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Differential effects of the loss of intrachain- versus interchain-disulfide bonds in the cystine-knot domain of von Willebrand factor on the clinical phenotype of von Willebrand disease.
Thromb Haemost. 2006 Dec;96(6):717-24. doi: 10.1160/th06-08-0460.
Thromb Haemost. 2006.
PMID: 17139364
G20210A is a functional mutation in the prothrombin gene; effect on protein levels and 3'-end formation.
Ceelie H, Spaargaren-van Riel CC, Bertina RM, Vos HL.
Ceelie H, et al. Among authors: spaargaren van riel cc.
J Thromb Haemost. 2004 Jan;2(1):119-27. doi: 10.1111/j.1538-7836.2003.00493.x.
J Thromb Haemost. 2004.
PMID: 14717975
Free article.
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Functional characterization of transcription factor binding sites for HNF1-alpha, HNF3-beta (FOXA2), HNF4-alpha, Sp1 and Sp3 in the human prothrombin gene enhancer.
Ceelie H, Spaargaren-Van Riel CC, De Jong M, Bertina RM, Vos HL.
Ceelie H, et al. Among authors: spaargaren van riel cc.
J Thromb Haemost. 2003 Aug;1(8):1688-98. doi: 10.1046/j.1538-7836.2003.00393.x.
J Thromb Haemost. 2003.
PMID: 12911579
Free article.
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Functional analysis of two polymorphisms in the 3'-UTR of the human prothrombin gene.
Ceelie H, Spaargaren-Van Riel CC, Lyon E, Bertina RM, Vos HL.
Ceelie H, et al. Among authors: spaargaren van riel cc.
J Thromb Haemost. 2005 Apr;3(4):806-8. doi: 10.1111/j.1538-7836.2005.01241.x.
J Thromb Haemost. 2005.
PMID: 15842380
Free article.
No abstract available.
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Functional analysis of two prothrombin 3'-untranslated region variants: the C20209T variant, mainly found among African-Americans, and the C20209A variant.
van der Putten HH, Spaargaren-van Riel CC, Bertina RM, Vos HL.
van der Putten HH, et al. Among authors: spaargaren van riel cc.
J Thromb Haemost. 2006 Oct;4(10):2285-7; author reply 2288-9. doi: 10.1111/j.1538-7836.2006.02102.x. Epub 2006 Jun 23.
J Thromb Haemost. 2006.
PMID: 16796711
Free article.
No abstract available.
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