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Page 1
Mutation analysis of the tyrosinase gene in oculocutaneous albinism.
Camand O, Marchant D, Boutboul S, Péquignot M, Odent S, Dollfus H, Sutherland J, Levin A, Menasche M, Marsac C, Dufier JL, Heon E, Abitbol M. Camand O, et al. Among authors: pequignot m. Hum Mutat. 2001 Apr;17(4):352. doi: 10.1002/humu.38. Hum Mutat. 2001. PMID: 11295837
Homozygous deletion in the coding sequence of the c-mer gene in RCS rats unravels general mechanisms of physiological cell adhesion and apoptosis.
Nandrot E, Dufour EM, Provost AC, Péquignot MO, Bonnel S, Gogat K, Marchant D, Rouillac C, Sépulchre de Condé B, Bihoreau MT, Shaver C, Dufier JL, Marsac C, Lathrop M, Menasche M, Abitbol MM. Nandrot E, et al. Among authors: pequignot mo. Neurobiol Dis. 2000 Dec;7(6 Pt B):586-99. doi: 10.1006/nbdi.2000.0328. Neurobiol Dis. 2000. PMID: 11114258
New splicing-site mutations in the SURF1 gene in Leigh syndrome patients.
Pequignot MO, Desguerre I, Dey R, Tartari M, Zeviani M, Agostino A, Benelli C, Fouque F, Prip-Buus C, Marchant D, Abitbol M, Marsac C. Pequignot MO, et al. J Biol Chem. 2001 May 4;276(18):15326-9. doi: 10.1074/jbc.M100388200. Epub 2001 Feb 6. J Biol Chem. 2001. PMID: 11279059 Free article.
Expression of SR-BI receptor and StAR protein in rat ocular tissues.
Provost AC, Péquignot MO, Sainton KM, Gadin S, Sallé S, Marchant D, Hales DB, Abitbol M. Provost AC, et al. Among authors: pequignot mo. C R Biol. 2003 Sep;326(9):841-51. doi: 10.1016/j.crvi.2003.09.001. C R Biol. 2003. PMID: 14694755 Free article.
A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium.
Meunier I, Lenaers G, Bocquet B, Baudoin C, Piro-Megy C, Cubizolle A, Quilès M, Jean-Charles A, Cohen SY, Merle H, Gaudric A, Labesse G, Manes G, Péquignot M, Cazevieille C, Dhaenens CM, Fichard A, Ronkina N, Arthur SJ, Gaestel M, Hamel CP. Meunier I, et al. Among authors: pequignot m. Hum Mol Genet. 2016 Mar 1;25(5):916-26. doi: 10.1093/hmg/ddv624. Epub 2016 Jan 6. Hum Mol Genet. 2016. PMID: 26744326
39 results