Associated Papers
Single-cell multi-omics data reveal heterogeneity in liver tissue microenvironment induced by hypertension.
Li H et al.
Molecular Therapy. Nucleic Acids, 2025
β-Cell Mitochondrial Dysfunction: Underlying Mechanisms and Potential Therapeutic Strategies.
Darwish R et al.
Cells, 2025
The Distribution of Sport Performance Gene Variations Through COVID-19 Disease Severity.
Yenmis G et al.
Diagnostics (basel, Switzerland), 2025
Single nucleotide polymorphisms: Implications in the early diagnosis and targeted intervention of coronary microvascular dysfunction.
Tian D et al.
Genes & Diseases, 2025
A systematic review and functional in-silico analysis of genes and variants associated with amyotrophic lateral sclerosis.
Arreola-Aldape CA et al.
Frontiers in Neuroscience, 2025
Genetic susceptibility to gestational diabetes and its mild modification by bisphenol A and thyroid-stimulating hormone: findings from a South Chinese pregnancy cohort.
Mao Y et al.
Frontiers in Nutrition, 2025
Association between the PPARGC1A Gly482Ser (rs8192678) polymorphism and endurance and power athlete status: a systematic review and meta-analysis.
Su W et al.
Frontiers in Physiology, 2025
Role of the PPARGC1A Gene and Its rs8192678 Polymorphism on Sport Performance, Aerobic Capacity, Muscle Adaptation and Metabolic Diseases: A Narrative Review.
Varillas-Delgado D
Genes, 2024
Influence of genetic polymorphism on sports talent performance versus non-athletes: a systematic review and meta-analysis.
Ferreira CP et al.
Bmc Sports Science, Medicine & Rehabilitation, 2024
Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.
Yang N et al.
Bmc Pediatrics, 2024
Association of Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1 Alpha Coding Variants with Hepatocellular Carcinoma Risk in the Moroccan Population: A Case-Control Study.
Tanouti IA et al.
Asian Pacific Journal of Cancer Prevention : Apjcp, 2023
Comparative physiological anthropogeny: exploring molecular underpinnings of distinctly human phenotypes.
Vaill M et al.
Physiological Reviews, 2023
Engineered allele substitution at PPARGC1A rs8192678 alters human white adipocyte differentiation, lipogenesis, and PGC-1α content and turnover.
Huang M et al.
Diabetologia, 2023
Association between Genotype and the Glycemic Response to an Oral Glucose Tolerance Test: A Systematic Review.
Bayer S et al.
Nutrients, 2023
The PPARGC1A Gly482Ser polymorphism is associated with elite long-distance running performance.
Hall ECR et al.
Journal of Sports Sciences, 2023
Association between the PPARGC1A Gly482Ser polymorphism and muscle fitness in Chinese schoolchildren.
Wei Q
Plos One, 2023
Association of rare PPARGC1A variants with Parkinson's disease risk.
Li LZ et al.
Journal of Human Genetics, 2022
Genetic Variants of VDR and PGC-1α Are Not Associated with the Risk of Endometriosis in Indian Women.
Beeram H et al.
Dna and Cell Biology, 2022
Genetics of long-distance runners and road cyclists-A systematic review with meta-analysis.
Konopka MJ et al.
Scandinavian Journal of Medicine & Science in Sports, 2022
Gene Polymorphism and Total Genetic Score in Martial Arts Athletes with Different Athletic Qualifications.
Vostrikova A et al.
Genes, 2022
Transmission Distortion of MCT1 rs1049434 among Polish Elite Athletes.
Dzitkowska-Zabielska M et al.
Genes, 2022
Unraveling Gut Microbiota Signatures Associated with PPARD and PARGC1A Genetic Polymorphisms in a Healthy Population.
Bailén M et al.
Genes, 2022
Deciphering the role of PGC-1α in neurological disorders: from mitochondrial dysfunction to synaptic failure.
Panes JD et al.
Neural Regeneration Research, 2022
Molecular Dynamics Simulation and Essential Dynamics of Deleterious Proline 12 Alanine Single-Nucleotide Polymorphism in PPARγ2 Associated with Type 2 Diabetes, Cardiovascular Disease, and Nonalcoholic Fatty Liver Disease.
Taghvaei S et al.
Ppar Research, 2022
Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis.
Schillemans T et al.
