Literature DB >> 2182033

The genetic dyslipoproteinemias--nosology update 1990.

G Schonfeld1.   

Abstract

The number of discrete disorders of lipid transport is growing. Concomitantly, the classification of the disorders is changing, from one based on altered concentrations of lipoproteins, to one based on current understanding of the genetics of the disorders and of lipoprotein biochemistry and physiology. Many disorders are now traceable to deficiencies of essential proteins such as apolipoproteins, enzymes, lipid transfer proteins and cellular receptors.

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Year:  1990        PMID： 2182033     DOI： 10.1016/0021-9150(90)90014-a

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN： 0021-9150            Impact factor:   5.162


  3 in total

Review 1.  Molecular aspects of pathological processes in the artery wall.

Authors:  J W van Neck; H P Bloemers
Journal:  Mol Biol Rep       Date:  1992-11       Impact factor: 2.316

2.  Approach to identification of a point mutation in apo B100 gene by means of a PCR-mediated site-directed mutagenesis.

Authors:  E I Schwartz; S P Shevtsov; A P Kuchinski; O V Plutalov
Journal:  Nucleic Acids Res       Date:  1991-07-11       Impact factor: 16.971

3.  High density lipoprotein deficiency with xanthomas. A defect in reverse cholesterol transport caused by a point mutation in the apolipoprotein A-I gene.

Authors:  K J Lackner; H Dieplinger; G Nowicka; G Schmitz
Journal:  J Clin Invest       Date:  1993-11       Impact factor: 14.808
  3 in total

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