Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Tomoko Andoh"'
Autor:
Miho Isoda, Tsukasa Sanosaka, Ryo Tomooka, Yo Mabuchi, Munehisa Shinozaki, Tomoko Andoh-Noda, Satoe Banno, Noriko Mizota, Ryo Yamaguchi, Hideyuki Okano, Jun Kohyama
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-15 (2023)
Abstract Although neural stem/progenitor cells derived from human induced pluripotent stem cells (hiPSC-NS/PCs) are expected to be a cell source for cell-based therapy, tumorigenesis of hiPSC-NS/PCs is a potential problem for clinical applications. T
Externí odkaz:
https://doaj.org/article/cfe8d14e05724bbf98a625f354acb147
Autor:
Tsukasa Sanosaka, Hironobu Okuno, Noriko Mizota, Tomoko Andoh-Noda, Miki Sato, Ryo Tomooka, Satoe Banno, Jun Kohyama, Hideyuki Okano
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract A mutation in the chromatin remodeler chromodomain helicase DNA-binding 7 (CHD7) gene causes the multiple congenital anomaly CHARGE syndrome. The craniofacial anomalies observed in CHARGE syndrome are caused by dysfunctions of neural crest c
Externí odkaz:
https://doaj.org/article/d18a0857a5604bd688e1ac7e1962f304
Autor:
Hideyuki Nakashima, Keita Tsujimura, Koichiro Irie, Takuya Imamura, Cleber A. Trujillo, Masataka Ishizu, Masahiro Uesaka, Miao Pan, Hirofumi Noguchi, Kanako Okada, Kei Aoyagi, Tomoko Andoh-Noda, Hideyuki Okano, Alysson R. Muotri, Kinichi Nakashima
Publikováno v:
Cell Reports, Vol 35, Iss 7, Pp 109124- (2021)
Summary: Rett syndrome (RTT) is a severe neurological disorder, with impaired brain development caused by mutations in MECP2; however, the underlying mechanism remains elusive. We know from previous work that MeCP2 facilitates the processing of a spe
Externí odkaz:
https://doaj.org/article/0fed81b11b5247d3a98746060e307b29
Autor:
Yoshikuni Tabata, Yoichi Imaizumi, Michiko Sugawara, Tomoko Andoh-Noda, Satoe Banno, MuhChyi Chai, Takefumi Sone, Kazuto Yamazaki, Masashi Ito, Kappei Tsukahara, Hideyuki Saya, Nobutaka Hattori, Jun Kohyama, Hideyuki Okano
Publikováno v:
Stem Cell Reports, Vol 11, Iss 5, Pp 1171-1184 (2018)
Summary: Parkinson disease (PD) is a progressive neurological disease caused by selective degeneration of dopaminergic (DA) neurons in the substantia nigra. Although most cases of PD are sporadic cases, familial PD provides a versatile research model
Externí odkaz:
https://doaj.org/article/fe1dd302708e4dc7827aa141f36e9904
Autor:
Takuya Matsumoto, Koki Fujimori, Tomoko Andoh-Noda, Takayuki Ando, Naoko Kuzumaki, Manabu Toyoshima, Hirobumi Tada, Kent Imaizumi, Mitsuru Ishikawa, Ryo Yamaguchi, Miho Isoda, Zhi Zhou, Shigeto Sato, Tetsuro Kobayashi, Manami Ohtaka, Ken Nishimura, Hiroshi Kurosawa, Takeo Yoshikawa, Takuya Takahashi, Mahito Nakanishi, Manabu Ohyama, Nobutaka Hattori, Wado Akamatsu, Hideyuki Okano
Publikováno v:
Stem Cell Reports, Vol 6, Iss 3, Pp 422-435 (2016)
Modeling of neurological diseases using induced pluripotent stem cells (iPSCs) derived from the somatic cells of patients has provided a means of elucidating pathogenic mechanisms and performing drug screening. T cells are an ideal source of patient-
Externí odkaz:
https://doaj.org/article/e6518bb7a49f4ff8af3ffc8d2cad638b
Autor:
Kunio Miyake, Chunshu Yang, Yohei Minakuchi, Kenta Ohori, Masaki Soutome, Takae Hirasawa, Yasuhiro Kazuki, Noboru Adachi, Seiko Suzuki, Masayuki Itoh, Yu-Ichi Goto, Tomoko Andoh, Hiroshi Kurosawa, Mitsuo Oshimura, Masayuki Sasaki, Atsushi Toyoda, Takeo Kubota
