Literature DB >> 3541514

Lecithin: cholesterol acyltransferase (LCAT) deficiency syndromes.

J Frohlich, R McLeod.   

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Year:  1986        PMID： 3541514     DOI： 10.1007/978-1-4684-1262-8_16

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN： 0065-2598            Impact factor:   2.622


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  3 in total

Review 1.  Analysis of familial hypoalphalipoproteinemia syndromes.

Authors:  J Frohlich; P H Pritchard
Journal:  Mol Cell Biochem       Date:  1992-08-18       Impact factor: 3.396

2.  A single G to A nucleotide transition in exon IV of the lecithin: cholesterol acyltransferase (LCAT) gene results in an Arg140 to His substitution and causes LCAT-deficiency.

Authors:  E Steyrer; S Haubenwallner; G Hörl; W Giessauf; G M Kostner; R Zechner
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

3.  The role of lecithin: cholesterol acyltransferase for lipoprotein (a) assembly. Structural integrity of low density lipoproteins is a prerequisite for Lp(a) formation in human plasma.

Authors:  E Steyrer; S Durovic; S Frank; W Giessauf; A Burger; H Dieplinger; R Zechner; G M Kostner
Journal:  J Clin Invest       Date:  1994-12       Impact factor: 14.808
  3 in total

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