Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yutaka Kurano"'
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:
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, 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