Zobrazeno 1 - 4
of 4
pro vyhledávání: '"genetics/metabolism, Transfection"'
Autor:
Henry Houlden, Victoria S Burchell, Andrea Calvo, Jessica Mandrioli, Cristina Moglia, Antonio Canosa, Colin J. Mahoney, Adriano Chiò, Selina Wray, Andrey Y. Abramov, Helene Plun-Favreau, Hsiu-Chuan Wu, Richard W. Orrell, Nick C. Fox, John Hardy, Fernando Bartolome, Elisavet Preza
Publikováno v:
Neuron
Neuron; Vol 78
Neuron; Vol 78
Summary Valosin-containing protein (VCP) is a highly expressed member of the type II AAA+ ATPase family. VCP mutations are the cause of inclusion body myopathy, Paget’s disease of the bone, and frontotemporal dementia (IBMPFD) and they account for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::846563b02156730769f60c95db7a858b
https://doi.org/10.1016/j.neuron.2013.02.028
https://doi.org/10.1016/j.neuron.2013.02.028
Autor:
Bénédicte Oulès, Patrizia Paterlini-Bréchot, Dolores Del Prete, Mounia Chami, Inger Lauritzen, Barbara Greco, Xuexin Zhang, Frédéric Checler, Sébastien Moreno, Mohamed Trebak, Jean Sevalle, Fabio Benfenati
Publikováno v:
The Journal of Neuroscience. 32:11820-11834
In Alzheimer disease (AD), the perturbation of the endoplasmic reticulum (ER) calcium (Ca2+) homeostasis has been linked to presenilins, the catalytic core in γ-secretase complexes cleaving the amyloid precursor protein (APP), thereby generating amy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b0c0f6ea578d7ddc16857385cd179e1
https://doi.org/10.1523/jneurosci.0875-12.2012
https://doi.org/10.1523/jneurosci.0875-12.2012
Publikováno v:
Cytogenetic and Genome Research, 122 (3-4)
The Ku heterodimer is a DNA end-binding protein that promotes the non-homologous end joining (NHEJ) pathway of DNA double strand break (DSB) repair by recruiting the catalytic subunit of the DNA-dependent protein kinase (DNA-PKcs). Ku is also a norma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::201b773531baa4e0f8769c10b3b4b33f
https://doi.org/10.1159/000167819
https://doi.org/10.1159/000167819
Autor:
D, Califano, C, Monaco, G, Santelli, A, Giuliano, M L, Veronese, M T, Berlingieri, V, de Franciscis, N, Berger, F, Trapasso, M, Santoro, G, Viglietto, A, Fusco
A subtractive thyroid cDNA library was constructed from two human thyroid carcinoma cell lines originating from an anaplastic carcinoma and a papillary thyroid carcinoma. The library was used to identify genes correlated with the progression to a hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::dc7d3030c12983562113df0783459931
http://hdl.handle.net/11588/484009
http://hdl.handle.net/11588/484009
