DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
about
Nonsynonymous polymorphic sites in the apolipoprotein (apo) A-IV gene are associated with changes in the concentration of apo B- and apo A-I-containing lipoproteins in a normal populationNon-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene.Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency.Lipoprotein lipase modulates net secretory output of apolipoprotein B in vitro. A possible pathophysiologic explanation for familial combined hyperlipidemia.Impaired activation of adipocyte lipolysis in familial combined hyperlipidemiaA unique genetic and biochemical presentation of fish-eye diseaseUniparental disomy for chromosome 16 in humans.Linkage disequilibrium and modification of risk for Huntington disease.Partial gene duplication involving exon-Alu interchange results in lipoprotein lipase deficiency.Characterization of six partial deletions in the low-density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH)A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene.Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.Improved predictive testing for Huntington disease by using three linked DNA markers.Gene and gene-product variation in the apolipoprotein A-I/C-III/A-IV cluster in the Dogrib Indians of the Northwest Territories.Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes.Linkage and association between distinct variants of the APOA1/C3/A4/A5 gene cluster and familial combined hyperlipidemia.Extended haplotypes and linkage disequilibrium between 11 markers at the APOA1-C3-A4 gene cluster on chromosome 11.Joint linkage and segregation analysis under multiallelic trait inheritance: simplifying interpretations for complex traits.
P2860
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P2860
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
description
1987 nî lūn-bûn
@nan
1987 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
@ast
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
@en
type
label
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
@ast
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
@en
prefLabel
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
@ast
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
@en
P2093
P2860
P1476
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias
@en
P2093
Frohlich J
P2860
P304
P407
P577
1987-05-01T00:00:00Z