Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Saya Satoh"'
Autor:
Francine Lianne Emralino, Saya Satoh, Nobuhiro Sakai, Masamichi Takami, Fumihiko Takeuchi, Nan Yan, Frank Rutsch, Takashi Fujita, Hiroki Kato
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 209(11)
Gain-of-function mutations in the viral dsRNA sensor melanoma differentiation–associated protein 5 (MDA5) lead to autoimmune IFNopathies, including Singleton–Merten syndrome (SMS) and Aicardi–Goutières syndrome. However, much remains unclear r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1fbf92b5cbcc41b11d2580f1fcece81
https://pubmed.ncbi.nlm.nih.gov/36426976
https://pubmed.ncbi.nlm.nih.gov/36426976
Autor:
Akihito Kira, Ichiko Tatsutomi, Keisuke Saito, Machiko Murata, Izumi Hattori, Haruna Kajita, Naoko Muraki, Yukako Oda, Saya Satoh, Yuta Tsukamoto, Seisuke Kimura, Hiroki Kato, Tsuyoshi Hirashima, Kohki Kawane
Cell extrusion is a universal mode of cell removal from tissues, and it plays an important role in regulating cell numbers and eliminating unwanted cells, such as apoptotic, unfit, or cancerous. During this process, cells delaminate from the cell lay
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6cc1022abe342baa40a186189fef081
https://doi.org/10.21203/rs.3.rs-257262/v2
https://doi.org/10.21203/rs.3.rs-257262/v2
Autor:
Taisuke Ohto, Ahmed Abu Tayeh, Ryuta Nishikomori, Hiroto Abe, Kyota Hashimoto, Shiro Baba, Anahi-Paula Arias-Loza, Nobumasa Soda, Saya Satoh, Masashi Matsuda, Yusuke Iizuka, Takashi Kondo, Haruhiko Koseki, Nan Yan, Takahiro Higuchi, Takashi Fujita, Hiroki Kato
Publikováno v:
Journal of autoimmunity. 127
Mutations in IFIH1 gene encoding viral RNA sensor MDA5 have been reported responsible for many interferonopathies, including Aicardi-Goutières syndrome (AGS) and monogenic lupus, however, the pathological link between IFIH1 mutations and various aut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::830163a7f5402e9cfe94cb3bfd3dd4c5
https://pubmed.ncbi.nlm.nih.gov/35168003
https://pubmed.ncbi.nlm.nih.gov/35168003
Psoriasis-like skin disorder in transgenic mice expressing a RIG-I Singleton-Merten syndrome variant
Autor:
Masahide Funabiki, Yoichiro Iwakura, Shota Shimizu, Lee Sumin, Ahmed Abu Tayeh, Takashi Fujita, Hiroki Kato, Saya Satoh
Publikováno v:
International immunology. 33(4)
Mutations in DDX58 (DExD/H-box helicase 58), which encodes the cytoplasmic RNA sensor retinoic acid-inducible gene I (RIG-I), were recently identified in the rare autoimmune disease Singleton–Merten syndrome (SMS). We report the spontaneous develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::345f3c2d5539750e1040afd7fc152d43
https://pubmed.ncbi.nlm.nih.gov/33119735
https://pubmed.ncbi.nlm.nih.gov/33119735