Zobrazeno 1 - 10 of 35 pro vyhledávání: '"Ohiko, HASHIMOTO"'
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The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism
Autor: Yukiko Kano, Nobumasa Kato, Toshiro Sugiyama, Kiyoto Kasai, Hideo Matsumoto, Ohiko Hashimoto, Seiichiro Jinde, Hisami Nishida, Kenji Yamamoto, Keiichiro Watanabe, Tetsuya Marui, Shinko Koishi, Ikuko Funatogawa
Publikováno v: Acta Psychiatrica Scandinavica. 123:118-124
Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Jinde S, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N. The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism. Obj
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d7f6de690fbab8656021770d2aa4f769
https://doi.org/10.1111/j.1600-0447.2010.01600.x
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5
Association study of the commonly recognized breakpoints in chromosome 15q11–q13 in Japanese autistic patients
Autor: Kenji Yamamoto, Hideo Matsumoto, Tsukasa Sasaki, Chieko Kato, Nobumasa Kato, Shinko Koishi, Mamoru Tochigi, Ohiko Hashimoto, Eiji Nanba, Yuki Kawakubo, Soo-Yung Kim, Keiichiro Watanabe, Yukiko Kano
Publikováno v: Psychiatric Genetics. 18:133-136
OBJECTIVE Chromosome 15q11-q13 has been proposed to harbor a gene for autism susceptibility because deletions of the region lead to Prader-Willi syndrome and Angelman syndrome, whose phenotypes overlap with autism. These deletions generally occur wit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4781bcf027d8ddd4d44be77cdc621bb
https://doi.org/10.1097/ypg.0b013e3282fb0064
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6
Plasma homovanillic acid levels in temporal lobe epilepsy
Autor: Shoji Nagakubo, Tomomichi Kameyama, Naoki Kumagai, Shin-Ichi Niwa, Nobuo Anzai, Masato Fukuda, Akinobu Hata, Ohiko Hashimoto, Yukihiko Shirayama
Publikováno v: Journal of Epilepsy. 11:383-388
The role of the central dopaminergic system in temporal lobe epilepsy (TLE) was investigated through measurement of plasma homovanillic acid (pHVA) levels. Plasma HVA levels in 30 patients with TLE were determined and compared with those in 53 health
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b27e77297f70831688f5ac35ce6049a6
https://doi.org/10.1016/s0896-6974(98)00031-0
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7
Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder
Autor: Tadashi Kaname, Kumiko Yanagi, Keiko Wakui, Yoshimitsu Fukushima, Kenji Naritomi, Ohiko Hashimoto
Publikováno v: Autism Research and Treatment
Autism Research and Treatment, Vol 2012 (2012)
Mutations in the X-linked genesneuroligin 3 (NLGN3)andneuroligin 4X (NLGN4X)were first implicated in the pathogenesis of X-linked autism in Swedish families. However, reports of mutations in these genes in autism spectrum disorder (ASD) patients from
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b0b88ba301b2d1355bd9433d6bcc8fe
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8
Brief report: Low frequency of the fragile X syndrome among Japanese autistic subjects
Autor: Yasuo Shimizu, Ohiko Hashimoto, Yoko Kawasaki
Publikováno v: Journal of Autism and Developmental Disorders. 23:201-209
The prevalence of Fra(X) among infantile autism in Japanese subjects was found to be no higher than in subject groups having nonspecific metal retardation, and thus it is concluded that Fra(X) does not constitute an etiologically valid autism subgrou
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40e957fb39733749a2d0901df653b535
https://doi.org/10.1007/bf01066429
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9
Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population
Autor: Nobumasa Kato, Yukiko Kano, Taku Miyagawa, Tadashi Umekage, Yoshiya Kawamura, Ryoichi Nakagami, Hisami Nishida, Shinko Koishi, Katsushi Tokunaga, Xiaoxi Liu, Tsukasa Sasaki, Ohiko Hashimoto, Takeshi Otowa, Takafumi Shimada, Mamoru Tochigi, Toshiro Sugiyama
Publikováno v: Journal of human genetics. 55(3)
The oxytocin receptor (OXTR) gene, which is located on chromosome 3p25.3, has been implicated as a candidate gene for susceptibility of autism spectrum disorder (ASD). Positive associations between OXTR and ASD have been reported in earlier studies.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e03d97d6eccb3d8183f04a73f77a3d1b
https://pubmed.ncbi.nlm.nih.gov/20094064
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10
Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene
Autor: Nobumasa Kato, Seiichiro Jinde, Kiyoto Kasai, Yukiko Kano, Toshiro Sugiyama, Hisami Nishida, Kenji Yamamoto, Ikuko Funatogawa, Ohiko Hashimoto, Keiichiro Watanabe, Hideo Matsumoto, Shinko Koishi, Tetsuya Marui
Publikováno v: The international journal of neuropsychopharmacology. 13(4)
Autism is a severe neurodevelopmental disorder with a complex genetic aetiology. The wingless-type MMTV integration site family member 2 (WNT2) gene has been considered as a candidate gene for autism. We conducted a case-control study and followed up
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e1686dc44c3f90e8eaebffbea71a9c4
https://pubmed.ncbi.nlm.nih.gov/19895723
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