Reitsma PH - Search Results

1

Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.

Pintao MC, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, Gandrille S, Reitsma PH. Pintao MC, et al. Among authors: reitsma ph. Hum Genet. 2009 Sep;126(3):449-56. doi: 10.1007/s00439-009-0687-9. Epub 2009 May 23. Hum Genet. 2009. PMID: 19466456 Free PMC article.

2

Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiency.

Pintao M, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, Gandrille S, Reitsma PH. Pintao M, et al. Among authors: reitsma ph. Hum Genet. 2010 Jan;127(1):121. Hum Genet. 2010. PMID: 20108435 No abstract available.

3

Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study.

Pintao MC, Ribeiro DD, Bezemer ID, Garcia AA, de Visser MC, Doggen CJ, Lijfering WM, Reitsma PH, Rosendaal FR. Pintao MC, et al. Among authors: reitsma ph. Blood. 2013 Oct 31;122(18):3210-9. doi: 10.1182/blood-2013-04-499335. Epub 2013 Sep 6. Blood. 2013. PMID: 24014240 Free article.

4

Two mutations in the promoter region of the human protein C gene both cause type I protein C deficiency by disruption of two HNF-3 binding sites.

Spek CA, Greengard JS, Griffin JH, Bertina RM, Reitsma PH. Spek CA, et al. Among authors: reitsma ph. J Biol Chem. 1995 Oct 13;270(41):24216-21. doi: 10.1074/jbc.270.41.24216. J Biol Chem. 1995. PMID: 7592627 Free article.

5

Identification of evolutionarily invariant sequences in the protein C gene promoter.

Spek CA, Bertina RM, Reitsma PH. Spek CA, et al. Among authors: reitsma ph. J Mol Evol. 1998 Dec;47(6):663-9. doi: 10.1007/pl00006424. J Mol Evol. 1998. PMID: 9847407

6

Genetic risk factors for venous thrombosis.

Spek CA, Reitsma PH. Spek CA, et al. Among authors: reitsma ph. Mol Genet Metab. 2000 Sep-Oct;71(1-2):51-61. doi: 10.1006/mgme.2000.3051. Mol Genet Metab. 2000. PMID: 11001795 Review. No abstract available.

7

High levels of protein C are determined by PROCR haplotype 3.

Pintao MC, Roshani S, de Visser MC, Tieken C, Tanck MW, Wichers IM, Meijers JC, Rosendaal FR, Middeldorp S, Reitsma PH. Pintao MC, et al. Among authors: reitsma ph. J Thromb Haemost. 2011 May;9(5):969-76. doi: 10.1111/j.1538-7836.2011.04256.x. J Thromb Haemost. 2011. PMID: 21392254 Free article.

8

VKORC1 and the vitamin K cycle.

Garcia AA, Reitsma PH. Garcia AA, et al. Among authors: reitsma ph. Vitam Horm. 2008;78:23-33. doi: 10.1016/S0083-6729(07)00002-7. Vitam Horm. 2008. PMID: 18374188 Review.

9

Genotypic variation in the promoter region of the protein C gene is associated with plasma protein C levels and thrombotic risk.

Spek CA, Koster T, Rosendaal FR, Bertina RM, Reitsma PH. Spek CA, et al. Among authors: reitsma ph. Arterioscler Thromb Vasc Biol. 1995 Feb;15(2):214-8. doi: 10.1161/01.atv.15.2.214. Arterioscler Thromb Vasc Biol. 1995. PMID: 7749828

10

Determination of the allelic and haplotype frequencies of three polymorphisms in the promoter region of the human protein C gene.

Spek CA, Poort SR, Bertina RM, Reitsma PH. Spek CA, et al. Among authors: reitsma ph. Blood Coagul Fibrinolysis. 1994 Apr;5(2):309-11. doi: 10.1097/00001721-199404000-00022. Blood Coagul Fibrinolysis. 1994. PMID: 8054464

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