„path polymorphism“
Suchergebnisse
870 Treffer
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Genetic Polymorphisms in FAS/FASL Apoptotic Pathway Genes Modulate Beta-Thalassemia Susceptibility and Oxidative Stress Response: A Case–Control Study
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Exploring the Association of MMP-7 Promoter Site Single Nucleotide Polymorphism with Risk of Diabetic Nephropathy
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Association of Genetic Polymorphisms of Glutathione S-Transferase (GSTM1, GSTT1, GSTP1) with Bladder Cancer Susceptibility in Iraqi Patients: A Case-Control Study
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Genetic Determinants of Apoptosis Regulate Liver Cirrhosis Risk: The FAS/FASL Polymorphism Connection in Iraqi Population
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Identification of Deleterious Missense Single Nucleotide Polymorphisms in Human ITK Gene: An In Silico Study
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Association Between Vitamin D Receptor Gene Polymorphism and Diabetic Nephropathy in Patients with Type 2 Diabetes Mellitus
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Association of MT1A rs11640851, rs8052394 and rs11076161 Polymorphisms with the Risk of Developing Breast Cancer: A Haplotype-Based Case-Control Study and in Silico Analysis
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Utility and Sensitivity of TLR10 Gene Polymorphism in Early Prediction and Association with Risk of Metabolic Primary Antiphospholipid Syndrome: Cohort Study
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Neural Cell Adhesion Molecule-1 Gene Polymorphism Increases the Risk of Cognitive Dysfunction in Schizophrenia Spectrum Disorder
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Tissue Inhibitor of Metalloproteinase 2 (TIMP 2) Promotor 418 G > C Polymorphism in Non-alcoholic Fatty Liver Disease (NAFLD) Patients of Eastern States of India
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An Updated Trial Sequential Meta-analysis of Vitamin D Receptor Gene Polymorphism (Fok1, Bsm1, Taq1 and Apa1) and Risk to Tuberculosis
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The KL genetic polymorphisms Associated with type 2 diabetes Mellitus
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Metabolic Analysis of Methylenetetrahydrofolate Reductase Single Nucleotide Polymorphisms (MTHFR 677C<T and MTHFR 1298A<C), Serum Folate and Vitamin B12 in Neural Tube Defects
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Impact of rs2107425 Polymorphism and Expression of lncH19 and miR-200a on the Susceptibility of Colorectal Cancer
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Association of Catechol-O-Methyltransferase Gene Polymorphisms and Haplotypes in the Levodopa-Induced Adverse Events in Subjects with Parkinson’s Disease
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Association of Angiotensin II Type 1 Receptor (AT1R) Gene Polymorphism with Angiotensin II Serum Levels in Patients with Essential Hypertension
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A Molecular Insight of the Role of PIN-1 Promoter Polymorphism (− 667C > T; rs2233679) in Chronic Kidney Disease Patients with Secondary Hyperparathyroidism
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Status of Vitamin D Receptor Gene Polymorphism and 25-Hydroxy Vitamin D Deficiency with Essential Hypertension
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Association of MTHFR C677T (rs1801133) and A1298C (rs1801131) Polymorphisms with Serum Homocysteine, Folate and Vitamin B12 in Patients with Young Coronary Artery Disease
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Dopamine Gene Polymorphism, Biochemical and Oxidative Stress Parameters in Geriatric Population with and Without Depression: A Pilot Study