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Further Characterization of Apolipoprotein B Genetic Variations in Taiwanese

Bibliographic Data

ID7990356
AuthorsJune Hsieh Wu, Yuan-Teh Lee, Hsiu-Ching Hsu, Ling-Ling Hsieh, Ming‐Shien Wen (0000-0002-0056-7985), Ming-Shien Wen, Ming‐Shyan Chern, Ming-Shyan Chern, Dan Y Wu, Delon Wu
Year2001
Volume73
Issue3
Pages451-460
Publication date2001-01-01
Peer ReviewedYes
Open AccessNo
TypeARTICLE
VenueHuman Biology (JOURNAL)
Journal identifiersISSN: 0018-7143 • E-ISSN: 1534-6617
PublisherProject MUSE (PUBLISHER • US)
DOI10.1353/hub.2001.0044
PMID11459425
OpenAlexW2031199616
LanguageEN

Apolipoprotein B (apoB, protein; APOB, gene) is the main protein component of low-density lipoprotein (LDL) and plays an important role in blood lipid metabolism. Previously, we have reported four APOB coding regions, 5' signal peptide, and 3' repeat sequence polymorphisms in our population. In this report, we further characterize other APOB genetic variations. The results illustrate that the mutation frequencies for Arg3500Gln (1/846 alleles), Arg4019Trp (2/786 alleles), -265 C/T promoter region (0/264 alleles), and intron 2 A/G (0/450 alleles) are very low. Our population showed a frequency of 68.9% for the B4311 Ser allele. The B4311 Asn allele was associated with a higher apoB level than the Ser group (p 200 mg/dL and apoB concentration > 85 mg/dL than in the group with a TC < 200 mg/dL and apoB < 85 mg/dL (p = 0.03 for TC comparison

Allele · Allele frequency · Apolipoprotein B · Biology · Cholesterol · Gene · Genotype · Lipoprotein · Population · Diabetes, Cardiovascular Risks, and Lipoproteins · Endocrinology · Genetic Associations and Epidemiology · Genetics · Lipoproteins and Cardiovascular Health · Medicine · Molecular Biology

Citation velocityhistorical
Highly citedNo

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