Associated Papers
Genetic association analysis-based networks and classification of human UCP1 polymorphisms.
Li D
Genes & Diseases, 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
Association of uncoupling protein (Ucp) gene polymorphisms with cardiometabolic diseases.
Pravednikova AE et al.
Molecular Medicine (cambridge, Mass.), 2020
Association of UCP1 polymorphisms with type 2 diabetes mellitus and their interaction with physical activity and sedentary behavior.
Dong C et al.
Gene, 2020
Analysis of association between common variants of uncoupling proteins genes and diabetic retinopathy in a Chinese population.
Jin P et al.
Bmc Medical Genetics, 2020
Association of Uncoupling Protein 1 (UCP1) gene polymorphism with obesity: a case-control study.
Chathoth S et al.
Bmc Medical Genetics, 2018
Sequence and Haplotypes Variation of the Ovine Uncoupling Protein-1 Gene (UCP1) and Their Association with Growth and Carcass Traits in New Zealand Romney Lambs.
An Q et al.
Genes, 2018
Genetic variants and the metabolic syndrome: a systematic review.
Povel CM et al.
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity, 2011
Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy.
Labruna G et al.
Journal of Obesity, 2011
A haplotype at the UCP1 gene locus contributes to genetic risk for type 2 diabetes in Asian Indians (CURES-72).
Vimaleswaran KS et al.
Metabolic Syndrome and Related Disorders, 2010
Absence of Association of Metabolic Syndrome with PPARGC1A, PPARG and UCP1 Gene Polymorphisms in Asian Indians.
Vimaleswaran KS et al.
Metabolic Syndrome and Related Disorders, 2007
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
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
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