Zobrazeno 1 - 10
of 1 241
pro vyhledávání: '"Iwatsubo Takeshi"'
Autor:
Abe, Tetsuro, Kuwahara, Tomoki, Suenaga, Shoichi, Sakurai, Maria, Takatori, Sho, Iwatsubo, Takeshi
Publikováno v:
In iScience 16 February 2024 27(2)
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Hampel, Harald, Hu, Yan, Cummings, Jeffrey, Mattke, Soeren, Iwatsubo, Takeshi, Nakamura, Akinori, Vellas, Bruno, O’Bryant, Sid, Shaw, Leslie M., Cho, Min, Batrla, Richard, Vergallo, Andrea, Blennow, Kaj, Dage, Jeffrey, Schindler, Suzanne E.
Publikováno v:
In Neuron 20 September 2023 111(18):2781-2799
Autor:
Watanabe, Hirotaka, Murakami, Rei, Tsumagari, Kazuya, Morimoto, Satoru, Hashimoto, Tadafumi, Imaizumi, Kent, Sonn, Iki, Yamada, Kaoru, Saito, Yuko, Murayama, Shigeo, Iwatsubo, Takeshi, Okano, Hideyuki
Publikováno v:
In Stem Cell Reports 12 September 2023 18(9):1854-1869
Autor:
Ryu, In Soo, Kim, Dae Hoon, Ro, Ju-Ye, Park, Byeong-Gyu, Kim, Seo Hyun, Im, Jong-Yeop, Lee, Jun-Young, Yoon, Soo Jin, Kang, Heeyoung, Iwatsubo, Takeshi, Teunissen, Charlotte E., Cho, Hyun-Jeong, Ryu, Jin-Hyeob
Publikováno v:
In Clinical Biochemistry August 2023 118
Autor:
Qiao Liyan, Hamamichi Shusei, Caldwell Kim A, Caldwell Guy A, Yacoubian Talene A, Wilson Scott, Xie Zuo-Lei, Speake Lisa D, Parks Rachael, Crabtree Donna, Liang Qiuli, Crimmins Stephen, Schneider Lonnie, Uchiyama Yasuo, Iwatsubo Takeshi, Zhou Yi, Peng Lisheng, Lu YouMing, Standaert David G, Walls Ken C, Shacka John J, Roth Kevin A, Zhang Jianhua
Publikováno v:
Molecular Brain, Vol 1, Iss 1, p 17 (2008)
Abstract α-synuclein (α-syn) is a main component of Lewy bodies (LB) that occur in many neurodegenerative diseases, including Parkinson's disease (PD), dementia with LB (DLB) and multi-system atrophy. α-syn mutations or amplifications are responsi
Externí odkaz:
https://doaj.org/article/e537a0cb3a7346ffbd10eea7ba929678
Autor:
Zhu Xiongwei, Babar Asim, Siedlak Sandra L, Yang Qiwei, Ito Genta, Iwatsubo Takeshi, Smith Mark A, Perry George, Chen Shu G
Publikováno v:
Molecular Neurodegeneration, Vol 1, Iss 1, p 17 (2006)
Abstract Background Mutations in LRRK2 encoding leucine-rich repeat kinase 2 are thus far the most frequent genetic cause associated with autosomal dominant and idiopathic Parkinson's disease (PD). To examine whether LRRK2 is directly associated with
Externí odkaz:
https://doaj.org/article/4893d92756ee40a9a591e1870ebb8133
Publikováno v:
Molecular Neurodegeneration, Vol 1, Iss 1, p 2 (2006)
Abstract Background Presenilin-dependent γ-secretase cleavage of several transmembrane proteins, including amyloid-β precursor protein and Notch, mediates the intramembrane proteolysis to liberate their intracellular domains that are involved in ce
Externí odkaz:
https://doaj.org/article/74b9ec4e62d74faca7ea81b0a609edf5
Autor:
Kasuga, Kensaku, Tsukie, Tamao, Kikuchi, Masataka, Tokutake, Takayoshi, Washiyama, Kazuo, Shimizu, Soichiro, Yoshizawa, Hiroshi, Kuroha, Yasuko, Yajima, Ryuji, Mori, Hiroshi, Arakawa, Yasuaki, Onda, Kiyoshi, Miyashita, Akinori, Onodera, Osamu, Iwatsubo, Takeshi, Ikeuchi, Takeshi
Publikováno v:
In Neurobiology of Aging July 2023 127:23-32