Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yurika Tsuji"'
Autor:
Yurika Tsuji, Shu Imaizumi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Individuals with the autism spectrum disorder (ASD) experience difficulties in perceiving speech in background noises with temporal dips; they also lack social orienting. We tested two hypotheses: (1) the higher the autistic traits, the lowe
Externí odkaz:
https://doaj.org/article/a80e35bc2f4f422da13086bce0642bdf
Autor:
Yurika Tsuji, Satoko Matsumoto, Aya Saito, Shu Imaizumi, Yoko Yamazaki, Tetsuyuki Kobayashi, Yoko Fujiwara, Mika Omori, Masumi Sugawara
Publikováno v:
BMC Psychology, Vol 10, Iss 1, Pp 1-10 (2022)
Abstract Background Sensory differences are related to the autistic traits, and previous studies have shown a positive correlation between sensory differences and internalizing problems. In this study, we hypothesized that sensory differences and suf
Externí odkaz:
https://doaj.org/article/05b8655072aa4fd5bbb5ffa1780f5eeb
Publikováno v:
Frontiers in Psychology, Vol 13 (2022)
Sensory symptoms are common in autism spectrum disorder (ASD). Previous studies have shown a positive correlation between sensory symptoms and internalizing problems; however, the role of the suffering due to sensory symptoms is not well understood.
Externí odkaz:
https://doaj.org/article/86e6c2c8d34045f18b79c1008e620cc1
Autor:
Rini Rossanti, Kandai Nozu, Daisuke Ichikawa, Kazuki Tanaka, Tomoko Horinouchi, China Nagano, Hiroaki Nagase, Koichi Kamei, Eri Okada, Yutaka Takaoka, Shinya Ishiko, Riku Hamada, Yurika Tsuji, Kazumoto Iijima, Nana Sakakibara, Yuko Noguchi, Yuya Aoto, Shingo Ishimori, Tomohiko Yamamura, Takeshi Ninchoji
Publikováno v:
Kidney International Reports
Introduction WT1 missense mutation in exon 8 or 9 causes infantile nephrotic syndrome with early progression to end-stage kidney disease (ESKD), Wilms tumor, and 46,XY female. However, some patients with missense mutations in exon 8 or 9 progress to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1400bd9ab54998d0858e899883afeda1
https://hdl.handle.net/20.500.14094/90008520
https://hdl.handle.net/20.500.14094/90008520
Autor:
Yurika Tsuji, Satoko Matsumoto, Aya Saito, Shu Imaizumi, Yoko Yamazaki, Tetsuyuki Kobayashi, Yoko Fujiwara, Mika Omori, Masumi Sugawara
Publikováno v:
BMC psychology. 10(1)
Background Sensory differences are related to the autistic traits, and previous studies have shown a positive correlation between sensory differences and internalizing problems. In this study, we hypothesized that sensory differences and suffering du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8657a7bdcb93c5c038b8cc97bdef48c
https://pubmed.ncbi.nlm.nih.gov/35698105
https://pubmed.ncbi.nlm.nih.gov/35698105
Autor:
Masafumi Matsuo, Yuko Shima, Eriko Tanaka, Koichi Nakanishi, Yurika Tsuji, Tomohiko Yamamura, China Nagano, Kandai Nozu, Kazumoto Iijima, Yoshinori Araki, Takayuki Okamoto, Hiroaki Nagase, Nana Sakakibara, Yuya Aoto, Eri Okada, Toshihiro Sawai, Shinya Ishiko, Koji Tsugawa, Tomoko Horinouchi, Rini Rossanti
Publikováno v:
Kidney International Reports
Introduction Frasier syndrome (FS) is a rare inherited kidney disease caused by intron 9 splicing variants of WT1. For wild-type WT1, 2 active splice donor sites in intron 9 cause a mixture of 2 essential transcripts (with or without lysine-threonine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17aac303460bda58eb0a2c04a77bde3d
https://pubmed.ncbi.nlm.nih.gov/34622098
https://pubmed.ncbi.nlm.nih.gov/34622098
Autor:
Masafumi Matsuo, Tomohiko Yamamura, Hiroshi Kaito, Yurika Tsuji, Shogo Minamikawa, Kazumoto Iijima, Mariko Taniguchi-Ikeda, Junya Fujimura, Naoya Morisada, Tomoko Horinouchi, Tadashi Sofue, Kandai Nozu, Keita Nakanishi, Yoshimi Nozu, Shigeo Hara, Ichiro Morioka
Publikováno v:
Nephron. 138(2):166
Background/Aims: Glomerulopathy with fibronectin deposits (GFND; OMIM: 601894) is a very rare inherited kidney disease caused by pathogenic variants in the FN1 gene. Only 9 exonic pathogenic variants in FN1, 9 at the heparin-binding site, and 1 at th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8df18ae11f0bc3a9a4359e5c3b6ba295
http://www.lib.kobe-u.ac.jp/handle_kernel/90007206
http://www.lib.kobe-u.ac.jp/handle_kernel/90007206