Andres CR - Search Results

1

Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis.

Blasco H, Vourc'h P, Nadjar Y, Ribourtout B, Gordon PH, Guettard YO, Camu W, Praline J, Meininger V, Andres CR, Corcia P; French ALS study group. Blasco H, et al. Among authors: andres cr. J Neurol Sci. 2011 Apr 15;303(1-2):124-7. doi: 10.1016/j.jns.2010.12.018. Epub 2011 Jan 26. J Neurol Sci. 2011. PMID: 21276595

2

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis.

Corcia P, Mayeux-Portas V, Khoris J, de Toffol B, Autret A, Müh JP, Camu W, Andres C; French ALS Research Group. Amyotrophic Lateral Sclerosis. Corcia P, et al. Ann Neurol. 2002 Feb;51(2):243-6. doi: 10.1002/ana.10104. Ann Neurol. 2002. PMID: 11835381

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

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. Among authors: andres cr. 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

9

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

Paubel A, Violette J, Amy M, Praline J, Meininger V, Camu W, Corcia P, Andres CR, Vourc'h P; French Amyotrophic Lateral Sclerosis (ALS) Study Group. Paubel A, et al. Among authors: andres cr. Arch Neurol. 2008 Oct;65(10):1333-6. doi: 10.1001/archneur.65.10.1333. Arch Neurol. 2008. PMID: 18852347

10

Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation.

Daoud H, Gruchy N, Constans JM, Moussaoui E, Saumureau S, Bayou N, Amy M, Védrine S, Vu PY, Rötig A, Laumonnier F, Vourc'h P, Andres CR, Leporrier N, Briault S. Daoud H, et al. Among authors: andres cr. Hum Genet. 2009 Jan;124(6):649-58. doi: 10.1007/s00439-008-0588-3. Epub 2008 Nov 16. Hum Genet. 2009. PMID: 19011903

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