies show that cpsf1 is essential for HSC survival and differentiation in caudal hematopoietic tissue.
- Published
- 2011
71. Asian Pacific Society of Cardiology Consensus Statements on the Diagnosis and Management of Obstructive Sleep Apnoea in Patients with Cardiovascular Disease
- Author
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Jack Wei Chieh Tan, Leong Chai Leow, Serene Wong, See Meng Khoo, Takatoshi Kasai, Pipin Kojodjojo, Duong-Quy Sy, Chuen Peng Lee, Naricha Chirakalwasan, Hsueh-Yu Li, Natalie Koh, Adeline Tan, Thun How Ong, Aye Thandar Aung, Song Tar Toh, and Chi-Hang Lee
- Subjects
Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Abstract
Obstructive sleep apnoea (OSA) is strongly associated with cardiovascular disease (CVD). However, evidence supporting this association in the Asian population is scarce. Given the differences in the epidemiology of CVD and cardiovascular risk factors, as well as differences in the availability of healthcare resources between Asian and Western countries, an Asian Pacific Society of Cardiology (APSC) working group developed consensus recommendations on the management of OSA in patients with CVD in the Asia-Pacific region. The APSC expert panel reviewed and appraised the available evidence using the Grading of Recommendations Assessment, Development, and Evaluation system. Consensus recommendations were developed and put to an online vote. Consensus was reached when 80% of votes for a given recommendation were in support of ‘agree’ or ‘neutral.’ The resulting statements provide guidance on the assessment and treatment of OSA in patients with CVD in the Asia-Pacific region. The APSC hopes for these recommendations to pave the way for screening, early diagnosis and treatment of OSA in the Asia-Pacific region.
- Published
- 2022
- Full Text
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72. Zebrafish blood stem cells
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Leonard I. Zon and Aye T. Chen
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Embryo, Nonmammalian ,Biochemistry ,Mesoderm ,Cell Movement ,medicine ,Animals ,Endothelium ,Progenitor cell ,Molecular Biology ,Zebrafish ,biology ,Lateral plate mesoderm ,fungi ,Hematopoietic Tissue ,Cell Biology ,biology.organism_classification ,Hematopoietic Stem Cells ,Cell biology ,Hematopoiesis ,Haematopoiesis ,medicine.anatomical_structure ,Immunology ,Myelopoiesis ,Bone marrow ,Stem cell - Abstract
Within the past two decades, the zebrafish (Danio rerio) has become an excellent model to study the development of hematopoietic stem cells (HSCs). All vertebrates including zebrafish have primitive and definitive waves of hematopoiesis, but self-renewing pluripotent HSCs are only produced by the definitive wave. The primitive wave occurs in two intraembryonic locations called the intermediate cell mass (ICM) and the anterior lateral mesoderm (ALM). Primitive erythropoiesis is in the ICM, whereas myelopoiesis initiates in the ALM. After circulation starts at 24 h post-fertilization, hematopoiesis shifts to the posterior blood island (PBI) for a brief period. The definitive wave starts in the aorta-gonad-mesonephros (AGM). There are three different HSC migration and colonization events that begin 2 days post-fertilization: AGM progenitor cells migrate to (1) the caudal hematopoietic tissue (CHT), which is an intermediate site of blood development; (2) the thymus, which is a site of lymphocyte maturation; and (3) the developing kidney marrow, which is the larval and adult location for production of all hematopoietic cell types, and is comparable to the bone marrow of mammals. Many of the transcription factors and signaling pathways that regulate the formation of HSCs in a zebrafish are conserved with mammals. Large-scale forward and reverse genetic screens have identified zebrafish blood and HSC mutants that represent models for known human diseases. Along with the technological advancements in the field of zebrafish research, future HSC studies in zebrafish will help us illuminate the genetic network controlling the development and function of stem cells in all vertebrates.
- Published
- 2009
73. A rhomboid-shaped printed monopole antenna for wideband circular polarization
- Author
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Lwin Zaw Myo and Aye Thae Su
- Subjects
circular polarization ,printed monopole antenna ,rhomboid shape ,wideband antenna ,Electrical engineering. Electronics. Nuclear engineering ,TK1-9971 - Abstract
This paper presents the design of a wideband circularly-polarized printed monopole antenna with a rhomboid shape. The rhomboid-shaped patch is fed by a microstrip line offset from the center to generate circular polarization (CP). The ground plane configuration is optimized for wide bandwidth operation. Bandwidth (satisfying both 10-dB return loss and 3-dB axial ratio) of 76% (1.92 - 4.27 GHz) is achieved in this research. The size of the proposed antenna is 0.386 2 0 l (55×66 mm2) where λ0 is the free space wavelength which corresponds to the center frequency of the bandwidth. The antenna has a fractional bandwidth-size ratio (BW/size) of 1.97 which is higher than most CP monopole antennas in the literature. This antenna is suitable for Wi-Fi, WiMAX, and other wireless applications which outperform using circular polarization.
