Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Pavitra Rengarajan"'
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
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