Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Takahide Okuyama"'
Autor:
Masaaki Ikeda, Ryosuke Yamagishi, Takahide Okuyama, Jiro Shimada, Yayoi Maruoka, Hiroki Kaneko
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 36:767-778
Oct4 is a master regulator of the induction and maintenance of cellular pluripotency, and has crucial roles in early stages of differentiation. It is the only factor that cannot be substituted by other members of the same protein family to induce plu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b9b53eb8bef349b834c995c5730d3a7
https://doi.org/10.1080/07391102.2017.1289124
https://doi.org/10.1080/07391102.2017.1289124
Autor:
Ryosuke Yamagishi, Hiroki Kaneko, Shigeru Chaen, Shuntaro Oba, Jiro Shimada, Takahide Okuyama
Publikováno v:
Biochemistry and Biophysics Reports
Most transcription and epigenetic factors in eukaryotic cells have nuclear localization signals (NLSs) and are transported to the nucleus by nuclear transport proteins. Understanding the features of NLSs and the mechanisms of nuclear transport might
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77e3125a89490fd0ffc83c48c6529285
https://doi.org/10.1016/j.bbrep.2015.11.001
https://doi.org/10.1016/j.bbrep.2015.11.001
Autor:
Takahide Okuyama, Yoichiro Takiguchi, Tomoko Shintani, Kazunori Namba, Tatsuo Matsunaga, Shuntaro Oba, Ryosuke Yamagishi, Kimitaka Kaga, Hiroki Kaneko, Hirotaka Yagi, Hideki Mutai
Publikováno v:
Otologyneurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 37(4)
Hypothesis Different missense mutations of the optic atrophy 1 gene (OPA1) identified in optic atrophy patients with auditory neuropathy spectrum disorder (ANSD) induce functional impairment through different molecular mechanisms. Background OPA1 is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8c180d70bffe93e35637465b02348f3
https://pubmed.ncbi.nlm.nih.gov/26905822
https://pubmed.ncbi.nlm.nih.gov/26905822