Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hisashi Oishi"'
Autor:
Yosuke Nishio, Kohji Kato, Frederic Tran Mau-Them, Hiroshi Futagawa, Chloé Quélin, Saori Masuda, Antonio Vitobello, Shiomi Otsuji, Hossam H. Shawki, Hisashi Oishi, Christel Thauvin-Robinet, Toshiki Takenouchi, Kenjiro Kosaki, Yoshiyuki Takahashi, Shinji Saitoh
Publikováno v:
HGG Advances, Vol 4, Iss 4, Pp 100238- (2023)
Summary: MYCN, a member of the MYC proto-oncogene family, regulates cell growth and proliferation. Somatic mutations of MYCN are identified in various tumors, and germline loss-of-function variants are responsible for Feingold syndrome, characterized
Externí odkaz:
https://doaj.org/article/500afd5a9bde413c8c9a8ccf0d6652d9
Publikováno v:
The FASEB Journal. 33
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 33(7)
Increased muscle contractile activity, as observed with regular exercise, prevents oxidative stress-induced muscle wasting, at least partially, by improving the antioxidant defense system. Phosphorylated p62/sequestosome1 competitively binds to the K
Autor:
Daisuke Ieda, Tomomi Miyamoto, Makoto Nakanishi, Yutaka Negishi, Kohji Kato, Shinya Ugawa, Hisashi Oishi, Natsuko Kumamoto, Shinji Saitoh, Ichiro Miyoshi, Yoshikazu Johmura
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0237814 (2020)
PLoS ONE
PLoS ONE
Schaaf-Yang syndrome (SYS) is a neurodevelopmental disorder caused by truncating variants in the paternal allele of MAGEL2, located in the Prader-Willi critical region, 15q11-q13. Although the phenotypes of SYS overlap those of Prader-Willi syndrome
Autor:
Abdelaziz E. Ibrahim, Youhei Hiromori, Megumi C. Katoh, Tsuyoshi Nakanishi, Hisashi Oishi, Al-Sayed Al-Soudy, Seiya Mizuno, Fumihiro Sugiyama, Atsushi Yoshiki, Walaa A Basha, Hossam H. Shawki, Satoru Takahashi, Yoshikazu Hasegawa, Hany A. El-Shemy, Hiroyoshi Iseki, Hisamitsu Nagase
Publikováno v:
genesis. 54:389-397
Spermatogenesis is a complex and highly regulated process by which spermatogonial stem cells differentiate into spermatozoa. To better understand the molecular mechanisms of the process, the Cre/loxP system has been widely utilized for conditional ge
Autor:
Hisashi Oishi, Shosei Yoshida, Ahmed A. H. Abdellatif, Toshiaki Usui, Yu Kitadate, Walaa A Basha, Satoru Takahashi, Masafumi Muratani, Risa Okada, Kazunori Hasegawa, Atsuo Ogura, Hany A. El-Shemy, Hossam H. Shawki, Keiji Mochida
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0190800 (2018)
PLoS ONE
PLoS ONE
The transcription factor MAFB is an important regulator of the development and differentiation of various organs and tissues. Previous studies have shown that MAFB is expressed in embryonic and adult mouse testes and is expected to act as the downstr
Autor:
Shinichi Mizuki, Satoru Takahashi, Tatsuhiko Miyazaki, Hisashi Oishi, Haruyasu Yamamoto, Masao Ono, Mingcai Zhang, Junji Kamogawa, Masato Nose
Publikováno v:
Pathology International. 60:430-437
A cumulative effect of the susceptibility genes with polymorphic alleles may be responsible for rheumatoid arthritis (RA). The objective of this study was to clarify whether susceptibility to RA is under the control of common allelic loci between two
Autor:
M. B. Shoaib, Yunshin Jung, Yukari Okita, Mesbah El-Sayed, Yoshikazu Hasegawa, Satoru Takahashi, Hiroyuki Suzuki, Hisashi Oishi, Fumihiro Sugiyama, Ahmed A. H. Abdellatif, Takahiro Itagaki, Salah E. El-Morsy, Hossam H. Shawki
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 2, p e0150010 (2016)
PLoS ONE, Vol 11, Iss 2, p e0150010 (2016)
The MAF family transcription factors are homologs of v-Maf, the oncogenic component of the avian retrovirus AS42. They are subdivided into 2 groups, small and large MAF proteins, according to their structure, function, and molecular size. MAFK is a m
Autor:
Natsuka Goto, Yuka Nakajima, Satoru Takahashi, Yoh-ichi Kawabe, Yuki Hayashi, Naoya Iwasaki, Tatsuya Watanabe, Ryohei Furumai, Masashi Kajiro, Masatsugu Ema, Hiroyuki Kishimoto, Akiko Murayama, Mai Tsuchiya, Miyuki Katano, Hisashi Oishi, Junn Yanagisawa
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 10, p e25871 (2011)
PLoS ONE, Vol 6, Iss 10, p e25871 (2011)
Protein ubiquitination is a post-translational protein modification that regulates many biological conditions [1], [2], [3], [4]. Trip12 is a HECT-type E3 ubiquitin ligase that ubiquitinates ARF and APP-BP1 [5], [6]. However, the significance of Trip
Autor:
Sakie Ohmura1, Seiya Mizuno2, Hisashi Oishi2, Chia-Jui Ku1, Mary Hermann1, Tomonori Hosoya1, Satoru Takahashi2, James Douglas Engel1 engel@umich.edu, Ohmura, Sakie (AUTHOR), Mizuno, Seiya (AUTHOR), Oishi, Hisashi (AUTHOR), Ku, Chia-Jui (AUTHOR), Hermann, Mary (AUTHOR), Hosoya, Tomonori (AUTHOR), Takahashi, Satoru (AUTHOR), Engel, James Douglas (AUTHOR)
Publikováno v:
Journal of Clinical Investigation. 3/1/2016, Vol. 126 Issue 3, p865-878. 14p. 1 Diagram, 3 Charts, 7 Graphs.