Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Eriko Fujita-Jimbo"'
Autor:
Taiju Hyuga, Kota Fujimoto, Daiki Hashimoto, Kazuya Tanabe, Taro Kubo, Shigeru Nakamura, Yuko Ueda, Eriko Fujita-Jimbo, Kazuhiro Muramatsu, Kentaro Suzuki, Hitoshi Osaka, Shinichi Asamura, Kimihiko Moriya, Hideo Nakai, Gen Yamada
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract The post-surgical fluid leakage from the tubular tissues is a critical symptom after gastrointestinal or urinary tract surgeries. Elucidating the mechanism for such abnormalities is vital in surgical and medical science. The exposure of the
Externí odkaz:
https://doaj.org/article/69cc720f13e44973848031dcdffdbf30
Autor:
Shinya Nakamura, Takuma Koyama, Naohiro Izawa, Seitaro Nomura, Takanori Fujita, Yasunori Omata, Takashi Minami, Morio Matsumoto, Masaya Nakamura, Eriko Fujita-Jimbo, Takashi Momoi, Takeshi Miyamoto, Hiroyuki Aburatani, Sakae Tanaka
Publikováno v:
PLoS ONE, Vol 12, Iss 4, p e0175632 (2017)
Trimethylation of histone H3 lysine 4 and lysine 27 (H3K4me3 and H3K27me3) at gene promoter regions critically regulates gene expression. Key developmental genes tend to exhibit changes in histone modification patterns from the H3K4me3/H3K27me3 bival
Externí odkaz:
https://doaj.org/article/25035f78986246198781dd29ab18eea8
Autor:
Eriko Fujita-Jimbo, Zhi-Ling Yu, Hong Li, Takanori Yamagata, Masato Mori, Takashi Momoi, Mariko Y Momoi
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e51155 (2012)
Little is known about the molecular pathogenesis of Autism spectrum disorder (ASD), a neurodevelopmental disorder. Here we identified two mutations in the G-protein-coupled receptor 37 gene (GPR37) localized on chromosome 7q31-33, called the AUTS1 re
Externí odkaz:
https://doaj.org/article/d3718463a9d64d91883277772c1ef1bb
Autor:
Khishigjargal Batjargal, Toshihiro Tajima, Eriko Fujita-Jimbo, Takeshi Yamaguchi, Akie Nakamura, Takanori Yamagata
Publikováno v:
Clinical Pediatric Endocrinology. 31:234-241
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a80496de3ba9759cb5d02cc7fd38f9f3
https://doi.org/10.1297/cpe.2021-0065
https://doi.org/10.1297/cpe.2021-0065
Autor:
Khishigjargal, Batjargal, Toshihiro, Tajima, Eriko, Fujita-Jimbo, Takeshi, Yamaguchi, Akie, Nakamura, Takanori, Yamagata
Publikováno v:
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology. 31(4)
Paired box transcription factor 8 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0760822c24958a0f0d5bb665cbf4f259
https://pubmed.ncbi.nlm.nih.gov/36405440
https://pubmed.ncbi.nlm.nih.gov/36405440
Autor:
Eriko Fujita-Jimbo1,2, Yuko Tanabe2, Zhiling Yu1,3, Karin Kojima1, Masato Mori1, Hong Li1,4, Sadahiko Iwamoto5, Takanori Yamagata1, Momoi, Mariko Y.1,2 mymomoi@iuhw.ac.jp, Takashi Momoi2 momoi@iuhw.ac.jp
Publikováno v:
Molecular Autism. 2015, Vol. 6 Issue 1, p1-10. 10p.
Publikováno v:
Cerebral cortex (New York, N.Y. : 1991). 27(7)
The molecular mechanisms underlying the formation of the thalamus during development have been investigated intensively. Although transcription factors distinguishing the thalamic primordium from adjacent brain structures have been uncovered, those i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4564dbf4efef0969dcf231556a8eba5
https://pubmed.ncbi.nlm.nih.gov/27384060
https://pubmed.ncbi.nlm.nih.gov/27384060
Autor:
Mariko Y. Momoi, Masato Mori, Takanori Yamagata, Karin Kojima, Hong Li, Eriko Fujita-Jimbo, Zhiling Yu, Yuko Tanabe, Sadahiko Iwamoto, Takashi Momoi
Publikováno v:
Molecular Autism
Background Autism spectrum disorder (ASD) has a complex genetic etiology. Some symptoms and mutated genes, including neuroligin (NLGN), neurexin (NRXN), and SH3 and multiple ankyrin repeat domains protein (SHANK), are shared by schizophrenia and ASD.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::595b657c31b0d74d7ca2654953d7e05d
http://europepmc.org/articles/PMC4360946
http://europepmc.org/articles/PMC4360946
Publikováno v:
Journal of neurochemistry. 134(4)
Autism spectrum disorder (ASD) is a developmental brain disorder. Mutations in synaptic components including synaptic adhesion molecules have been found in ASD patients. Contactin-associated protein-like 2 (CASPR2) is one of the synaptic adhesion mol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5456cfc4d0bb2197f72c355325bd7e35
https://pubmed.ncbi.nlm.nih.gov/25977097
https://pubmed.ncbi.nlm.nih.gov/25977097
Autor:
Akira Shiota, Haruki Senoo, Yuko Tanabe, Koko Urase, Takashi Momoi, Kana Takahashi, Yoriko Kouroku-Murakami, Eriko Fujita-Jimbo, Yoshihiro Mezaki
Publikováno v:
Neuroscience letters. 576
Src kinase-associated phosphoprotein 2 (Ra70/scap2), which was originally isolated as a retinoic acid (RA)-induced gene, associates with molecules that modulate integrin-survival signals. Although RA is essential for vertebrate organogenesis in the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4e9c240be1f4141aded5ae6b66c10fe
https://pubmed.ncbi.nlm.nih.gov/24846415
https://pubmed.ncbi.nlm.nih.gov/24846415