Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nell Rebowe"'
Autor:
Samantha T. Reyes, Robert M. J. Deacon, Scarlett G. Guo, Francisco J. Altimiras, Jessa B. Castillo, Berend van der Wildt, Aimara P. Morales, Jun Hyung Park, Daniel Klamer, Jarrett Rosenberg, Lindsay M. Oberman, Nell Rebowe, Jeffrey Sprouse, Christopher U. Missling, Christopher R. McCurdy, Patricia Cogram, Walter E. Kaufmann, Frederick T. Chin
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Fragile X syndrome (FXS), a disorder of synaptic development and function, is the most prevalent genetic form of intellectual disability and autism spectrum disorder. FXS mouse models display clinically-relevant phenotypes, such as increased
Externí odkaz:
https://doaj.org/article/3fe726770d9a49e4a8f47d5b5a43daca
Autor:
Patricia Cogram, Robert M. J. Deacon, Daniel Klamer, Nell Rebowe, Jeffrey Sprouse, Samantha T. Reyes, Christopher U. Missling, Walter E. Kaufmann
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 188(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa27f9d6ff88dad7a2e96f6535d442e7
https://pubmed.ncbi.nlm.nih.gov/35661397
https://pubmed.ncbi.nlm.nih.gov/35661397
Autor:
Berend van der Wildt, Daniel Klamer, Samantha T. Reyes, Jeffrey Sprouse, Robert M. J. Deacon, Nell Rebowe, Walter E. Kaufmann, Aimara P. Morales, Lindsay M. Oberman, Jarrett Rosenberg, Frederick T. Chin, Jun Hyung Park, Scarlett G. Guo, Francisco Altimiras, Christopher U. Missling, Jessa B. Castillo, Patricia Cogram, Christopher R. McCurdy
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports
Scientific Reports
Fragile X syndrome (FXS), a disorder of synaptic development and function, is the most prevalent genetic form of intellectual disability and autism spectrum disorder. FXS mouse models display clinically-relevant phenotypes, such as increased anxiety
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c948229589818defff7cde088fec673
https://doi.org/10.1038/s41598-021-94079-7
https://doi.org/10.1038/s41598-021-94079-7
Autor:
Reyes, Samantha T.1, Deacon, Robert M. J.2,3,4, Guo, Scarlett G.1, Altimiras, Francisco J.2,5, Castillo, Jessa B.1, van der Wildt, Berend1, Morales, Aimara P.1, Park, Jun Hyung1, Klamer, Daniel6, Rosenberg, Jarrett1, Oberman, Lindsay M.7, Rebowe, Nell6, Sprouse, Jeffrey6, Missling, Christopher U.6, McCurdy, Christopher R.8, Cogram, Patricia2,3,4, Kaufmann, Walter E.6,9 walter.e.kaufmann@emory.edu, Chin, Frederick T.1 chinf@stanford.edu
Publikováno v:
Scientific Reports. 8/25/2021, Vol. 11 Issue 1, p1-14. 14p.
Autor:
Cogram, Patricia, Deacon, Robert M. J., Klamer, Daniel, Rebowe, Nell, Sprouse, Jeffrey, Reyes, Samantha T., Missling, Christopher U., Kaufmann, Walter E.
Publikováno v:
American Journal of Medical Genetics. Part A; Aug2022, Vol. 188 Issue 8, p2497-2500, 4p
Publikováno v:
Glamour; Feb2015, Vol. 113 Issue 2, p41-46, 3p, 4 Color Photographs