- Published
- 2021
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74. Fine-needle aspiration cytology of metaplastic carcinoma of the breast
- Author
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Gita Jayaram, Puay Hoon Tan, Aye T. Khin, Gary M.K. Tse, Philip C.W. Lui, Benjaporn Chaiwun, Thomas C. Putti, Norman H.L. Chan, Patrick P. L. Lau, and K.L. Mak
- Subjects
Adult ,Pathology ,medicine.medical_specialty ,Stromal cell ,Metaplastic carcinoma ,Biopsy, Fine-Needle ,Breast Neoplasms ,Pathology and Forensic Medicine ,Breast cancer ,Metaplasia ,Cytology ,Carcinoma ,Medicine ,Humans ,Aged ,Retrospective Studies ,business.industry ,Cell Differentiation ,General Medicine ,Middle Aged ,medicine.disease ,Squamous carcinoma ,Mixed Tumor, Malignant ,Carcinoma, Squamous Cell ,Female ,Original Article ,medicine.symptom ,business ,Breast carcinoma - Abstract
Background: Metaplastic carcinoma of the breast encompasses a heterogeneous group of tumours with variable components of sarcomatoid, squamous or poorly differentiated carcinomas. Aim: To review a series of 19 cytological preparations of metaplastic carcinomas to assess diagnostic cytological features. Methods: 17 cases of fine-needle aspirates of histologically proven metaplastic carcinomas (4 monophasic spindle cell carcinomas, 4 squamous cell carcinomas and 11 biphasic tumours) were reviewed, with an emphasis on the presence of poorly differentiated carcinoma, squamous cell carcinoma, atypical spindle cells, benign stromal fragments and necrosis. Results: All cases were diagnosed as malignant, with 68% of cases showing moderate to high cellularity, and 47% showing necrosis. If the tumours were analysed according to the constituting components histologically, 7, 15 and 8 cases, respectively, possess poorly differentiated carcinoma cells, sarcomatoid malignant cells and squamous carcinoma cells, whereas these components were cytologically identified in 11, 10 and 7 cases, respectively. Dual tumour populations were identified in only 5 of the 11 biphasic carcinomas in the cytological preparations; and the stromal material was cytologically identified in the only case with chondroid stroma. Conclusions: Identification of metaplastic carcinoma in cytology remains problematic. There seems to be morphological overlap between various components. The identification of dual components, unequivocal squamous carcinoma cells and chondroid stroma is helpful for diagnosis, but it is uncommon. The presence of poorly differentiated carcinoma cells with a suggestion of focal spindle morphology is another clue to the suggestion of metaplastic carcinoma.
- Published
- 2006
75. Women's intergenerational intimate partner violence and household child abuse in Burma (Myanmar)
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Stephanie Spaid Miedema and Aye Thiri Kyaw
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Burma (Myanmar) ,Child discipline ,Child abuse ,Intergenerational violence ,Intimate partner violence ,Public aspects of medicine ,RA1-1270 ,Social sciences (General) ,H1-99 - Abstract
Intimate partner violence (IPV) and child abuse are prevalent in Burma (Myanmar). However, gaps exist in our understanding of intergenerational cycles and co-occurrence of violence, and whether patterns of violence vary by women and children's life course transitions and developmental stages. Using data from the 2015–2016 Demographic and Health Survey, we estimated structural equation models to evaluate the pathways between women's exposure to IPV perpetrated by her father against her mother (maternal abuse), her own past-year experiences of IPV, attitudes toward IPV, and household child discipline practices. We ran stratified analyses by women's age at first birth and child's age to assess whether intergenerational cycles and co-occurrence of violence in the household vary by pivotal life events and development stages. Maternal abuse was directly and indirectly associated with women's past-year exposure to physical and/or sexual IPV and children's exposure to physical or emotional child abuse by a caregiver in the household. Stratified models indicated significant intergenerational cycles of IPV and co-occurrence of IPV and child abuse among women who experienced first childbirth before age 23, and among women living with older children. We conclude that synchronized efforts to prevent violence against women and violence against children are integral to addressing cyclical and co-occurring patterns of violence in Burma (Myanmar). Violence prevention efforts might consider developmental stage and life course factors that may intensify risk of intergenerational violence.
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- 2022
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76. The presence of an alternative food source changes the tending behavior of the big-headed ant, Pheidole megacephala(Hymenoptera: Formicidae) on Dysmicoccus brevipes(Homoptera: Pseudococcidae)
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Win, Aye T., Kinoshita, Tetsu, and Tsuji, Kazuki
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The mutualistic association between ants and hemipterans is often facultative and can be affected by the availability of other food sources. In the present study we tested whether the tending behavior of the big-headed ant, Pheidole megacephala(Fabricius), had a negative impact on the pink pineapple mealybug, Dysmicoccus brevipes(Cockerell), when alternative food sources: (1) sugar solution, (2) purified water + mealworms and (3) sugar solution + mealworms versus with purified water (control) were provided to the ant colonies. We found that the frequency of ant tending on D. brevipesdecreased when ants were provided with alternative food sources. However, we did not see any aggressive behaviors and predation of ants on D. brevipes.Also, the survival of D. brevipeswas not different among food condition treatments. These results suggest that the decreased tending frequency of ants can lead to the decline in ant protection service to mealybugs.
