Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery disease.
about
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.Benefits and risks assessment of simvastatin in familial hypercholesterolaemia.New Approaches in Detection and Treatment of Familial HypercholesterolemiaThe plasma concentration of HDL-associated apoM is influenced by LDL receptor-mediated clearance of apoB-containing particles.Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.Apolipoprotein polymorphisms and familial hypercholesterolemia.Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries.Strengthening causal inference in cardiovascular epidemiology through Mendelian randomization.Sib-pair analysis detects elevated Lp(a) levels and large variation of Lp(a) concentration in subjects with familial defective ApoBDefining the role of lipoprotein apheresis in the management of familial hypercholesterolemia.Molecular characterization of Iranian patients with possible familial hypercholesterolemiaMolecular diagnostics for cardiovascular disease.Familial defective apolipoprotein B-100: a cause of hypercholesterolemia and early coronary heart disease.Randomised by (your) god: robust inference from an observational study design.Detection of apoB-100 R3500Q mutation by competitive allele-specific polymerase chain reaction.Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry.Molecular description of familial defective APOB-100 in Malaysia.Association between apolipoprotein B genetic polymorphism and the risk of calcific aortic stenosis in Chinese subjects, in Xinjiang, China.
P2860
Q30419436-563F1BF8-48FD-447D-A8BA-DD4340AE47A8Q36081978-F0226B83-3516-4E4C-85D5-729534D38F77Q36177473-C2405CAC-0248-4EE8-9D2B-AAE0A941B7A8Q36213916-9FC145A1-78BC-4E2C-988E-4C11EFA5CDF7Q36249248-7F5629E9-020B-4F2F-A6C3-DCE481C20754Q36966031-BD0D0AFA-0ABD-4C40-B0DE-54DB8BB8E074Q36966952-8C27385D-D6DC-43F8-BDF8-1981A1A676A3Q37209749-473D426A-989E-4AD6-8554-9474190B85E0Q37366904-088B2FE9-5A7F-4127-8FED-94D2947A141CQ37965588-651E6173-2A2A-41EA-8996-EB01261AD287Q38266454-01C5CD36-A33C-4CB7-BC0A-5585E72683C9Q40836393-EC977CAD-1E74-425B-A9DE-AA8265A29185Q40874969-ACF748E1-75A3-43C5-B03E-F72F0F6F90EAQ43159238-B7AF248B-C2E0-464F-ACDB-DD4F04EFB184Q43749230-795593A0-1E14-45DE-BACC-FB35FAF5768AQ45041602-2F58F2C0-84C3-4530-B778-C4D0AC1B53E4Q50899557-1D9EB80F-2764-44BC-9D7F-6F89B45D2E90Q52668852-84F04E50-CB23-4595-8A73-52ED128095ED
P2860
Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery disease.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Familial defective apolipoprot ...... ature coronary artery disease.
@ast
Familial defective apolipoprot ...... ature coronary artery disease.
@en
type
label
Familial defective apolipoprot ...... ature coronary artery disease.
@ast
Familial defective apolipoprot ...... ature coronary artery disease.
@en
prefLabel
Familial defective apolipoprot ...... ature coronary artery disease.
@ast
Familial defective apolipoprot ...... ature coronary artery disease.
@en
P1433
P1476
Familial defective apolipoprot ...... ature coronary artery disease.
@en
P2093
Humphries SE
Tybjaerg-Hansen A
P304
P356
10.1016/0021-9150(92)90056-M
P577
1992-10-01T00:00:00Z