Associated Papers
Sequencing and functional characterization of SCARB1 variants in subjects with extreme HDL cholesterol levels.
Gracia-Rubio I et al.
Journal of Clinical Lipidology, 2025
Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma.
Villa M et al.
British Journal of Cancer, 2024
Influence of the rs4238001 Genetic Polymorphism of the SR-B1 Gene on Serum Lipid Levels and Response to Rosuvastatin in Myocardial Infarction Iraqi Patients.
Abdulfattah SY et al.
Biochemical Genetics, 2024
ACE Phenotyping in Human Blood and Tissues: Revelation of ACE Outliers and Sex Differences in ACE Sialylation.
Enyedi EE et al.
Biomedicines, 2024
Rare and common coding variants in lipid metabolism-related genes and their association with coronary artery disease.
Li W et al.
Bmc Cardiovascular Disorders, 2024
Hunting for the elusive target antigen in gestational alloimmune liver disease (GALD).
Rieneck K et al.
Plos One, 2023
Identification of genetic variants related to metabolic syndrome by next-generation sequencing.
Lee S et al.
Diabetology & Metabolic Syndrome, 2022
Genome-Wide Characterization of a Highly Penetrant Form of Hyperlipoprotein(a)emia Associated With Genetically Elevated Cardiovascular Risk.
Coassin S et al.
Circulation. Genomic and Precision Medicine, 2022
Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts.
Dagli-Hernandez C et al.
Pharmacological Reports : Pr, 2022
Investigation of Scavenger Receptor Class B Type I gene variants in patients with coronary heart disease with a history of early myocardial infarction.
Çaykara B et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir, 2021
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
Targeted transcriptome analysis using synthetic long read sequencing uncovers isoform reprograming in the progression of colon cancer.
Liu S et al.
Communications Biology, 2021
Identification and characterization of a rare variant in apolipoprotein A-IV, p.(V336M), and evaluation of HDL functionality in a Greek cohort with extreme HDL cholesterol levels.
Chroni A et al.
Archives of Biochemistry and Biophysics, 2020
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease.
Helgadottir A et al.
European Heart Journal, 2018
SCARB1 Gene Variants Are Associated With the Phenotype of Combined High High-Density Lipoprotein Cholesterol and High Lipoprotein (a).
Yang X et al.
Circulation. Cardiovascular Genetics, 2016
Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study.
Niemsiri V et al.
Bmc Medical Genetics, 2015
Association of the Lipoprotein Receptor SCARB1 Common Missense Variant rs4238001 with Incident Coronary Heart Disease.
Manichaikul A et al.
Plos One, 2015
Impact of genetic variants in human scavenger receptor class B type I (SCARB1) on plasma lipid traits.
Niemsiri V et al.
Circulation. Cardiovascular Genetics, 2014
Flow-mediated dilation, carotid wall thickness and HDL function in subjects with hyperalphalipoproteinemia.
Vigna GB et al.
Nutrition, Metabolism, and Cardiovascular Diseases : Nmcd, 2014
Functional genomics of the human high-density lipoprotein receptor scavenger receptor BI: an old dog with new tricks.
Chadwick AC et al.
Current Opinion in Endocrinology, Diabetes, and Obesity, 2013
[Influence of genetic combinations on HDL-C levels in a Southern Brazilian population].
Andrade FM et al.
Arquivos Brasileiros De Cardiologia, 2010
Influence of SCARB1 polymorphisms on serum lipids of hypercholesterolemic individuals treated with atorvastatin.
Cerda A et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2010
A synonymous variant in scavenger receptor, class B, type I gene is associated with lower SR-BI protein expression and function.
Constantineau J et al.
Atherosclerosis, 2010
Scavenger receptor class B type I protein as an independent predictor of high-density lipoprotein cholesterol levels in subjects with hyperalphalipoproteinemia.
West M et al.
The Journal of Clinical Endocrinology and Metabolism, 2009
Scavenger receptor class B type I (SCARB1) c.1119C>T polymorphism affects postprandial triglyceride metabolism in men.
Tanaka T et al.
The Journal of Nutrition, 2007
Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels.
Boekholdt SM et al.
Clinical Genetics, 2006
Polymorphisms in APOA1 and LPL genes are statistically independently associated with fasting TG in men with CAD.
Souverein OW et al.
European Journal of Human Genetics : Ejhg, 2005
Population-based study of SR-BI genetic variation and lipid profile.
Morabia A et al.
Atherosclerosis, 2004
Genetic diversity patterns in the SR-BI/II locus can be explained by a recent selective sweep.
Le Jossec M et al.
Molecular Biology and Evolution, 2004
Association of the 3' UTR transcription factor LBP-1c/CP2/LSF polymorphism with late-onset Alzheimer's disease.
Luedecking-Zimmer E et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2003
Polymorphisms at the SRBI locus are associated with lipoprotein levels in subjects with heterozygous familial hypercholesterolemia.
Tai ES et al.
Clinical Genetics, 2003
Candidate genes and confirmed genetic polymorphisms associated with cardiovascular diseases: a tabular assessment.
Tang Z et al.
Journal of Thrombosis and Thrombolysis, 2001