Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Chihiro Hisatsune"'
Autor:
Takaaki Inaba, Chihiro Hisatsune, Yasumasa Sasaki, Yoko Ogawa, Etsuko Ebisui, Naoko Ogawa, Minoru Matsui, Tsutomu Takeuchi, Katsuhiko Mikoshiba, Kazuo Tsubota
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e99205 (2014)
Tear secretion is important as it supplies water to the ocular surface and keeps eyes moist. Both the parasympathetic and sympathetic pathways contribute to tear secretion. Although intracellular Ca2+ elevation in the acinar cells of lacrimal glands
Externí odkaz:
https://doaj.org/article/55f3bca5939b411b85acbf975d3b1450
Publikováno v:
The Journal of Neuroscience. 41:8134-8149
Tuberous sclerosis complex (TSC) is a multisystem developmental disorder characterized by hamartomas in various organs such as the brain, lungs, and kidneys. Epilepsy, along with autism and intellectual disability, is one of the neurological impairme
Publikováno v:
Encyclopedia of Biological Chemistry III ISBN: 9780128220405
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8676336f984e6ae8c1c116a875094b38
https://doi.org/10.1016/b978-0-12-819460-7.00237-1
https://doi.org/10.1016/b978-0-12-819460-7.00237-1
Publikováno v:
J Neurosci
Tuberous sclerosis complex (TSC) is a multisystem developmental disorder characterized by hamartomas in various organs, such as the brain, lungs, and kidneys. Epilepsy, along with autism and intellectual disability, is one of the neurologic impairmen
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1865:1733-1744
Spinocerebellar ataxia (SCA) is a neural disorder, which is caused by degenerative changes in the cerebellum. SCA is primarily characterized by gait ataxia, and additional clinical features include nystagmus, dysarthria, tremors and cerebellar atroph
Autor:
Jillian P. Casey, B O’hIci, Chihiro Hisatsune, Bryan Lynch, Sean Ennis, Sally Ann Lynch, Aimee M Dunne, Nick van der Spek, Taisei Hirouchi, Akitoshi Miyamoto, Katsuhiko Mikoshiba, Raymond P. Murphy
Publikováno v:
Journal of Neurology. 264:1444-1453
We report three affected members, a mother and her two children, of a non-consanguineous Irish family who presented with a suspected autosomal dominant spinocerebellar ataxia characterized by early motor delay, poor coordination, gait ataxia, and dys
Autor:
Chihiro Hisatsune, Katsuhiko Mikoshiba
Publikováno v:
Journal of Neurochemistry. 141:790-807
The inositol 1,4,5-trisphosphate receptor (IP3 R) is a huge Ca2+ channel that is localized at the endoplasmic reticulum. The IP3 R releases Ca2+ from the endoplasmic reticulum upon binding to IP3 , which is produced by various extracellular stimuli t
Autor:
John L. Sherwood, Hiroko Bannai, Chihiro Hisatsune, Misa Arizono, Katsuhiko Mikoshiba, Aude Panatier, Mark W. Sherwood, Stéphane H. R. Oliet, Etsuko Ebisui
Publikováno v:
Glia. 65:502-513
Astrocytes regulate hippocampal synaptic plasticity by the Ca2+ dependent release of the N-methyl d-aspartate receptor (NMDAR) co-agonist d-serine. Previous evidence indicated that d-serine release would be regulated by the intracellular Ca2+ release
Publikováno v:
Journal of Neuroscience; 9/29/2021, Vol. 41 Issue 39, p8134-8149, 16p
Publikováno v:
Biochimica et biophysica acta. Molecular cell research. 1865(11 Pt)
Spinocerebellar ataxia (SCA) is a neural disorder, which is caused by degenerative changes in the cerebellum. SCA is primarily characterized by gait ataxia, and additional clinical features include nystagmus, dysarthria, tremors and cerebellar atroph