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http://dx.doi.org/10.1016/j.numecd.2012.05.001 | DOI Listing |
Int J Mol Sci
August 2024
Department of Human Genetics, Punjabi University, Patiala 147002, India.
Rev Assoc Med Bras (1992)
March 2023
Karabük Üniversitesi, Medical Faculty, Department of Medical Biology - Samsun, Turkey.
Objective: The aim of this study was to determine frequency and associations between APOA5 c.56C>G, -1131T>C, c.553G>T, and APOC3 -482C>T and SstI gene polymorphisms with hypertriglyceridemia.
View Article and Find Full Text PDFPharmacogenet Genomics
April 2022
Unidad de Investigación Médica en Enfermedades Infecciosas y Parasitarias, UMAE Hospital de Pediatría, Centro Médico Nacional Siglo XXI. Instituto Mexicano del Seguro Social, IMSS.
J Pers Med
March 2021
Department of Bio-Convergence System, Hoseo University, Asan 31499, Korea.
3GO is a condition in which hypertension, hyperglycemia, and dyslipidemia co-occur, and these conditions are related to each other and genetic and environmental factors. We hypothesized that common genetic variants and their interactions with lifestyles influenced 3GO risk. We aimed to explore common genetic variants to affect 3GO risk and their haplotype interaction with lifestyles in a city hospital-based cohort in 58,701 Koreans > 40 years.
View Article and Find Full Text PDFJ Genet Genomics
December 2020
Department of Genetics, Shanghai-MOST Key Laboratory of Health and Disease Genomics, Chinese National Human Genome Center at Shanghai and Shanghai Academy of Science and Technology, Shanghai 200025, China. Electronic address:
The unusual chromosome 11q23.3 harboring the apolipoprotein (APO) gene cluster has been well documented for its essential roles in plasma lipid-related traits and atherosclerotic cardiovascular diseases. However, its genetic architecture and the potential biological mechanisms underlying complex phenotypes have not been well assessed.
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