Literature DB >> 207903

Familial hypobetalipoproteinemia. Absence of atherosclerosis in a postmortem study.

J A Kahn, C J Glueck.   

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Year:  1978        PMID： 207903     DOI： 10.1001/jama.240.1.47

Source DB:  PubMed          Journal:  JAMA        ISSN： 0098-7484            Impact factor:   56.272


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  5 in total

1.  Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.

Authors:  S G Young; S T Hubl; R S Smith; S M Snyder; J F Terdiman
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808

Review 2.  The response-to-retention hypothesis of early atherogenesis.

Authors:  K J Williams; I Tabas
Journal:  Arterioscler Thromb Vasc Biol       Date:  1995-05       Impact factor: 8.311

3.  A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia.

Authors:  F K Welty; S T Hubl; V R Pierotti; S G Young
Journal:  J Clin Invest       Date:  1991-05       Impact factor: 14.808

4.  Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100.

Authors:  S G Young; S J Bertics; L K Curtiss; B W Dubois; J L Witztum
Journal:  J Clin Invest       Date:  1987-06       Impact factor: 14.808

5.  Clinicopathological Phenotype of Autosomal Recessive Cholesterol Deficiency in Holstein Cattle.

Authors:  T Mock; K Mehinagic; F Menzi; E Studer; A Oevermann; M H Stoffel; C Drögemüller; M Meylan; N Regenscheit
Journal:  J Vet Intern Med       Date:  2016-06-08       Impact factor: 3.333
  5 in total

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