Zobrazeno 1 - 10
of 340
pro vyhledávání: '"Morrow Eric M"'
Autor:
Wu, Qing1,2,3 (AUTHOR), Morrow, Eric M.1,2,3,4 (AUTHOR), Uzun, Ece D. Gamsiz2,3,5,6 (AUTHOR) dilber_gamsiz@brown.edu
Publikováno v:
PLoS Computational Biology. 11/8/2024, Vol. 20 Issue 11, p1-18. 18p.
Publikováno v:
In Journal of Biological Chemistry August 2024 300(8)
Autor:
Klei Lambertus, Sanders Stephan J, Murtha Michael T, Hus Vanessa, Lowe Jennifer K, Willsey A, Moreno-De-Luca Daniel, Yu Timothy W, Fombonne Eric, Geschwind Daniel, Grice Dorothy E, Ledbetter David H, Lord Catherine, Mane Shrikant M, Martin Christa, Martin Donna M, Morrow Eric M, Walsh Christopher A, Melhem Nadine M, Chaste Pauline, Sutcliffe James S, State Matthew W, Cook Edwin H, Roeder Kathryn, Devlin Bernie
Publikováno v:
Molecular Autism, Vol 3, Iss 1, p 9 (2012)
Abstract Background Autism spectrum disorders (ASD) are early onset neurodevelopmental syndromes typified by impairments in reciprocal social interaction and communication, accompanied by restricted and repetitive behaviors. While rare and especially
Externí odkaz:
https://doaj.org/article/e00a785ffaf64e9a812e2922484cd74e
Publikováno v:
Neural Development, Vol 3, Iss 1, p 2 (2008)
Abstract Background Retinal bipolar cells comprise a diverse group of neurons. Cone bipolar cells and rod bipolar cells are so named for their connections with cone and rod photoreceptors, respectively. Morphological criteria have been established th
Externí odkaz:
https://doaj.org/article/47ef5a9d32fb44afb4c88c6922bf421c
Publikováno v:
Annals of General Psychiatry, Vol 5, Iss 1, p 9 (2006)
Abstract Background Postictal psychosis (PIP), an episode of psychosis occurring after a cluster of seizures, is common and may be associated with profound morbidity, including chronic psychosis. Symptoms are often pleomorphic, involving a range of p
Externí odkaz:
https://doaj.org/article/a54319ae7d0c4e73b6a066f8b2915048
Publikováno v:
BMC Neuroscience, Vol 6, Iss 1, p 5 (2005)
Abstract Background In Leber's congenital amaurosis (LCA), affected individuals are blind, or nearly so, from birth. This early onset suggests abnormal development of the neural retina. Mutations in genes that affect the development and/or function o
Externí odkaz:
https://doaj.org/article/526109f6f35849d29c7b3a329856cb9d
Akademický článek
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Publikováno v:
Molecular Brain; 11/27/2024, Vol. 17 Issue 1, p1-21, 21p
Akademický článek
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Autor:
Ouyang, Qing, Nakayama, Tojo, Baytas, Ozan, Davidson, Shawn M., Yang, Chendong, Schmidt, Michael, Lizarraga, Sofia B., Mishra, Sasmita, EI-Quessny, Malak, Niaz, Saima, Butt, Mirrat Gul, Murtaza, Syed Imran, Javed, Afzal, Chaudhry, Haroon Rashid, Vaughan, Dylan J., Hill, R. Sean, Partlow, Jennifer N., Yoo, Seung-Yun, Lam, Anh-Thu N., Nasir, Ramzi, Al-Saffar, Muna, Barkovich, A. James, Schwede, Matthew, Nagpal, Shailender, Rajab, Anna, DeBerardinis, Ralph J., Housman, David E., Mochida, Ganeshwaran H., Morrow, Eric M.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2016 Sep . 113(38), E5598-E5607.
Externí odkaz:
https://www.jstor.org/stable/26471664