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- 2018
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77. Association between body mass index and ready-to-eat food consumption among sedentary staff in Nay Pyi Taw union territory, Myanmar
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Thin Zar Thike, Yu Mon Saw, Htin Lin, Khin Chit, Aung Ba Tun, Hein Htet, Su Myat Cho, Aye Thazin Khine, Thu Nandar Saw, Tetsuyoshi Kariya, Eiko Yamamoto, and Nobuyuki Hamajima
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Ready-to-eat food ,Sedentary staffs ,Physical exercise ,Nay Pyi Taw ,Myanmar ,Public aspects of medicine ,RA1-1270 - Abstract
Abstract Background Ready-to-eat (RTE) food consumption has become popular in the working community with the increase in full-time jobs and the limited time to prepare food. Although RTE food is essential for this community, its consumption causes obesity. In Myanmar, obesity is a modifiable risk factor for non-communicable diseases, causing increases in morbidity and mortality. This study aimed to identify the association between body mass index (BMI) and RTE food consumption among sedentary staff in Nay Pyi Taw Union Territory, Myanmar. Methods A cross-sectional study was conducted in 2018, in which 400 respondents participated in face-to-face interviews. The study area was selected using simple random sampling and drawing method. Measuring tape and digital weighing scale were used to measure the height and weight of the respondents. BMI was calculated by dividing the weight by height squared (kg/m2). Overweight and obesity were categorized by World Health Organization cut-off points. The collected data were analyzed using multiple logistic regression to estimate the adjusted odds ratio (AOR), and the 95% confidence interval (CI). Results This study revealed that sedentary staff who consumed RTE food once or more per month were nearly five times more likely to be overweight and obese (AOR = 4.78, 95% CI 1.44–15.85) than those who consumed RTE food less frequently. In addition, five factors namely being older than 32 years (AOR = 3.97, 95% CI 1.82–8.69), preference for RTE food (AOR = 8.93, 95% CI 2.54–31.37), light-intensity of physical exercise (AOR = 3.55, 95% CI 1.63–7.73), sedentary leisure activities (AOR = 3.32, 95% CI 1.22–9.03), and smoking (AOR = 5.62, 95% CI 1.06–29.90) were positively associated with overweight and obesity. Conclusion Frequent consumers of RTE food and less physically active sedentary staff were more likely to be overweight and obese. This study highlights the urgent need to raise awareness regarding healthy lifestyle behaviors among the working community to reduce the burden of obesity-related chronic diseases. Moreover, sedentary workers should be aware of the food-based dietary guidelines of the country. Policy makers should strictly enforce nutritional labeling of RTE food, and strictly prohibit over-branding of RTE food.
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- 2020
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78. Three new fossil records of Equisetum (Equisetaceae) from the Neogene of south-western China and northern Vietnam
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Aye Thida Aung, Jian Huang, Truong Van Do, Ai Song, Jia Liu, Zhe-Kun Zhou, and Tao Su
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Botany ,QK1-989 - Abstract
Three fossil species of Equisetum (Equisetaceae) were reported from the Neogene of south-western China and northern Vietnam, based on well-preserved rhizomes with tubers. Equisetum cf. pratense Ehrhart from the middle Miocene of Zhenyuan County, Yunnan Province, China is characterised by a bunch of three ovate tubers with longitudinal ridges on the surface. Equisetum yenbaiense A.T. Aung, T. Su, T.V. Do & Z.K. Zhou, sp. nov. from the late Miocene of Yenbai Province, Vietnam is characterised by four bunches of elongate tubers arranged in a whorl on a node. Equisetum yongpingense A.T. Aung, T. Su & Z.K. Zhou, sp. nov. from the late Pliocene of Yunnan is characterised by fibrous roots on most nodes and two to four bunches of large cylindrical tubers arranged in a whorl on a node. Floristic assemblages suggest that these species might have grown near a riverside or lakeshore. These new fossil records improve our understanding of species richness of Equisetum and their distribution range during the Neogene in Asia.
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- 2020
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79. An annotated checklist of Myanmar orchid flora
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Ye Lwin Aung, Aye Thin Mu, Mung Htoi Aung, Qiang Liu, and Xiao-Hua Jin
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Botany ,QK1-989 - Abstract
Myanmar is situated in Southeast Asia, where species richness and diversity are very high. Myanmar orchid flora is very rich, but still poorly known because botanical explorations have sharply decreased in Myanmar since 1950. The present study provides a checklist of Myanmar orchid flora which includes 1040 species and 151 genera currently known from Myanmar, based on the herbarium specimens, literature and online databases. The number of species is increased by approximately 200 species more than that given in the checklist of Kress et al. (2003), mainly due to recent discoveries of new species to science and new records for Myanmar. There are 76 endemic species of Orchidaceae in Myanmar. It is estimated that ca. 150–300 species still remain as unidentified and are expected to be discovered in further studies on Myanmar orchid flora.
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- 2020
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80. Single Nucleotide Polymorphism at rs7903146 of Transcription Factor 7-like 2 gene Among Subjects with Type 2 Diabetes Mellitus in Myanmar
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Sagawah Phu, Aye Thida, Kyu Kyu Maung, and Tet Tun Chit
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TCF7L2 ,SNP ,Myanmar ,Diseases of the endocrine glands. Clinical endocrinology ,RC648-665 - Abstract
Objectives. To investigate the association between the single nucleotide polymorphism (SNP) rs7903146 in the transcription factor 7-like 2 (TCF7L2) gene and type 2 diabetes mellitus (T2DM) and to examine the impact of this variant on pancreatic beta-cell function in the Myanmar population. Methodology. A case-control study was undertaken in 100 subjects with T2DM and 113 controls. The SNP rs7903146 was genotyped using the allele-specific polymerase chain reaction method. Plasma glucose and serum insulin levels were determined using the enzymatic colorimetric method and ELISA respectively. Beta-cell function was calculated by the HOMA-β formula. Results. The frequencies of carrier genotypes (CT and TT) were higher in subjects with T2DM than in controls. The minor T alleles of rs7903146 were found to statistically increase type 2 diabetes risk than the C allele with an allelic odds ratio of 2.07 (95% CI 1.39-3.09, p=0.0004). The mean HOMA-β level of the group with non-carrier genotype (CC) was significantly higher than that of the groups with carrier genotypes (CT and TT) in subjects with T2DM and controls with a p-value of 0.0003 and less than 0.0001, respectively. Conclusion. The rs7903146 variant of the TCF7L2 gene was found to be associated with T2DM and low β-cell function among Myanmar subjects.
