184 related articles for article (PubMed ID: 17849047)
1. Exclusion of the alpha2 subunit of platelet-activating factor acetylhydrolase 1b (PAFAH1B2) as a prothrombotic gene in a protein C-deficient kindred and population-based case-control sample.
Hasstedt SJ; Scott BT; Rosendaal FR; Callas PW; Vossen CY; Long GL; Bovill EG
Thromb Haemost; 2007 Sep; 98(3):587-92. PubMed ID: 17849047
[TBL] [Abstract][Full Text] [Related]
2. Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.
Scott BT; Bovill EG; Callas PW; Hasstedt SJ; Leppert MF; Valliere JE; Varvil TS; Long GL
Thromb Haemost; 2001 Jan; 85(1):82-7. PubMed ID: 11204593
[TBL] [Abstract][Full Text] [Related]
3. Cell adhesion molecule 1: a novel risk factor for venous thrombosis.
Hasstedt SJ; Bezemer ID; Callas PW; Vossen CY; Trotman W; Hebbel RP; Demers C; Rosendaal FR; Bovill EG
Blood; 2009 Oct; 114(14):3084-91. PubMed ID: 19643986
[TBL] [Abstract][Full Text] [Related]
4. Genome scan of venous thrombosis in a pedigree with protein C deficiency.
Hasstedt SJ; Scott BT; Callas PW; Vossen CY; Rosendaal FR; Long GL; Bovill EG
J Thromb Haemost; 2004 Jun; 2(6):868-73. PubMed ID: 15140118
[TBL] [Abstract][Full Text] [Related]
5. Polymorphisms in the protein C gene as risk factor for venous thrombosis.
Pomp ER; Doggen CJ; Vos HL; Reitsma PH; Rosendaal FR
Thromb Haemost; 2009 Jan; 101(1):62-7. PubMed ID: 19132190
[TBL] [Abstract][Full Text] [Related]
6. The G20210A prothrombin polymorphism is not associated with increased thromboembolic risk in a large protein C deficient kindred.
Bovill EG; Hasstedt SJ; Callas PW; Valliere JE; Scott BT; Bauer KA; Long GL
Thromb Haemost; 2000 Mar; 83(3):366-70. PubMed ID: 10744139
[TBL] [Abstract][Full Text] [Related]
7. Haplotypes of IL1B, IL1RN, IL1R1, and IL1R2 and the risk of venous thrombosis.
van Minkelen R; de Visser MC; Houwing-Duistermaat JJ; Vos HL; Bertina RM; Rosendaal FR
Arterioscler Thromb Vasc Biol; 2007 Jun; 27(6):1486-91. PubMed ID: 17413037
[TBL] [Abstract][Full Text] [Related]
8. Hereditary basis of protein C deficiency (PCD) in thrombosis patients: first report from India.
Pai N; Shetty S; Idicula-Thomas S; Kulkarni B; Ghosh K
Thromb Haemost; 2009 Apr; 101(4):785-7. PubMed ID: 19350130
[No Abstract] [Full Text] [Related]
9. Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.
Tjeldhorn L; Sandset PM; Haugbro K; Skretting G
Thromb Res; 2010 Mar; 125(3):230-4. PubMed ID: 19535131
[TBL] [Abstract][Full Text] [Related]
10. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.
Ireland H; Thompson E; Lane DA
Thromb Haemost; 1996 Dec; 76(6):867-73. PubMed ID: 8972002
[TBL] [Abstract][Full Text] [Related]
11. P-selectin gene haplotypes modulate soluble P-selectin concentrations and contribute to the risk of venous thromboembolism.
Ay C; Jungbauer LV; Kaider A; Koder S; Panzer S; Pabinger I; Mannhalter C
Thromb Haemost; 2008 May; 99(5):899-904. PubMed ID: 18449419
[TBL] [Abstract][Full Text] [Related]
12. Haplotypes encoding the factor VIII 1241 Glu variation, factor VIII levels and the risk of venous thrombosis.
Nossent AY; Eikenboom JC; Vos HL; Bakker E; Tanis BC; Doggen CJ; Bertina RM; Rosendaal FR
Thromb Haemost; 2006 Jun; 95(6):942-8. PubMed ID: 16732372
[TBL] [Abstract][Full Text] [Related]
13. Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients.
Altinisik J; Ates O; Ulutin T; Cengiz M; Buyru N
Clin Appl Thromb Hemost; 2008 Oct; 14(4):415-20. PubMed ID: 18160601
[TBL] [Abstract][Full Text] [Related]
14. Candidate gene approach in association studies: would the factor V Leiden mutation have been found by this approach?
van Hylckama Vlieg A; Sandkuijl LA; Rosendaal FR; Bertina RM; Vos HL
Eur J Hum Genet; 2004 Jun; 12(6):478-82. PubMed ID: 15054398
[TBL] [Abstract][Full Text] [Related]
15. Evidence of a founder effect for the protein C gene 3363 inserted C mutation in thrombophilic pedigrees of French origin.
Couture P; Bovill EG; Demers C; Simard J; Delage R; Scott BT; Valliere JE; Callas PW; Jomphe M; Rosendaal FR; Aiach M; Long GL
Thromb Haemost; 2001 Oct; 86(4):1000-6. PubMed ID: 11686315
[TBL] [Abstract][Full Text] [Related]
16. R147W mutation of PROC gene is common in venous thrombotic patients in Taiwanese Chinese.
Tsay W; Shen MC
Am J Hematol; 2004 May; 76(1):8-13. PubMed ID: 15114590
[TBL] [Abstract][Full Text] [Related]
17. Thrombin generation in first-degree relatives of patients with venous thromboembolism who have factor V Leiden. A pilot study.
Couturaud F; Duchemin J; Leroyer C; Delahousse B; Abgrall JF; Mottier D;
Thromb Haemost; 2008 Jan; 99(1):223-8. PubMed ID: 18217158
[TBL] [Abstract][Full Text] [Related]
18. [Type I protein C deficiency caused by a novel protein C gene mutation].
Zheng Y; Zhu D; Zhou B
Zhonghua Xue Ye Xue Za Zhi; 1998 Mar; 19(3):138-42. PubMed ID: 11243145
[TBL] [Abstract][Full Text] [Related]
19. [A point mutation of protein C gene in a congenital protein C deficiency pedigree].
Liu L; Guo WR; He LS; Mu H; Jiang Y; Huang FQ; Li JZ
Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):115-8. PubMed ID: 12697119
[TBL] [Abstract][Full Text] [Related]
20. Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
Boinot C; Borgel D; Kitzis A; Guicheteau M; Aiach M; Alhenc-Gelas M
Blood Coagul Fibrinolysis; 2003 Feb; 14(2):191-6. PubMed ID: 12632031
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]