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Human Molecular Genetics|November 2, 2013
Systems biology analysis of Drosophila in vivo screen data elucidates core networks for DNA damage repair in SCA1Sam S Barclay, Takuya Tamura, Hikaru Ito, et al.
Molecular Psychiatry|October 5, 2018
The intellectual disability gene PQBP1 rescues Alzheimer's disease pathologyHikari Tanaka, Kanoh Kondo, Xigui Chen, et al.
The European Journal of Neuroscience|July 30, 2008
Omi / HtrA2 is relevant to the selective vulnerability of striatal neurons in Huntington's diseaseReina Inagaki, Kazuhiko Tagawa, Mei-Ling Qi, et al.
Communications Medicine|November 28, 2023
AAV-mediated editing of PMP22 rescues Charcot-Marie-Tooth disease type 1A features in patient-derived iPS Schwann cellsYuki Yoshioka, Juliana Bosso Taniguchi, Hidenori Homma, et al.
Thyroid : Official Journal of the American Thyroid Association|February 9, 2018
Mild Maternal Hypothyroxinemia During Pregnancy Induces Persistent DNA Hypermethylation in the Hippocampal Brain-Derived Neurotrophic Factor Gene in Mouse OffspringKenichi Kawahori, Koshi Hashimoto, Xunmei Yuan, et al.
Nature Cell Biology|March 27, 2007
Proteome analysis of soluble nuclear proteins reveals that HMGB1/2 suppress genotoxic stress in polyglutamine diseasesMei-Ling Qi, Kazuhiko Tagawa, Yasushi Enokido, et al.
Human Molecular Genetics|February 8, 2017
RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repairJuliana Bosso Taniguchi, Kanoh Kondo, Kyota Fujita, et al.
ACS Chemical Neuroscience|July 28, 2021
Hepta-Histidine Inhibits Tau AggregationKanoh Kondo, Teikichi Ikura, Hikari Tanaka, et al.
Human Molecular Genetics|February 8, 2017
Targeting TEAD/YAP-transcription-dependent necrosis, TRIAD, ameliorates Huntington's disease pathologyYing Mao, Xigui Chen, Min Xu, et al.
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