Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Madoka Iizumi"'
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
AMPA receptors are responsible for fast excitatory synaptic transmission in the mammalian brain. Post-translational protein S-palmitoylation of AMPA receptor subunits GluA1-4 reversibly regulates synaptic AMPA receptor expression, resulting in long-l
Externí odkaz:
https://doaj.org/article/22ef18d899834060a8a684e3431d55a2
Autor:
Ichiro Fukunaga, Yoko Oe, Keiko Danzaki, Sayaka Ohta, Cheng Chen, Madoka Iizumi, Takahiro Shiga, Rina Matsuoka, Takashi Anzai, Remi Hibiya-Motegi, Shori Tajima, Katsuhisa Ikeda, Wado Akamatsu, Kazusaku Kamiya
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102290- (2021)
The gap junction beta-2 (GJB2) gene is the most common genetic cause of hereditary deafness worldwide. Among them, the G45E/Y136X mutation in GJB2 is the third most prevalent in Japan. In this study, we generated two induced pluripotent stem cell (iP
Externí odkaz:
https://doaj.org/article/3f4ede43415d429eac1f2147b38eb85c
Autor:
Takashi Anzai, Takahiro Shiga, Cheng Chen, Sayaka Ohta, Ichiro Fukunaga, Madoka Iizumi, Wado Akamatsu, Keiko Danzaki, Remi Hibiya-Motegi, Kazusaku Kamiya, Shori Tajima, Katsuhisa Ikeda, Yoko Oe, Rina Matsuoka
Publikováno v:
Stem Cell Research, Vol 53, Iss, Pp 102290-(2021)
The gap junction beta-2 (GJB2) gene is the most common genetic cause of hereditary deafness worldwide. Among them, the G45E/Y136X mutation in GJB2 is the third most prevalent in Japan. In this study, we generated two induced pluripotent stem cell (iP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f835f5047e0b3e1138990d604bb44beb
https://pubmed.ncbi.nlm.nih.gov/33780732
https://pubmed.ncbi.nlm.nih.gov/33780732