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Selective Neuromuscular Denervation in Taiwanese Severe SMA Mouse Can Be Reversed by Morpholino Antisense Oligonucleotides

Spinal muscular atrophy (SMA) is an autosomal recessive motor neuron disease caused by deficiency of the survival of motor neuron (SMN) protein, which leads to synaptic defects and spinal motor neuron death. Neuromuscular junction (NMJ) abnormalities have been found to be involved in SMA pathogenesi...

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Podrobná bibliografie
Vydáno v:PLoS One
Hlavní autoři: Lin, Te-Lin, Chen, Tai-Heng, Hsu, Ya-Yun, Cheng, Yu-Hua, Juang, Bi-Tzen, Jong, Yuh-Jyh
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2016
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4849667/
https://ncbi.nlm.nih.gov/pubmed/27124114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0154723
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