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- 2021
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81. International multicenter evaluation of the clinical utility of a dipstick assay for detection of Leptospira-specific immunoglobulin M antibodies in human serum specimens
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Smits, H. L., Ananyina, Y. V., Chereshsky, A., Dancel, L., Lai-A-Fat, R. F., Chee, H. D., Levett, P. N., Masuzawa, T., Yanagihara, Y., Muthusethupathi, M. A., Sanders, E. J., Sasaki, D. M., Domen, H., Yersin, C., Aye, T., Bragg, S. L., Gussenhoven, G. C., Goris, M. G., Terpstra, W. J., Hartskeerl, R. A., and Other departments
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parasitic diseases - Abstract
We performed a multicenter evaluation of a robust and easily performed dipstick assay for the serodiagnosis of human leptospirosis. The assay is aimed at the detection of Leptospira-specific immunoglobulin M (IgM) antibodies. The study involved 2,665 serum samples collected from 2,057 patients with suspected leptospirosis in 12 countries on five continents with different levels of endemicity and different surveillance systems. The patients were grouped as laboratory-confirmed leptospirosis case patients and noncase patients based on the results of culturing and the microscopic agglutination test. Paired samples from 27.7% of the subjects were tested. Of the 485 case patients, 87.4% had a positive dipstick result for one or more samples. Of the 1,513 noncase patients, only 7.2% had a positive result. Whereas most (88.4%) of the positive samples from the case patients showed moderate to strong (2+ to 4+) staining in the dipstick assay, most (68.1%) of the positive samples from the noncase patients showed weak (1+) staining. The sensitivity of the dipstick assay increased from 60.1% for acute-phase serum samples to 87.4% for convalescent-phase samples. The specificities for these two groups of samples were 94.1 and 92.7%, respectively. The dipstick assay detected a broad variety of serogroups. The results of the dipstick assay were concordant (observed agreement, 93.2%; kappa value, 0.76) with the results of an enzyme-linked immunosorbent assay for the detection of specific IgM antibodies, a test which is often used in the laboratory diagnosis of current or recent leptospirosis. This study demonstrated that this easily performed dipstick assay is a valuable and useful test for the quick screening for leptospirosis; has a wide applicability in different countries with different degrees of endemicity; can be used at all levels of the health care system, including the field; and will be useful for detecting and monitoring outbreaks of leptospirosis
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- 1999
82. Sequence Analyses and Phenotypic Characterization Revealed Multidrug Resistant Gene Insertions in the Genomic Region Encompassing Phase 2 Flagellin Encoding fljAB Genes in Monophasic Variant Salmonella enterica Serovar 4,5,12:i:- Isolates From Various Sources in Thailand
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Aye Thida Win, Sirirak Supa-amornkul, Renato H. Orsi, Jaclyn H. Carey, William J. Wolfgang, and Soraya Chaturongakul
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monophasic S. Typhimurium ,fljAB region ,antimicrobial resistance ,WGS—whole-genome sequencing ,STM2759 and iroB ,Microbiology ,QR1-502 - Abstract
Salmonella enterica serovar 4,5,12:i:- (S. 4,5,12:i:-), a monophasic variant of Salmonella Typhimurium (STm) lacking the phase 2 flagellin encoding genes fljAB, has become increasingly prevalent worldwide. The increasing trends in multidrug resistant (MDR) S. 4,5,12:i:- prevalence also pose an important global health threat. Though many reports have characterized phenotypic and genotypic drug resistance of this serovar, few studies have characterized antimicrobial resistance of this serovar in Thailand. In this study, 108 S. 4,5,12:i:- isolates from various sources in Thailand and four international S. 4,5,12:i:- isolates were screened using polymerase chain reaction (PCR) to detect the presence of five target regions which are associated with antimicrobial resistant (AMR) genes, in the genomic region that contained fljAB genes in STm. We determined AMR phenotypes of all isolates by Kirby-Bauer disk diffusion method. Whole genome sequencing (WGS) was performed on 53 representative isolates (based on differences in the pulsed filed gel electrophoresis profiles, the sources of isolate, and the PCR and AMR patterns) to characterize the genetic basis of AMR phenotype and to identify the location of AMR determinants. Based on PCR screening, nine PCR profiles showing distinct deletion patterns of the five target regions have been observed. Approximately 76% of isolates (or 85 of 112 isolates), all of which were Thai isolates, contained five target regions inserted between STM2759 and iroB gene. A total of 21 phenotypic AMR patterns were identified with the predominant AmpST resistant phenotype [i.e., 84% (or 94 of 112) tested positive for resistance to ampicillin, streptomycin, and tetracycline], and 89% (or 100 of 112) were found to be MDR (defined here as resistant to at least three classes of tested antimicrobials). Using WGS data, a total of 24 genotypic AMR determinants belonging to seven different antimicrobial groups were found. AMR determinants (i.e., blaTEM–1, strB-A, sul2, and tetB, conferring resistance to ampicillin, streptomycin, sulfonamides, and tetracycline, respectively) were found to be inserted in a region typically occupied by the phase 2 flagellin encoding genes in STm. These resistant genes were flanked by a number of insertion sequences (IS), and co-localized with mercury tolerance genes. Our findings identify AMR genes, possibly associated with multiple IS26 copies, in the genetic region between STM2759 and iroB genes replacing phase 2 flagellin encoding fljAB genes in Thai S. 4,5,12:i:- isolates.
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- 2021
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83. Myocardial strain in a health and disease: CMR feature tracking analysis in cardiac hypertrophy
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Barison, Andrea, primary, Cobb, Vanessa, additional, Hline, Aye T, additional, Sado, Daniel, additional, White, Steven K, additional, Flett, Andrew, additional, Banypersad, Sanjay M, additional, Treibel, Thomas A, additional, Herrey, Anna S, additional, and Moon, James, additional
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- 2013
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84. RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processes
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Bennett, Alexis H., O’Donohue, Marie-Francoise, Gundry, Stacey R., Chan, Aye T., Widrick, Jeffrey, Draper, Isabelle, Chakraborty, Anirban, Zhou, Yi, Zon, Leonard I., Gleizes, Pierre-Emmanuel, Beggs, Alan H., and Gupta, Vandana A.
