Borgel D - Search Results

1

Expression and characterization of recombinant protein S with the Ser 460 Pro mutation.

Morboeuf O, Borgel D, Aiach M, Kaabache T, Gandrille S, Gaussem P. Morboeuf O, et al. Among authors: borgel d. Thromb Res. 2000 Oct 1;100(1):81-8. doi: 10.1016/s0049-3848(00)00296-6. Thromb Res. 2000. PMID: 11053620

2

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: borgel d. Blood. 1995 Nov 1;86(9):3436-43. Blood. 1995. PMID: 7579448 Free article.

3

Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene.

Gandrille S, Borgel D, Eschwege-Gufflet V, Aillaud M, Dreyfus M, Matheron C, Gaussem P, Abgrall JF, Jude B, Sie P, et al. Gandrille S, et al. Among authors: borgel d. Blood. 1995 Jan 1;85(1):130-8. Blood. 1995. PMID: 7803790 Free article.

4

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. Blood Coagul Fibrinolysis. 1994 Aug;5(4):593-600. Blood Coagul Fibrinolysis. 1994. PMID: 7841316

5

Five novel mutations of the protein S active gene (PROS 1) in 8 Norman families.

Duchemin J, Borg JY, Borgel D, Vasse M, Lévèque H, Aiach M, Gandrille S. Duchemin J, et al. Among authors: borgel d. Thromb Haemost. 1996 Mar;75(3):437-44. Thromb Haemost. 1996. PMID: 8701404

6

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. 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.

7

First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484-->Pro, in the protein S active gene (PROS1).

Borgel D, Jude B, Aiach M, Gandrille S. Borgel D, et al. Thromb Haemost. 1996 Jun;75(6):883-6. Thromb Haemost. 1996. PMID: 8822580

8

Protein S deficiency.

Borgel D, Gandrille S, Aiach M. Borgel D, et al. Thromb Haemost. 1997 Jul;78(1):351-6. Thromb Haemost. 1997. PMID: 9198178 Review.

9

Protein C and protein S deficiencies.

Aiach M, Borgel D, Gaussem P, Emmerich J, Alhenc-Gelas M, Gandrille S. Aiach M, et al. Among authors: borgel d. Semin Hematol. 1997 Jul;34(3):205-16. Semin Hematol. 1997. PMID: 9241706 Review.

10

Protein S deficiency: a database of mutations. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Gandrille S, Borgel D, Ireland H, Lane DA, Simmonds R, Reitsma PH, Mannhalter C, Pabinger I, Saito H, Suzuki K, Formstone C, Cooper DN, Espinosa Y, Sala N, Bernardi F, Aiach M. Gandrille S, et al. Among authors: borgel d. Thromb Haemost. 1997 Jun;77(6):1201-14. Thromb Haemost. 1997. PMID: 9241758 No abstract available.

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