Associated Papers
Genetic association analysis-based networks and classification of human UCP1 polymorphisms.
Li D
Genes & Diseases, 2024
Genotypes of the UCP1 gene polymorphisms and cardiometabolic diseases: A multifactorial study of association with disease probability.
Pravednikova AE et al.
Biochimie, 2024
Indicators of HSV1 Infection, ECM-Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia.
Huang YC et al.
Journal of Personalized Medicine, 2023
NGS Sequencing Reveals New UCP1 Gene Variants Potentially Associated with MetS and/or T2DM Risk in the Polish Population-A Preliminary Study.
Andrzejczak A et al.
Genes, 2023
Prevalence of uncoupling protein one genetic polymorphisms and their relationship with cardiovascular and metabolic health.
Dinas PC et al.
Plos One, 2022
Association of uncoupling protein (Ucp) gene polymorphisms with cardiometabolic diseases.
Pravednikova AE et al.
Molecular Medicine (cambridge, Mass.), 2020
Association of Uncoupling Protein 1 (UCP1) gene polymorphism with obesity: a case-control study.
Chathoth S et al.
Bmc Medical Genetics, 2018
Association of oxidative stress gene polymorphisms with presbycusis.
Manche SK et al.
Gene, 2016
The role of uncoupling proteins in diabetes mellitus.
Liu J et al.
Journal of Diabetes Research, 2013
Association of the UCP-1 single nucleotide polymorphism A-3826G with the dampness-phlegm pattern among Korean stroke patients.
Lim JH et al.
Bmc Complementary and Alternative Medicine, 2012
Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy.
Labruna G et al.
Journal of Obesity, 2011
Triangulation of the human, chimpanzee, and Neanderthal genome sequences identifies potentially compensated mutations.
Zhang G et al.
Human Mutation, 2010
The polymorphisms of UCP1 genes associated with fat metabolism, obesity and diabetes.
Jia JJ et al.
Molecular Biology Reports, 2010
The uncoupling protein 1 gene, UCP1, is expressed in mammalian islet cells and associated with acute insulin response to glucose in African American families from the IRAS Family Study.
Sale MM et al.
Bmc Endocrine Disorders, 2007
[Chimpanzee genome sequencing and comparative analysis with the human genome].
Watanabe H et al.
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme, 2006
A study to survey susceptible genetic factors responsible for troglitazone-associated hepatotoxicity in Japanese patients with type 2 diabetes mellitus.
Watanabe I et al.
Clinical Pharmacology and Therapeutics, 2003
Uncoupling protein 1 and 3 polymorphisms are associated with waist-to-hip ratio.
Herrmann SM et al.
Journal of Molecular Medicine (berlin, Germany), 2003
Frequency and significance of the A-->G (-3826) polymorphism in the promoter of the gene for uncoupling protein-1 with regard to metabolic parameters and adipocyte transcription factor binding in a large population-based Caucasian cohort.
Schäffler A et al.
European Journal of Clinical Investigation, 1999
Analysis of the uncoupling protein-1 (UCP1) gene in obese and lean subjects: identification of four amino acid variants.
Hamann A et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity, 1998
The human mitochondrial transport/carrier protein family. Nonsynonymous single nucleotide polymorphisms (nsSNPs) and mutations that lead to human diseases.
Wohlrab H
Biochimica Et Biophysica Acta, 0
Oxidative stress pathway genes and chronic renal insufficiency in Asian Indians with Type 2 diabetes.
Tiwari AK et al.
Journal of Diabetes and Its Complications, 0