Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Olugbenga M Doherty"'
Autor:
Noriko Wakabayashi-Ito, Olugbenga M Doherty, Hideaki Moriyama, Xandra O Breakefield, James F Gusella, Janis M O'Donnell, Naoto Ito
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26183 (2011)
Dystonia represents the third most common movement disorder in humans. At least 15 genetic loci (DYT1-15) have been identified and some of these genes have been cloned. TOR1A (formally DYT1), the gene responsible for the most common primary hereditar
Externí odkaz:
https://doaj.org/article/f577069ad7a34a17a0a5af6311ff640a
Autor:
Noriko Wakabayashi-Ito, Rami R. Ajjuri, Benjamin W. Henderson, Olugbenga M. Doherty, Xandra O. Breakefield, Janis M. O'Donnell, Naoto Ito
Publikováno v:
Biology Open, Vol 4, Iss 5, Pp 585-595 (2015)
Dystonia represents the third most common movement disorder in humans with over 20 genetic loci identified. TOR1A (DYT1), the gene responsible for the most common primary hereditary dystonia, encodes torsinA, an AAA ATPase family protein. Most cases
Externí odkaz:
https://doaj.org/article/393daecd50f04d25a31ca190b07d6e3f
Autor:
Noriko Wakabayashi-Ito, Olugbenga M. Doherty, Hideaki Moriyama, Xandra O. Breakefield, James F. Gusella, Janis M. O'Donnell, Naoto Ito
Publikováno v:
PLoS ONE, Vol 6, Iss 10 (2011)
Externí odkaz:
https://doaj.org/article/c413924d167d45eba7cfc1742a8676eb
Autor:
Janis M. O'Donnell, Xandra O. Breakefield, Noriko Wakabayashi-Ito, Olugbenga M. Doherty, Benjamin W. Henderson, Rami R. Ajjuri, Naoto Ito
Publikováno v:
Biology Open, Vol 4, Iss 5, Pp 585-595 (2015)
Biology Open
Biology Open
Dystonia represents the third most common movement disorder in humans with over 20 genetic loci identified. TOR1A (DYT1), the gene responsible for the most common primary hereditary dystonia, encodes torsinA, an AAA ATPase family protein. Most cases
Autor:
Zhinong Huang, Zhe Wang, Olugbenga M. Doherty, Iyare Izevbaye, Dean G. Stathakis, Jerrad Thomas, J. Gavin Daigle, Janis M. O'Donnell, Faiza Ferdousy, Hakeem Lawal
Publikováno v:
Journal of Neurochemistry. 119:1294-1305
Dopamine (DA) regulates movement, cognition, attention and reward (Calabresi et al., 2007; Palmiter, 2007; Sillitoe and Vogel, 2008), while dysfunction of dopaminergic signaling has been implicated in numerous neurological diseases and abnormal behav
Autor:
Noriko Wakabayashi-Ito, Olugbenga M. Doherty, Hideaki Moriyama, Xandra O. Breakefield, James F. Gusella, Janis M. O'Donnell, Naoto Ito
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 10 (2011)
PLoS ONE, Vol 6, Iss 10 (2011)
Autor:
Olugbenga M. Doherty, James F. Gusella, Xandra O. Breakefield, Janis M. O'Donnell, Noriko Wakabayashi-Ito, Naoto Ito, Hideaki Moriyama
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 10, p e26183 (2011)
PLoS ONE, Vol 6, Iss 10, p e26183 (2011)
Dystonia represents the third most common movement disorder in humans. At least 15 genetic loci (DYT1-15) have been identified and some of these genes have been cloned. TOR1A (formally DYT1), the gene responsible for the most common primary hereditar
Autor:
Oneil A. Wright, Lawrence T. Reiter, George M. Hilliard, Faiza Ferdousy, Janis M. O'Donnell, Nahed Elsisi, Olugbenga M. Doherty, William J. Bodeen, Kyle C. Summers
Publikováno v:
Neurobiology of Disease, Vol 41, Iss 3, Pp 669-677 (2011)
The underlying defects in Angelman syndrome (AS) and autism spectrum disorder (ASD) may be in part due to basic defects in synaptic plasticity and function. In some individuals serotonin reuptake inhibitors, which decrease pre-synaptic re-uptake of s