Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Syouichi, Katayama"'
Publikováno v:
Neural Plasticity, Vol 2020 (2020)
Cyclin-dependent kinase-like 5 (CDKL5, also known as STK9) is a serine/threonine protein kinase originally identified in 1998 during a transcriptional mapping project of the human X chromosome. Thereafter, a mutation in CDKL5 was reported in individu
Externí odkaz:
https://doaj.org/article/ba0749e2d520435ab656c205a9ab6d4f
Publikováno v:
Heliyon, Vol 5, Iss 10, Pp e02662- (2019)
Yokukansan (YKS), a traditional Japanese Kampo medicine, affects neurological and psychiatric disorders. It ameliorates hippocampal neurogenesis in animals. However, its effect on neuronal cell differentiation remains unclear. Therefore, we investiga
Externí odkaz:
https://doaj.org/article/c7f75e90d45249a98f9fce74a2ce5d9d
Autor:
Yasunori Sugiyama, Syouichi Katayama, Isamu Kameshita, Keiko Morisawa, Takuma Higuchi, Hiroshi Todaka, Eiji Kinoshita, Emiko Kinoshita-Kikuta, Tohru Koike, Taketoshi Taniguchi, Shuji Sakamoto
Publikováno v:
MethodsX, Vol 2, Iss C, Pp 469-474 (2015)
Protein kinase expression and activity play important roles in diverse cellular functions through regulation of phosphorylation signaling. The most commonly used tools for detecting the protein kinase are protein kinase-specific antibodies, and phosp
Externí odkaz:
https://doaj.org/article/1d4949930c884dbfa0f3a4a90c32f4de
Autor:
Syouichi Katayama
Publikováno v:
Electrophoresis Letters. 64:41-44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0bcc64945c4c5d34ff05fccf7948d853
https://doi.org/10.2198/electroph.64.41
https://doi.org/10.2198/electroph.64.41
Autor:
Hisashi Takatsuka, Yukihiko Kubota, Gen Yasui, Tetsuya Inazu, Masahiro Ito, Syouichi Katayama
Publikováno v:
Biochemical and biophysical research communications. 568
Rett syndrome (OMIM # 312750 ) is a developmental neurological disorder that is caused by a mutation in methyl-CpG-binding protein 2 (MeCP2). MeCP2 localizes to the nucleus, binds to methylated DNA, and regulates gene expression during neuronal devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0fa4b6268cadf29896168c9fcf6e4f7
https://pubmed.ncbi.nlm.nih.gov/34192606
https://pubmed.ncbi.nlm.nih.gov/34192606
Publikováno v:
Biologicalpharmaceutical bulletin. 43(7)
P19 pluripotent embryonic carcinoma (EC) stem cells are derived from pluripotent germ cell tumours and can differentiate into three germ layers. Treatment of these cells in suspension culture with retinoic acid induces their differentiation into neur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cff6fb884a3e605b86e8fc29a770a38
https://pubmed.ncbi.nlm.nih.gov/32612072
https://pubmed.ncbi.nlm.nih.gov/32612072
Autor:
Isamu Kameshita, Hiroki Yamada, Noriyuki Sueyoshi, Yukako Senga, Syouichi Katayama, Masashi Yamashita, Yasushi Shigeri, Yasuhiro Takenaka, Atsuhiko Ishida
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 82:1335-1343
We surveyed genome sequences from the basidiomycetous mushroom Coprinopsis cinerea and isolated a cDNA homologous to CMKA, a calmodulin-dependent protein kinase (CaMK) in Aspergillus nidulans. We designated this sequence, encoding 580 amino acids wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf4bc97cba665c09d53b207f24206d20
https://doi.org/10.1080/09168451.2018.1462692
https://doi.org/10.1080/09168451.2018.1462692
Autor:
Juliet O. Makanga, Atsushi Morii, Naoki Miyata, Tetsuya Inazu, Takayoshi Suzuki, Syouichi Katayama
Publikováno v:
Biochemical and Biophysical Research Communications. 498:45-51
Histone acetylation and deacetylation correlate with diverse biological phenomena through gene transcription. Histone deacetylases (HDACs) regulate deacetylation of histones and other proteins. However, as a member of the HDAC family, HDAC8 function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5495f78e5f4b348f934894b2b32d73ba
https://doi.org/10.1016/j.bbrc.2018.02.195
https://doi.org/10.1016/j.bbrc.2018.02.195
Autor:
Gen Yasui, Masahiro Ito, Takako Kaneko-Kawano, Muhamad Fahmi, Yukihiko Kubota, Tetsuya Inazu, Kaito Seki, Syouichi Katayama
Rett syndrome (RTT), a neurodevelopmental disorder, is mainly caused by mutations in methyl CpG-binding protein 2 (MECP2), which alter the functions of domains to either bind to methylated DNA or interact with a transcriptional co-repressor complex.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd2a267d8e6ae429408b0d1969047838
Autor:
Yukihiko Kubota, Tetsuya Inazu, Muhamad Fahmi, Masahiro Ito, Syouichi Katayama, Takako Kaneko-Kawano, Kaito Seki, Gen Yasui
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 22, p 5593 (2019)
International Journal of Molecular Sciences
Volume 20
Issue 22
International Journal of Molecular Sciences
Volume 20
Issue 22
Rett syndrome (RTT), a neurodevelopmental disorder, is mainly caused by mutations in methyl CpG-binding protein 2 (MECP2), which has multiple functions such as binding to methylated DNA or interacting with a transcriptional co-repressor complex. It h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b107a8351882b952e1f772ea5a5c272
https://www.mdpi.com/1422-0067/20/22/5593
https://www.mdpi.com/1422-0067/20/22/5593