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The European Journal of Neuroscience|September 30, 2005
PQBP-1 is expressed predominantly in the central nervous system during developmentYunglong Qi, Masataka Hoshino, Yo-ichi Wada, et al.Eneuro|September 19, 2018
Ser46-Phosphorylated MARCKS Is a Marker of Neurite Degeneration at the Pre-aggregation Stage in PD/DLB PathologyKyota Fujita, Hidenori Homma, Kanoh Kondo, et al.Brain Research. Molecular Brain Research|November 19, 2004
Oct-3/4 repression accelerates differentiation of neural progenitor cells in vitro and in vivoTomohiro Okuda, Kazuhiko Tagawa, Mei-Ling Qi, et al.Biochemical and Biophysical Research Communications|June 11, 2002
Enhanced SUMOylation in polyglutamine diseasesHiroko Ueda, Jun Goto, Hideji Hashida, et al.Acta Neuropathologica Communications|March 10, 2017
A novel form of necrosis, TRIAD, occurs in human Huntington's diseaseEmiko Yamanishi, Kazuko Hasegawa, Kyota Fujita, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 22, 2010
Drosophila PQBP1 regulates learning acquisition at projection neurons in aversive olfactory conditioningTakuya Tamura, Daisuke Horiuchi, Yi-Chung Chen, et al.Journal of Neurochemistry|August 18, 2005
Polyglutamine tract-binding protein-1 dysfunction induces cell death of neurons through mitochondrial stressShigeki Marubuchi, Yo-Ichi Wada, Tomohiro Okuda, et al.Journal of Neurochemistry|May 14, 2004
Distinct aggregation and cell death patterns among different types of primary neurons induced by mutant huntingtin proteinKazuhiko Tagawa, Masataka Hoshino, Tomohiro Okuda, et al.Human Molecular Genetics|March 26, 2003
PQBP-1 transgenic mice show a late-onset motor neuron disease-like phenotypeTomohiro Okuda, Hiroshi Hattori, Sousuke Takeuchi, et al.Journal of Neurochemistry|September 13, 2003
Histone deacetylase activity is retained in primary neurons expressing mutant huntingtin proteinMasataka Hoshino, Kazuhiko Tagawa, Tomohiro Okuda, et al.Pageof 11