Vourc'h P - Search Results

1

Mutation in the RRM2 domain of TDP-43 in Amyotrophic Lateral Sclerosis with rapid progression associated with ubiquitin positive aggregates in cultured motor neurons.

Maurel C, Madji-Hounoum B, Thepault RA, Marouillat S, Brulard C, Danel-Brunaud V, Camdessanche JP, Blasco H, Corcia P, Andres CR, Vourc'h P. Maurel C, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Feb;19(1-2):149-151. doi: 10.1080/21678421.2017.1349152. Epub 2017 Jul 13. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 28705014

2

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

Vourc'h P, Bienvenu T, Beldjord C, Chelly J, Barthélémy C, Müh JP, Andres C. Vourc'h P, et al. Eur J Hum Genet. 2001 Jul;9(7):556-8. doi: 10.1038/sj.ejhg.5200660. Eur J Hum Genet. 2001. PMID: 11464249

3

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder.

Vourc'h P, Martin I, Marouillat S, Adrien JL, Barthélémy C, Moraine C, Müh JP, Andres C. Vourc'h P, et al. Neurosci Lett. 2003 Feb 27;338(2):115-8. doi: 10.1016/s0304-3940(02)01338-1. Neurosci Lett. 2003. PMID: 12566166

4

Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine-rich repeat domain, not its glycosylphosphatidyl-inositol anchor.

Vourc'h P, Moreau T, Arbion F, Marouillat-Védrine S, Müh JP, Andres C. Vourc'h P, et al. J Neurochem. 2003 May;85(4):889-97. doi: 10.1046/j.1471-4159.2003.01764.x. J Neurochem. 2003. PMID: 12716421 Free article.

5

The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system.

Vourc'h P, Dessay S, Mbarek O, Marouillat Védrine S, Müh JP, Andres C. Vourc'h P, et al. Brain Res Dev Brain Res. 2003 Sep 10;144(2):159-68. doi: 10.1016/s0165-3806(03)00167-6. Brain Res Dev Brain Res. 2003. PMID: 12935913

6

Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder.

Vourc'h P, Martin I, Bonnet-Brilhault F, Marouillat S, Barthélémy C, Pierre Müh J, Andres C. Vourc'h P, et al. Psychiatr Genet. 2003 Dec;13(4):221-5. doi: 10.1097/00041444-200312000-00005. Psychiatr Genet. 2003. PMID: 14639049

7

Oligodendrocyte myelin glycoprotein (OMgp): evolution, structure and function.

Vourc'h P, Andres C. Vourc'h P, et al. Brain Res Brain Res Rev. 2004 May;45(2):115-24. doi: 10.1016/j.brainresrev.2004.01.003. Brain Res Brain Res Rev. 2004. PMID: 15145622 Review.

8

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.

Corcia P, Camu W, Halimi JM, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres CR; French ALS Study Group. Corcia P, et al. Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Neurology. 2006. PMID: 16931506 Clinical Trial.

9

Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband.

Martin I, Gauthier J, D'Amelio M, Védrine S, Vourc'h P, Rouleau GA, Persico AM, Andres CR. Martin I, et al. Neurosci Res. 2007 Dec;59(4):426-30. doi: 10.1016/j.neures.2007.08.009. Epub 2007 Aug 19. Neurosci Res. 2007. PMID: 17897745

10

[Genetics of motor neuron disorders].

Corcia P, Praline J, Vourc'h P, Andres C. Corcia P, et al. Rev Neurol (Paris). 2008 Feb;164(2):115-30. doi: 10.1016/j.neurol.2007.10.002. Epub 2008 Feb 20. Rev Neurol (Paris). 2008. PMID: 18358870 Review. French.

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