19 results on '"Emma Burt"'
Search Results
2. In Ph+BCR-ABL1P210+ acute lymphoblastic leukemia the e13a2 (B2A2) transcript is prevalent
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Daniel Coriu, Audrey Bidet, BJ Milner, Michele Baccarani, Ilaria Iacobucci, Sabina Chiaretti, Samia Menif, A Ayala, Stephen E. Langabeer, Beatrice Borsellino, Elisabeth Paietta, Emma Burt, Ana Ines Prado, Lorenzo Comba, Sabine Jeromin, Orietta Spinelli, Mario Luppi, Barbara Scappini, Monica Crugnola, Jiri Mayer, Letizia Foroni, Jacqueline Maier, Sara Galimberti, Irena Preložnik Zupan, Francesco Passamonti, Francesca Lunghi, Neelam Varma, Anna Candoni, Jeroen Janssen, Mario Annunziata, Francesco Albano, Poonkuzhali Balasubramanian, Thomas Lion, Giovanna Rege-Cambrin, Valentina Polli, Carolina Terragna, Behzad Poopak, Ombretta Annibali, Barbara Izzo, Renata Zadro, Victor Salinas-Viedma, Francesco Di Raimondo, Tulika Seth, Robin Foà, Baccarani, M., Iacobucci, I., Chiaretti, S., Foa', R., Balasubramanian, P., Paietta, E., Foroni, L., Jeromin, S., Izzo, B., Spinelli, O., Varma, N., Menif, S., Terragna, C., Seth, T., Bidet, A., Coriu, D., Lunghi, F., Mayer, J., Scappini, B., Langabeer, S., Maier, J., Burt, E., Candoni, A., Albano, F., Luppi, M., Zupan, I., Lion, T., Zadro, R., di Raimondo, F., Poopak, B., Rege-Cambrin, G., Annunziata, M., Ayala, A., Salinas-Viedma, V., Ines Prado, A., Milner, B., Galimberti, S., Janssen, J., Polli, V., Comba, L., Borsellino, B., Annibali, O., Crugnola, M., Passamonti, F., Hematology, and CCA - Cancer biology and immunology
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Adult ,Male ,Cancer Research ,Adolescent ,Lymphoblastic Leukemia ,bcr-abl ,Fusion Proteins, bcr-abl ,Young Adult ,Myelogenous ,Text mining ,Leukemia, Myelogenous, Chronic, BCR-ABL Positive ,medicine ,Humans ,Age Factor ,Chronic ,Young adult ,Child ,Proto-Oncogene Proteins c-abl ,Aged ,B-Lymphocytes ,Leukemia ,business.industry ,B-Lymphocyte ,Age Factors ,breakpoint cluster region ,Fusion Proteins ,Hematology ,Middle Aged ,Precursor Cell Lymphoblastic Leukemia-Lymphoma ,medicine.disease ,Fusion protein ,Oncology ,Multicenter study ,Cancer research ,Female ,BCR-ABL Positive ,business ,Human - Published
- 2019
3. In Ph+BCR-ABL1
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Michele, Baccarani, Ilaria, Iacobucci, Sabina, Chiaretti, Robin, Foà', Poonkuzhali, Balasubramanian, Elisabeth, Paietta, Letizia, Foroni, Sabine, Jeromin, Barbara, Izzo, Orietta, Spinelli, Neelam, Varma, Samia, Menif, Carolina, Terragna, Tulika, Seth, Audrey, Bidet, Daniel, Coriu, Francesca, Lunghi, Jiri, Mayer, Barbara, Scappini, Stephen, Langabeer, Jacqueline, Maier, Emma, Burt, Anna, Candoni, Francesco, Albano, Mario, Luppi, Irena, Zupan, Thomas, Lion, Renata, Zadro, Francesco, di Raimondo, Behzad, Poopak, Giovanna, Rege-Cambrin, Mario, Annunziata, Ana, Ayala, Victor, Salinas-Viedma, Ana, Ines Prado, Benedict, Milner, Sara, Galimberti, Jeroen, Janssen, Valentina, Polli, Lorenzo, Comba, Beatrice, Borsellino, Ombretta, Annibali, Monica, Crugnola, and Francesco, Passamonti
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Adult ,Male ,B-Lymphocytes ,Adolescent ,Age Factors ,Fusion Proteins, bcr-abl ,Middle Aged ,Precursor Cell Lymphoblastic Leukemia-Lymphoma ,Young Adult ,Leukemia, Myelogenous, Chronic, BCR-ABL Positive ,Humans ,Female ,Child ,Proto-Oncogene Proteins c-abl ,Aged - Published
- 2019
4. Guidelines for the measurement of BCR-ABL1 transcripts in chronic myeloid leukaemia
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Emma Burt, Abida Awan, Stephen E. Langabeer, Nicholas C.P. Cross, Sproul Am, BJ Milner, Lihui Wang, Gareth Gerrard, Tim Clench, Guillermina Nickless, Anna Schuh, Helen E. White, David Grimwade, Letizia Foroni, Alexandra E. Irvine, Stephen Austin, Jeremy Hancock, Caroline Wickham, Gill Wilson, Joanne Mason, Aytug Kizilors, Joanna Farruggia, and David Gonzalez de Castro
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Oncology ,medicine.medical_specialty ,ABL ,medicine.drug_class ,breakpoint cluster region ,Context (language use) ,Imatinib ,Hematology ,Biology ,medicine.disease ,Tyrosine-kinase inhibitor ,Myelogenous ,Internal medicine ,Molecular genetics ,Immunology ,medicine ,Chronic myelogenous leukemia ,medicine.drug - Abstract
