Fujigasaki H - Search Results

1

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.

Fujigasaki H, Verma IC, Camuzat A, Margolis RL, Zander C, Lebre AS, Jamot L, Saxena R, Anand I, Holmes SE, Ross CA, Dürr A, Brice A. Fujigasaki H, et al. Ann Neurol. 2001 Jan;49(1):117-21. Ann Neurol. 2001. PMID: 11198281

2

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Stevanin G, Fujigasaki H, Lebre AS, Camuzat A, Jeannequin C, Dode C, Takahashi J, San C, Bellance R, Brice A, Durr A. Stevanin G, et al. Among authors: fujigasaki h. Brain. 2003 Jul;126(Pt 7):1599-603. doi: 10.1093/brain/awg155. Epub 2003 May 6. Brain. 2003. PMID: 12805114

3

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

Fujigasaki H, Martin JJ, De Deyn PP, Camuzat A, Deffond D, Stevanin G, Dermaut B, Van Broeckhoven C, Dürr A, Brice A. Fujigasaki H, et al. Brain. 2001 Oct;124(Pt 10):1939-47. doi: 10.1093/brain/124.10.1939. Brain. 2001. PMID: 11571212

4

Two populations of neuronal intranuclear inclusions in SCA7 differ in size and promyelocytic leukaemia protein content.

Takahashi J, Fujigasaki H, Zander C, El Hachimi KH, Stevanin G, Dürr A, Lebre AS, Yvert G, Trottier Y, de Thé H, Hauw JJ, Duyckaerts C, Brice A. Takahashi J, et al. Among authors: fujigasaki h. Brain. 2002 Jul;125(Pt 7):1534-43. doi: 10.1093/brain/awf154. Brain. 2002. PMID: 12077003

5

Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions.

Lebre AS, Jamot L, Takahashi J, Spassky N, Leprince C, Ravisé N, Zander C, Fujigasaki H, Kussel-Andermann P, Duyckaerts C, Camonis JH, Brice A. Lebre AS, et al. Among authors: fujigasaki h. Hum Mol Genet. 2001 May 15;10(11):1201-13. doi: 10.1093/hmg/10.11.1201. Hum Mol Genet. 2001. PMID: 11371513

6

Zander C, Takahashi J, El Hachimi KH, Fujigasaki H, Albanese V, Lebre AS, Stevanin G, Duyckaerts C, Brice A. Zander C, et al. Among authors: fujigasaki h. Hum Mol Genet. 2001 Oct 15;10(22):2569-79. doi: 10.1093/hmg/10.22.2569. Hum Mol Genet. 2001. PMID: 11709544

7

Spinocerebellar ataxia type 10 in the French population.

Fujigasaki H, Tardieu S, Camuzat A, Stevanin G, LeGuern E, Matsuura T, Ashizawa T, Dürr A, Brice A. Fujigasaki H, et al. Ann Neurol. 2002 Mar;51(3):408-9. doi: 10.1002/ana.10126. Ann Neurol. 2002. PMID: 11891842 No abstract available.

8

Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions.

Seilhean D, Takahashi J, El Hachimi KH, Fujigasaki H, Lebre AS, Biancalana V, Dürr A, Salachas F, Hogenhuis J, de Thé H, Hauw JJ, Meininger V, Brice A, Duyckaerts C. Seilhean D, et al. Among authors: fujigasaki h. Acta Neuropathol. 2004 Jul;108(1):81-7. doi: 10.1007/s00401-004-0855-x. Epub 2004 Apr 27. Acta Neuropathol. 2004. PMID: 15114487

9

SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7.

Janer A, Werner A, Takahashi-Fujigasaki J, Daret A, Fujigasaki H, Takada K, Duyckaerts C, Brice A, Dejean A, Sittler A. Janer A, et al. Among authors: fujigasaki h. Hum Mol Genet. 2010 Jan 1;19(1):181-95. doi: 10.1093/hmg/ddp478. Hum Mol Genet. 2010. PMID: 19843541

10

PML nuclear bodies and neuronal intranuclear inclusion in polyglutamine diseases.

Takahashi J, Fujigasaki H, Iwabuchi K, Bruni AC, Uchihara T, El Hachimi KH, Stevanin G, Dürr A, Lebre AS, Trottier Y, de Thé H, Tanaka J, Hauw JJ, Duyckaerts C, Brice A. Takahashi J, et al. Among authors: fujigasaki h. Neurobiol Dis. 2003 Aug;13(3):230-7. doi: 10.1016/s0969-9961(03)00080-9. Neurobiol Dis. 2003. PMID: 12901837

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