| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1991PNAS...88.4855F |
| P356 | DOI | 10.1073/PNAS.88.11.4855 |
| P932 | PMC publication ID | 51765 |
| P698 | PubMed publication ID | 2052566 |
| P5875 | ResearchGate publication ID | 21102595 |
| P2093 | author name string | J J Albers | |
| P H Pritchard | |||
| G Assmann | |||
| H Funke | |||
| J J Kastelein | |||
| A von Eckardstein | |||
| C Droste | |||
| P2860 | cites work | Designed diagnostic restriction fragment length polymorphisms for the detection of point mutations in ras oncogenes | Q69371372 |
| Human plasma lecithin-cholesterol acyltransferase. An elucidation of the catalytic mechanism | Q69491747 | ||
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| Evidence for the presence in human plasma of lecithin: cholesterol acyltransferase activity (beta-LCAT) specifically esterifying free cholesterol of combined pre-beta- and beta-lipoproteins. Studies of fish eye disease patients and control subjects | Q41505971 | ||
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| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | eye disease | Q3041498 |
| P304 | page(s) | 4855-9 | |
| P577 | publication date | 1991-06-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity | |
| P478 | volume | 88 |
| Q63979951 | A molecular approach to inherited kidney disorders |
| Q36387268 | A physiologically based in silico kinetic model predicting plasma cholesterol concentrations in humans |
| Q24336518 | A plasma lipoprotein containing only apolipoprotein E and with gamma mobility on electrophoresis releases cholesterol from cells |
| Q47655146 | A retractable lid in lecithin:cholesterol acyltransferase provides a structural mechanism for activation by apolipoprotein A-I. |
| Q34386276 | A unique genetic and biochemical presentation of fish-eye disease |
| Q39812837 | An apoA-I mimetic peptide increases LCAT activity in mice through increasing HDL concentration |
| Q37357561 | An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease). |
| Q35797202 | Analysis of familial hypoalphalipoproteinemia syndromes |
| Q40716232 | Analysis of glomerulosclerosis and atherosclerosis in lecithin cholesterol acyltransferase-deficient mice. |
| Q73129821 | Analysis of human lecithin-cholesterol acyltransferase activity by carboxyl-terminal truncation |
| Q35370268 | ApoE regulates hematopoietic stem cell proliferation, monocytosis, and monocyte accumulation in atherosclerotic lesions in mice |
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| Q48069326 | Chicken lecithin-cholesterol acyltransferase. Molecular characterization reveals unusual structure and expression pattern |
| Q72992419 | Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144 |
| Q34362195 | Clinical and histopathological features of a suspected case of fish-eye disease |
| Q24598765 | Common variants at 30 loci contribute to polygenic dyslipidemia |
| Q44361735 | Deletion of N-terminal amino acids from human lecithin:cholesterol acyltransferase differentially affects enzyme activity toward alpha- and beta-substrate lipoproteins |
| Q82443808 | Disturbed apolipoprotein A-I-containing lipoproteins in fish-eye disease are improved by the lecithin:cholesterol acyltransferase produced by gene-transduced adipocytes in vitro |
| Q41962268 | Familial lecithin-cholesterol acyltransferase (LCAT) deficiency; a differential of proteinuria |
| Q34114305 | Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis |
| Q33891534 | Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease |
| Q40266047 | Genetics of corneal disease for the ocular surface clinician. |
| Q34869723 | Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse |
| Q38197735 | HDL quality and functionality: what can proteins and genes predict? |
| Q36766976 | High density lipoprotein cholesterol: an evolving target of therapy in the management of cardiovascular disease |
| Q30406862 | High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in The Netherlands: identification and characterization of eight novel mutations |
| Q52509864 | In vitro expression of structural defects in the lecithin-cholesterol acyltransferase gene. |
| Q34021570 | Lecithin: cholesterol acyltransferase--from biochemistry to role in cardiovascular disease |
| Q43719479 | Lecithin:cholesterol acyl transferase G30S: association with atherosclerosis, hypoalphalipoproteinemia and reduced in vivo enzyme activity |
| Q36723319 | Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations |
| Q47788413 | Lipid-free apolipoprotein (apo) A-I is converted into alpha-migrating high density lipoproteins by lipoprotein-depleted plasma of normolipidemic donors and apo A-I-deficient patients but not of Tangier disease patients |
| Q37544267 | Lipoproteins, cholesterol homeostasis and cardiac health |
| Q35665689 | Mapping the eye diseases |
| Q34120460 | Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease |
| Q40836393 | Molecular diagnostics for cardiovascular disease |
| Q24670184 | Nonsynonymous polymorphic sites in the apolipoprotein (apo) A-IV gene are associated with changes in the concentration of apo B- and apo A-I-containing lipoproteins in a normal population |
| Q33791444 | Remodeling adipose tissue through in silico modulation of fat storage for the prevention of type 2 diabetes. |
| Q34404589 | Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol |
| Q28626773 | Structural and functional properties of two mutants of lecithin-cholesterol acyltransferase (T123I and N228K) |
| Q41041206 | T-->G or T-->A mutation introduced in the branchpoint consensus sequence of intron 4 of lecithin:cholesterol acyltransferase (LCAT) gene: intron retention causing LCAT deficiency |
| Q28263895 | The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families |
| Q53750486 | The low down on lipoprotein lipase. |
| Q36307357 | The use of PCR in diagnosing lipoprotein disorders |
| Q24564900 | Two 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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