Associated Papers
Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder.
Wang T et al.
Computational and Structural Biotechnology Journal, 2023
38213898 (PubMed )
Supplement: mmc2.xlsx › RIVs_in_VARGs
SR-B1's Next Top Model: Structural Perspectives on the Functions of the HDL Receptor.
Powers HR et al.
Current Atherosclerosis Reports, 2022
Genetics and regulation of HDL metabolism.
Kardassis D et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids, 2022
SR-B1, a Key Receptor Involved in the Progression of Cardiovascular Disease: A Perspective from Mice and Human Genetic Studies.
Gracia-Rubio I et al.
Biomedicines, 2021
Human variant of scavenger receptor BI (R174C) exhibits impaired cholesterol transport functions.
May SC et al.
Journal of Lipid Research, 2021
Rare P376L variant in the SR-BI gene associates with HDL dysfunction and risk of cardiovascular disease.
Samadi S et al.
Clinical Biochemistry, 2019
Association of Endonuclease G Gene Variants with Cardiovascular Disease Risk Factors.
Etehad Roodi N et al.
Reports of Biochemistry & Molecular Biology, 2019
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease.
Helgadottir A et al.
European Heart Journal, 2018
iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers.
Wang M et al.
Scientific Reports, 2016
27527004 (PubMed )
Supplement: srep31321-s5.xls › VaribenchSelectedPure
Single nucleotide polymorphisms in genes that are common targets of luteotropin and luteolysin in primate corpus luteum: computational exploration.
Suresh PS et al.
Gene, 2012
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