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Nature Biotechnology|March 2, 2010
Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin proteinPeter O Bauer, Anand Goswami, Hon Kit Wong, et al.Scientific Reports|October 1, 2016
Differential roles of NF-Y transcription factor in ER chaperone expression and neuronal maintenance in the CNSTomoyuki Yamanaka, Asako Tosaki, Haruko Miyazaki, et al.Journal of Neurochemistry|June 30, 2006
Sodium channel beta4 subunit: down-regulation and possible involvement in neuritic degeneration in Huntington's disease transgenic miceFumitaka Oyama, Haruko Miyazaki, Naoaki Sakamoto, et al.The Journal of Biological Chemistry|June 29, 2017
Parallel homodimer structures of the extracellular domains of the voltage-gated sodium channel β4 subunit explain its role in cell-cell adhesionHideaki Shimizu, Asako Tosaki, Noboru Ohsawa, et al.Acta Neuropathologica Communications|September 21, 2018
Rapid dissemination of alpha-synuclein seeds through neural circuits in an in-vivo prion-like seeding experimentAyami Okuzumi, Masaru Kurosawa, Taku Hatano, et al.Acta Neuropathologica Communications|April 25, 2015
FUS/TLS deficiency causes behavioral and pathological abnormalities distinct from amyotrophic lateral sclerosisYoshihiro Kino, Chika Washizu, Masaru Kurosawa, et al.Scientific Reports|May 25, 2016
Structure-based site-directed photo-crosslinking analyses of multimeric cell-adhesive interactions of voltage-gated sodium channel β subunitsHideaki Shimizu, Haruko Miyazaki, Noboru Ohsawa, et al.Scientific Reports|November 25, 2016
Acidic mammalian chitinase is a proteases-resistant glycosidase in mouse digestive systemMisa Ohno, Masahiro Kimura, Haruko Miyazaki, et al.The International Journal of Eating Disorders|September 24, 2025
DSOK-0011 Potentially Regulates Circadian Misalignment and Affects Gut Microbiota Composition in Activity-Based Anorexia ModelHiroki Kawai, Nanami Wada, Shinji Sakamoto, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 28, 2009
A functional null mutation of SCN1B in a patient with Dravet syndromeGustavo A Patino, Lieve R F Claes, Luis F Lopez-Santiago, et al.Pageof 6