Lataa...

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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Neurosci
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Society for Neuroscience 2005
Aiheet:
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!