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S Gandrille

Showing results (51-60 of 64) with videos related to

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Thrombosis and Haemostasis|March 4, 1999
The factor V gene A4070G mutation and the risk of venous thrombosisM Alhenc-Gelas, V Nicaud, S Gandrille, et al.
Blood|July 1, 1995
Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. The French Network on the behalf of INSERMS Gandrille, J S Greengard, M Alhenc-Gelas, et al.
Human Mutation|January 1, 1992
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresisS Gandrille, M Vidaud, M Aiach, et al.
Blood|November 1, 1995
The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiencyJ Duchemin, S Gandrille, D Borgel, et al.
The Journal of Biological Chemistry|November 5, 1990
Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamineS Gandrille, M Aiach, D A Lane, et al.
Blood|January 1, 1995
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 geneS Gandrille, D Borgel, V Eschwege-Gufflet, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiencyMaria Pintao, A A Garcia, D Borgel, et al.
The Biochemical Journal|November 22, 2001
Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domainD Borgel, P Gaussem, C Garbay, et al.
Human Genetics|May 26, 2009
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiencyMaria C Pintao, A A Garcia, D Borgel, et al.
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain functionM Baroni, G Mazzola, T Kaabache, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Thrombosis and Haemostasis|March 4, 1999
The factor V gene A4070G mutation and the risk of venous thrombosisM Alhenc-Gelas, V Nicaud, S Gandrille, et al.
Blood|July 1, 1995
Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. The French Network on the behalf of INSERMS Gandrille, J S Greengard, M Alhenc-Gelas, et al.
Human Mutation|January 1, 1992
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresisS Gandrille, M Vidaud, M Aiach, et al.
Blood|November 1, 1995
The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiencyJ Duchemin, S Gandrille, D Borgel, et al.
The Journal of Biological Chemistry|November 5, 1990
Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamineS Gandrille, M Aiach, D A Lane, et al.
Blood|January 1, 1995
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 geneS Gandrille, D Borgel, V Eschwege-Gufflet, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiencyMaria Pintao, A A Garcia, D Borgel, et al.
The Biochemical Journal|November 22, 2001
Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domainD Borgel, P Gaussem, C Garbay, et al.
Human Genetics|May 26, 2009
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiencyMaria C Pintao, A A Garcia, D Borgel, et al.
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain functionM Baroni, G Mazzola, T Kaabache, et al.
Pageof 7