Screening for functional sequence variations and mutations in ABCA1.
about
Isolated low high density lipoprotein-cholesterol (HDL-C): implications of global risk reduction. Case report and systematic scientific reviewGenetic causes of high and low serum HDL-cholesterol.Epigenetic variation during the adult lifespan: cross-sectional and longitudinal data on monozygotic twin pairs.Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms.Histone Methyltransferase Enhancer of Zeste Homolog 2-Mediated ABCA1 Promoter DNA Methylation Contributes to the Progression of Atherosclerosis.Targeted next-generation sequencing to diagnose disorders of HDL cholesterol.Molecular diagnosis of ATP-binding cassette transporter-related diseases.Lipidomic strategies to study structural and functional defects of ABC-transporters in cellular lipid trafficking.Hypermethylation at loci sensitive to the prenatal environment is associated with increased incidence of myocardial infarction.24(S)-hydroxycholesterol is actively eliminated from neuronal cells by ABCA1.A Comprehensive In Silico Analysis of the Functional and Structural Impact of Nonsynonymous SNPs in the ABCA1 Transporter Gene.Position 834 in TM6 plays an important role in cholesterol and phosphatidylcholine transport by ABCA1.
P2860
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P2860
Screening for functional sequence variations and mutations in ABCA1.
description
2004 nî lūn-bûn
@nan
2004 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Screening for functional sequence variations and mutations in ABCA1.
@ast
Screening for functional sequence variations and mutations in ABCA1.
@en
type
label
Screening for functional sequence variations and mutations in ABCA1.
@ast
Screening for functional sequence variations and mutations in ABCA1.
@en
prefLabel
Screening for functional sequence variations and mutations in ABCA1.
@ast
Screening for functional sequence variations and mutations in ABCA1.
@en
P2093
P1433
P1476
Screening for functional sequence variations and mutations in ABCA1.
@en
P2093
Charalampos Aslanidis
Christa Buechler
Christiane Keller
Francisco E Baralle
Geesje M Dallinga-Thie
Harald Thumann
Jürgen Geisel
Mario C O Probst
Thomas Langmann
Valentine C Menys
P304
P356
10.1016/J.ATHEROSCLEROSIS.2004.02.019
P50
P577
2004-08-01T00:00:00Z