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e66729 (2013)
Monozygotic (identical) twins have been widely used in genetic studies to determine the relative contributions of heredity and the environment in human diseases. Discordance in disease manifestation between affected monozygotic twins has been attribu
Externí odkaz:
https://doaj.org/article/9050d526d07243489bf95e66c5b60318
Autor:
Hideyuki Okano, Tomoko Andoh-Noda, Kanako Okada, Masataka Ishizu, Keita Tsujimura, Hideyuki Nakashima, Takuya Imamura, Miao Pan, Masahiro Uesaka, Kinichi Nakashima, Koichiro Irie, Kei Aoyagi, Cleber A. Trujillo, Alysson R. Muotri, Hirofumi Noguchi
Publikováno v:
Cell Reports, Vol 35, Iss 7, Pp 109124-(2021)
Summary: Rett syndrome (RTT) is a severe neurological disorder, with impaired brain development caused by mutations in MECP2; however, the underlying mechanism remains elusive. We know from previous work that MeCP2 facilitates the processing of a spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ded250cdfac294e9489824f5c778a4f1
https://pubmed.ncbi.nlm.nih.gov/34010654
https://pubmed.ncbi.nlm.nih.gov/34010654
Autor:
Takefumi Sone, Muh Chyi Chai, Yoichi Imaizumi, Yoshikuni Tabata, Michiko Sugawara, Kappei Tsukahara, Satoe Banno, Jun Kohyama, Nobutaka Hattori, Masashi Ito, Tomoko Andoh-Noda, Hideyuki Saya, Kazuto Yamazaki, Hideyuki Okano
Publikováno v:
Stem Cell Reports, Vol 11, Iss 5, Pp 1171-1184 (2018)
Stem Cell Reports
Stem Cell Reports
Summary Parkinson disease (PD) is a progressive neurological disease caused by selective degeneration of dopaminergic (DA) neurons in the substantia nigra. Although most cases of PD are sporadic cases, familial PD provides a versatile research model
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c07aa98760e5b7c104992ea75aaafaf5
https://doi.org/10.1016/j.stemcr.2018.09.006
https://doi.org/10.1016/j.stemcr.2018.09.006
Autor:
Takeo Kubota, Kunio Miyake, Michiko O. Inouye, Hideyuki Okano, Wado Akamatsu, Tomoko Andoh-Noda
Publikováno v:
CNS & Neurological Disorders - Drug Targets. 15:544-550
Rett syndrome (RTT) is one of a group of neurodevelopmental disorders typically characterized by deficits in the X-linked gene MECP2 (methyl-CpG binding protein 2). The MECP2 gene encodes a multifunctional protein involved in transcriptional repressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e62af6a475e2ba21c69b41c822c6d360
https://doi.org/10.2174/1871527315666160413120156
https://doi.org/10.2174/1871527315666160413120156
Autor:
Takeo Yoshikawa, Zhi Zhou, Wado Akamatsu, Koki Fujimori, Hirobumi Tada, Tomoko Andoh-Noda, Mahito Nakanishi, Ryo Yamaguchi, Takuya Takahashi, Miho Isoda, Kent Imaizumi, Manabu Toyoshima, Mitsuru Ishikawa, Takuya Matsumoto, Hiroshi Kurosawa, Nobutaka Hattori, Manabu Ohyama, Takayuki Ando, Naoko Kuzumaki, Tetsuro Kobayashi, Hideyuki Okano, Shigeto Sato, Ken Nishimura, Manami Ohtaka
Publikováno v:
Stem Cell Reports, Vol 6, Iss 3, Pp 422-435 (2016)
Stem Cell Reports
Stem Cell Reports
Summary Modeling of neurological diseases using induced pluripotent stem cells (iPSCs) derived from the somatic cells of patients has provided a means of elucidating pathogenic mechanisms and performing drug screening. T cells are an ideal source of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76480f03474ac55483941a723781392f