五十嵐 修一

S.Igarashi, H.Morita, K.M.Bennett(その他7名) Inducible PC12 cell model of Huntington's disease shows toxicity and decreased histone acetylation 

Neuroreport 14:565-568, 2003年  

H . Date, O. Onodera, H. Tanaka, K. Iwabuchi, K. Uekawa, S. Igarashi, R. Koike, et.al. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene 

Nature Genetics 29(2):184-8, 2001年  

S. Igarashi, R. koide, T. Shimohata, et. al. Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine strech 

Nature Genetics 18(2):111-117, 1998年  

S. Igarashi, Y. Yonemoti, K. Tanaka,et.al.; Atipical clinical presentation of X-linked spinal and bulbar muscular atrophy in patients with mild CAG expansions in androgen receptor gene 

Europian Neurology 38: 310-312, 1997年  

K. Sanpei, H. Takano, S.Igarashi, et. al. ; Identification of the spinocereberllar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT 

Nature Genetics 14(3); 277-284, 1996年  

S. Igarashi, Y. Takiyama, G. Cancel, et.al.; Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implication for molecular mechanisms of the instability of ・・・ 

Human Molecular Genetics 5(7); 923-932, 1996年  

Y. Takiyama, S. Igarashi, E.A.Rogaeva,et.al.;Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease 

Human Molecular Genetics 4(7); 1137-1146, 1995年  

R.Koide, T.Ikeuti, O. Onodera, H.Tanaka, S. Igarashi, et al. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) 

Nature Genetics 6;9-13, 1994年  

S. Igarashi, Y. Tanno, O. Onodera, M. （その他10名） Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrohy 

Neurology 42 (12); 2300-2302 1992年  

S. Naruse, S. Igarashi, H. Kobayashi,（その他8名） Mis-sense mutation Val->Ile in exon 17 of amyroid precursor protein gene in Japanese familial Alzheimer’s disease 

Lancet 337 (20); 978-979 1991年