Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Cynthia Moncada"'
Autor:
Qin Huang, Albert T Chen, Ken Y Chan, Hikari Sorensen, Andrew J Barry, Bahar Azari, Qingxia Zheng, Thomas Beddow, Binhui Zhao, Isabelle G Tobey, Cynthia Moncada-Reid, Fatma-Elzahraa Eid, Christopher J Walkey, M Cecilia Ljungberg, William R Lagor, Jason D Heaney, Yujia A Chan, Benjamin E Deverman
Publikováno v:
PLoS Biology, Vol 21, Iss 7, p e3002112 (2023)
Viruses have evolved the ability to bind and enter cells through interactions with a wide variety of cell macromolecules. We engineered peptide-modified adeno-associated virus (AAV) capsids that transduce the brain through the introduction of de novo
Externí odkaz:
https://doaj.org/article/1e261ffbb0154ecb9a09e3105cd10b51
Autor:
Minjin Jeong, Karen E. Ocwieja, Dongjun Han, P. Ashley Wackym, Yichen Zhang, Alyssa Brown, Cynthia Moncada, Andrea Vambutas, Theodore Kanne, Rachel Crain, Noah Siegel, Valerie Leger, Felipe Santos, D. Bradley Welling, Lee Gehrke, Konstantina M. Stankovic
Publikováno v:
Communications Medicine, Vol 1, Iss 1, Pp 1-14 (2021)
Plain language summary Coronavirus disease 2019 (COVID-19) is an infectious disease caused by the novel coronavirus SARS-CoV-2. A growing number of sensory symptoms have been linked to this illness. Here, we describe patients with COVID-19 and new-on
Externí odkaz:
https://doaj.org/article/caaa18033e444b8284794201f082d3fe
Autor:
Rachel Crain, Karen E. Ocwieja, Noah S. Siegel, Lee Gehrke, Valerie Leger, D. Bradley Welling, Cynthia Moncada, Andrea Vambutas, Theodore Kanne, Felipe Santos, Yichen Zhang, Minjin Jeong, Dongjun Han, P. Ashley Wackym, Alyssa Brown, Konstantina M. Stankovic
Publikováno v:
Communications Medicine, Vol 1, Iss 1, Pp 1-14 (2021)
Communications Medicine
Communications Medicine
Background COVID-19 is a pandemic respiratory and vascular disease caused by SARS-CoV-2 virus. There is a growing number of sensory deficits associated with COVID-19 and molecular mechanisms underlying these deficits are incompletely understood. Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cb4f0ed903740ddac5402356cbcf835
https://doaj.org/article/caaa18033e444b8284794201f082d3fe
https://doaj.org/article/caaa18033e444b8284794201f082d3fe
Autor:
Hongjie Li, Mark A. Gillespie, Maria C. Marchetto, Hirotaka Shoji, Gerald R. Crabtree, Zohar Shipony, Erik L. Miller, Lu Wang, Seung Tae Baek, Liqun Luo, Laura Elias, Cynthia Moncada, Wendy Wenderski, Andrey Krokhotin, Esther Y. Son, Jessica J. Walsh, Fred H. Gage, Tipu Sultan, Valentina Stanley, Shereen G. Ghosh, Jeffrey A. Ranish, Tsuyoshi Miyakawa, Renee D. George, Brett T. Staahl, Maha S. Zaki, Dillon Y. Chen, Joseph G. Gleeson, Sara B. Linker, Robert C. Malenka
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, vol 117, iss 18
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America
Significance Autism is a complex neurodevelopmental disorder whose causative mechanisms are unclear. Taking advantage of a unique cohort with recessively inherited autism, we identified six families with biallelic mutation of the neuronal-specific su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94cdae66df1cbf408e3b12b6df577943
https://escholarship.org/uc/item/65w0b3xr
https://escholarship.org/uc/item/65w0b3xr
