Long GL - Search Results

1

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. Bovill EG, et al. Among authors: long gl. Thromb Haemost. 2000 Mar;83(3):366-70. Thromb Haemost. 2000. PMID: 10744139

2

No effect of the prothrombin G20210A mutation on protein C activation in a large kindred with type I protein C deficiency.

Vossen CY, Strandberg K, Stenflo J, Rosendaal FR, Callas PW, Long GL, Bovill EG. Vossen CY, et al. Among authors: long gl. Blood Coagul Fibrinolysis. 2004 Oct;15(7):573-6. doi: 10.1097/00001721-200410000-00007. Blood Coagul Fibrinolysis. 2004. PMID: 15389124

3

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. Hasstedt SJ, et al. Among authors: long gl. Thromb Haemost. 2007 Sep;98(3):587-92. Thromb Haemost. 2007. PMID: 17849047

4

Genetic analysis of a large kindred exhibiting type I protein C deficiency and associated thrombosis.

Tomczak JA, Ando RA, Sobel HG, Bovill EG, Long GL. Tomczak JA, et al. Among authors: long gl. Thromb Res. 1994 May 1;74(3):243-54. doi: 10.1016/0049-3848(94)90112-0. Thromb Res. 1994. PMID: 7913773

5

Hereditary thrombophilia as a model for multigenic disease.

Bovill EG, Hasstedt SJ, Leppert MF, Long GL. Bovill EG, et al. Among authors: long gl. Thromb Haemost. 1999 Aug;82(2):662-6. Thromb Haemost. 1999. PMID: 10605765 Review. No abstract available.

6

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. Scott BT, et al. Among authors: long gl. Thromb Haemost. 2001 Jan;85(1):82-7. Thromb Haemost. 2001. PMID: 11204593

7

Characterization of the human prostaglandin H synthase 1 gene (PTGS1): exclusion by genetic linkage analysis as a second modifier gene in familial thrombosis.

Scott BT, Hasstedt SJ, Bovill EG, Callas PW, Valliere JE, Wang L, Wu KK, Long GL. Scott BT, et al. Among authors: long gl. Blood Coagul Fibrinolysis. 2002 Sep;13(6):519-31. doi: 10.1097/00001721-200209000-00007. Blood Coagul Fibrinolysis. 2002. PMID: 12192304

8

Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C-deficient family.

Vossen CY, Hasstedt SJ, Rosendaal FR, Callas PW, Bauer KA, Broze GJ, Hoogendoorn H, Long GL, Scott BT, Bovill EG. Vossen CY, et al. Among authors: long gl. J Thromb Haemost. 2004 Feb;2(2):242-7. doi: 10.1111/j.1538-7933.2003.00592.x. J Thromb Haemost. 2004. PMID: 14995985 Free article.

9

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. Hasstedt SJ, et al. Among authors: long gl. J Thromb Haemost. 2004 Jun;2(6):868-73. doi: 10.1111/j.1538-7836.2004.00663.x. J Thromb Haemost. 2004. PMID: 15140118 Free article.

10

A genetic basis for the interrelation of coagulation factors.

Vossen CY, Callas PW, Hasstedt SJ, Long GL, Rosendaal FR, Bovill EG. Vossen CY, et al. Among authors: long gl. J Thromb Haemost. 2007 Sep;5(9):1930-5. doi: 10.1111/j.1538-7836.2007.02678.x. J Thromb Haemost. 2007. PMID: 17723132 Free article.

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