Defective Neuromuscular Synapses in Mice Lacking Amyloid Precursor Protein (APP) and APP-Like Protein 2

Biochemical and genetic studies place the amyloid precursor protein (APP) at the center stage of Alzheimer's disease (AD) pathogenesis. Although mutations in the APP gene lead to dominant inheritance of familial AD, the normal function of APP remains elusive. Here, we report that the APP family...

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Foilsithe in:J Neurosci
Main Authors: Wang, Pei, Yang, Guang, Mosier, Dennis R., Chang, Paul, Zaidi, Tahire, Gong, Yan-Dao, Zhao, Nan-Ming, Dominguez, Bertha, Lee, Kuo-Fen, Gan, Wen-Biao, Zheng, Hui
Formáid: Artigo
Teanga:Inglês
Foilsithe: Society for Neuroscience 2005
Ábhair:
Neurobiology of Disease
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6725967/
https://ncbi.nlm.nih.gov/pubmed/15689559
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4660-04.2005
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