Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Christine M. LaPash Daniels"'
Autor:
Christine M LaPash Daniels, Elizabeth Paffenroth, Elizabeth V Austin, Konstantin Glebov, Diana Lewis, Jochen Walter, Albee Messing
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0138132 (2015)
Alexander disease is a fatal neurodegenerative disease caused by mutations in the astrocyte intermediate filament glial fibrillary acidic protein (GFAP). The disease is characterized by elevated levels of GFAP and the formation of protein aggregates,
Externí odkaz:
https://doaj.org/article/6766d9e586b844719369d9eda10cc5be
Autor:
Heather M. Christensen, Sally R. McIver, Mingjie Li, David A. Harris, Nada Husic, Christine M. LaPash Daniels, Ibrahim Malik, Paul T. Kotzbauer, Ying Lin, Mark P. Goldberg, B. Joy Snider
Publikováno v:
Journal of Neuroscience Methods. 189:56-64
Lentiviral vectors transduce both dividing and non-dividing cells and can support sustained expression of transgenes. These properties make them attractive for the transduction of neurons and other neural cell types in vitro and in vivo. Lentiviral v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a19569b3bf9b2d298dfb3849768fe25
https://doi.org/10.1016/j.jneumeth.2010.03.019
https://doi.org/10.1016/j.jneumeth.2010.03.019
Autor:
Mark P. Goldberg, Joseph P. Culver, Kathryn L. Ayers, Amanda M. Finley, Christine M. LaPash Daniels
Publikováno v:
Neuroscience Letters. 450:191-195
Functional reorganization of brain cortical areas occurs following stroke in humans, and many instances of this plasticity are associated with recovery of function. Rodent studies have shown that following a cortical stroke, neurons in uninjured area
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abaf408b729150fac264581e5169ce84
https://doi.org/10.1016/j.neulet.2008.11.017
https://doi.org/10.1016/j.neulet.2008.11.017
Autor:
Jochen Walter, Diana Lewis, Christine M. LaPash Daniels, Albee Messing, Elizabeth V. Austin, Elizabeth Paffenroth, Konstantin Glebov
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0138132 (2015)
PLoS ONE
PLoS ONE
Alexander disease is a fatal neurodegenerative disease caused by mutations in the astrocyte intermediate filament glial fibrillary acidic protein (GFAP). The disease is characterized by elevated levels of GFAP and the formation of protein aggregates,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e4d4ff1b8e4b4367bb1e5ca306b8efd
http://europepmc.org/articles/PMC4574949?pdf=render
http://europepmc.org/articles/PMC4574949?pdf=render
Autor:
Christine M. LaPash Daniels, James E. Goldman, John Q. Trojanowski, Virginia M.-Y. Lee, Adam K. Walker, Albee Messing
Alexander disease (AxD) is a rare neurodegenerative disorder characterized pathologically by the presence of eosinophilic inclusions known as Rosenthal fibers (RFs) within astrocytes, and is caused by dominant mutations in the coding region of the ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ef5de15bff3337d53888c3f636cb014
https://europepmc.org/articles/PMC4012304/
https://europepmc.org/articles/PMC4012304/
Autor:
Tracy L. Hagemann, Albee Messing, Danica E. Rockney, Elizabeth M. Jacka, Jeffrey A. Johnson, Christine M. LaPash Daniels, Delinda A. Johnson, Elizabeth V. Austin
Alexander disease is a fatal neurodegenerative disease caused by dominant mutations in glial fibrillary acidic protein (GFAP). The disease is characterized by protein inclusions called Rosenthal fibers within astrocyte cell bodies and processes, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60c87e65c368dcffd44c968ae32095b
https://europepmc.org/articles/PMC3448488/
https://europepmc.org/articles/PMC3448488/
Publikováno v:
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics. 7(4)
Alexander disease is a rare and generally fatal disorder of the CNS, originally classified among the leukodystrophies because of the prominent myelin deficits found in young patients. The most common form of this disease affects infants, who often ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eec2f89e4c949c04f55e09b524ec30a
https://pubmed.ncbi.nlm.nih.gov/20880512
https://pubmed.ncbi.nlm.nih.gov/20880512