Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mieko MATSUDA"'
Autor:
Hiroaki Asai, Isamu Nashiyama, Mieko Matsuda, Yoshio Miyazaki, Yoshiya Iide, Kensuke Shiba, Kenji Sugimoto
Publikováno v:
IEEE Transactions on Nuclear Science. 59:880-885
Tolerance against single-event burnout (SEB) caused by terrestrial neutrons is one of the urgent issues in practical application of SiC power devices. This paper presents evaluation results of neutron-induced SEB in SiC power diodes and differences b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::835c61fcbf0a757507dfc707c082471b
https://doi.org/10.1109/tns.2012.2203145
https://doi.org/10.1109/tns.2012.2203145
Autor:
Nari Shiokawa, Yoko Tomiyasu, Masayuki Nakamura, Mieko Matsuda, Fujio Umehara, Takehiro Hayashi, Kimiyoshi Arimura, Satsuki Mori, Takanori Ishizuka, Mio Ichiba, Yukie Inamori, Akira Sano, Yuji Okamoto, Yoshiaki Nakabeppu, Akiyuki Tomiyasu, Maiko Kato, Hirochika Shimo
Publikováno v:
Psychiatry and Clinical Neurosciences. 65:105-108
Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease caused by a deficiency of arylsulfatase A. MLD is a heterogeneous disease with variable age at onset and variable clinical features. We evaluated a 33-year-old fem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74c1215ad4cb912d7de0a700971df9ba
https://doi.org/10.1111/j.1440-1819.2010.02169.x
https://doi.org/10.1111/j.1440-1819.2010.02169.x
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:
Takehiro, Hayashi, Masayuki, Nakamura, Mio, Ichiba, Mieko, Matsuda, Maiko, Kato, Nari, Shiokawa, Hirochika, Shimo, Akiyuki, Tomiyasu, Satsuki, Mori, Yoko, Tomiyasu, Takanori, Ishizuka, Yukie, Inamori, Yuji, Okamoto, Fujio, Umehara, Kimiyoshi, Arimura, Yoshiaki, Nakabeppu, Akira, Sano
Publikováno v:
Psychiatry and clinical neurosciences. 65(1)
Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease caused by a deficiency of arylsulfatase A. MLD is a heterogeneous disease with variable age at onset and variable clinical features. We evaluated a 33-year-old fem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9becf1b348bc96c85b6e75bafda9c58e
https://pubmed.ncbi.nlm.nih.gov/21265945
https://pubmed.ncbi.nlm.nih.gov/21265945
Autor:
M. Katoh, K. Yutaka, Shu-ichi Ueno, Y. Katoh, Mio Ichiba, Akira Sano, Mieko Matsuda, Yutaka Kurano, Masayuki Nakamura
Publikováno v:
Neuroacanthocytosis Syndromes II ISBN: 9783540716921
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fa56bc6cb56ca2b511b5c9b77b1f06a
https://doi.org/10.1007/978-3-540-71693-8_12
https://doi.org/10.1007/978-3-540-71693-8_12
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
Publikováno v:
International journal of urology : official journal of the Japanese Urological Association. 6(7)
Background: Intrarenal pelvic Wilms’ tumor in a papillary growth is rare in children. A case of a two-year-old infant with Wilms’ tumor associated with congenital aniridia is reported. Results: A chromosomal abnormality (11p13 deletion) was found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f6b624925d8524de8c6c2a3522f6f9b
https://pubmed.ncbi.nlm.nih.gov/10445307
https://pubmed.ncbi.nlm.nih.gov/10445307
Publikováno v:
Nihon Naika Gakkai Zasshi. 63:643-650
近年免疫学の進歩とともに,免疫不全症,自己免疫疾患およびリンパ系悪性腫瘍の共存が注目されてきた.われわれは無γ-グロブリン血症に粘液水腫を合併し,種々な免疫学的異常を呈した症
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfdbd006fa26e5413d4a8824cc33e9b4
https://doi.org/10.2169/naika.63.643
https://doi.org/10.2169/naika.63.643