The isolation and characterisation of a cDNA clone for human lecithin:cholesterol acyl transferase and its use to analyse the genes in patients with LCAT deficiency and fish eye disease

scientific article

The isolation and characterisation of a cDNA clone for human lecithin:cholesterol acyl transferase and its use to analyse the genes in patients with LCAT deficiency and fish eye disease is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/0006-291X(87)91090-4
P698PubMed publication ID2823801

P50authorSissel RogneQ17106868
Ola MyklebostQ41845092
P2093author name stringG Skretting
H Prydz
E Gjone
L A Carlson
L Holmquist
F Larsen
B Mevåg
P433issue1
P407language of work or nameEnglishQ1860
P921main subjecteye diseaseQ3041498
P304page(s)161-169
P577publication date1987-10-01
P1433published inBiochemical and Biophysical Research CommunicationsQ864228
P1476titleThe isolation and characterisation of a cDNA clone for human lecithin:cholesterol acyl transferase and its use to analyse the genes in patients with LCAT deficiency and fish eye disease
P478volume148

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cites work (P2860)
Q67577150A physical map of a 1.3-Mb region on the long arm of chromosome 12, spanning the GLI and LRP loci
Q68164317Association analysis of lipid levels and apolipoprotein restriction fragment length polymorphisms
Q48069326Chicken lecithin-cholesterol acyltransferase. Molecular characterization reveals unusual structure and expression pattern
Q39606692Familial LCAT deficiency and fish-eye disease
Q39565195Familial lecithin: cholesterol acyltransferase (LCAT) deficiency. An updated review Spring 1988.
Q52509864In vitro expression of structural defects in the lecithin-cholesterol acyltransferase gene.
Q36422036Rat liver carboxylesterase: cDNA cloning, sequencing, and evidence for a multigene family
Q28263895The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families
Q33593510The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5.
Q24564900Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met)

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