Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Natsumi Ohsawa"'
Autor:
Takumi Nakamura, Natsumi Ohsawa-Yoshida, Yimeng Zhao, Michinori Koebis, Kosuke Oana, Hiroaki Mitsuhashi, Shoichi Ishiura
Publikováno v:
Biochemistry and Biophysics Reports, Vol 5, Iss C, Pp 63-69 (2016)
Expression of chloride channel 1 (CLCN1/ClC-1) in skeletal muscle is driven by alternative splicing, a process regulated in part by RNA-binding protein families MBNL and CELF. Aberrant splicing of CLCN1 produces many mRNAs, which were translated into
Externí odkaz:
https://doaj.org/article/c61dc747d6cc402c8d3927898810aa10
Autor:
Kosuke Oana, Natsumi Ohsawa-Yoshida, Shoichi Ishiura, Yimeng Zhao, Takumi Nakamura, Michinori Koebis, Hiroaki Mitsuhashi
Publikováno v:
Biochemistry and Biophysics Reports
Biochemistry and Biophysics Reports, Vol 5, Iss C, Pp 63-69 (2016)
Biochemistry and Biophysics Reports, Vol 5, Iss C, Pp 63-69 (2016)
Expression of chloride channel 1 (CLCN1/ClC-1) in skeletal muscle is driven by alternative splicing, a process regulated in part by RNA-binding protein families MBNL and CELF. Aberrant splicing of CLCN1 produces many mRNAs, which were translated into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33eda6e7e6ea8ea9c8643cab10449516
http://europepmc.org/articles/PMC5600464
http://europepmc.org/articles/PMC5600464
Autor:
Yasuko Toyoshima, Shoichi Ishiura, Taisuke Otsuki, Yoshikazu Ugawa, Norio Kanesawa, Yutaka Suzuki, Akira Tamaoka, Yuji Takahashi, Masashi Hamada, Ryoko Koike, Hiroshi Akiyama, Ritsuko Hanajima, Jun Shimizu, Hitoshi Takahashi, Koji Abe, Takashi Matsukawa, Takefumi Hitomi, Jun Mitsui, Mieko Otsuka, Yasuo Terao, Shota Shibata, Mutsuo Sasagawa, Shoji Tsuji, Yutaka Saito, Takeshi Yasuda, Takayuki Kondo, Wei Qu, Koichiro Higasa, Masaki Tanaka, Asao Fujiyama, Sumio Sugano, Akira Sano, Hideaki Yurino, Hidetoshi Date, Miho Matsukawa, Junko Kanda, Osamu Onodera, Satomi Inomata-Terada, Masayuki Nakamura, Yuichiro Shirota, Akatsuki Kubota, Jun Yoshimura, Toshihiro Hayashi, Ryo Yamasaki, K. Kaida, Akio Ikeda, Akiyoshi Kakita, Yoshio Sakiyama, Kazuhiro Sanpei, Jun Goto, Yasuko Kuroha, Aki Mitsue, Naoya Hasegawa, Masatoyo Nishizawa, Hiroki Takano, Akira Ueki, Kazuki Ichikawa, Fumiko Kusunoki Nakamoto, Mana Higashihara, Yoshihisa Takiyama, Shinichi Morishita, Koichiro Doi, Yaeko Ichikawa, Natsumi Ohsawa-Yoshida, Kishin Koh, Hiroyuki Ishiura, Masayoshi Tada
Publikováno v:
Nature genetics. 50(4)
Epilepsy is a common neurological disorder, and mutations in genes encoding ion channels or neurotransmitter receptors are frequent causes of monogenic forms of epilepsy. Here we show that abnormal expansions of TTTCA and TTTTA repeats in intron 4 of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0667ba844436dc89160e64c454605b
https://pubmed.ncbi.nlm.nih.gov/30254519
https://pubmed.ncbi.nlm.nih.gov/30254519
Publikováno v:
Genes to Cells. 20:121-134
Myotonic dystrophy type 1 (DM1) is an RNA-mediated disorder characterized by muscle weakness, cardiac defects and multiple symptoms and is caused by expanded CTG repeats within the 3' untranslated region of the DMPK gene. In this study, we found abno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16b6ab94c0505998dd9ddc77b06804df
https://doi.org/10.1111/gtc.12201
https://doi.org/10.1111/gtc.12201
Autor:
Shoichi Ishiura, Ichizo Nishino, Michinori Koebis, Yoshihiro Kino, Noboru Sasagawa, Natsumi Ohsawa
Publikováno v:
Genes to Cells. 16:961-972
Myotonic dystrophy type 1 (DM1) is a multisystemic disease caused by a CTG repeat expansion in the 3′-UTR of dystrophia myotonica-protein kinase. Aberrant regulation of alternative splicing is a characteristic feature of DM. Dozens of genes have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3bfa9925663118636a5e868a007b855
https://doi.org/10.1111/j.1365-2443.2011.01542.x
https://doi.org/10.1111/j.1365-2443.2011.01542.x
Publikováno v:
Biochemical and Biophysical Research Communications. 409:64-69
Myotonic dystrophy type 1 (DM1) is an autosomal dominant disorder of muscular dystrophy characterized by muscle weakness and wasting. DM1 is caused by expansion of CTG repeats in the 3'-untranslated region (3'-UTR) of DM protein kinase (DMPK) gene. S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8ce9c218be68ad2152ee752d35c6051
https://doi.org/10.1016/j.bbrc.2011.04.106
https://doi.org/10.1016/j.bbrc.2011.04.106
Autor:
Michinori, Koebis, Natsumi, Ohsawa, Yoshihiro, Kino, Noboru, Sasagawa, Ichizo, Nishino, Shoichi, Ishiura
Publikováno v:
Genes to cells : devoted to molecularcellular mechanisms. 16(9)
Myotonic dystrophy type 1 (DM1) is a multisystemic disease caused by a CTG repeat expansion in the 3'-UTR of dystrophia myotonica-protein kinase. Aberrant regulation of alternative splicing is a characteristic feature of DM. Dozens of genes have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b67e23add3ec72203d65d0cb3ee390f0
https://pubmed.ncbi.nlm.nih.gov/21794030
https://pubmed.ncbi.nlm.nih.gov/21794030