Scott BT - Search Results

1

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: scott bt. 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.

2

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: scott bt. Thromb Haemost. 2000 Mar;83(3):366-70. Thromb Haemost. 2000. PMID: 10744139

3

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. Thromb Haemost. 2001 Jan;85(1):82-7. Thromb Haemost. 2001. PMID: 11204593

4

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. Blood Coagul Fibrinolysis. 2002 Sep;13(6):519-31. doi: 10.1097/00001721-200209000-00007. Blood Coagul Fibrinolysis. 2002. PMID: 12192304

5

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: scott bt. 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.

6

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: scott bt. Thromb Haemost. 2007 Sep;98(3):587-92. Thromb Haemost. 2007. PMID: 17849047

7

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. Couture P, et al. Among authors: scott bt. Thromb Haemost. 2001 Oct;86(4):1000-6. Thromb Haemost. 2001. PMID: 11686315

8

A genome search for genetic determinants of markers of protein C activation.

Vossen CY, Hasstedt SJ, Scott BT, Rosendaal FR, Bovill EG. Vossen CY, et al. Among authors: scott bt. J Thromb Haemost. 2006 Mar;4(3):706-8. doi: 10.1111/j.1538-7836.2006.01810.x. J Thromb Haemost. 2006. PMID: 16460468 Free article. No abstract available.

9

Novel isoforms of intracellular platelet activating factor acetylhydrolase (PAFAH1b2) in human testis; encoded by alternatively spliced mRNAs.

Scott BT, Olson N, Long GL, Bovill EG. Scott BT, et al. Prostaglandins Other Lipid Mediat. 2008 Mar;85(3-4):69-80. doi: 10.1016/j.prostaglandins.2007.10.005. Epub 2007 Nov 9. Prostaglandins Other Lipid Mediat. 2008. PMID: 18155631 Free PMC article.

10

HuR/Cx40 downregulation causes coronary microvascular dysfunction in type 2 diabetes.

Si R, Cabrera JTO, Tsuji-Hosokawa A, Guo R, Watanabe M, Gao L, Lee YS, Moon JS, Scott BT, Wang J, Ashton AW, Rao JN, Wang JY, Yuan JX, Makino A. Si R, et al. Among authors: scott bt. JCI Insight. 2021 Nov 8;6(21):e147982. doi: 10.1172/jci.insight.147982. JCI Insight. 2021. PMID: 34747371 Free PMC article.

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