His Allele research is covered under the topics of Trinucleotide repeat expansion and Haplotype. The study of Trinucleotide repeat expansion is intertwined with the study of Gene in a number of ways. Osamu Onodera undertakes multidisciplinary investigations into Gene and Penetrance in his work. He carries out multidisciplinary research, doing studies in Haplotype and Allele. His Phenotype study is within the categories of Penetrance and Clinical phenotype. Clinical phenotype is closely attributed to Phenotype in his study. Osamu Onodera connects Genetics with Molecular biology in his study. His work blends Molecular biology and Genetics studies together. His study on Disease is mostly dedicated to connecting different topics, such as Dementia.
Frameshift mutation and Missense mutation are the areas that his Mutation study falls under. Osamu Onodera performs multidisciplinary studies into Missense mutation and Mutation in his work. Osamu Onodera performs multidisciplinary study in Internal medicine and Endocrinology in his work. He combines Endocrinology and Internal medicine in his research. He performs integrative Gene and Phenotype research in his work. He integrates many fields in his works, including Phenotype and Gene. Osamu Onodera performs multidisciplinary study in Genetics and Frameshift mutation in his work. His research ties Spinocerebellar ataxia and Disease together. His study in Disease extends to Spinocerebellar ataxia with its themes.
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Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)
R. Koide;T. Ikeuchi;O. Onodera;H. Tanaka.
Nature Genetics (1994)
Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease
Shoji Tsuji;Osamu Onodera.
The New England Journal of Medicine (2010)
Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription.
Takayoshi Shimohata;Toshihiro Nakajima;Mitsunori Yamada;Chiharu Uchida.
Nature Genetics (2000)
TDP-43 mutation in familial amyotrophic lateral sclerosis
Akio Yokoseki;Atsushi Shiga;Chun-Feng Tan;Asako Tagawa.
Annals of Neurology (2008)
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;Kiyoshi Iwabuchi.
Nature Genetics (2001)
Mutations in COQ2 in familial and sporadic multiple-system atrophy the multiple-system atrophy research collaboration
Jun Mitsui;Takashi Matsukawa;Hiroyuki Ishiura;Yoko Fukuda;Yoko Fukuda.
The New England Journal of Medicine (2013)
TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.
Chun-Feng Tan;Hiroto Eguchi;Asako Tagawa;Osamu Onodera.
Acta Neuropathologica (2007)
Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients
Naoki Hattori;Masahiko Yamamoto;Tsuyoshi Yoshihara;Haruki Koike.
Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic.
Toshiaki Takahashi;Shinya Kikuchi;Shinichi Katada;Yoshitaka Nagai.
Human Molecular Genetics (2008)
Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease.
Kaoru Okuizumi;Osamu Onodera;Yoshio Namba;Kazuhiko Ikeda.
Nature Genetics (1995)
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