45 results on '"Zhang, Channa"'
Search Results
2. Spectrum and genotype–phenotype relationship of ALPK3 variants in Chinese patients with hypertrophic cardiomyopathy
3. Role of Biomarkers of Myocardial Injury to Predict Adverse Outcomes in Hypertrophic Cardiomyopathy
4. Abstract 18721: Increased Predisposition to Hypertrophic Cardiomyopathy in Mitochondria Gene CYP2E1 Rare Variant Carriers
5. Abstract 12016: Rare Variants in APOE Gene Are Associated With Disease-Onset and Outcomes of Hypertrophic Cardiomyopathy
6. Effects of the stress hyperglycemia ratio on long-term mortality in patients with triple-vessel disease and acute coronary syndrome
7. A genome-wide association study identifies a novel association between SDC3 and apparent treatment-resistant hypertension
8. Correction: A genome-wide association study identifies a novel association between SDC3 and apparent treatment-resistant hypertension
9. Abstract 12506: Assessment of the Left Ventricular Trabeculation Phenotype Contributes to Risk Stratification in Hypertrophic Cardiomyopathy Patients
10. Titin-Truncating Variants Increase the Risk of Cardiovascular Death in Patients With Hypertrophic Cardiomyopathy
11. East Asian–Specific Common Variant in TNNI3 Predisposes to Hypertrophic Cardiomyopathy
12. Prognostic value of neutrophil gelatinase-associated lipocalin and glycosylated hemoglobin for non-ST-segment elevation myocardial infarction patients with single concomitant chronic total occlusion following primary percutaneous coronary intervention: A prospective observational study
13. Effect of Cis-Compound Variants in MYH7 on Hypertrophic Cardiomyopathy With a Mild Phenotype
14. Truncating Variants in OBSCN Gene Associated With Disease-Onset and Outcomes of Hypertrophic Cardiomyopathy
15. Variants of COL3A1 Are Associated with the Risk of Stroke Recurrence and Prognosis in the Chinese Population: a Prospective Study
16. Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy
17. VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification
18. Variant Spectrum of Formin Homology 2 Domain‐Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy
19. Prediction of all-cause mortality with hypoalbuminemia in patients with heart failure: a meta-analysis
20. Variant Spectrum of Formin Homology 2 Domain-Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy.
21. Low Estimated Glomerular Filtration Rate is Associated with High Recurrence Rate and Poor Prognosis of Hemorrhage Stroke
22. East Asian-Specific Common Variant in Predisposes to Hypertrophic Cardiomyopathy.
23. Prognostic value of neutrophil gelatinase-associated lipocalin and glycosylated hemoglobin for non-ST-segment elevation myocardial infarction patients with single concomitant chronic total occlusion following primary percutaneous coronary intervention: A prospective observational study.
24. East Asian–Specific Common Variant in TNNI3Predisposes to Hypertrophic Cardiomyopathy
25. The genotype-phenotype correlation of the MYH7 gene c.1273G > A mutation in familial hypertrophic cardiomyopathy
26. A Variant in the Endoglin Gene is Associated with the Development of Sporadic Intracranial Aneurysms
27. Prevalence and risk factors of abnormal left ventricular geometrical patterns in untreated hypertensive patients
28. Association of Kallikrein gene polymorphisms with sporadic intracranial aneurysms in the Chinese population
29. Common Genetic Variants of MGP Are Associated With Calcification on the Arterial Wall but Not With Calcification Present in the Atherosclerotic Plaques
30. Short telomere length in blood leucocytes contributes to the presence of atherothrombotic stroke and haemorrhagic stroke and risk of post-stroke death
31. TNNT2Gene Polymorphisms Are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in the Han Chinese Population
32. Functional Haplotypes of the hTERT Gene, Leukocyte Telomere Length Shortening, and the Risk of Peripheral Arterial Disease
33. VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification
34. Abstract 8783: Methylation of FOXP3 In Regulatory T Cells is Related to the Severity of Coronary Atherosclerosis
35. Lack of association between lymphotoxin-α, galectin-2 polymorphisms and coronary artery disease: A meta-analysis
36. Cyclooxygenase-2 (COX-2) G-765C is a protective factor for coronary artery disease but not for ischemic stroke: A meta-analysis
37. The haplotype of the growth-differentiation factor 15 gene is associated with left ventricular hypertrophy in human essential hypertension
38. Novel promoter and exon mutations of the BMPR2 gene in Chinese patients with pulmonary arterial hypertension
39. KCTD10 interacts with proliferating cell nuclear antigen and its down-regulation could inhibit cell proliferation
40. QiHong Prevents Death in Coxsackievirus B3–Induced Murine Myocarditis Through Inhibition of Virus Attachment and Penetration
41. VKORC1 Haplotypes Are Associated With Arterial Vascular Diseases (Stroke, Coronary Heart Disease, and Aortic Dissection)
42. Vitamin K Epoxide Reductase: A Protein Involved in Angiogenesis
43. Common Genetic Variants of MGPAre Associated With Calcification on the Arterial Wall but Not With Calcification Present in the Atherosclerotic Plaques
44. TNNT2 Gene Polymorphisms Are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in the Han Chinese Population.
45. Lack of association between lymphotoxin-alpha, galectin-2 polymorphisms and coronary artery disease: a meta-analysis.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.