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Treatment with trichostatin A initiated after disease onset delays disease progression and increases survival in a mouse model of amyotrophic lateral sclerosis
Authors:Yoo Young-Eun  Ko Chien-Ping
Affiliation:aSection of Neurobiology, Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089-2520, USA
Abstract:
Keywords:Amyotrophic lateral sclerosis (ALS)   Mouse model   Treatment   HDAC inhibitor   Histone acetylation   Motoneurons   Astrocyte   Microglia   Neuromuscular junction   Motor function
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