Morel F - Search Results

1

Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells.

Bionda C, Li XJ, van Bruggen R, Eppink M, Roos D, Morel F, Stasia MJ. Bionda C, et al. Among authors: morel f. Hum Genet. 2004 Oct;115(5):418-27. doi: 10.1007/s00439-004-1173-z. Epub 2004 Aug 24. Hum Genet. 2004. PMID: 15338276 Free article.

2

Characterization of six novel mutations in the CYBB gene leading to different sub-types of X-linked chronic granulomatous disease.

Stasia MJ, Bordigoni P, Floret D, Brion JP, Bost-Bru C, Michel G, Gatel P, Durant-Vital D, Voelckel MA, Li XJ, Guillot M, Maquet E, Martel C, Morel F. Stasia MJ, et al. Among authors: morel f. Hum Genet. 2005 Jan;116(1-2):72-82. doi: 10.1007/s00439-004-1208-5. Epub 2004 Nov 6. Hum Genet. 2005. PMID: 15538631

3

Crucial role of two potential cytosolic regions of Nox2, 191TSSTKTIRRS200 and 484DESQANHFAVHHDEEKD500, on NADPH oxidase activation.

Li XJ, Grunwald D, Mathieu J, Morel F, Stasia MJ. Li XJ, et al. Among authors: morel f. J Biol Chem. 2005 Apr 15;280(15):14962-73. doi: 10.1074/jbc.M500226200. Epub 2005 Jan 31. J Biol Chem. 2005. PMID: 15684431 Free article.

4

Leu505 of Nox2 is crucial for optimal p67phox-dependent activation of the flavocytochrome b558 during phagocytic NADPH oxidase assembly.

Li XJ, Fieschi F, Paclet MH, Grunwald D, Campion Y, Gaudin P, Morel F, Stasia MJ. Li XJ, et al. Among authors: morel f. J Leukoc Biol. 2007 Jan;81(1):238-49. doi: 10.1189/jlb.0905541. Epub 2006 Oct 23. J Leukoc Biol. 2007. PMID: 17060362

5

New insights into the membrane topology of the phagocyte NADPH oxidase: characterization of an anti-gp91-phox conformational monoclonal antibody.

Campion Y, Paclet MH, Jesaitis AJ, Marques B, Grichine A, Berthier S, Lenormand JL, Lardy B, Stasia MJ, Morel F. Campion Y, et al. Among authors: morel f. Biochimie. 2007 Sep;89(9):1145-58. doi: 10.1016/j.biochi.2007.01.010. Epub 2007 Feb 20. Biochimie. 2007. PMID: 17397983

6

A novel and unusual case of chronic granulomatous disease in a child with a homozygous 36-bp deletion in the CYBA gene (A22(0)) leading to the activation of a cryptic splice site in intron 4.

Stasia MJ, Bordigoni P, Martel C, Morel F. Stasia MJ, et al. Among authors: morel f. Hum Genet. 2002 May;110(5):444-50. doi: 10.1007/s00439-002-0720-8. Epub 2002 Apr 9. Hum Genet. 2002. PMID: 12073015

7

An unusual case of sarcoidosis.

Cathébras P, Sauron C, Morel F, Stasia MJ. Cathébras P, et al. Among authors: morel f. Lancet. 2001 Jul 28;358(9278):294. doi: 10.1016/S0140-6736(01)05485-X. Lancet. 2001. PMID: 11498217 No abstract available.

8

Aspartate aminotransferase macroenzyme complex in serum identified and characterized.

Stasia MJ, Surla A, Renversez JC, Pene F, Morel-Femelez A, Morel F. Stasia MJ, et al. Among authors: morel f, morel femelez a. Clin Chem. 1994 Jul;40(7 Pt 1):1340-3. Clin Chem. 1994. PMID: 8013110

9

[Comparative study of two methods permitting the detection of macroamylases. Application to the evaluation of macroamylasemia in a hospitalized population].

Stasia MJ, Cohen-Tanugi Cholley L, Laporte F, Coudray C, Cartier A, Chabert M, Champavier S, Gérard G, Maquet E, Morel F. Stasia MJ, et al. Among authors: morel f. Ann Biol Clin (Paris). 1993;51(9):801-6. Ann Biol Clin (Paris). 1993. PMID: 8166393 French.

10

Molecular and functional characterization of a new X-linked chronic granulomatous disease variant (X91+) case with a double missense mutation in the cytosolic gp91phox C-terminal tail.

Stasia MJ, Lardy B, Maturana A, Rousseau P, Martel C, Bordigoni P, Demaurex N, Morel F. Stasia MJ, et al. Among authors: morel f. Biochim Biophys Acta. 2002 Apr 24;1586(3):316-30. doi: 10.1016/s0925-4439(01)00110-7. Biochim Biophys Acta. 2002. PMID: 11997083 Free article.

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