About: Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families

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About: Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families Goto Sponge NotDistinct Permalink

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description	article (en) wetenschappelijk artikel (nl) wüsseschaftlicher Artikel, wo im Johr 2000 veröffentlicht worden isch (gsw) наукова стаття, опублікована в грудні 2001 (uk) im Januar 2000 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56982669-62334EE6-654C-4D3E-9F72-C74420AF01B5
publication date	2000-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q56982669-09361FFE-4A75-4F30-B646-3863B67816A6 wds:Q56982669-0D8EB26C-9FF8-4A89-A76A-5B59EC5BBB08 wds:Q56982669-0E5F8570-2253-4E36-943E-56F609458528 wds:Q56982669-1736440A-4B11-43E9-9DDC-74B669D061C8 wds:Q56982669-1E21D5F6-18F0-47E5-80F7-2C46FE0712FD wds:Q56982669-288A0E34-A4B1-4472-BFA5-151065A3EB67 wds:Q56982669-3A89B1E5-302F-4015-932E-96AB674C4A15 wds:Q56982669-480F7E19-1057-489A-985A-CF6FCC20DA13 wds:Q56982669-4A5EBE36-8036-4903-A94B-00B6AE8C52B2 wds:Q56982669-4F6447B7-1656-47CE-B6B1-F081E20870F3 wds:Q56982669-62DBD3BF-806D-4ED4-8308-1E3A37721783 wds:Q56982669-64946921-381F-49CB-9B80-3B2EECB7280F wds:Q56982669-65CB5BE3-A8B8-4CFA-845E-E3B17C1DF090 wds:Q56982669-75590A18-0731-4B58-B56F-83D402278952 wds:Q56982669-7B595C26-00C1-4579-90FC-71C89FAD38A7 wds:Q56982669-830A231F-52D1-4457-AA20-68B14EFD13E6 wds:Q56982669-8316E85B-1FEA-4303-9856-5E61D9DBF0DE wds:Q56982669-8B816BF3-C101-4B39-9381-73C290E48390 wds:Q56982669-A6730BEA-FE0D-414C-B787-EAA463AB9E68 wds:Q56982669-A82917F1-FB89-4B49-936D-5D2BA81E8FBF wds:Q56982669-B201E197-0CBA-4853-83C9-7135E3CECF5D wds:Q56982669-B54D15E5-B52E-40BA-827E-AC0A648E566F wds:Q56982669-BACB7C22-8ABA-46ED-AE1B-29208A92B079 wds:Q56982669-CAC37F20-1E98-4062-B4CB-A25CFA0D9616 wds:Q56982669-CB694D1F-5BBA-41E0-BA6A-DC367BA8CFFB wds:Q56982669-D1E82498-27DD-46AD-9CDD-008D4DC60F67 wds:Q56982669-E6DC57AC-65FD-47E0-A8FB-23F38233FCC8 wds:Q56982669-E7C8E8E1-A076-4546-97DA-0D768BC914AC wds:Q56982669-F048ED5C-EB5E-42A2-B48A-A7977ACC396B
cites work	Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes Model misspecification and multipoint linkage analysis Efficient computation of lod scores: genotype elimination, genotype redefinition, and hybrid maximum likelihood algorithms. Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23 Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia Familial lipoprotein disorders in patients with premature coronary artery disease Mapping a gene for combined hyperlipidaemia in a mutant mouse strain. Family study of serum lipids and lipoproteins in coronary heart-disease An extended transmission/disequilibrium test (TDT) for multi-allele marker loci. Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24 Association of coronary atherosclerosis with hyperapobetalipoproteinemia [increased protein but normal cholesterol levels in human plasma low density (beta) lipoproteins] Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results Linkage of atherogenic lipoprotein phenotype to the low density lipoprotein receptor locus on the short arm of chromosome 19 Plasma triglyceride as a risk factor for coronary heart disease. The epidemiologic evidence and beyond Ath-1, a gene determining atherosclerosis susceptibility and high density lipoprotein levels in mice Retinoid-induced hypertriglyceridemia in rats is mediated by retinoic acid receptors Abnormal spermatogenesis in RXR beta mutant mice. Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels RXR agonists activate PPARalpha-inducible genes, lower triglycerides, and raise HDL levels in vivo Peroxisome proliferator-activated receptor gamma gene locus is related to body mass index and lipid values in healthy nonobese subjects. Oligonucleotide ligation assay (OLA) for the diagnosis of familial hypercholesterolemia. Familial dyslipidemic hypertension. Evidence from 58 Utah families for a syndrome present in approximately 12% of patients with essential hypertension Inhibition of the metabolism of endogenous retinoic acid as treatment for severe psoriasis: an open study with oral liarozole. A bootstrap approach to estimating power for linkage heterogeneity Heritability analysis of lipids and three gene loci in twins link the macrophage scavenger receptor to HDL cholesterol concentrations A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype. Approaches to the genetics of cardiovascular disease through genetic field work.
author name string	wds:Q56982669-01E54CF7-F4E5-4324-B16C-41D06AB6DA73 wds:Q56982669-3092D93A-0EAD-44C2-8E2B-6ECC4EA19146 wds:Q56982669-34E3A0D5-A40C-4F1B-BD27-EE2EDAEABB70 wds:Q56982669-4FE2293C-A690-45EA-A2FF-448B7742FF3A wds:Q56982669-8F363BFD-A3DC-4CCE-BAE8-C2EEFFE664D6 wds:Q56982669-B9626BFE-9B96-4F69-90BF-9325B9A655D4 wds:Q56982669-CEB2CF29-17A0-4F0C-A966-046AA162A224 wds:Q56982669-E1EE4F38-8697-449B-A8FE-2B46EA501411 wds:Q56982669-FE47A4A0-8BEF-4480-9844-DEBF8E31CA20
author name string	X Wu L Liu B Müller-Myhsok W Pei R Hui H Schuster H Baron H Knoblauch S A Al-Yahyaee
rdfs:label	Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families (en) Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families (nl)
skos:prefLabel	Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families (en) Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families (nl)
name	Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families (en) Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families (nl)
author	wds:Q56982669-773D5A67-6BB5-468A-9C2D-09F81D051FCE wds:Q56982669-B9F6091F-CBF1-4030-B7C0-8FF4AF723CE1
author	Andreas Busjahn Friedrich C. Luft
title	wds:Q56982669-F7D4FF40-67D7-4F78-BE1E-4C6A5C1D24F7
title	Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families (en)
page(s)	wds:Q56982669-F74FF039-EAE0-441E-9DD6-0290A4ECA384
page(s)	29-34
instance of	wds:Q56982669-DAF33E5C-3FD2-4FD6-989B-FFF957A6AA3F
instance of	scholarly article

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