Molecular testing for the BCR-ABL1 fusion gene by real time quantitative polymerase chain reaction (RT-qPCR) is the most sensitive routine approach for monitoring the response to therapy of patients with chronic myeloid leukaemia. In the context of tyrosine kinase inhibitor (TKI) therapy, the technique is most appropriate for patients who have achieved complete cytogenetic remission and can be used to define specific therapeutic milestones. To achieve this effectively, standardization of the laboratory procedures and the interpretation of results are essential. We present here consensus best practice guidelines for RT-qPCR testing, data interpretation and reporting that have been drawn up and agreed by a consortium of 21 testing laboratories in the United Kingdom and Ireland in accordance with the procedures of the UK Clinical Molecular Genetics Society.
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- 2011
5. Export of ice-nucleating particles from watersheds: results from the Amazon and Tocantins river plumes
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Annika Einbock, Emma Burtscher, Claudia Frey, and Franz Conen
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ice-nucleating particles ,river plume ,Amazon ,Tocantins ,watershed ,atmosphere ,Science - Abstract
We examined ice-nucleating particles (INPs) in the plumes of the Tocantins and Amazon rivers, which drain watersheds with different proportions of degraded land. The concentration of INPs active at −15°C (INP−15) was an order of magnitude lower in the Tocantins (mean = 13.2 ml−1; s.d. = 7.8 ml−1), draining the more degraded watershed, compared with the Amazon (mean = 175.8 ml−1; s.d. = 11.2 ml−1), where the concentration was also significantly higher than in Atlantic surface waters (mean = 3.2 ml−1; s.d. = 2.3 ml−1). Differences in heat tolerance suggest that INPs emitted by the Amazon rainforest to the atmosphere or washed into the river might originate from contrasting sources on top of and below the rainforest canopy, respectively. For the Amazon River, we estimate a daily discharge of 1018 INP−15 to Atlantic waters. Rivers in cooler climate zones tend to have much higher concentrations of INPs and could, despite a smaller water volume discharged, transfer even larger absolute numbers of INP−15 to shelf waters than does the Amazon. To what extent these terrestrial INPs become aerosolized by breaking waves and bubble-bursting remains an open question.
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- 2023
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6. Caenorhabditis elegans in the study of SMN-interacting proteins: a role for SMI-1, an orthologue of human Gemin2 and the identification of novel components of the SMN complex
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Paula R. Towers, Emma Burt, and David B. Sattelle
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animal diseases ,Two-hybrid screening ,Molecular Sequence Data ,Nerve Tissue Proteins ,Cellular and Molecular Neuroscience ,Developmental Neuroscience ,SMN complex ,RNA interference ,SMN Complex Proteins ,Two-Hybrid System Techniques ,Genetic model ,medicine ,Animals ,Humans ,Amino Acid Sequence ,Cloning, Molecular ,RNA, Small Interfering ,Caenorhabditis elegans ,Caenorhabditis elegans Proteins ,Cyclic AMP Response Element-Binding Protein ,Gene ,Genetics ,Sequence Homology, Amino Acid ,biology ,Reverse Transcriptase Polymerase Chain Reaction ,RNA-Binding Proteins ,Spinal muscular atrophy ,biology.organism_classification ,medicine.disease ,nervous system diseases ,nervous system - Abstract
Spinal muscular atrophy is a common neuromuscular disorder caused by mutations in the survival motor neuron (SMN) gene. In mammals, SMN is tightly associated with Gemin2. To gain further insight into the functions of SMN and Gemin2, we have cloned and sequenced smi-1 (Survival of Motor neuron-Interacting protein 1), a C. elegans homologue of the human Gemin2 gene. We show that the SMI-1 expression pattern and RNA interference phenotype show considerable overlap with that previously reported for SMN-1. Finally, we demonstrate that the SMN-1 and SMI-1 proteins directly interact. Having demonstrated the utility of the C. elegans genetic model for investigating genes encoding SMN-interacting proteins, we have undertaken a yeast two-hybrid screen of a C. elegans cDNA library to identify novel proteins that interact with SMN-1. We show the direct interaction of SMN-1 with nine novel proteins, several of which may be involved in RNA metabolism.
