Néri C - Search Results

1

CAG repeat sequences in bipolar affective disorder: no evidence for association in a French population.

Zander C, Schürhoff F, Laurent C, Chavand O, Bellivier F, Samolyk D, Leboyer M, Allilaire JF, Cann H, Néri C, Mallet J. Zander C, et al. Among authors: neri c. Am J Med Genet. 1998 Jul 10;81(4):338-41. Am J Med Genet. 1998. PMID: 9674981

2

Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic cases.

Laurent C, Zander C, Thibaut F, Bonnet-Brilhault F, Chavand O, Jay M, Samolyk D, Petit M, Martinez M, Campion D, Néri C, Mallet J, Cann H. Laurent C, et al. Among authors: neri c. Am J Med Genet. 1998 Jul 10;81(4):342-6. doi: 10.1002/(sici)1096-8628(19980710)81:4<342::aid-ajmg12>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9674982

3

Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders.

Néri C, Albanèse V, Lebre AS, Holbert S, Saada C, Bougueleret L, Meier-Ewert S, Le Gall I, Millasseau P, Bui H, Giudicelli C, Massart C, Guillou S, Gervy P, Poullier E, Rigault P, Weissenbach J, Lennon G, Chumakov I, Dausset J, Lehrach H, Cohen D, Cann HM. Néri C, et al. Hum Mol Genet. 1996 Jul;5(7):1001-9. doi: 10.1093/hmg/5.7.1001. Hum Mol Genet. 1996. PMID: 8817338

4

Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.

Cancel G, Abbas N, Stevanin G, Dürr A, Chneiweiss H, Néri C, Duyckaerts C, Penet C, Cann HM, Agid Y, et al. Cancel G, et al. Among authors: neri c. Am J Hum Genet. 1995 Oct;57(4):809-16. Am J Hum Genet. 1995. PMID: 7573040 Free PMC article.

5

CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: outcome in searching for new dynamic mutations.

Albanese V, Holbert S, Saada C, Meier-Ewert S, Lebre AS, Moriniere S, Bougueleret L, Le Gall I, Weissenbach J, Lennon G, Lehrach H, Cohen D, Cann HM, Neri C. Albanese V, et al. Among authors: neri c. Genomics. 1998 Feb 1;47(3):414-8. doi: 10.1006/geno.1997.5130. Genomics. 1998. PMID: 9480757

6

Detection of polyglutamine expansion in a new acidic protein: a candidate for childhood onset schizophrenia?

Moriniere S, Saada C, Holbert S, Sidransky E, Galat A, Ginns E, Rapoport JL, Neri C. Moriniere S, et al. Among authors: neri c. Mol Psychiatry. 1999 Jan;4(1):58-63. doi: 10.1038/sj.mp.4000448. Mol Psychiatry. 1999. PMID: 10089010

7

The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: neuropathologic and genetic evidence for a role in Huntington's disease pathogenesis.

Holbert S, Denghien I, Kiechle T, Rosenblatt A, Wellington C, Hayden MR, Margolis RL, Ross CA, Dausset J, Ferrante RJ, Néri C. Holbert S, et al. Among authors: neri c. Proc Natl Acad Sci U S A. 2001 Feb 13;98(4):1811-6. doi: 10.1073/pnas.98.4.1811. Epub 2001 Jan 30. Proc Natl Acad Sci U S A. 2001. PMID: 11172033 Free PMC article.

8

Cdc42-interacting protein 4 binds to huntingtin: neuropathologic and biological evidence for a role in Huntington's disease.

Holbert S, Dedeoglu A, Humbert S, Saudou F, Ferrante RJ, Néri C. Holbert S, et al. Among authors: neri c. Proc Natl Acad Sci U S A. 2003 Mar 4;100(5):2712-7. doi: 10.1073/pnas.0437967100. Epub 2003 Feb 25. Proc Natl Acad Sci U S A. 2003. PMID: 12604778 Free PMC article.

9

Expanded polyglutamines in Caenorhabditis elegans cause axonal abnormalities and severe dysfunction of PLM mechanosensory neurons without cell death.

Parker JA, Connolly JB, Wellington C, Hayden M, Dausset J, Neri C. Parker JA, et al. Among authors: neri c. Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):13318-23. doi: 10.1073/pnas.231476398. Epub 2001 Oct 30. Proc Natl Acad Sci U S A. 2001. PMID: 11687635 Free PMC article.

10

Resveratrol rescues mutant polyglutamine cytotoxicity in nematode and mammalian neurons.

Parker JA, Arango M, Abderrahmane S, Lambert E, Tourette C, Catoire H, Néri C. Parker JA, et al. Among authors: neri c. Nat Genet. 2005 Apr;37(4):349-50. doi: 10.1038/ng1534. Epub 2005 Mar 27. Nat Genet. 2005. PMID: 15793589

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