Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Fumiko Arima-Yoshida"'
Autor:
Tetsuo Ohnishi, Yuji Kiyama, Fumiko Arima‐Yoshida, Mitsutaka Kadota, Tomoe Ichikawa, Kazuyuki Yamada, Akiko Watanabe, Hisako Ohba, Kaori Tanaka, Akihiro Nakaya, Yasue Horiuchi, Yoshimi Iwayama, Manabu Toyoshima, Itone Ogawa, Chie Shimamoto‐Mitsuyama, Motoko Maekawa, Shabeesh Balan, Makoto Arai, Mitsuhiro Miyashita, Kazuya Toriumi, Yayoi Nozaki, Rumi Kurokawa, Kazuhiro Suzuki, Akane Yoshikawa, Tomoko Toyota, Toshihiko Hosoya, Hiroyuki Okuno, Haruhiko Bito, Masanari Itokawa, Shigehiro Kuraku, Toshiya Manabe, Takeo Yoshikawa
Publikováno v:
EMBO Molecular Medicine, Vol 13, Iss 4, Pp 1-21 (2021)
Abstract Genomic defects with large effect size can help elucidate unknown pathologic architecture of mental disorders. We previously reported on a patient with schizophrenia and a balanced translocation between chromosomes 4 and 13 and found that th
Externí odkaz:
https://doaj.org/article/c3d643b8363c4222821faa0e5c5dffd8
Autor:
Tsutomu Nakamura, Fumiko Arima-Yoshida, Fumika Sakaue, Yukiko Nasu-Nishimura, Yasuko Takeda, Ken Matsuura, Natacha Akshoomoff, Sarah N. Mattson, Paul D. Grossfeld, Toshiya Manabe, Tetsu Akiyama
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-16 (2016)
The molecular underpinning of autism is unclear. Here the authors show PX-RICS deficient mice exhibit autism-like social behavioural abnormalities and impaired GABAA receptor trafficking, and enhancing inhibitory synaptic transmission with a GABAArec
Externí odkaz:
https://doaj.org/article/111e3b7f27194d44a435bfedacde52eb
Autor:
Ken Matsuura, Shizuka Kobayashi, Kohtarou Konno, Miwako Yamasaki, Takahiro Horiuchi, Takao Senda, Tomoatsu Hayashi, Kiyotoshi Satoh, Fumiko Arima-Yoshida, Kei Iwasaki, Lumi Negishi, Naomi Yasui-Shimizu, Kazuyoshi Kohu, Shigenori Kawahara, Yutaka Kirino, Tsutomu Nakamura, Masahiko Watanabe, Tadashi Yamamoto, Toshiya Manabe, Tetsu Akiyama
Publikováno v:
J Neurosci
Signal-induced proliferation-associated 1 (SIPA1)-like 1 (SIPA1L1; also known as SPAR1) has been proposed to regulate synaptic functions that are important in maintaining normal neuronal activities, such as regulating spine growth and synaptic scalin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89059b4b8bb5b8a4c264909839843927
https://doi.org/10.1523/jneurosci.0569-21.2022
https://doi.org/10.1523/jneurosci.0569-21.2022
Autor:
Shigenori Kawahara, Kiyotoshi Satoh, Tomoatsu Hayashi, Yohei Kirino, Tadashi Yamamoto, Kohtarou Konno, Fumiko Arima-Yoshida, Kazuyoshi Kohu, Terumi Horiuchi, Negishi L, Kiyotaka Iwasaki, Masahiko Watanabe, Toshiya Manabe, Shizuka Kobayashi, Michimasa Yamasaki, Takao Senda, Matsuura K, Takahisa Nakamura, Yasui-Shimizu N, Tetsu Akiyama
SIPA1L1 (also known as SPAR1) has been proposed to regulate synaptic functions that are important in maintaining normal neuronal activities, such as regulating spine growth and synaptic scaling, as a component of the postsynaptic density (PSD)-95/N-m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::addfc32bd64b3c422055f708df64e8b2
https://doi.org/10.1101/2021.02.12.430872
https://doi.org/10.1101/2021.02.12.430872
Autor:
Kazuya Toriumi, Toshihiko Hosoya, Fumiko Arima-Yoshida, Yuji Kiyama, Shigehiro Kuraku, Motoko Maekawa, Chie Shimamoto-Mitsuyama, Akiko Watanabe, Kazuhiro Suzuki, Tetsuo Ohnishi, Makoto Arai, Mitsuhiro Miyashita, Tomoko Toyota, Kaori Tanaka, Akane Yoshikawa, Mitsutaka Kadota, Yasue Horiuchi, Yayoi Nozaki, Yoshimi Iwayama, Kazuyuki Yamada, Hisako Ohba, Manabu Toyoshima, Takeo Yoshikawa, Itone Ogawa, Masanari Itokawa, Rumi Kurokawa, Akihiro Nakaya, Haruhiko Bito, Shabeesh Balan, Tomoe Ichikawa, Toshiya Manabe, Hiroyuki Okuno
Publikováno v:
