Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Peter Bannerman"'
Autor:
Florian Mayrhofer, Zhanna Dariychuk, Anthony Zhen, Daniel J. Daugherty, Peter Bannerman, Angela M. Hanson, David Pleasure, Athena Soulika, Wenbin Deng, Olga V. Chechneva
Publikováno v:
Neurobiology of Disease, Vol 161, Iss , Pp 105556- (2021)
Multiple sclerosis (MS) is a chronic autoimmune demyelinating disease with high variability of clinical symptoms. In most cases MS appears as a relapsing-remitting disease course that at a later stage transitions into irreversible progressive decline
Externí odkaz:
https://doaj.org/article/302d5ae29ee14ef795820b683ac8af09
Publikováno v:
PLoS ONE, Vol 13, Iss 9, p e0204536 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0167573.].
Externí odkaz:
https://doaj.org/article/a0f28c54c2944e759631a31fd0f5c776
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0167573 (2016)
Charcot-Marie-Tooth disease type 2A (CMT2A), the most common axonal form of hereditary sensory motor neuropathy, is caused by mutations of mitofusin-2 (MFN2). Mitofusin-2 is a GTPase required for fusion of mitochondrial outer membranes, repair of dam
Externí odkaz:
https://doaj.org/article/164a7964088747d0b17872301df0558a
Autor:
Florian, Mayrhofer, Zhanna, Dariychuk, Anthony, Zhen, Daniel J, Daugherty, Peter, Bannerman, Angela M, Hanson, David, Pleasure, Athena, Soulika, Wenbin, Deng, Olga V, Chechneva
Publikováno v:
Neurobiology of disease. 161
Multiple sclerosis (MS) is a chronic autoimmune demyelinating disease with high variability of clinical symptoms. In most cases MS appears as a relapsing-remitting disease course that at a later stage transitions into irreversible progressive decline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a94650319e747d98554c443f5b56bc73
https://pubmed.ncbi.nlm.nih.gov/34752925
https://pubmed.ncbi.nlm.nih.gov/34752925
Autor:
Christopher Croteau, Jie Xu, Xuehong Gui, Sheng Zhang, Peter Bannerman, Lanying Song, Fuzheng Guo, Aijun Wang, Xiaoqing Zhu
Publikováno v:
The Journal of Neuroscience. 38:1802-1820
In the CNS, myelination and remyelination depend on the successful progression and maturation of oligodendroglial lineage cells, including proliferation and differentiation of oligodendroglial progenitor cells (OPCs). Previous studies have reported t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::897cddc26a3400dca162e56f24b892e6
https://doi.org/10.1523/jneurosci.1291-17.2018
https://doi.org/10.1523/jneurosci.1291-17.2018
Autor:
Jiho Sohn, Peter Bannerman, Fuzheng Guo, Travis Burns, Laird Miers, Christopher Croteau, Naveen K. Singhal, Jennifer A. McDonough, David Pleasure
Publikováno v:
The Journal of Neuroscience. 37:413-421
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9f5d5749aa5b1044c2a65bccb5f984b
https://doi.org/10.1523/jneurosci.2013-16.2017
https://doi.org/10.1523/jneurosci.2013-16.2017
Autor:
Christopher Croteau, Jiho Sohn, Travis Burns, Naveen Kumar Singhal, David E Pleasure, Laird Miers, Jennifer McDonough, Fuzheng Guo, Peter Bannerman
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience, vol 37, iss 2
Canavan disease is a leukodystrophy caused by aspartoacylase (ASPA) deficiency. The lack of functional ASPA, an enzyme enriched in oligodendroglia that cleavesN-acetyl-l-aspartate (NAA) to acetate andl-aspartic acid, elevates brain NAA and causes “
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba19cfd1d5cc83c3b61084f2a62e2d28
https://doi.org/10.1523/jneurosci.2013-16.2016
https://doi.org/10.1523/jneurosci.2013-16.2016
Autor:
Aijun Wang, Sheng Zhang, Athena M. Soulika, Danayit Tsegaye, Abeer Rasai, Fuzheng Guo, Xiangjiang Zhan, Peter Bannerman, Daffcar Erol, Jie Xu, Yan Wang
Publikováno v:
Molecular neurobiology, vol 55, iss 12
Myelination in the central nervous system takes place predominantly during the postnatal development of humans and rodents by myelinating oligodendrocytes (OLs), which are differentiated from oligodendrocyte progenitor cells (OPCs). We recently repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdfb72cbc3bcd925241fb1b23c6df58f
https://escholarship.org/uc/item/0kh2w8p5
https://escholarship.org/uc/item/0kh2w8p5
Autor:
A. Daniels, Leah P. Shriver, Robert Clements, E. E. Kooijman, Peter Bannerman, Shuo Li, Jennifer McDonough, He Huang, Naveen Kumar Singhal, Fuzheng Guo, Travis Burns, David E Pleasure, Ernest J. Freeman, J. Gadd
Publikováno v:
Experimental brain research, vol 235, iss 1
The neuronal mitochondrial metabolite N-acetylaspartate (NAA) is decreased in the multiple sclerosis (MS) brain. NAA is synthesized in neurons by the enzyme N-acetyltransferase-8-like (NAT8L) and broken down in oligodendrocytes by aspartoacylase (ASP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bd06266b136544009eab064e13aa81e
https://doi.org/10.1007/s00221-016-4789-z
https://doi.org/10.1007/s00221-016-4789-z
Autor:
Gregory Kujawski, J. Kent Leach, Travis Burns, Fernando A. Fierro, Alan J. Man, Peter Bannerman, Elaine N. Miller
Publikováno v:
Cellular and Molecular Bioengineering. 9:96-106
Numerous signaling molecules are altered following nerve injury, serving as a blueprint for drug delivery approaches that promote nerve repair. However, challenges with achieving the appropriate temporal duration of recombinant protein delivery have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af6262490d0dce85d81c9aab639e251e
https://doi.org/10.1007/s12195-015-0425-4
https://doi.org/10.1007/s12195-015-0425-4