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Biology and Life Sciences ,Anatomy ,Musculoskeletal System ,Muscles ,Skeletal Muscles ,Medicine and Health Sciences ,Developmental Biology ,Morphogenesis ,Muscle Differentiation ,Experimental Organism Systems ,Model Organisms ,Zebrafish ,Animal Models ,Organisms ,Eukaryota ,Animals ,Vertebrates ,Fish ,Osteichthyes ,Biology and life sciences ,Biochemistry ,Nucleic acids ,RNA ,Non-coding RNA ,Ribosomal RNA ,Ribosomes ,Cell biology ,Cellular structures and organelles ,Cell Biology ,Cellular Types ,Animal Cells ,Stem Cells ,Myoblasts ,Cellular Structures and Organelles ,Regeneration ,Muscle Regeneration ,Organism Development ,Immunologic Techniques ,Immunoassays ,Immunofluorescence - Abstract
Gene expression in a tissue-specific context depends on the combined efforts of epigenetic, transcriptional and post-transcriptional processes that lead to the production of specific proteins that are important determinants of cellular identity. Ribosomes are a central component of the protein biosynthesis machinery in cells; however, their regulatory roles in the translational control of gene expression in skeletal muscle remain to be defined. In a genetic screen to identify critical regulators of myogenesis, we identified a DEAD-Box RNA helicase, DDX27, that is required for skeletal muscle growth and regeneration. We demonstrate that DDX27 regulates ribosomal RNA (rRNA) maturation, and thereby the ribosome biogenesis and the translation of specific transcripts during myogenesis. These findings provide insight into the translational regulation of gene expression in myogenesis and suggest novel functions for ribosomes in regulating gene expression in skeletal muscles.
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- 2018
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85. Design and Construction of Compressive Force Measuring Device for Engineering and Biomaterials
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Ajiboye, Aye T., primary and E. Ahaneku, Isiguzo, additional
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- 2012
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86. Ccdc94 Protects Cells from Ionizing Radiation by Inhibiting the Expression of p53
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Sorrells, Shelly, primary, Carbonneau, Seth, additional, Harrington, Erik, additional, Chen, Aye T., additional, Hast, Bridgid, additional, Milash, Brett, additional, Pyati, Ujwal, additional, Major, Michael B., additional, Zhou, Yi, additional, Zon, Leonard I., additional, Stewart, Rodney A., additional, Look, A. Thomas, additional, and Jette, Cicely, additional
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- 2012
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87. A Splice Site Mutation in Laminin-α2 Results in a Severe Muscular Dystrophy and Growth Abnormalities in Zebrafish
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Gupta, Vandana A., primary, Kawahara, Genri, additional, Myers, Jennifer A., additional, Chen, Aye T., additional, Hall, Thomas E., additional, Manzini, M. Chiara, additional, Currie, Peter D., additional, Zhou, Yi, additional, Zon, Leonard I., additional, Kunkel, Louis M., additional, and Beggs, Alan H., additional
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- 2012
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88. Ccdc94 Protects Cells from Ionizing Radiation by Inhibiting the Expression of p53
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Erik B. Harrington, Michael B. Major, Shelly Sorrells, Cicely A. Jette, Rodney A. Stewart, Leonard I. Zon, Ujwal J. Pyati, Seth Carbonneau, Yi Zhou, Aye T. Chen, A. Thomas Look, Brett Milash, and Bridgid E. Hast
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Cancer Research ,Programmed cell death ,lcsh:QH426-470 ,DNA damage ,DNA repair ,Embryonic Development ,Apoptosis ,Genes, Recessive ,Biology ,medicine.disease_cause ,Radiation Tolerance ,03 medical and health sciences ,Model Organisms ,0302 clinical medicine ,Radiation, Ionizing ,Radioresistance ,Molecular Cell Biology ,Genetics ,medicine ,Animals ,DNA Breaks, Double-Stranded ,Molecular Biology ,Zebrafish ,Genetics (clinical) ,Ecology, Evolution, Behavior and Systematics ,030304 developmental biology ,Neurons ,0303 health sciences ,Mutation ,Gene knockdown ,Radiobiology ,Zebrafish Proteins ,Molecular biology ,3. Good health ,Cell biology ,lcsh:Genetics ,Gene Expression Regulation ,030220 oncology & carcinogenesis ,Cancer cell ,Tumor Suppressor Protein p53 ,Research Article ,Developmental Biology ,Genetic screen - Abstract
DNA double-strand breaks (DSBs) represent one of the most deleterious forms of DNA damage to a cell. In cancer therapy, induction of cell death by DNA DSBs by ionizing radiation (IR) and certain chemotherapies is thought to mediate the successful elimination of cancer cells. However, cancer cells often evolve to evade the cytotoxicity induced by DNA DSBs, thereby forming the basis for treatment resistance. As such, a better understanding of the DSB DNA damage response (DSB–DDR) pathway will facilitate the design of more effective strategies to overcome chemo- and radioresistance. To identify novel mechanisms that protect cells from the cytotoxic effects of DNA DSBs, we performed a forward genetic screen in zebrafish for recessive mutations that enhance the IR–induced apoptotic response. Here, we describe radiosensitizing mutation 7 (rs7), which causes a severe sensitivity of zebrafish embryonic neurons to IR–induced apoptosis and is required for the proper development of the central nervous system. The rs7 mutation disrupts the coding sequence of ccdc94, a highly conserved gene that has no previous links to the DSB–DDR pathway. We demonstrate that Ccdc94 is a functional member of the Prp19 complex and that genetic knockdown of core members of this complex causes increased sensitivity to IR–induced apoptosis. We further show that Ccdc94 and the Prp19 complex protect cells from IR–induced apoptosis by repressing the expression of p53 mRNA. In summary, we have identified a new gene regulating a dosage-sensitive response to DNA DSBs during embryonic development. Future studies in human cancer cells will determine whether pharmacological inactivation of CCDC94 reduces the threshold of the cancer cell apoptotic response., Author Summary Radiation therapy and most chemotherapies elicit cancer cell death through the induction of excessive DNA damage. However, cancer cells can harbor genetic defects that confer resistance to these therapies. To identify cellular components whose targeted therapeutic inactivation could potentially enhance the sensitivity of treatment-resistant cancer cells to DNA–damaging therapies, we have chosen an unbiased genetic approach in live whole zebrafish embryos to identify genes that normally protect cells from the lethal effects of DNA damage. This approach has yielded the discovery of a novel radioprotective gene called ccdc94. Upon inactivation of ccdc94, cells become more sensitive to radiation-induced cell death. Our further analysis revealed that the Ccdc94 protein functions in the Prp19 complex, which is known to regulate gene expression and repair of damaged DNA. We found that this complex normally represses radiation-induced cell death by inhibiting the expression of the p53 gene, a critical mediator of DNA damage–induced cell death. Future experiments that inactivate Ccdc94 and Prp19 complex proteins in human cancer cells will determine if inactivation of this complex represents a novel therapeutic strategy that could increase p53 expression to enhance sensitivity to DNA damaging therapies in chemo- and radio-resistant cancer cells.
