Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Hideo Taniura"'
Autor:
Shuhei Soeda, Daiki Ito, Tomoe Ogushi, Yui Sano, Ryosuke Negoro, Takuya Fujita, Ryo Saito, Hideo Taniura
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Prader-Willi syndrome (PWS), which is a complex epigenetic disorder caused by the deficiency of paternally expressed genes in chromosome 15q11-q13, is associated with several psychiatric dimensions, including autism spectrum disorder. We hav
Externí odkaz:
https://doaj.org/article/fe1f53e544044a61b1f7652b592c2aa6
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102351- (2021)
DNA methylation is a common method of gene expression regulation, and this form of regulation occurs in the neurodevelopmental disorder Prader-Willi syndrome (PWS). Gene expression regulation via methylation is important for humans, although there is
Externí odkaz:
https://doaj.org/article/65ddc2217fe64273b0ba48e1c6b00969
Publikováno v:
Heliyon, Vol 5, Iss 3, Pp e01301- (2019)
Sirtuin interacts with many regulatory proteins involved in energy homeostasis, DNA repair, cell survival, and lifespan extension. We investigated the functional roles of Sir2D during early Dictyostelium development upon starvation. We found that ect
Externí odkaz:
https://doaj.org/article/c4b3ff74e7984e7b955dba04d5d5e839
Autor:
Shin-Ichiro Yamaguchi, Qilin Xie, Fumiya Ito, Kazuki Terao, Yoshinobu Kato, Miki Kuroiwa, Satoshi Omori, Hideo Taniura, Kengo Kinoshita, Takuya Takahashi, Shinya Toyokuni, Kota Kasahara, Masafumi Nakayama
Publikováno v:
Nature Nanotechnology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14089aa6ea4b4d9f2c0e028e39397311
https://doi.org/10.1038/s41565-023-01363-w
https://doi.org/10.1038/s41565-023-01363-w
Publikováno v:
Stem Cell Research, Vol 53, Iss, Pp 102351-(2021)
DNA methylation is a common method of gene expression regulation, and this form of regulation occurs in the neurodevelopmental disorder Prader-Willi syndrome (PWS). Gene expression regulation via methylation is important for humans, although there is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e755f6f7f10796326497a46662ed6b08
https://pubmed.ncbi.nlm.nih.gov/33895503
https://pubmed.ncbi.nlm.nih.gov/33895503
Publikováno v:
SSRN Electronic Journal.
DNA methylation is a common method of gene expression regulation, and this form of regulation occurs in the neurodevelopmental disorder Prader Willi syndrome (PWS). Gene expression regulation via methylation is important for humans, although the role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::179efab68f87ce59e66f38bfbccf2341
https://doi.org/10.2139/ssrn.3616899
https://doi.org/10.2139/ssrn.3616899
Publikováno v:
Heliyon, Vol 5, Iss 3, Pp e01301-(2019)
Sirtuin interacts with many regulatory proteins involved in energy homeostasis, DNA repair, cell survival, and lifespan extension. We investigated the functional roles of Sir2D during early Dictyostelium development upon starvation. We found that ect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5effe130db58d966674150d46dbfa2d
http://www.sciencedirect.com/science/article/pii/S2405844018352642
http://www.sciencedirect.com/science/article/pii/S2405844018352642
Publikováno v:
Neuroscience letters. 703
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by a lack of expression of paternally inherited genes located in the15q11.2-q13 chromosome region. An obstacle in the study of human neurological diseases is the inaccessibility of b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8981136bae74f535a75b75bddb33a3b1
https://pubmed.ncbi.nlm.nih.gov/30902571
https://pubmed.ncbi.nlm.nih.gov/30902571
Publikováno v:
Cell Biology. 9:1
Sirtuin involves in cellular processes to adapt to starvation in the endocrine and metabolic systems. We examined Sir2B function during early Dictyostelium development upon starvation. GFP-tagged Sir2B was expressed and the immunoreactivity was detec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4a781ea2a85ef43f902a6b770bb85c7
https://doi.org/10.11648/j.cb.20210901.11
https://doi.org/10.11648/j.cb.20210901.11
Autor:
Shuhei Soeda, Aya Igeta, Futa Shimizu, Yuka Tokumura, Hideo Taniura, Shusei Tojo, Ai Fujii, Yui Sano, Minori Nakamura, Yoshiaki Nakagawara, Daisuke Fukuoka, Rio Kawamoto
Publikováno v:
Proceedings for Annual Meeting of The Japanese Pharmacological Society. 93:2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16157bbbd8a8962d3d0b2c0c03acd09f
https://doi.org/10.1254/jpssuppl.93.0_2-p-251
https://doi.org/10.1254/jpssuppl.93.0_2-p-251