Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Naoko T. Fujito"'
Autor:
Sundaramoorthy Revathidevi, Kazuyoshi Hosomichi, Toyoaki Natsume, Hirofumi Nakaoka, Naoko T. Fujito, Hisako Akatsuka, Takehito Sato, Arasambattu Kannan Munirajan, Ituro Inoue
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11124 (2022)
Cowden syndrome (CS) is a rare autosomal dominant disorder associated with multiple hamartomatous and neoplastic lesions in various organs. Most CS patients have been found to have germline mutations in the PTEN tumor suppressor. In the present study
Externí odkaz:
https://doaj.org/article/03e10c0e999743b3ab8488e525c34a86
Autor:
Toshiyuki Hayakawa, Zahra Khedri, Flavio Schwarz, Corinna Landig, Suh-Yuen Liang, Hai Yu, Xi Chen, Naoko T. Fujito, Yoko Satta, Ajit Varki, Takashi Angata
Publikováno v:
BMC Evolutionary Biology, Vol 17, Iss 1, Pp 1-11 (2017)
Abstract Background Siglecs-11 and -16 are members of the sialic acid recognizing Ig-like lectin family, and expressed in same cells. Siglec-11 functions as an inhibitory receptor, whereas Siglec-16 exhibits activating properties. In humans, SIGLEC11
Externí odkaz:
https://doaj.org/article/6d3bfaa1ab564971b6dafea15b540306
Autor:
Naoko T Fujito, Yoko Satta, Masaya Hane, Atsushi Matsui, Kenta Yashima, Ken Kitajima, Chihiro Sato, Naoyuki Takahata, Toshiyuki Hayakawa
Publikováno v:
PLoS ONE, Vol 13, Iss 7, p e0200278 (2018)
A number of loci are associated with highly heritable schizophrenia and the prevalence of this mental illness has had considerable negative fitness effects on human populations. Here we focused on one particular schizophrenia-associated gene that enc
Externí odkaz:
https://doaj.org/article/a93d08bd28a4454ca3a2dc175e227d99
Autor:
Toshiyuki Hayakawa, Masahiro Terahara, Naoko T. Fujito, Takumi Matsunaga, Kosuke M. Teshima, Masaya Hane, Ken Kitajima, Chihiro Sato, Naoyuki Takahata, Yoko Satta
Publikováno v:
PLoS ONE
ST8SIA2 is an important molecule regulating expression of the phenotype involved in schizophrenia. Lowered promoter activity of the ST8SIA2 gene is considered to be protective against schizophrenia by conferring tolerance to psychosocial stress. Here
Autor:
Rauri C. K. Bowie, Jeffrey D. Wall, Pui-Yan Kwok, Zachary R. Hanna, Michal Levy-Sakin, John P. Dumbacher, Naoko T. Fujito
Publikováno v:
Genome biology and evolution, vol 13, iss 5
Genome Biology and Evolution
Genome Biology and Evolution
Spotted owls (SOs, Strix occidentalis) are a flagship species inhabiting old-growth forests in western North America. In recent decades, their populations have declined due to ongoing reductions in suitable habitat caused by logging, wildfires, and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19f500bfe510b828d2153055dbb538d6
https://escholarship.org/uc/item/9nz903h4
https://escholarship.org/uc/item/9nz903h4
Autor:
Chihiro Sato, Masaya Hane, Matsunaga T, Yoko Satta, Terahara M, Naoko T. Fujito, Toshiyuki Hayakawa, Naoyuki Takahata, Ken Kitajima, Teshima K
ST8SIA2 is the main factor regulating expression of the phenotype involved in schizophrenia. Lowered promoter activity of the ST8SIA2 gene is considered to be protective against schizophrenia by conferring tolerance to psychosocial stress. Here, we e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5bc65099780d88f507ce47040ef206e
https://doi.org/10.1101/2021.04.11.439101
https://doi.org/10.1101/2021.04.11.439101
Autor:
Pui-Yan Kwok, Zachary R. Hanna, Jeffrey D. Wall, John P. Dumbacher, Naoko T. Fujito, Michal Levy-Sakin, Rauri C. K. Bowie
Spotted owls (SO,Strix occidentalis) are a keystone species inhabiting old-growth forests in Western North America. In recent decades, their populations have declined due to ongoing reductions in suitable habitat caused by logging, wildfires, and com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87948737e05b508c4eb45bab4a5d96b5
https://doi.org/10.1101/2020.02.18.954685
https://doi.org/10.1101/2020.02.18.954685
Autor:
Naoko T. Fujito, Toshiyuki Hayakawa, Wanjing Zheng, Yoko Satta, Kumiko V. Nishiyama, Risa L. Iwasaki, Naoyuki Takahata
Publikováno v:
Genesgenetic systems. 94(6)
The two-dimensional site frequency spectrum (2D SFS) was investigated to describe the intra-allelic variability (IAV) maintained within a derived allele (D) group that has undergone an incomplete selective sweep against an ancestral allele group. We
Publikováno v:
Molecular biology and evolution. 35(6)
Selective sweep is a phenomenon of reduced variation at presumably neutrally evolving sites (hitchhikers) in the genome that is caused by the spread of a selected allele at a linked focal site, and is widely used to test for action of positive select
Autor:
Corinna S. Landig, Naoko T. Fujito, Yoko Satta, Suh Yuen Liang, Hai Yu, Flavio Schwarz, Toshiyuki Hayakawa, Ajit Varki, Zahra Khedri, Takashi Angata, Xi Chen
Publikováno v:
BMC evolutionary biology, vol 17, iss 1
BMC Evolutionary Biology
BMC Evolutionary Biology, Vol 17, Iss 1, Pp 1-11 (2017)
BMC Evolutionary Biology
BMC Evolutionary Biology, Vol 17, Iss 1, Pp 1-11 (2017)
Background Siglecs-11 and -16 are members of the sialic acid recognizing Ig-like lectin family, and expressed in same cells. Siglec-11 functions as an inhibitory receptor, whereas Siglec-16 exhibits activating properties. In humans, SIGLEC11 and SIGL