Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Emiko Mizuno"'
Publikováno v:
Neuropsychopharmacology Reports, Vol 42, Iss 2, Pp 183-190 (2022)
Abstract Aim Supporting patients upon discharge following prolonged hospitalization in private psychiatric hospitals in Japan have long been an issue. This study evaluated the efficacy of clozapine in treating long‐stay patients with treatment‐re
Externí odkaz:
https://doaj.org/article/fc530a2614be41b28c421f8b9a6aa503
Autor:
Yutaka Kurano, Mio Ichiba, Mieko Matsuda, Emiko Mizuno, Akira Sano, Shuji Izumo, Asumi Agemura, Masayuki Nakamura, Maiko Kato
Publikováno v:
Biochemical and Biophysical Research Communications. 353:431-435
Chorea-acanthocytosis (ChAc) is a hereditary neurodegenerative disorder caused by loss of function mutations in the VPS13A gene encoding chorein. In this study, we produced an antibody against chorein and examined its protein-level expression and loc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d8ac6c5c37636c95ba7897874cab85d
https://doi.org/10.1016/j.bbrc.2006.12.059
https://doi.org/10.1016/j.bbrc.2006.12.059
Autor:
Shoichi Suzuki, Yasuki Asada, Tetsuya Kamei, Kazuta Nishi, Emiko Mizuno, Natsue Hara, Takeo Orito, Sukehiko Koga
Publikováno v:
JAPANES JOURNAL OF MEDICAL INSTRUMENTATION. 70:229-233
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b03383e0e40f81231cb180b0aea27fb
https://doi.org/10.4286/ikakikaigaku.70.5_229
https://doi.org/10.4286/ikakikaigaku.70.5_229
Autor:
Emiko Mizuno, Hiroyuki Masuda, Minoru Fujimori, Shinya Kobayashi, Masayuki Haniuda, Akira Sugenoya, Yoshio Kasuga, Futoshi Iida
Publikováno v:
Acta Endocrinologica. 124:115-120
The presence of thyroid hormone autoantibodies was investigated in a 48-year-old non-goitrous woman with high levels of serum total T3 and free T3. Her other thyroid function tests were normal. The presence of thyroid hormone autoantibodies were asse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d054254b8de4ac80755d4ddf7fa38016
https://doi.org/10.1530/acta.0.1240115
https://doi.org/10.1530/acta.0.1240115
Autor:
Yutaka Kurano, Akira Kusumoto, Shinji Muroya, Emiko Mizuno, Masayuki Nakamura, Asumi Agemura, Akira Sano, Mio Ichiba
Publikováno v:
Biochemical and biophysical research communications. 353(4)
Mutations in vacuolar protein sorting 13A (VPS13A) gene are responsible for chorea-acanthocytosis (ChAc). We previously determined the full-length sequence and exon-intron structure of mouse VPS13A and generated a ChAc model mouse by using the gene t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::166173ee06b84e3ad6bb80f86b4550a2
https://pubmed.ncbi.nlm.nih.gov/17196930
https://pubmed.ncbi.nlm.nih.gov/17196930
Autor:
Yutaka Kurano, Maiko Kato, Mieko Matsuda, Masayuki Nakamura, Mio Ichiba, Akira Sano, Shuji Izumo, Emiko Mizuno
Publikováno v:
Biochemical and biophysical research communications. 351(2)
Chorea-acanthocytosis (ChAc) is a hereditary neurodegenerative disorder caused by loss of function mutations in the VPS13A gene encoding chorein. Recently, using a gene-targeting technique to delete exons 60-61, we produced a ChAc-model mouse that co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f6dd625ba7c02d4cb4cb1823a76eb9d
https://pubmed.ncbi.nlm.nih.gov/17070500
https://pubmed.ncbi.nlm.nih.gov/17070500
Autor:
Emiko Mizuno, Yoshiaki Nakabeppu, Asumi Agemura, Mieko Matsuda, Akira Sano, Mio Ichiba, Masayuki Nakamura, Maiko Kato, Yuko Tomemori, Yutaka Kurano, Akira Kusumoto, Shinji Muroya
Publikováno v:
Journal of the neurological sciences. 263(1-2)
Background Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene. There are only few reports that studied clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5080e3af05564d6c3a5acb627cba44b
https://pubmed.ncbi.nlm.nih.gov/17673232
https://pubmed.ncbi.nlm.nih.gov/17673232
Autor:
Shu-ichi Ueno, Akira Kusumoto, Shinji Muroya, Atsu Aiba, Mio Ichiba, Emiko Mizuno, Kenji Nakamura, Akira Sano, Hiroaki Kawaguchi, Yuko Tomemori, Motoya Katsuki, Kazuki Nakao, Hiroki Yoshida, Masayuki Nakamura, Daisuke Sato
Publikováno v:
Journal of neurochemistry. 92(4)
Chorea-acanthocytosis (CHAC) is a hereditary neurodegenerative disorder with autosomal recessive transmission, in which selective degeneration of striatum has been reported in brain pathology. Clinically, CHAC shows Huntington's disease-like neuropsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b99cc8ac5943cda4848b8ea23ff1075
https://pubmed.ncbi.nlm.nih.gov/15686477
https://pubmed.ncbi.nlm.nih.gov/15686477
Autor:
Masayuki Haniuda, Rinko Sakai, Emiko Mizuno, Michimasa Kato, Akira Sugenoya, Futoshi Iida, Mitsuaki Kameko
Publikováno v:
Folia Endocrinologica Japonica. 64:677-686
A 48-year-old non-goitrous woman, who had undergone cardiac surgery for mitral stenosis under the extracorporeal circulation, showed high levels of serum T3 and free T3 in a recent follow-up study, employing antibody coated-bead RIA for T3 and -Amerl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b610daefd877455289862b5d6c7ccf7
https://doi.org/10.1507/endocrine1927.64.8_677
https://doi.org/10.1507/endocrine1927.64.8_677
Publikováno v:
Chemical and Pharmaceutical Bulletin. 31:2936-2939
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9398b41e2de77a80c547e566dc573391
https://doi.org/10.1248/cpb.31.2936
https://doi.org/10.1248/cpb.31.2936