56 results on '"Si, Nuo"'
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2. Melatonin regulates circadian clock proteins expression in allergic airway inflammation
3. Genetic and clinical characterization of familial renal glucosuria
4. Model development and validation of noninvasive parameters based on coronary computed tomography angiography to predict culprit lesions in acute coronary syndromes within 3 years: value of plaque characteristics, hemodynamics and pericoronary adipose tissue
5. Assessing the Content Quality of Industry Technology Roadmaps
6. Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect
7. Characteristics and patterns of residential energy consumption for space cooling in China: Evidence from appliance-level data
8. Patterns of organic carbon and nitrogen stocks in soil particle-size fractions along an aridity gradient in Northern China’s deserts
9. Transcriptomic analysis of the upper lip and primary palate development in mice
10. Cu-Catalyzed Decarboxylative Annulation of Proline Derivatives: Multi-component Synthesis of Functionalized Chromeno[2,3-c]pyrrol-9(1H)-one Derivatives
11. Identification of patients with acute coronary syndrome and representation of their degree of inflammation: application of pericoronary adipose tissue within different radial distances of the proximal coronary arteries
12. Cyanobacterial‐ and moss‐forming biocrusts consistently decrease the temperature sensitivity of microbial respiration along a continental precipitation gradient
13. Electroencephalogram and Electrocardiogram in Human-Computer Interaction
14. Mechanistic Basis for the High Enantioselectivity and Activity in the Multichiral Bimetallic Complex-Mediated Enantioselective Copolymerization of meso-Epoxides
15. Functional Pathway and Process Enrichment Analysis of Genes Associated With Morphological Abnormalities of the Outer Ear
16. Effect of 320-row CT reconstruction technology on fractional flow reserve derived from coronary CT angiography based on machine learning: single- versus multiple-cardiac periodic images
17. Identification of patients with acute myocardial infarction based on coronary CT angiography: the value of pericoronary adipose tissue radiomics
18. Nature and evolution of the Late Cretaceous lithospheric mantle beneath the eastern Jiangnan orogenic belt: constraints from peridotite xenoliths
19. De novo 22q11.2 deletions and auricular findings in two Chinese patients with microtia
20. Generation of a human induced pluripotent stem cell line (PSHi002-A) from a Treacher-Collins syndrome patient carrying a TCOF1 gene mutation (c.1966_1969dup)
21. Heterogeneity of Accompanying Phenotypes and Genomic Variants Involved in Microtia
22. Clinical and genetic findings in patients with congenital cataract and heart diseases
23. FSGS in Chinese twins with a de novo PAX2 mutation: a case report and review of the literature
24. Generation of an induced pluripotent stem cell line from a congenital microtia patient with 4p16.1 microduplication involving the long-range enhancer of HMX1
25. Slc20a2-Deficient Mice Exhibit Multisystem Abnormalities and Impaired Spatial Learning Memory and Sensorimotor Gating but Normal Motor Coordination Abilities
26. Identification of loss-of-function HOXA2 mutations in Chinese families with dominant bilateral microtia
27. Duplications involving the long range HMX1 enhancer are associated with human isolated bilateral concha-type microtia
28. Keratin 5-Cre-driven deletion of Ncstn in an acne inversa-like mouse model leads to a markedly increased IL-36a and Sprr2 expression
29. A Novel COL4A5 Splicing Mutation Causes Skipping of Exon 14 in a Chinese Family with Alport Syndrome
30. TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
31. Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease
32. A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype
33. A novel MAF missense mutation leads to congenital nuclear cataract by impacting the transactivation of crystallin and noncrystallin genes
34. A four-generation pedigree of vascular-type Ehlers–Danlos syndrome with spontaneous aortic dissections and multiple aneurysms: A case report and literature review
35. A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family
36. Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies
37. Cow raising in the Mekong Delta - The current status of waste treatment and risk of greenhouse gas emissions
38. 17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype
39. The renal manifestations of type 4 familial partial lipodystrophy: a case report and review of literature
40. Surface Tension Model Based on Implicit Incompressible Smoothed Particle Hydrodynamics for Fluid Simulation
41. Gross deletions in FBN1 results in variable phenotypes of Marfan syndrome
42. Genetic Testing of the mucin 1 gene-Variable Number Tandem Repeat Single Cytosine Insertion Mutation in a Chinese Family with Medullary Cystic Kidney Disease
43. Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome
44. Recommendations for acupuncture in clinical practice guidelines of the national guideline clearinghouse
45. Clinical practice guidelines of using acupuncture for low back pain
46. Analysis on Influencing Factors of Community Logistics Development Based on ISM
47. Clinical practice guidelines for using acupuncture to treat depression
48. Identification of a Novel Four and a Half LIM Domain 1 Mutation in a Chinese Male Presented with Hypertrophic Cardiomyopathy and Mild Skeletal Muscle Hypertrophy
49. Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome
50. Familial Aggregation of a Chinese Female Premenopausal Gout
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