Clinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor function

scientific article published on May 1, 1991

Clinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor function is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1161/01.ATV.11.3.691
P953full work available at URLhttps://www.ahajournals.org/doi/pdf/10.1161/01.ATV.11.3.691
P698PubMed publication ID1674216

P50authorAnders HamstenQ30421754
Stephen E HumphriesQ51751590
Johan FrostegardQ60314762
P2093author name stringJ. Nilsson
J. J. Gallagher
B. L. Knight
N. B. Myant
P. Talmud
S. N. McCarthy
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectCardiology and cardiovascular medicineQ96320350
hypercholesterolemiaQ762713
familial hypercholesterolemiaQ2711291
P304page(s)691-703
P577publication date1991-05-01
P1433published inArteriosclerosis and thrombosis : a journal of vascular biologyQ27709770
P1476titleClinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor function
P478volume11

Reverse relations

cites work (P2860)
Q33910296Accumulation of "small dense" low density lipoproteins (LDL) in a homozygous patients with familial defective apolipoprotein B-100 results from heterogenous interaction of LDL subfractions with the LDL receptor
Q79908962Diagnosis of families with familial hypercholesterolaemia and/or Apo B-100 defect by means of DNA analysis of LDL-receptor gene mutations
Q73349296Effects of Ava II and Hinc II polymorphisms at the LDL receptor gene on serum lipid levels of Brazilian individuals with high risk for coronary heart disease
Q36186468Familial defective apolipoprotein B-100: a common cause of primary hypercholesterolemia
Q35553545Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity
Q53393462First International Workshop on Familial Defective apo B-100, Munich, November 1991
Q72912457Four new nucleotide sequence polymorphisms in the LDL receptor gene detected by SSCP analysis
Q57452975How Genomics Is Personalizing the Management of Dyslipidemia and Cardiovascular Disease Prevention
Q40303557Metabolism of triglyceride-rich lipoproteins during alimentary lipemia
Q33595177Six DNA polymorphisms in the low density lipoprotein receptor gene: their genetic relationship and an example of their use for identifying affected relatives of patients with familial hypercholesterolaemia
Q27021950The roles of genetic polymorphisms and human immunodeficiency virus infection in lipid metabolism
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
Q40335473Variation in lipoprotein(a) concentration associated with different apolipoprotein(a) alleles

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