Familial HDL deficiency due to marked hypercatabolism of normal apoA-I

scientific article published on 01 September 1993

Familial HDL deficiency due to marked hypercatabolism of normal apoA-I is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1161/01.ATV.13.9.1299
P698PubMed publication ID8364014

P2093author name stringH B Brewer
S Santamarina-Fojo
J Emmerich
I Tauveron
B Vergès
D Rader
P Thiéblot
M Ayrault-Jarrier
J Shaefer
P433issue9
P304page(s)1299-1306
P577publication date1993-09-01
P1433published inArteriosclerosis and thrombosis : a journal of vascular biologyQ27709770
P1476titleFamilial HDL deficiency due to marked hypercatabolism of normal apoA-I
P478volume13

Reverse relations

cites work (P2860)
Q73130601Apolipoprotein AI isoforms in serum determined by isoelectric focusing and immunoblotting
Q72992419Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144
Q44329447Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol
Q74348218Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations
Q34558799Dynamics of reverse cholesterol transport: protection against atherosclerosis
Q37058273Effect of obesity on high-density lipoprotein metabolism
Q43546756Enhanced fractional catabolic rate of apo A-I and apo A-II in heterozygous subjects for apo A-I(Zaragoza) (L144R).
Q73359069Fish-eye disease: structural and in vivo metabolic abnormalities of high-density lipoproteins
Q47788413Lipid-free apolipoprotein (apo) A-I is converted into alpha-migrating high density lipoproteins by lipoprotein-depleted plasma of normolipidemic donors and apo A-I-deficient patients but not of Tangier disease patients
Q34120460Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease
Q57241088Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

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