32 results on '"Zhang, Channa"'
Search Results
2. Role of Biomarkers of Myocardial Injury to Predict Adverse Outcomes in Hypertrophic Cardiomyopathy
3. An elevated triglyceride-glucose index predicts adverse outcomes and interacts with the treatment strategy in patients with three-vessel disease
4. Abstract 18721: Increased Predisposition to Hypertrophic Cardiomyopathy in Mitochondria Gene CYP2E1 Rare Variant Carriers
5. Correction: A genome-wide association study identifies a novel association between SDC3 and apparent treatment-resistant hypertension
6. A genome-wide association study identifies a novel association between SDC3 and apparent treatment-resistant hypertension
7. Effect of Cis-Compound Variants in MYH7 on Hypertrophic Cardiomyopathy With a Mild Phenotype
8. Truncating Variants in OBSCN Gene Associated With Disease-Onset and Outcomes of Hypertrophic Cardiomyopathy
9. Variant Spectrum of Formin Homology 2 Domain‐Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy
10. East Asian–Specific Common Variant in TNNI3 Predisposes to Hypertrophic Cardiomyopathy
11. 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
12. Prediction of all-cause mortality with hypoalbuminemia in patients with heart failure: a meta-analysis
13. Titin-Truncating Variants Increase the Risk of Cardiovascular Death in Patients With Hypertrophic Cardiomyopathy
14. A Variant in the Endoglin Gene is Associated with the Development of Sporadic Intracranial Aneurysms
15. Prevalence and risk factors of abnormal left ventricular geometrical patterns in untreated hypertensive patients
16. Association of Kallikrein gene polymorphisms with sporadic intracranial aneurysms in the Chinese population
17. Variants of COL3A1 Are Associated with the Risk of Stroke Recurrence and Prognosis in the Chinese Population: a Prospective Study
18. Common Genetic Variants of MGP Are Associated With Calcification on the Arterial Wall but Not With Calcification Present in the Atherosclerotic Plaques
19. Short telomere length in blood leucocytes contributes to the presence of atherothrombotic stroke and haemorrhagic stroke and risk of post-stroke death
20. Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy
21. TNNT2Gene Polymorphisms Are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in the Han Chinese Population
22. Functional Haplotypes of the hTERT Gene, Leukocyte Telomere Length Shortening, and the Risk of Peripheral Arterial Disease
23. VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification
24. Abstract 8783: Methylation of FOXP3 In Regulatory T Cells is Related to the Severity of Coronary Atherosclerosis
25. Lack of association between lymphotoxin-α, galectin-2 polymorphisms and coronary artery disease: A meta-analysis
26. Cyclooxygenase-2 (COX-2) G-765C is a protective factor for coronary artery disease but not for ischemic stroke: A meta-analysis
27. The haplotype of the growth-differentiation factor 15 gene is associated with left ventricular hypertrophy in human essential hypertension
28. Novel promoter and exon mutations of the BMPR2 gene in Chinese patients with pulmonary arterial hypertension
29. KCTD10 interacts with proliferating cell nuclear antigen and its down-regulation could inhibit cell proliferation
30. QiHong Prevents Death in Coxsackievirus B3–Induced Murine Myocarditis Through Inhibition of Virus Attachment and Penetration
31. VKORC1 Haplotypes Are Associated With Arterial Vascular Diseases (Stroke, Coronary Heart Disease, and Aortic Dissection)
32. Vitamin K Epoxide Reductase: A Protein Involved in Angiogenesis
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.