Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Baraa S, Nawash"'
Autor:
Matthew S. Elitt, H. Elizabeth Shick, Mayur Madhavan, Kevin C. Allan, Benjamin L.L. Clayton, Chen Weng, Tyler E. Miller, Daniel C. Factor, Lilianne Barbar, Baraa S. Nawash, Zachary S. Nevin, Angela M. Lager, Yan Li, Fulai Jin, Drew J. Adams, Paul J. Tesar
Publikováno v:
Stem Cell Reports, Vol 11, Iss 3, Pp 711-726 (2018)
Summary: Pelizaeus-Merzbacher disease (PMD) is a fatal X-linked disorder caused by loss of myelinating oligodendrocytes and consequent hypomyelination. The underlying cellular and molecular dysfunctions are not fully defined, but therapeutic enhancem
Externí odkaz:
https://doaj.org/article/85ceab688bb44f7d8336a4d35cb11973
Autor:
Ronald A. Conlon, Berit Powers, Matthew S. Elitt, Daniela Schlatzer, H. Elizabeth Shick, Yuka Maeno-Hikichi, Lilianne Barbar, David F. LePage, Weihong Jiang, Hannah E. Olsen, Hien T Zhao, Stevephen Hung, Adam Swayze, Frank Rigo, Paul J. Tesar, Kevin C. Allan, Zachary S. Nevin, Baraa S. Nawash, Masahiro Hitomi, Artur S. Gevorgyan, Mayur Madhavan
Publikováno v:
Nature
Mutations in PLP1, the gene that encodes proteolipid protein (PLP), result in failure of myelination and neurological dysfunction in the X-chromosome-linked leukodystrophy Pelizaeus–Merzbacher disease (PMD)1,2. Most PLP1 mutations, including point
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::316136b1462be634a5e5c31e077ee96d
http://europepmc.org/articles/PMC7810164
http://europepmc.org/articles/PMC7810164
Autor:
Mahmoud, Omar, Anas M, Qatanani, Nerone O, Douglas, Baraa S, Nawash, Tamara, Ibrahim, Syed Z, Kaleem, Brian J, McKinnon
Publikováno v:
American Journal of Otolaryngology. 43:103608
To determine the impact of sociodemographic factors on post-operative performance outcomes among PCI recipients across the world.A qualitative systematic review of PubMed, Scopus, Web of Science, and Embase was undertaken for studies analyzing the as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8564d69ae6ad2c343a4f9ab09428a691
https://doi.org/10.1016/j.amjoto.2022.103608
https://doi.org/10.1016/j.amjoto.2022.103608
Autor:
Yan Li, Matthew S. Elitt, Zachary S. Nevin, Paul J. Tesar, Angela M. Lager, H. Elizabeth Shick, Chen Weng, Drew J. Adams, Mayur Madhavan, Tyler E. Miller, Kevin C. Allan, Lilianne Barbar, Fulai Jin, Daniel C. Factor, Baraa S. Nawash, Benjamin L.L. Clayton
Publikováno v:
Stem Cell Reports, Vol 11, Iss 3, Pp 711-726 (2018)
Summary: Pelizaeus-Merzbacher disease (PMD) is a fatal X-linked disorder caused by loss of myelinating oligodendrocytes and consequent hypomyelination. The underlying cellular and molecular dysfunctions are not fully defined, but therapeutic enhancem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::667b09ef40330db9dbda4a2c78c57762
http://www.sciencedirect.com/science/article/pii/S2213671118303205
http://www.sciencedirect.com/science/article/pii/S2213671118303205
Autor:
Masahiro Hitomi, Ronald A. Conlon, Berit Powers, Matthew S. Elitt, Baraa S. Nawash, Zachary S. Nevin, Frank Rigo, David F. LePage, H. Elizabeth Shick, Weihong Jiang, Mayur Madhavan, Paul J. Tesar, Hannah E. Olsen, Kevin C. Allan, Lilianne Barbar, Yuka Maeno-Hikichi
Mutations in proteolipid protein 1 (PLP1) result in failure of myelination and severe neurological dysfunction in the X-linked pediatric leukodystrophy Pelizaeus-Merzbacher disease (PMD). The majority of PLP1 variants, including supernumerary copies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bb9aef0fb00a04d13ee97f5b90e39d5