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- 2012
89. Cleavage and Polyadenylation Specificity Factor 1 Is Required for Definitive Hematopoietic Stem Cell Survival In Zebrafish.
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Bolli, Niccolo, primary, Payne, Elspeth, additional, Rhodes, Jennifer, additional, Johnston, Adam, additional, Guo, Feng, additional, Lee, Jeong-Soo, additional, Kanki, John, additional, Chen, Aye T., additional, Zhou, Yi, additional, Zon, Leonard I., additional, and Look, A. Thomas, additional
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- 2010
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90. Zebrafish blood stem cells
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Chen, Aye T., primary and Zon, Leonard I., additional
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- 2009
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91. Geographical heterogeneity in prevalence of subclinical malaria infections at sentinel endemic sites of Myanmar
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Ziling Liu, Than Naing Soe, Yan Zhao, Aye Than, Cho Cho, Pyae Linn Aung, Yuling Li, Lin Wang, Huilin Yang, Xiangnan Li, Danni Li, Zhiping Peng, Jiangang Wang, Yan Li, Zhaoqing Yang, Hongning Zhou, Qinghui Wang, Myat Phone Kyaw, Yaming Cao, and Liwang Cui
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Myanmar ,Malaria ,Prevalence ,Subclinical ,Pooling strategy ,Infectious and parasitic diseases ,RC109-216 - Abstract
Abstract Background The malaria burden of Myanmar still remains high within the Greater Mekong Subregion of Southeast Asia. An important indicator of progress towards malaria elimination is the prevalence of parasite infections in endemic populations. Information about malaria epidemiology is mostly derived from reports of confirmed acute malaria cases through passive case detection, whereas the prevalence of baseline subclinical malaria infections is much less known. Methods In this study, cross-sectional surveys were conducted during the rainy season of 2017 in four townships (Bilin, Thabeikkyin, Banmauk and Paletwa) of Myanmar with divergent annual malaria incidences. A total of 1991 volunteers were recruited from local villages and Plasmodium subclinical infections were estimated by light microscopy (LM), rapid diagnostic tests (RDTs) and nested PCR. The nested PCR analysis was performed with a modified pooling strategy that was optimized based on an initial estimate the infection prevalence. Results The overall malaria infection prevalence based on all methods was 13.9% (277/1991) and it differed drastically among the townships, with Paletwa in the western border having the highest infection rate (22.9%) and Thabeikkyin in central Myanmar having the lowest (3.9%). As expected, nested PCR was the most sensitive and identified 226 (11.4%) individuals with parasite infections. Among the parasite species, Plasmodium vivax was the most prevalent in all locations, while Plasmodium falciparum also accounted for 32% of infections in the western township Paletwa. Two RDTs based on the detection of the hrp2 antigen detected a total of 103 P. falciparum infections, and the ultrasensitive RDT detected 20% more P. falciparum infections than the conventional RDT. In contrast, LM missed the majority of the subclinical infections and only identified 14 Plasmodium infections. Conclusions Cross-sectional surveys identified considerable levels of asymptomatic Plasmodium infections in endemic populations of Myanmar with P. vivax becoming the predominant parasite species. Geographical heterogeneity of subclinical infections calls for active surveillance of parasite infections in endemic areas. The pooling scheme designed for nested PCR analysis offers a more practical strategy for large-scale epidemiological studies of parasite prevalence. Such information is important for decision-makers to put forward a more realistic action plan for malaria elimination.
