Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Kosuke Jozaki"'
Autor:
MD. Mijanur Rahman, Riho Matsuda, Tomoe Matsuda, Yuki Nishiyama, Kosuke Jozaki, Kajio Anann, Yasuhiko Wada
Publikováno v:
The Journal of Poultry Science, Vol 51, Iss 2, Pp 138-143 (2014)
Silkie fowl are very famous in China and Japan, however the egg production rate of the Silkie fowl is very low because of broodiness. Authors have examined the polymorphisms of the 5′-flanking region of the prolactin gene in Taihe Silkie fowl and i
Externí odkaz:
https://doaj.org/article/4a6d1a19e37844f890a7620d06b1d238
FABP7 Regulates Acetyl-CoA Metabolism Through the Interaction with ACLY in the Nucleus of Astrocytes
Autor:
Yuji Owada, Masayuki Kanamori, Kosuke Jozaki, Shuhei Kobayashi, Subrata Kumar Shil, Ryo Zama, Hiroshi Kogo, Ariful Islam, Kazuhiko Igarashi, Hirofumi Miyazaki, Chie Shimamoto-Mitsuyama, Yoshiteru Kagawa, Shin Ichiro Kanno, Banlanjo Abdulaziz Umaru, Shun Sato, Ryo Ito, Teiji Tominaga, Hiroki Shima, Akira Yasui, Kohji Fukunaga, Yui Yamamoto, Takeo Yoshikawa, Norihiro Sugino, Akira Sugawara
Publikováno v:
Molecular Neurobiology
Fatty acid binding protein 7 (FABP7) is an intracellular fatty acid chaperon that is highly expressed in astrocytes, oligodendrocyte-precursor cells, and malignant glioma. Previously, we reported that FABP7 regulates the response to extracellular sti
Autor:
Hiromi Asada, Masahiro Shinagawa, Ryo Maekawa, Shun Sato, Hiroshi Tamura, Yuichiro Shirafuta, Isao Tamura, Norihiro Sugino, Kosuke Jozaki, Toshiaki Taketani
Publikováno v:
Journal of Biological Chemistry. 293:5270-5280
We have previously shown that decidualization of human endometrial stromal cells (ESCs) causes a genome-wide increase in the levels of acetylation of histone-H3 Lys-27 (H3K27ac). We also reported that the distal gene regions, more than 3 kb up- or do
Autor:
Norihiro Sugino, Yumiko Mihara, Yuichiro Shirafuta, Isao Tamura, Yasuyuki Ohkawa, Toshiaki Taketani, Yumiko Doi-Tanaka, Ryo Maekawa, Shun Sato, Kosuke Jozaki, Hiroshi Tamura, Haruka Takagi
Publikováno v:
Molecular and Cellular Endocrinology. 520:111085
We previously reported that H3K27 acetylation (H3K27ac) increases throughout the genome during decidualization of human endometrial stromal cells (ESCs). However, its mechanisms have not been clarified. We also reported that C/EBPβ acts as a pioneer
Autor:
Ryo Maekawa, Takuya Kajimura, Shun Sato, Hiromi Asada, Yoshiaki Yamagata, Shigeru Yamamoto, Hiroshi Tamura, Kosuke Jozaki, Norihiro Sugino, Isao Tamura, Maki Okada, Lifa Lee
Publikováno v:
Molecular Endocrinology. 30:335-347
The mechanism controlling tissue-specific expression of estrogen receptor 1 (ESR1) is unclear. In other genes, DNA methylation of a region called the tissue-dependent and differentially methylated region (T-DMR) has been associated with tissue-specif
Autor:
Ryo Maekawa, Kosuke Jozaki, Shun Sato, Yuichiro Shirafuta, Hiromi Asada, Masahiro Shinagawa, Haruka Takagi, Norihiro Sugino, Toshiaki Taketani, Hiroshi Tamura, Isao Tamura, Yumiko Mihara
Publikováno v:
Reproduction (Cambridge, England). 157(5)
Decidualization stimuli activate the insulin signaling pathway and increase the glucose uptake in human endometrial stromal cells (ESCs). The inductions of prolactin (PRL) and IGF-binding protein-1 (IGFBP1), specific markers of decidualization, were
Autor:
Yoshio Makita, Kazuhiko Nakabayashi, Tsutomu Ogata, Yuhei Hamasaki, Makoto Migita, Nobuhiko Okamoto, Kosuke Jozaki, Hitomi Yatsuki, Keiko Matsubara, Toshiyuki Maeda, Kenichiro Hata, Muneaki Matsuo, Hidefumi Tonoki, Hidenobu Soejima, Kenichi Nishioka, Hirofumi Ohashi, Rika Kosaki, Tsunehiro Mukai, Fumio Takada, Yasufumi Ohtsuka, Keiichiro Joh, Ken Higashimoto
Publikováno v:
Genetics in Medicine
Purpose: Expression of imprinted genes is regulated by DNA methylation of differentially methylated regions (DMRs). Beckwith–Wiedemann syndrome is an imprinting disorder caused by epimutations of DMRs at 11p15.5. To date, multiple methylation defec
Autor:
Ken Higashimoto, Yuichi Takama, Hidenobu Soejima, Akio Kubota, Masahiro Nakayama, Kosuke Jozaki
Publikováno v:
Pediatrics International. 56:931-934
Herein is described a case of breast fibroadenomas in a 16-year-old girl with Beckwith-Wiedemann syndrome (BWS) and uniparental disomy (UPD) of chromosome 11p15.5. She was clinically diagnosed with BWS and direct closure was performed for an omphaloc
Autor:
Yasufumi Ohtsuka, Nobuhiko Okamoto, Koh-ichiro Yoshiura, Hitomi Yatsuki, Yuichi Takama, Kensaku Sasaki, Akio Kubota, Tsunehiro Mukai, Hidenobu Soejima, H. Yoshinaga, Ken Higashimoto, Kosuke Jozaki, M. Nakayama, Keiichiro Joh, Kenichi Nishioka
Publikováno v:
Clinical Genetics. 88:261-266
Approximately 20% of Beckwith-Wiedemann syndrome (BWS) cases are caused by mosaic paternal uniparental disomy of chromosome 11 (pUPD11). Although pUPD11 is usually limited to the short arm of chromosome 11, a small minority of BWS cases show genome-w
Autor:
Hiromi Asada, Hiroshi Tamura, Ryo Maekawa, Norihiro Sugino, Shun Sato, Isao Tamura, Takuya Kajimura, Yumiko Mihara, Kosuke Jozaki, Maki Okada, Toshiaki Taketani, Akihisa Takasaki
Publikováno v:
Reproductive Medicine and Biology
Aim Although a thin endometrium has been well recognized as a critical factor in implantation failure, little information is available regarding the molecular mechanisms. The present study investigated these mechanisms by using genome-wide mRNA expre