The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.
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The role of genetics in the risk of thromboembolism: prothrombin 20210A and oral contraceptive therapy.The effect of factor V Leiden carriage on maternal and fetal healthReview and management of patients with the prothrombin G20210A polymorphism.Thrombophilia, polymorphisms, and vascular diseaseGene polymorphisms of the haemostatic system and the risk of arterial thrombotic disease.Update on selected inherited venous thrombotic disorders.Clinical significance of gene-diagnosis for defects in coagulation factors and inhibitors.G20210A prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects.Implications of polyadenylation in health and disease.Different outcome of six homozygotes for prothrombin A20210A gene variantFactor VLeiden and prothrombin G20210A gene polymorphisms in patients with coronary artery disease.Elevated prothrombin promotes venous, but not arterial, thrombosis in mice.Association of C677T MTHFR and G20210A FII prothrombin polymorphisms with susceptibility to myocardial infarctionFrequency and association of 1691 (G>A) FVL, 20210 (G>A) PT and 677 (C>T) MTHFR with deep vein thrombosis in the population of Bosnia and Herzegovina.Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controlsGenetic aspects of ischemic stroke: coagulation, homocysteine, and lipoprotein metabolism as potential risk factors.The prothrombin 20209 C-->T mutation in Jewish-Moroccan Caucasians: molecular analysis of gain-of-function of 3' end processing.Which are the most common thrombophilic genetic nucleotide polymorphisms in infertile women undergoing an IVF cycle?G20210A is a functional mutation in the prothrombin gene; effect on protein levels and 3'-end formation.VKORC1 -1639 G>A Polymorphism in Romanian Patients With Deep Vein Thrombosis.The relationship between factor V Leiden, prothrombin G20210A, and MTHFR mutations and the first major thrombotic episode in polycythemia vera and essential thrombocythemia.Thrombophilic risk factors in patients with severe carotid atherosclerosis.Prothrombin G20210A and factor V Leiden polymorphisms in stroke.Varied association of prothrombin G20210A polymorphism with coronary artery disease susceptibility in different ethnic groups: evidence from 15,041 cases and 21,507 controls.Prothrombotic coagulation defects and cardiovascular risk factors in young women with acute myocardial infarction.Venous thromboembolism, oral contraceptives and high prothrombin levels.Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster.The factor V Glu1608Lys mutation is recurrent in familial thrombophilia.
P2860
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P2860
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
The heterozygous 20210 G/A pro ...... n frequency in artery disease.
@en
The heterozygous 20210 G/A pro ...... n frequency in artery disease.
@nl
type
label
The heterozygous 20210 G/A pro ...... n frequency in artery disease.
@en
The heterozygous 20210 G/A pro ...... n frequency in artery disease.
@nl
prefLabel
The heterozygous 20210 G/A pro ...... n frequency in artery disease.
@en
The heterozygous 20210 G/A pro ...... n frequency in artery disease.
@nl
P2093
P1476
The heterozygous 20210 G/A pro ...... n frequency in artery disease.
@en
P2093
Ardissino D
Bernardi F
Castoldi E
Cavallari E
Ferraresi P
Marchetti G
Palareti G
P304
P356
10.1161/01.ATV.17.11.2418
P407
P577
1997-11-01T00:00:00Z