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- 2019
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92. Cleavage and Polyadenylation Specificity Factor 1 Is Required for Definitive Hematopoietic Stem Cell Survival In Zebrafish
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Jeong-Soo Lee, Feng Guo, Niccolo Bolli, Aye T. Chen, A. Thomas Look, Yi Zhou, Elspeth Payne, Jennifer Rhodes, John P. Kanki, Leonard I. Zon, and Adam Johnston
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animal structures ,Myeloid ,biology ,Immunology ,Neural crest ,Hematopoietic stem cell ,GATA1 ,Cell Biology ,Hematology ,In situ hybridization ,biology.organism_classification ,Biochemistry ,Cell biology ,Haematopoiesis ,medicine.anatomical_structure ,medicine ,Stem cell ,Zebrafish - Abstract
Abstract 1606 Hematopoiesis is a tightly regulated process requiring the differential activation of specific genetic programs. Inactivating mutations of genes involved in normal hematopoiesis have been implicated in bone marrow failure syndromes, myelodysplastic syndromes and hematopoietic neoplasms. Despite recent advances, many genes regulating normal hematopoiesis are still unknown and innovative gene-discovery approaches can benefit our understanding of the molecular mechanisms underlying this complex developmental process. The combined genetic and embryologic strengths of the zebrafish model system are ideal for studying factors regulating hematopoiesis, which is highly conserved with mammals. We have used ENU-mutated zebrafish lines to screen for genes whose inactivation results in the loss of definitive hematopoiesis. Here, we report the identification and analysis of the zebrafish mutant grechetto, caused by a lethal, recessive, inactivating mutation (grcl8a12) of the cleavage and specificity factor 1 (cpsf1) gene. Cpsf1 encodes a protein required for processing the 3’UTR of a subset of pre-mRNAs. Cpsf1 is maternally expressed ubiquitously through the first five days of development including primitive myeloid and erythroid cells and definitive hematopoietic stem cells (HSC). Although grechetto mutants fail to express cspf1 already at 24 hpf, they appear to develop normally until 72 hpf, when they first become morphologically distinct from wild-type siblings with a smaller head and the absence of a protruding jaw. Importantly, primitive hematopoiesis appears normal, as shown by expression of the myeloid and erythroid markers mpx and band3, respectively, at 24 and 48 hpf by whole mount RNA in situ hybridization (WISH). By 120 hpf the phenotype is more marked and embryos have a curved body, cardiac edema, development defects in the jaw and gut and a reduction in the number of iridophores. While many of these affected tissues represent derivatives of the neural crest (NC), the expression of markers of NC specification (sox10 and foxd3 at 15,5 hpf, crestin at 24 hpf), migration (dlx2 at 36 and 48 hpf) and differentiation (pax9a at 48 hpf) are normal. When definitive hematopoiesis was assayed for markers of mature blood cells by WISH at 120 hpf, grechetto mutants exhibit a loss of myeloid (mpx, lysC, l-plastin), erythroid (band3, gata1) and lymphoid cells (rag1, lck). Since myeloid and erythroid cells are normal at 24 hpf, but severely reduced at 120 hpf, we investigated whether the absence of HSC could explain the loss of definitive hematopoiesis in grechetto mutants. Interestingly, WISH staining for the HSC marker c-myb showed that in mutant embryos HSCs are normally specified and represented in the ventral wall of the dorsal aorta at 36 and 48 hpf. Nevertheless, at 72 hpf the numbers of HSCs are reduced in grechetto mutants upon their migration to the caudal hematopoietic tissue (CHT) and by 120 hpf very few remain. To investigate the fate of these HSCs we crossed the grechetto line with the Tg(c-myb:EGFP) reporter line, that expresses EGFP under the control of the c-myb promoter. By whole mount immunostaining, we were able to find increased co-localization of activated caspase3 and TUNEL staining in the c-myb:EGFP positive cells in the CHT in grechetto mutants compared to WT siblings at 72 and 96 hpf, suggesting that HSCs undergo apoptosis during this stage. Furthermore, PI cell cycle profile of sorted c-myb:EGFP+ cells from 96 hpf mutants shows a sub-G1 peak, representing pyknotic cell nuclei undergoing advanced stages of apoptosis. Importantly, both activated caspase3 staining and TUNEL assay did not show increased apoptosis in the tissue immediately surrounding the CHT. These studies show that cpsf1 is not required for primitive hematopoiesis or definitive HSC specification, however, it is essential for HSC survival in the CHT. The fact that grechetto embryos do not undergo generalized apoptotic cell death suggests that, despite ubiquitous cpsf1 expression and the general development defects of grechetto mutants, the prosurvival pathways in the HSC compartment are particularly dependent on Cpsf1 activity. Disclosures: Zon: FATE, Inc.: Consultancy, Equity Ownership, Membership on an entity's Board of Directors or advisory committees, Patents & Royalties; Stemgent: Consultancy, Equity Ownership, Membership on an entity's Board of Directors or advisory committees.
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- 2010
93. Noninvasive NMR/MRS Metabolic Parameters to Evaluate Metabolic Syndrome in Rats
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Khin Thandar Htun, Krit Jaikumkao, Jie Pan, Aye Thidar Moe Moe, Nuttawadee Intachai, Sasivimon Promsan, Anusorn Lungkaphin, Monruedee Tapanya, Duanghathai Pasanta, Montree Tungjai, Siriprapa Kaewjaeng, Hong Joo Kim, Jakrapong Kaewkhao, Christopher Lai, and Suchart Kothan
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MRI ,1H MRS ,1H NMR ,HFD ,metabolic syndrome ,Medicine (General) ,R5-920 - Abstract
(1) Background: Ectopic fat deposition and its effects, metabolic syndrome, have been significantly correlated to lifestyle and caloric consumption. There is no specific noninvasive evaluation tool being used in order to establish clinical markers for tracing the metabolic pathway implicated in obesity-related abnormalities that occur in the body as a result of a high-fat diet (HFD). The purpose of this work is to investigate in vivo ectopic fat distribution and in vitro metabolite profiles given by HFDs, as well as how they are inter-related, in order to find surrogate metabolic biomarkers in the development of metabolic syndrome utilizing noninvasive approaches. (2) Methods: Male Wistar rats were divided into a standard normal chow diet, ND group, and HFD group. After 16 weeks of different diet administration, blood samples were collected for proton nuclear magnetic resonance (1H NMR) and biochemical analysis. Magnetic resonance imaging/proton magnetic resonance spectroscopy (MRI/1H MRS) was performed on the abdomen, liver, and psoas muscle of the rats. (3) Results: Visceral fat showed the strongest relationship with blood cholesterol. Although liver fat content (LFC) was not associated with any biophysical profiles, it had the highest correlation with metabolites such as (-CH2)n very-low-density lipoprotein/low-density lipoprotein (VLDL/LDL), lactate, and N-acetyl glycoprotein of serum 1H NMR. HFD showed no obvious influence on muscle fat accumulation. Acetoacetate, N-acetyl glycoprotein, lactate, (-CH2)n VLDL/LDL, and valine were the five possible metabolic biomarkers used to differentiate HFD from ND in the present study. (4) Conclusions: Our study has validated the influence of long-term HFD-induced ectopic fat on body metabolism as well as the metabolic profile deterioration both in vivo and in vitro.
