Aiach M - Search Results

1

Functional properties of the sex-hormone-binding globulin (SHBG)-like domain of the anticoagulant protein S.

Saposnik B, Borgel D, Aiach M, Gandrille S. Saposnik B, et al. Among authors: aiach m. Eur J Biochem. 2003 Feb;270(3):545-55. doi: 10.1046/j.1432-1033.2003.03423.x. Eur J Biochem. 2003. PMID: 12542704 Free article.

2

The gamma-carboxyglutamic acid domain of anticoagulant protein S is involved in activated protein C cofactor activity, independently of phospholipid binding.

Saller F, Villoutreix BO, Amelot A, Kaabache T, Le Bonniec BF, Aiach M, Gandrille S, Borgel D. Saller F, et al. Among authors: aiach m. Blood. 2005 Jan 1;105(1):122-30. doi: 10.1182/blood-2004-06-2176. Epub 2004 Aug 12. Blood. 2005. PMID: 15308562 Free article.

3

Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain.

Borgel D, Gaussem P, Garbay C, Bachelot-Loza C, Kaabache T, Liu WQ, Brohard-Bohn B, Le Bonniec B, Aiach M, Gandrille S. Borgel D, et al. Among authors: aiach m. Biochem J. 2001 Dec 1;360(Pt 2):499-506. doi: 10.1042/0264-6021:3600499. Biochem J. 2001. PMID: 11716779 Free PMC article.

4

Cleaved protein S (PS), total PS, free PS, and activated protein C cofactor activity as risk factors for venous thromboembolism.

Borgel D, Reny JL, Fischelis D, Gandrille S, Emmerich J, Fiessinger JN, Aiach M. Borgel D, et al. Among authors: aiach m. Clin Chem. 2003 Apr;49(4):575-80. doi: 10.1373/49.4.575. Clin Chem. 2003. PMID: 12651809

5

Alternative mRNA is favored by the A3 haplotype of the EPCR gene PROCR and generates a novel soluble form of EPCR in plasma.

Saposnik B, Lesteven E, Lokajczyk A, Esmon CT, Aiach M, Gandrille S. Saposnik B, et al. Among authors: aiach m. Blood. 2008 Apr 1;111(7):3442-51. doi: 10.1182/blood-2007-08-104968. Epub 2007 Dec 11. Blood. 2008. PMID: 18073349 Free PMC article.

6

The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency.

Duchemin J, Gandrille S, Borgel D, Feurgard P, Alhenc-Gelas M, Matheron C, Dreyfus M, Dupuy E, Juhan-Vague I, Aiach M. Duchemin J, et al. Among authors: aiach m. Blood. 1995 Nov 1;86(9):3436-43. Blood. 1995. PMID: 7579448 Free article.

7

First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiency.

Borgel D, Gandrille S, Gouault-Heilmann M, Aiach M. Borgel D, et al. Among authors: aiach m. Blood Coagul Fibrinolysis. 1994 Aug;5(4):593-600. Blood Coagul Fibrinolysis. 1994. PMID: 7841316

8

Scanning method to establish the molecular basis of protein C deficiencies.

Gandrille S, Goossens M, Aiach M. Gandrille S, et al. Among authors: aiach m. Hum Mutat. 1994;4(1):20-30. doi: 10.1002/humu.1380040104. Hum Mutat. 1994. PMID: 7951255

9

Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.

Borgel D, Duchemin J, Alhenc-Gelas M, Matheron C, Aiach M, Gandrille S. Borgel D, et al. Among authors: aiach m. J Lab Clin Med. 1996 Aug;128(2):218-27. doi: 10.1016/s0022-2143(96)90015-3. J Lab Clin Med. 1996. PMID: 8765219 Clinical Trial.

10

Molecular basis for protein C hereditary deficiency.

Aiach M, Gandrille S. Aiach M, et al. Haemostasis. 1996 Oct;26 Suppl 4:9-19. doi: 10.1159/000217280. Haemostasis. 1996. PMID: 8979107 Review.

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