Associated Papers
Genetic association analysis-based networks and classification of human UCP1 polymorphisms.
Li D
Genes & Diseases, 2024
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia.
Dong W et al.
Journal of Lipid Research, 2022
35460704 (PubMed )
Supplement: mmc1.pdf
Association of uncoupling protein (Ucp) gene polymorphisms with cardiometabolic diseases.
Pravednikova AE et al.
Molecular Medicine (cambridge, Mass.), 2020
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
Select a paper to view details