Zobrazeno 1 - 7
of 7
pro vyhledávání: '"David Kalikhman"'
Autor:
Thomas Portmann, Mu Yang, Rong Mao, Georgia Panagiotakos, Jacob Ellegood, Gul Dolen, Patrick L. Bader, Brad A. Grueter, Carleton Goold, Elaine Fisher, Katherine Clifford, Pavitra Rengarajan, David Kalikhman, Darren Loureiro, Nay L. Saw, Zhou Zhengqui, Michael A. Miller, Jason P. Lerch, R. Mark Henkelman, Mehrdad Shamloo, Robert C. Malenka, Jacqueline N. Crawley, Ricardo E. Dolmetsch
Publikováno v:
Cell Reports, Vol 7, Iss 4, Pp 1077-1092 (2014)
A deletion on human chromosome 16p11.2 is associated with autism spectrum disorders. We deleted the syntenic region on mouse chromosome 7F3. MRI and high-throughput single-cell transcriptomics revealed anatomical and cellular abnormalities, particula
Externí odkaz:
https://doaj.org/article/2b15e4f053b64684bb0d398a07072ba2
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e81401 (2013)
Neurosurgical therapeutic interventions include components that are presumed to be therapeutically inert, such as craniotomy and electrode implantation. Because these procedures may themselves exert neuroactive actions, with anecdotal evidence sugges
Externí odkaz:
https://doaj.org/article/bd843086967541d1a455d6dabfbf0023
Publikováno v:
Epilepsia. 55:1374-1379
Summary Objective To compare manual and automated preoperative and postoperative hippocampal volume measurements in patients with intractable epilepsy. Methods We studied 34 patients referred to the Clinical Epilepsy Section, National Institute of Ne
Autor:
Darren Loureiro, Nay L. Saw, Thomas Portmann, Georgia Panagiotakos, Katherine M Clifford, Gül Dölen, Elaine M. Fisher, Robert C. Malenka, Rong Mao, David Kalikhman, Zhou Zhengqui, Mu Yang, Pavitra Rengarajan, Jacob Ellegood, Jacqueline N. Crawley, Jason P. Lerch, Brad A. Grueter, Carleton Goold, Patrick Bader, Michael A. Miller, Mehrdad Shamloo, R. Mark Henkelman, Ricardo E. Dolmetsch
Publikováno v:
Cell Reports, Vol 7, Iss 4, Pp 1077-1092 (2014)
A deletion on human chromosome 16p11.2 is associated with autism spectrum disorders. We deleted the syntenic region on mouse chromosome 7F3. MRI and high-throughput single-cell transcriptomics revealed anatomical and cellular abnormalities, particula
Autor:
Mu Yang, Mark J. Harris, David Kalikhman, Maria Luisa Scattoni, Leuk Woldeyohannes, Harrison Simon, Markus Wöhr, Jacqueline N. Crawley, Florence I. Roullet, Joseph D. Buxbaum, Ozlem Bozdagi, James Zhang, Jill L. Silverman, Danielle N. Abrams, Adam M. Katz, Roheeni Saxena
Publikováno v:
The Journal of Neuroscience. 32:6525-6541
Mutations in the synaptic scaffolding protein geneSHANK3are strongly implicated in autism and Phelan–McDermid 22q13 deletion syndrome. The precise location of the mutation within theShank3gene is key to its phenotypic outcomes. Here, we report the
Male mice emit distinct ultrasonic vocalizations when the female leaves the social interaction arena
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 7 (2013)
Frontiers in Behavioral Neuroscience
Frontiers in behavioral neuroscience, vol 7, iss NOV
Frontiers in Behavioral Neuroscience
Frontiers in behavioral neuroscience, vol 7, iss NOV
Adult male mice emit large number of complex ultrasonic vocalizations (USVs) when interacting with adult females. Call numbers and call categories differ greatly among inbred mouse strains. Little is known about USV emissions when the social partner
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e81401 (2013)
PLoS ONE
PLoS ONE
Neurosurgical therapeutic interventions include components that are presumed to be therapeutically inert, such as craniotomy and electrode implantation. Because these procedures may themselves exert neuroactive actions, with anecdotal evidence sugges