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- 2022
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94. Effect of organic and inorganic phosphate fertilizers and their combination on maize yield and phosphorus availability in a Yellow Earth in Myanmar
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Aye, T. M., primary, Hedley, M. J., additional, Loganathan, P., additional, Lefroy, R. D. B., additional, and Bolan, N. S., additional
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- 2008
- Full Text
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95. Evaluation of endotracheal tube intubation using different laryngoscopic methods
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Lim, S.H., primary, Ng, Y.Y., additional, Choa, G., additional, Chan, K.P., additional, and Aye, T., additional
- Published
- 2008
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96. Hypothyroxinemia and Prematurity
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Forghani, N., primary and Aye, T., additional
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- 2008
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97. The long-term impact of the Leprosy Post-Exposure Prophylaxis (LPEP) program on leprosy incidence: A modelling study.
- Author
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David J Blok, Peter Steinmann, Anuj Tiwari, Tanja Barth-Jaeggi, Mohammad A Arif, Nand Lal Banstola, Rabindra Baskota, David Blaney, Marc Bonenberger, Teky Budiawan, Arielle Cavaliero, Zaahira Gani, Helena Greter, Eliane Ignotti, Deusdedit V Kamara, Christa Kasang, Pratap R Manglani, Liesbeth Mieras, Blasdus F Njako, Tiara Pakasi, Unnati R Saha, Paul Saunderson, W Cairns S Smith, René Stäheli, Nayani D Suriyarachchi, Aye Tin Maung, Tin Shwe, Jan van Berkel, Wim H van Brakel, Bart Vander Plaetse, Marcos Virmond, Millawage S D Wijesinghe, Ann Aerts, and Jan Hendrik Richardus
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Arctic medicine. Tropical medicine ,RC955-962 ,Public aspects of medicine ,RA1-1270 - Abstract
BackgroundThe Leprosy Post-Exposure Prophylaxis (LPEP) program explored the feasibility and impact of contact tracing and the provision of single dose rifampicin (SDR) to eligible contacts of newly diagnosed leprosy patients in Brazil, India, Indonesia, Myanmar, Nepal, Sri Lanka and Tanzania. As the impact of the programme is difficult to establish in the short term, we apply mathematical modelling to predict its long-term impact on the leprosy incidence.MethodologyThe individual-based model SIMCOLEP was calibrated and validated to the historic leprosy incidence data in the study areas. For each area, we assessed two scenarios: 1) continuation of existing routine activities as in 2014; and 2) routine activities combined with LPEP starting in 2015. The number of contacts per index patient screened varied from 1 to 36 between areas. Projections were made until 2040.Principal findingsIn all areas, the LPEP program increased the number of detected cases in the first year(s) of the programme as compared to the routine programme, followed by a faster reduction afterwards with increasing benefit over time. LPEP could accelerate the reduction of the leprosy incidence by up to six years as compared to the routine programme. The impact of LPEP varied by area due to differences in the number of contacts per index patient included and differences in leprosy epidemiology and routine control programme.ConclusionsThe LPEP program contributes significantly to the reduction of the leprosy incidence and could potentially accelerate the interruption of transmission. It would be advisable to include contact tracing/screening and SDR in routine leprosy programmes.
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- 2021
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98. Female Condition-dependent Allocation of Nuptial Gifts by Males in the Moth Ostrinia scapulalis (Lepidoptera: Crambidae).
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WIN, AYE T., WATARU KOJIMA, and YUKIO ISHIKAWA
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CRAMBIDAE , *SEXUAL behavior in insects , *SPERMATOPHORES , *COURTSHIP , *FEMALE physiology , *INSECTS - Abstract
The males of many insect species transfer a spermatophore, i.e., a proteinaceous capsule containing sperm, to females during copulation, and this may also function as a nuptial gift. If production of the spermatophore is costly and variations in the quality of females are large, males may strategically allocate their investment based on the quality of the mate to maximize their own reproductive success. We examined the size and protein content of spermatophores transferred to females of different ages and body sizes, and also to water-deprived and water-replete females in the moth Ostrinia scapulalis (Walker). Males transferred a spermatophore of a smaller size or with less protein to older females, smaller females, and water-deprived females. These results indicated that O. scapulalis males manipulated their reproductive investment based on the conditions of the mate. We also demonstrated that older males varied their resource allocation to a greater extent in response to female conditions than younger males. Thus, resource allocation by the males of this species is modulated by both female conditions and the age of the males. [ABSTRACT FROM AUTHOR]
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- 2015
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99. Phosphorus in soils of riparian and non‐riparian wetland and buffer strips in the Waikato area, New Zealand
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Aye, T. M., primary, Nguyen, M. L., additional, Bolan, N. S., additional, and Hedley, M. J., additional
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- 2006
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100. An Improved Procedure for Determining Magnesium Fertilizer Dissolution in Field Soils
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Loganathan, P., primary, Mitchell, A. D., additional, Hanly, J. A., additional, and Aye, T. M., additional
- Published
- 2005
- Full Text
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