Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Richard Smeyne"'
Autor:
Junning Yang, Claire Simonneau, Robert Kilker, Laura Oakley, Matthew D Byrne, Zuzana Nichtova, Ioana Stefanescu, Fnu Pardeep‐Kumar, Sushil Tripathi, Eric Londin, Pascale Saugier‐Veber, Belinda Willard, Mathew Thakur, Stephen Pickup, Hiroshi Ishikawa, Horst Schroten, Richard Smeyne, Arie Horowitz
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 1, Pp 1-19 (2018)
Abstract Though congenital hydrocephalus is heritable, it has been linked only to eight genes, one of which is MPDZ. Humans and mice that carry a truncated version of MPDZ incur severe hydrocephalus resulting in acute morbidity and lethality. We show
Externí odkaz:
https://doaj.org/article/9e7dfd6574c64708bffe246dee632cbb
Autor:
Samuel O Adeosun, Xu Hou, Yun Jiao, Baoying Zheng, Sherry Henry, Rosanne Hill, Zhi He, Amar Pani, Patrick Kyle, Xiaoming Ou, Thomas Mosley, Jerry M Farley, Craig Stockmeier, Ian Paul, Steven Bigler, Roberta Diaz Brinton, Richard Smeyne, Jun Ming Wang
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e50040 (2012)
Restorative/protective therapies to restore dopamine neurons in the substantia nigra pars compacta (SNpc) are greatly needed to effectively change the debilitating course of Parkinson's disease. In this study, we tested the therapeutic potential of a
Externí odkaz:
https://doaj.org/article/59d821c9f03f4717ba7f657db3177b07
Autor:
Junning Yang, Claire Simonneau, Robert Kilker, Laura Oakley, Matthew D Byrne, Zuzana Nichtova, Ioana Stefanescu, Fnu Pardeep‐Kumar, Sushil Tripathi, Eric Londin, Pascale Saugier‐Veber, Belinda Willard, Mathew Thakur, Stephen Pickup, Hiroshi Ishikawa, Horst Schroten, Richard Smeyne, Arie Horowitz
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 1, Pp n/a-n/a (2019)
Though congenital hydrocephalus is heritable, it has been linked only to eight genes, one of which is MPDZ. Humans and mice that carry a truncated version of MPDZ incur severe hydrocephalus resulting in acute morbidity and lethality. We show by magne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::d220c04d80925615277c0e17425484f5
https://doaj.org/article/9e7dfd6574c64708bffe246dee632cbb
https://doaj.org/article/9e7dfd6574c64708bffe246dee632cbb
Autor:
Junning, Yang, Claire, Simonneau, Robert, Kilker, Laura, Oakley, Matthew D, Byrne, Zuzana, Nichtova, Ioana, Stefanescu, Fnu, Pardeep-Kumar, Sushil, Tripathi, Eric, Londin, Pascale, Saugier-Veber, Belinda, Willard, Mathew, Thakur, Stephen, Pickup, Hiroshi, Ishikawa, Horst, Schroten, Richard, Smeyne, Arie, Horowitz
Publikováno v:
EMBO Molecular Medicine
Though congenital hydrocephalus is heritable, it has been linked only to eight genes, one of which is MPDZ. Humans and mice that carry a truncated version of MPDZ incur severe hydrocephalus resulting in acute morbidity and lethality. We show by magne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cadab8f6e98b4d2a22f527dfe52aa6d5
https://pubmed.ncbi.nlm.nih.gov/30518636
https://pubmed.ncbi.nlm.nih.gov/30518636
Autor:
Richard Smeyne
Publikováno v:
Molecular Brain Research. 134:1-2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0c66686f59a6e65a5deb4f948bf9027
https://doi.org/10.1016/j.molbrainres.2005.01.001
https://doi.org/10.1016/j.molbrainres.2005.01.001