Frontiers in Physiology, 2022
Influence of Peroxisome Proliferator-Activated Receptor (PPAR)-gamma Coactivator (PGC)-1 alpha gene rs8192678 polymorphism by gender on different health-related parameters in healthy young adults.
Montes-de-Oca-García A et al.
Frontiers in Physiology, 2022
Case report: Whole-exome sequencing identifies a novel DES mutation (p. E434K) in a Chinese family with cardiomyopathy and sudden cardiac death.
Liu YX et al.
Frontiers in Cardiovascular Medicine, 2022
Effects of PPARG and PPARGC1A gene polymorphisms on obesity markers.
Muntean C et al.
Frontiers in Public Health, 2022
Genotype Score for Iron Status Is Associated with Muscle Fiber Composition in Women.
Takaragawa M et al.
Genes, 2021
Candidate Genes of Regulation of Skeletal Muscle Energy Metabolism in Athletes.
Balberova OV et al.
Genes, 2021
PPARGC1A rs8192678 G>A polymorphism affects the severity of hepatic histological features and nonalcoholic steatohepatitis in patients with nonalcoholic fatty liver disease.
Zhang RN et al.
World Journal of Gastroenterology, 2021
Genetic Basis for the Dominance of Israeli Long-Distance Runners of Ethiopian Origin.
Ben-Zaken S et al.
Journal of Strength and Conditioning Research, 2021
Associations among perfluorooctanesulfonic/perfluorooctanoic acid levels, nuclear receptor gene polymorphisms, and lipid levels in pregnant women in the Hokkaido study.
Kobayashi S et al.
Scientific Reports, 2021
Association of Genetic Variances in ADRB1 and PPARGC1a with Two-Kilometre Running Time-Trial Performance in Australian Football League Players: A Preliminary Study.
Jacob Y et al.
Sports (basel, Switzerland), 2021
Effects of Genetic Variation on Endurance Performance, Muscle Strength, and Injury Susceptibility in Sports: A Systematic Review.
Appel M et al.
Frontiers in Physiology, 2021
Computational Analysis of Gly482Ser Single-Nucleotide Polymorphism in PPARGC1A Gene Associated with CAD, NAFLD, T2DM, Obesity, Hypertension, and Metabolic Diseases.
Taghvaei S et al.
Ppar Research, 2021
Pharmacogenomics and Personalized Medicine in Type 2 Diabetes Mellitus: Potential Implications for Clinical Practice.
Venkatachalapathy P et al.
Pharmacogenomics and Personalized Medicine, 2021
Associations between nine candidate genetic polymorphisms with coronary heart disease : A meta-analysis.
Li Q et al.
Herz, 2020
Gene-environment interaction in chronic kidney disease among people with type 2 diabetes from The Malaysian Cohort project: a case-control study.
Ahmad N et al.
Diabetic Medicine : a Journal of the British Diabetic Association, 2020
Association of Candidate Gene Polymorphism with Metabolic Syndrome among Mongolian Subjects: A Case-Control Study.
Chuluun-Erdene A et al.
Medical Sciences (basel, Switzerland), 2020
PPARGC1A rs8192678 and NRF1 rs6949152 Polymorphisms Are Associated with Muscle Fiber Composition in Women.
Yvert T et al.
Genes, 2020
UCP2-866G/A Polymorphism is Associated with Prediabetes and Type 2 Diabetes.
Hou G et al.
Archives of Medical Research, 2020
PPARG (Pro12Ala) genetic variant and risk of T2DM: a systematic review and meta-analysis.
Sarhangi N et al.
Scientific Reports, 2020
Mitochondrial dysfunction: An emerging link in the pathophysiology of polycystic ovary syndrome.
Shukla P et al.
Mitochondrion, 2020
Association of the SH2B1 rs7359397 Gene Polymorphism with Steatosis Severity in Subjects with Obesity and Non-Alcoholic Fatty Liver Disease.
Perez-Diaz-Del-Campo N et al.
Nutrients, 2020
Meta-analysis demonstrates Gly482Ser variant of PPARGC1A is associated with components of metabolic syndrome within Asian populations.
Bhatta P et al.
Genomics, 2020
Genetic Variants in the Activation of the Brown-Like Adipocyte Pathway and the Risk for Severe Obesity.
da Fonseca ACP et al.
Obesity Facts, 2020