Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Wulan Apridita Sebastian"'
Autor:
Shaohong Lai, Hiroshi Shiraishi, Wulan Apridita Sebastian, Nobuyuki Shimizu, Ryohei Umeda, Mayo Ikeuchi, Kyoko Kiyota, Takashi Takeno, Shuya Miyazaki, Shinji Yano, Tatsuo Shimada, Akihiko Yoshimura, Reiko Hanada, Toshikatsu Hanada
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-15 (2024)
Abstract SMG9 is an essential component of the nonsense-mediated mRNA decay (NMD) machinery, a quality control mechanism that selectively degrades aberrant transcripts. Mutations in SMG9 are associated with heart and brain malformation syndrome (HBMS
Externí odkaz:
https://doaj.org/article/69b86210ae654ce4bc27a66b71939425
Autor:
Masanori Inoue, Wulan Apridita Sebastian, Shota Sonoda, Hiroaki Miyahara, Nobuyuki Shimizu, Hiroshi Shiraishi, Miwako Maeda, Kumiko Yanagi, Tadashi Kaname, Reiko Hanada, Toshikatsu Hanada, Kenji Ihara
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-14 (2024)
Abstract Background Biallelic pathogenic variants of LARS1 cause infantile liver failure syndrome type 1 (ILFS1), which is characterized by acute hepatic failure with steatosis in infants. LARS functions as a protein associated with mTORC1 and plays
Externí odkaz:
https://doaj.org/article/53ef72dfa87b4e6d82ec5d817e1bf0f2
Autor:
Wulan Apridita Sebastian, Hiroshi Shiraishi, Nobuyuki Shimizu, Ryohei Umeda, Shaohong Lai, Mayo Ikeuchi, Ikuko Morisaki, Shinji Yano, Akihiko Yoshimura, Reiko Hanada, Toshikatsu Hanada
Publikováno v:
Biochemical and biophysical research communications. 624
Autosomal recessive primary microcephaly (MCPH) is a rare congenital disorder characterized by a below average brain volume at birth and is associated with neurodevelopmental disorders such as growth retardation and intellectual disability. Mutations
Publikováno v:
ICCD. 1:688-691
Children are susceptible to be passive smokers as a consequence of exposure to cigarette smoke when they are in the surroundings of smokers. Nearly 70% of children aged 13-15 years are exposed to cigarette smoke inside their homes, while 78 percent a
Autor:
Tohru Ishitani, Ryohei Umeda, Kazumasa Hada, Hiroyuki Yatsuka, Nobuyuki Shimizu, Wulan Apridita Sebastian, Reiko Hanada, Hiroshi Shiraishi, Takatoshi Hikida, Kenichi Kimoto, Toshiaki Kubota, Tatsuo Shimada, Toshikatsu Hanada, Ikuko Morisaki, Hirotaro Urushibata
Publikováno v:
Biochemical and biophysical research communications. 533(4)
Exosc2 is one of the components of the exosome complex involved in RNA 3′ end processing and degradation of various RNAs. Recently, EXOSC2 mutation has been reported in German families presenting short stature, hearing loss, retinitis pigmentosa, a
Autor:
Kazumasa Hada, Takatoshi Hikida, Reiko Hanada, Hiroyuki Yatsuka, Ikuko Morisaki, Tohru Ishitani, Toshiaki Kubota, Hirotaro Urushibata, Toshikatsu Hanada, Kenichi Kimoto, Nobuyuki Shimizu, Wulan Apridita Sebastian, Tatsuo Shimada, Hiroshi Shiraishi, Ryohei Umeda
Publikováno v:
Biochemical and Biophysical Research Communications. 546:200
Publikováno v:
Jurnal Ilmiah dan Teknologi Kedokteran Gigi. 13:22
Karies awal pada masa kanak-kanak atau ECC adalah suatu bentuk awal dari karies gigi yang disebabkan oleh banyak faktor. Hal ini menjadi sasaran utama dalam menentukan promosi kesehatan masyarakat. Menurut World Health Organization (WHO), menyusui me