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- 2006
7. A Novel Phenotype of Glycogen Storage Disease Presenting as Gastrointestinal Neuromuscular Disease
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Pauline M. Levey, Finbarr E. Cotter, Mohammed M. Rahman, Joanne E. Martin, Asma Fikree, Philip J. Rowburrey, Qasim Aziz, Austin J. Hymas, Richard W. Pickersgill, Gareth J. Sanger, Liz Allen, David B.A. Silk, John Broad, Alice A. Thomas, Christopher A. Evagora, Shaun Bevan, ATMDilshad H. Chowdhury, Charles H. Knowles, Murphy Elaine, Sheldon C. Cooper, Katie Bainbridge, Emma Burt, Suzanne McElwaine, and Yan Yiannakou
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Wavefront ,medicine.medical_specialty ,Neuromuscular disease ,Materials science ,Hepatology ,Wave propagation ,Circumferential velocity ,Diabetic gastroparesis ,Gastroenterology ,Gastric pacing ,medicine.disease ,Internal medicine ,medicine ,Cardiology ,Glycogen storage disease ,Antrum - Abstract
Introduction Gastric smooth muscle layers are electrically excited by slow waves. In the normal stomach, slow waves propagate longitudinally in ring wavefronts from the upper corpus to the distal antrum. Circumferential propagation does not appear to occur, likely because there is no excitable tissue available circumferentially in these rings. However, rapid circumferential propagation has been observed in isolated gastric tissues and during gastric pacing. In this study, the propagation profiles of slow wave behaviors in diabetic gastroparesis were defined at high resolution (HR). The hypothesis was that circumferential propagation occurs during dysrhythmia, presenting a novel marker of gastric electrical dysfunction. Methods HR (multi-electrode) mapping was performed in 7 patients with diabetic gastroparesis undergoing laparotomy for stimulator implantation. Anterior serosal recordings were taken using flexible PCB arrays (256 electrodes; 4 mm spacing; 36cm2), and activation mapping was performed. Velocity fields were calculated using a finite difference approach incorporating a Gaussian filter smoothing function. Amplitudes were calculated using a peak-trough detection algorithm. Longitudinal and circumferential propagation data from corpus recordings were compared with Student's t-test. Means±SEM are reported. Results Atypical or dysrhythmic propagation was observed in 6/7 patients, including incomplete conduction block, complete block with escape, ectopic pacemaking in the corpus and antral tachygastria (freq range: 2.7-4.2 cpm). Circumferential propagation was associated with all of these events (circumferential velocity 6.6 ± 0.9 mm/s vs longitudinal velocity 2.9 ± 0.2 mm/s; p
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- 2011
8. Scholarly productivity and citation impact of Australian academic psychologists
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Trevor G. Mazzucchelli, Emma Burton, and Lynne Roberts
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academic psychologists ,citations ,h‐index ,impact ,productivity ,publication rates ,Psychology ,BF1-990 - Abstract
Objective This study sought to provide up‐to‐date normative data on the productivity and citation impact of publications by Australian academic psychologists at each academic level (lecturer to professor) and for each university grouping (e.g., Group of Eight [Go8], Australian Technology Network, etc.). Method Publication and citation data for a representative sample of 732 psychology academics were extracted using the Scopus database. Norms for lifetime publications, citations, and h‐index were developed for each academic level and were compared with those reported in previous studies. Results Judgements of academic level based on number of publications, citations and h‐indexes are highly reliable with publication means for the ranks roughly doubling, and citation means more than doubling, for each successive level. Lifetime publication means have increased by a factor of 2 to 3 since the norms published in 2010, consistent with the suggestion that rates of scholarly publication have increased over the last decade. Academics at the research‐intensive Go8 universities had, as a group, significantly higher publication averages at every level than academics at other universities; however, these differences varied considerably in size across the university groupings. Conclusions Indices of research productivity and impact are important when evaluating academic psychologists' performance, and the present article provides up‐to‐date, comprehensive, and representative norms of Australian academic psychologists.
