Shuichi Igarashi

p53 Mediates Cellular Dysfunction and Behavioral Abnormalities in Huntington’s Disease

Byoung-Il Bae, Hong Xu, Shuichi Igarashi et al. · Neuron · 2005 · 481 citations · Full text

Neurodegenerative Diseases, Medicine, Degenerative Disease +6

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

Hidetoshi Date, Osamu Onodera, Hajime Tanaka et al. · Nature Genetics · 2001 · 382 citations

New Hit, Mendelian Disorder, Ophthalmology +10

Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch

Shuichi Igarashi, Reiji Koide, Takayoshi Shimohata et al. · Nature Genetics · 1998 · 357 citations

Polyglutamine Stretch, Drpla Protein, Protein Function +9

Dentatorubral‐pallidoluysian atrophy: Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat

Takeshi Ikeuchi, Reiji Koide, Hajime Tanaka et al. · Annals of Neurology · 1995 · 168 citations

Spinocerebellar ataxia type 6: CAG repeat expansion in α_1a voltage‐dependent calcium channel gene and clinical variations in japanese population

Takeshi Ikeuchi, Hiroki Takano, Reiji Koide et al. · Annals of Neurology · 1997 · 136 citations