Négrier C - Search Results

1

Early septic shock induces loss of oxidative phosphorylation yield plasticity in liver mitochondria.

Eyenga P, Roussel D, Morel J, Rey B, Romestaing C, Teulier L, Sheu SS, Goudable J, Négrier C, Viale JP. Eyenga P, et al. Among authors: negrier c. J Physiol Biochem. 2014 Jun;70(2):285-96. doi: 10.1007/s13105-013-0280-5. Epub 2014 Feb 26. J Physiol Biochem. 2014. PMID: 24570093

2

The potential role of synovial thrombomodulin in the pathophysiology of joint bleeds in haemophilia.

Dargaud Y, Simpson H, Chevalier Y, Scoazec JY, Hot A, Guyen O, Baglin T, Négrier C. Dargaud Y, et al. Among authors: negrier c. Haemophilia. 2012 Sep;18(5):818-23. doi: 10.1111/j.1365-2516.2012.02809.x. Epub 2012 Apr 25. Haemophilia. 2012. PMID: 22533488

3

Usefulness of an in vitro cellular expression model for haemophilia A carrier diagnosis: illustration with five novel mutations in the F8 gene in women with isolated factor VIII:C deficiency.

Roualdes O, Nougier C, Fretigny M, Talagrand E, Durand B, Negrier C, Vinciguerra C. Roualdes O, et al. Among authors: negrier c. Haemophilia. 2015 May;21(3):e202-e209. doi: 10.1111/hae.12651. Epub 2015 Feb 24. Haemophilia. 2015. PMID: 25708597

4

Potential limits of AAV-based gene therapy with the use of new transgenes expressing factor IX fusion proteins.

Le Quellec S, Dane A, Enjolras N, McIntosh J, Rosales C, Negrier C, Nathwani A. Le Quellec S, et al. Among authors: negrier c. Haemophilia. 2019 Jan;25(1):e11-e18. doi: 10.1111/hae.13651. Epub 2018 Dec 6. Haemophilia. 2019. PMID: 30520547

5

Recombinant Adeno-Associated Viral Vectors Expressing Human Coagulation FIX-E456H Variant in Hemophilia B Mice.

Le Quellec S, Dane AP, Barbon E, Bordet JC, Mingozzi F, Dargaud Y, Marais T, Biferi MG, Négrier C, Nathawani AC, Enjolras N. Le Quellec S, et al. Among authors: negrier c. Thromb Haemost. 2019 Dec;119(12):1956-1967. doi: 10.1055/s-0039-1697658. Epub 2019 Oct 28. Thromb Haemost. 2019. PMID: 31659733

6

Characterization of an autosomal dominant bleeding disorder caused by a thrombomodulin mutation.

Dargaud Y, Scoazec JY, Wielders SJ, Trzeciak C, Hackeng TM, Négrier C, Hemker HC, Lindhout T, Castoldi E. Dargaud Y, et al. Among authors: negrier c. Blood. 2015 Feb 26;125(9):1497-501. doi: 10.1182/blood-2014-10-604553. Epub 2015 Jan 6. Blood. 2015. PMID: 25564403 Free PMC article.

7

Human hepatoma cell line HuH-7 is an effective cellular system to produce recombinant factor IX with improved post-translational modifications.

Enjolras N, Dargaud Y, Pérot E, Guillaume F, Becchi M, Négrier C. Enjolras N, et al. Among authors: negrier c. Thromb Res. 2012 Nov;130(5):e266-73. doi: 10.1016/j.thromres.2012.08.313. Epub 2012 Sep 25. Thromb Res. 2012. PMID: 23021500

8

In vivo efficacy of human recombinant factor IX produced by the human hepatoma cell line HuH-7.

Enjolras N, Perot E, Le Quellec S, Indalecio A, Girard J, Negrier C, Dargaud Y. Enjolras N, et al. Among authors: negrier c. Haemophilia. 2015 Jul;21(4):e317-21. doi: 10.1111/hae.12688. Epub 2015 May 15. Haemophilia. 2015. PMID: 25981983

9

Protein S: A multifunctional anticoagulant vitamin K-dependent protein at the crossroads of coagulation, inflammation, angiogenesis, and cancer.

Suleiman L, Négrier C, Boukerche H. Suleiman L, et al. Among authors: negrier c. Crit Rev Oncol Hematol. 2013 Dec;88(3):637-54. doi: 10.1016/j.critrevonc.2013.07.004. Epub 2013 Aug 16. Crit Rev Oncol Hematol. 2013. PMID: 23958677 Review.

10

Increased thrombosis incidence in a family with an inherited protein S deficiency and a high oxygen affinity hemoglobin variant.

Berruyer M, Francina A, Ffrench P, Negrier C, Boneu B, Dechavanne M. Berruyer M, et al. Among authors: negrier c. Am J Hematol. 1994 Jul;46(3):214-7. doi: 10.1002/ajh.2830460310. Am J Hematol. 1994. PMID: 8192151

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