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- 2019
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9. Discussing lifestyle behaviors: perspectives and experiences of general practitioners
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Kyra Hamilton, Joanna Henderson, Emma Burton, and Martin S. Hagger
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general practitioners ,general practice ,lifestyle behaviors ,health promotion ,health communication ,Medicine ,Psychology ,BF1-990 - Abstract
Background: Initiatives aimed at increasing participation in preventive health behaviors has been identified as a priority for addressing the increasing incidence of non-communicable chronic disease. General practice is an existing network that can be leveraged to intervene and promote messages for health behavior change. We aimed to explore the extent to which ‘lifestyle’ behaviors are discussed by general practitioners (GPs) with their patients in their practices, and the context and content of these discussions. Methods: GPs (N = 26) practising in Australian clinics participated in semi-structured interviews. Data were analyzed using an inductive thematic analysis. Results: Results showed discussions of lifestyle behaviors were brief, but relatively frequent and often initiated by the GP. GPs generally provided basic advice and education that was often ad-hoc and in reaction to prompts from the patient. GPs recognized the importance of addressing lifestyle behaviors in practice, but also highlighted substantive barriers that limit the initiation of these discussions. These included patient readiness for change, patient acceptance and openness, patient accountability and responsibility, patient background factors, GPs’ role and knowledge, GP financial implications, GP-patient relationship, and lack of time. Conclusions: Current findings provide important preliminary knowledge on the extent to which Australian GPs discuss lifestyle behavior change with patients during routine consultations, the context and content of these discussions, and barriers to initiating these discussions. Further research should seek to gain a better understanding of barriers and identify strategies to mitigate their impact. This might maximize the potential for GPs to promote adaptive lifestyle behavior change for improving patient health.
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- 2019
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10. Transchromosomic cell model of Down syndrome shows aberrant migration, adhesion and proteome response to extracellular matrix
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Joris D Veltman, Emma Burt, Dean Nizetic, Finbarr E. Cotter, Frederic Delom, Jürgen Groet, and Alexander Hoischen
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Genetics ,Down syndrome ,Genetics and epigenetic pathways of disease [NCMLS 6] ,lcsh:Cytology ,Research ,Cell migration ,Biology ,medicine.disease ,Biochemistry ,Cell biology ,Genomic disorders and inherited multi-system disorders [IGMD 3] ,Extracellular matrix ,Translational research [ONCOL 3] ,Collagen VI ,Proteome ,medicine ,Atrioventricular canal ,lcsh:QH573-671 ,Trisomy ,Chromosome 21 ,Molecular Biology - Abstract
Background Down syndrome (DS), caused by trisomy of human chromosome 21 (HSA21), is the most common genetic birth defect. Congenital heart defects (CHD) are seen in 40% of DS children, and >50% of all atrioventricular canal defects in infancy are caused by trisomy 21, but the causative genes remain unknown. Results Here we show that aberrant adhesion and proliferation of DS cells can be reproduced using a transchromosomic model of DS (mouse fibroblasts bearing supernumerary HSA21). We also demonstrate a deacrease of cell migration in transchromosomic cells independently of their adhesion properties. We show that cell-autonomous proteome response to the presence of Collagen VI in extracellular matrix is strongly affected by trisomy 21. Conclusion This set of experiments establishes a new model system for genetic dissection of the specific HSA21 gene-overdose contributions to aberrant cell migration, adhesion, proliferation and specific proteome response to collagen VI, cellular phenotypes linked to the pathogenesis of CHD.
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- 2009
11. James and Henry Leonard
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Library and Information Sciences ,Language and Linguistics - Published
- 1924
12. Couvert leonard of West Wickham
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Library and Information Sciences ,Language and Linguistics - Published
- 1925
13. Burt of Alford, England, and Taunton, U.S.A
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Library and Information Sciences ,Language and Linguistics - Published
- 1930
14. Martin, emigrant to America
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Library and Information Sciences ,Language and Linguistics - Published
- 1925
15. Calvert: Leonard
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Library and Information Sciences ,Language and Linguistics - Published
- 1928
16. James Leonard, british settler in America
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Library and Information Sciences ,Language and Linguistics - Published
- 1925
17. Leonard Family of America: Lennard of Brede
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Library and Information Sciences ,Language and Linguistics - Published
- 1928
18. Leonard: Meaning of name
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Philosophy ,Meaning (existential) ,Library and Information Sciences ,Language and Linguistics ,Linguistics - Published
- 1928
19. Leonards in Hammersmith
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M. Emma Burt
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Linguistics and Language ,Literature and Literary Theory ,Library and Information Sciences ,Language and Linguistics - Published
- 1925
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