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MOESM4 of A robust TDP-43 knock-in mouse model of ALS

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posted on 2020-01-22, 08:36 authored by Shih-Ling Huang, Lien-Szu Wu, Min Lee, Chin-Wen Chang, Wei-Cheng Cheng, Yu-Sheng Fang, Yun-Ru Chen, Pei-Lin Cheng, Che-Kun Shen
Additional file 4: Figure S4. Increase of phosphorylated TDP-43 (pTDP-43) in the spinal cord, and loss of NeuN(+) neurons of primary motor cortex of the old N390D/+ male mice.

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    Acta Neuropathologica Communications

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    Amyotrophic lateral sclerosis (ALS)TAR DNA-binding protein 43 (TDP-43)Homologous knock-in mouse models with ALS-associated TDP-43 mutationsALS-TDP pathogenesisAutonomous spinal cord motor neuron degenerationMis-splicing of Bcl-2 pre-mRNA

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