Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia.
about
A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT projectThe epidemiology of venous thromboembolismProgress in research into the genes associated with venous thromboembolismA genome-wide association study of the Protein C anticoagulant pathwayGenetics of venous thrombosis: insights from a new genome wide association studyGenetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke.Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.Design and establishment of a biobank in a multicenter prospective cohort study of elderly patients with venous thromboembolism (SWITCO65+).Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies.Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes.Genome-wide investigation of DNA methylation marks associated with FV Leiden mutation.Study of associated genetic variants in Indian subjects reveals the basis of ethnicity related differences in susceptibility to venous thromboembolism.Modifier genes in haemophilia: their expansion in the human genome.Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins?Genetic variants of coagulation factor XI show association with ischemic stroke up to 70 years of age.Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolismMultilocus genetic risk scores for venous thromboembolism risk assessment.Novel family-based approaches to genetic risk in thrombosis.The 3' end prothrombin gene variants in serbian patients with idiopathic thrombophilia.A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels.Genetic Determinants of Thrombin Generation and Their Relation to Venous Thrombosis: Results from the GAIT-2 ProjectGenetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery diseaseA genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.Venous thromboembolism: disease burden, outcomes and risk factors.The Central Role of KNG1 Gene as a Genetic Determinant of Coagulation Pathway-Related Traits: Exploring Metaphenotypes.Dissecting the genetic determinants of hemostasis and thrombosisGenetic risk factors in patients with deep venous thrombosis, a retrospective case control study on Iranian populationIdentification of quantitative trait loci for fibrin clot phenotypes: the EuroCLOT studyGenetic polymorphisms associated with carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention StudyPersonalized genomic medicine: a future prerequisite for the prevention of coronary artery disease.Common genetic risk factors for venous thrombosis in the Chinese populationGenetic association of PROC variants with pulmonary embolism in Northern Chinese Han population.Ischemic stroke is associated with the ABO locus: the EuroCLOT studyUSAT: A Unified Score-Based Association Test for Multiple Phenotype-Genotype Analysis.Novel genetic predictors of venous thromboembolism risk in African Americans.Elevated factor VIII level and stroke in patients without traditional risk factors associated with cardiovascular diseases.A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels
P2860
Q24530955-CE912733-4744-4113-AC21-1400C4C2E229Q28067893-4672FE26-A80A-4D00-996E-6B3F6ACF5146Q28084640-B16AABD0-C63E-4952-8D16-54469A856483Q28478614-BCEA54B9-A217-44B2-8FD9-39F42254006AQ28744518-C79CC945-50B0-4035-B055-C34CA5C5986EQ30279042-ED83F653-0355-43D2-81EE-8BC3A5011518Q30300355-4FE4D6F3-48E3-48E5-A658-9D086FD25D38Q31113588-D2CFD86A-1601-401C-832C-982FDF621819Q31115221-38876378-DC32-4B4B-8EC8-6EE73AED8A89Q33772986-1F8876A2-64C5-4504-9CE6-DDFBC6E229BAQ33782720-6E59F2E2-6D35-4D9E-A523-F7D1D297B56CQ33931897-2F83E40F-9EC5-45CA-87FD-B0C2DC3EFD0EQ34165506-F26FBE19-39FF-4FBB-8F76-687239929AF1Q34263842-1416E9CC-6E32-47E8-B5F8-974F5C5C4ED9Q34346972-D73652F8-9C67-4F42-8DEF-E2E27AFA43A6Q34636953-EB5EB0D0-991D-42FC-9933-44B6A7B638D7Q34738273-3F4273D8-CBE4-45B2-BE16-DB36F8DF4826Q35005516-11C8FBD1-9BC9-47A2-803A-2D45BC0AA18DQ35032797-A45B3750-2F2B-4A1F-97CC-BB4874511BF0Q35070627-76687158-2D7F-4D12-93BC-1AFC6A024319Q35181584-B8CCDFC9-05CF-424E-AF1F-564DF83AB69BQ35549649-07A60871-371E-4BD9-998A-A13CBBADF054Q35804461-0B19BC03-A756-4EAB-9A1E-D6A0670CEA41Q35897688-B4D8681C-4316-4724-BE82-DD167A6A34EBQ36096131-21EDE64F-CF14-4F3C-820A-9A08BF733936Q36166323-FFDFA522-953F-42E5-B4D6-9780AFBCDF34Q36230821-898F2C92-1F3F-4548-BCAA-D704E2914F40Q36231412-A48296F6-8026-4CAB-82D7-59815B1861D0Q36259417-CEA6D78C-923D-4BDA-8E66-31344DD88D01Q36267584-0BE8D8B0-8F1C-4C32-B582-9816CD5CDB5BQ36429404-64B48975-5C17-4922-B7BB-0907CA0F39A1Q36537470-4FCF8DA4-ECF2-4D27-AA84-972747301758Q36559160-0706B21C-E0A0-459E-B402-5FCC5DF82874Q36595087-BB9D4241-0CD6-42F8-A7A7-6C9CCC1E1201Q36610096-D14F6CCA-2F1B-4415-9BC5-A5D9F7CA85F1Q36637803-7D4D8A74-DAEE-445E-AF1E-0B609D54C747Q36671949-639388D3-59B5-48B0-BAD4-351EA1CD48CFQ36800467-10E9AAD9-3DF0-41ED-AD20-6F17643FCC69Q36944538-FAE1A159-DA69-4D7B-819D-AF3A2DA9FFD7Q36992117-8544C010-5977-43C8-9C37-4CCA458275A3
P2860
Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia.
description
2000 nî lūn-bûn
@nan
2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@ast
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@en
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@nl
type
label
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@ast
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@en
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@nl
prefLabel
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@ast
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@en
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@nl
P2093
P2860
P356
P1476
Genetic susceptibility to thro ...... s of Idiopathic Thrombophilia.
@en
P2093
F Blanco-Vaca
J Blangero
J Fontcuberta
P2860
P304
P356
10.1086/316903
P407
P50
P577
2000-10-19T00:00:00Z