Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Motoi Yoshimura"'
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Akademický článek
Characteristic distribution and molecular properties of normal cellular prion protein in human endocrine and exocrine tissues
Autor: Sachiko Koyama, Hideko Noguchi, Kaoru Yagita, Hideomi Hamasaki, Masahiro Shijo, Motoi Yoshimura, Kohei Inoshita, Naokazu Sasagasako, Hiroyuki Honda
Publikováno v: Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Prion disease is an infectious and fatal neurodegenerative disease. Human prion disease autopsy studies have revealed abnormal prion protein (PrPSc) deposits in the central nervous system and systemic organs. In deer, chronic wasting disease
Externí odkaz: https://doaj.org/article/30347cd5ad9240edac04a0de0ecbee83
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2
Mutated FUS in familial amyotrophic lateral sclerosis involves multiple hnRNPs in the formation of neuronal cytoplasmic inclusions
Autor: Hiroyuki Honda, Motoi Yoshimura, Hajime Arahata, Kaoru Yagita, Shoko Sadashima, Hideomi Hamasaki, Masahiro Shijo, Sachiko Koyama, Hideko Noguchi, Naokazu Sasagasako
Publikováno v: Journal of Neuropathology & Experimental Neurology. 82:231-241
Fused in sarcoma (FUS), coded by FUS, is a heterogeneous nuclear ribonucleoprotein (hnRNP). FUS mutations are among the major mutations in familial amyotrophic lateral sclerosis (ALS-FUS: ALS6). The pathological hallmarks of ALS-FUS are FUS-positive
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d030af15b45c87aee00f3d598f001aae
https://doi.org/10.1093/jnen/nlac124
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3
Cerebral Tuberculoma with Mild Posterior Cervical Pain as the Main Symptom Despite Extensive Brain Lesions
Autor: Ban-yu Saitoh, Takahisa Tateishi, Motoi Yoshimura, Satoshi O. Suzuki, Noriko Isobe, Toru Iwaki, Jun-ichi Kira
Publikováno v: Internal Medicine. 61:2941-2945
A 59-year-old woman with a diabetes history experienced mild neck pain. A neurological examination revealed only mild neck stiffness. Magnetic resonance imaging showed extensive T2-weighted high-intensity lesions with patchy gadolinium enhancement ma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfe45f7fa0553200d46f3213ada81c32
https://doi.org/10.2169/internalmedicine.9020-21
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5
PCBP2 Is Downregulated in Degenerating Neurons and Rarely Observed in TDP-43-Positive Inclusions in Sporadic Amyotrophic Lateral Sclerosis
Autor: Toshiharu Ninomiya, Shinichiro Mori, Toru Iwaki, Satoshi O. Suzuki, Motoi Yoshimura, Hiroyuki Honda, Hideomi Hamasaki, Jun Ichi Kira, Naokazu Sasagasako, Takashi Ishii
Publikováno v: Journal of Neuropathology & Experimental Neurology. 80:220-228
Various heterogeneous nuclear ribonucleoproteins (hnRNPs) are deposited in pathological inclusions of amyotrophic lateral sclerosis (ALS) and related diseases, such as frontotemporal lobar degeneration (FTLD). Recently, poly (rC)-binding protein 2 (P
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87b6cf908058ac9daa9cfa0514c621ec
https://doi.org/10.1093/jnen/nlaa148
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8
Expanded polyglutamine impairs normal nuclear distribution of fused in sarcoma and poly (rC)‐binding protein 1 in Huntington's disease
Autor: Motoi Yoshimura, Naokazu Sasagasako, Takashi Ishii, Satoshi O. Suzuki, Shinichiro Mori, Takayuki Taniwaki, Hiroyuki Honda, Toru Iwaki
Publikováno v: Neuropathology. 39:358-367
Huntington's disease (HD) is an inherited neurodegenerative disease caused by a polyglutamine repeat expansion in the huntingtin protein. Immunohistochemical studies using the 1C2 antibody for polyglutamine expansion have detected characteristic intr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fc352936519cbf8861545dc65cee548
https://doi.org/10.1111/neup.12600
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