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 13, Iss 4, Pp n/a-n/a (2021)
EMBO Molecular Medicine, Vol 13, Iss 4, Pp n/a-n/a (2021)
Genomic defects with large effect size can help elucidate unknown pathologic architecture of mental disorders. We previously reported on a patient with schizophrenia and a balanced translocation between chromosomes 4 and 13 and found that the breakpo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d37e801540257fc3b482ef56f847f0cf
https://pubmed.ncbi.nlm.nih.gov/33656268
https://pubmed.ncbi.nlm.nih.gov/33656268
Autor:
Fumiko, Arima-Yoshida, Matthieu, Raveau, Atsushi, Shimohata, Kenji, Amano, Akihiro, Fukushima, Masashi, Watanave, Shizuka, Kobayashi, Satoko, Hattori, Masaya, Usui, Haruhiko, Sago, Nobuko, Mataga, Tsuyoshi, Miyakawa, Kazuhiro, Yamakawa, Toshiya, Manabe
Publikováno v:
Scientific Reports
Down syndrome is a complex genetic disorder caused by the presence of three copies of the chromosome 21 in humans. The most common models, carrying extra-copies of overlapping fragments of mouse chromosome 16 that is syntenic to human chromosome 21,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::172b7cdfb6c187b90b68130d2f881fc0
https://pubmed.ncbi.nlm.nih.gov/32843708
https://pubmed.ncbi.nlm.nih.gov/32843708
Autor:
Sarah N. Mattson, Yasuko Takeda, Tetsu Akiyama, Yukiko Nasu-Nishimura, Natacha Akshoomoff, Toshiya Manabe, Ken Matsuura, Fumiko Arima-Yoshida, Fumika Sakaue, Tsutomu Nakamura, Paul Grossfeld
Publikováno v:
Nature Communications
Nature Communications, Vol 7, Iss 1, Pp 1-16 (2016)
Nature Communications, Vol 7, Iss 1, Pp 1-16 (2016)
Jacobsen syndrome (JBS) is a rare congenital disorder caused by a terminal deletion of the long arm of chromosome 11. A subset of patients exhibit social behavioural problems that meet the diagnostic criteria for autism spectrum disorder (ASD); howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6db142e8b255fa41f0e126e6858117f
https://doi.org/10.1038/ncomms10861
https://doi.org/10.1038/ncomms10861
Publikováno v:
European Journal of Neuroscience. 33:1637-1646
The hippocampus is essential for the formation of certain types of memory, and synaptic plasticity such as long-term potentiation (LTP) is widely accepted as a cellular basis of hippocampus-dependent memory. Although LTP in both perforant path-dentat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e45a89973257385540f80750071eedb
https://doi.org/10.1111/j.1460-9568.2011.07657.x
https://doi.org/10.1111/j.1460-9568.2011.07657.x
Autor:
Masahiko Watanabe, Shoji Komai, Yoichiro Iwakura, Reiko Horai, Yuji Kiyama, Fumiko Arima-Yoshida, Hisashi Umemori, Kazumi Ebine, Toshiya Manabe, June Goto, Takanobu Nakazawa, Tadashi Yamamoto, Tohru Tezuka, Masahiro Fukaya, Ayako M. Watabe, Mina Delawary, Katsuko Sudo
Publikováno v:
The EMBO Journal. 25:2867-2877
Phosphorylation of neural proteins in response to a diverse array of external stimuli is one of the main mechanisms underlying dynamic changes in neural circuitry. The NR2B subunit of the NMDA receptor is tyrosine-phosphorylated in the brain, with Ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3300d2126fe1f457aa473d50ac3b61b2
https://doi.org/10.1038/sj.emboj.7601156
https://doi.org/10.1038/sj.emboj.7601156
Publikováno v:
The European journal of neuroscience. 33(9)
The hippocampus is essential for the formation of certain types of memory, and synaptic plasticity such as long-term potentiation (LTP) is widely accepted as a cellular basis of hippocampus-dependent memory. Although LTP in both perforant path-dentat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::530a2365285e76ff8a16f25718b00e77
https://pubmed.ncbi.nlm.nih.gov/21535245
https://pubmed.ncbi.nlm.nih.gov/21535245