Identification of the base substitution responsible for the Ag(x/y) polymorphism of apolipoprotein B-100.

scientific article

Identification of the base substitution responsible for the Ag(x/y) polymorphism of apolipoprotein B-100. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1161/01.ATV.11.2.379
P698PubMed publication ID1998655

P50authorMing-Jiuan WuQ40474628
P2093author name stringV N Schumaker
R Bütler
E Bütler
P433issue2
P304page(s)379-384
P577publication date1991-03-01
P1433published inArteriosclerosis and thrombosis : a journal of vascular biologyQ27709770
P1476titleIdentification of the base substitution responsible for the Ag(x/y) polymorphism of apolipoprotein B-100.
P478volume11

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cites work (P2860)
Q35900953Bovine apolipoprotein B-100 is a dominant immunogen in therapeutic cell populations cultured in fetal calf serum in mice and humans
Q73229414Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK
Q35553545Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity
Q54242561Frequency of the XbaI, EcoRI, PvuII and MspI polymorphisms of the apolipoprotein B gene in relation to hypercholesterolaemia in the general population
Q34210824Molecular and metabolic basis for the metabolic disorder normotriglyceridemic abetalipoproteinemia
Q38312923Screening for mutations in the exon 26 of the apolipoprotein B gene in hypercholesterolemic Finnish families by the single-strand conformation polymorphism method.
Q73111107Screening of the 3' two-thirds of the coding area of the apo B gene in Finnish hypercholesterolemic patients report of six new genetic variants
Q43952048The effect of six polymorphisms in the Apolipoprotein B gene on parameters of lipid metabolism in a Danish population
Q35195246Two amino acid substitutions in apolipoprotein B are in complete allelic association with the antigen group (x/y) polymorphism: evidence for little recombination in the 3' end of the human gene

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