Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cenfu Wei"'
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 17, p 9549 (2022)
The HER2/neu signaling pathway is one of the most frequently mutated in human cancer. Although therapeutics targeting this pathway have good efficacy, cancer cells frequently develop resistance. The HER2 gene encodes the full-length HER2 protein, as
Externí odkaz:
https://doaj.org/article/ba29ab2fb76f46398b7c83b58b5a4dde
Autor:
Xiaofei Du, Giorgio Grasselli, Dana H. Simmons, Christopher M. Gomez, Justine Shih, Christian Hansel, Heather K. Titley, Silas E. Busch, Claire Piochon, Cenfu Wei
Publikováno v:
Biological Psychiatry Global Open Science. 2:450-459
Background Autism spectrum disorder (ASD) patients often show altered responses to sensory stimuli as well as motor deficits, including an impairment of delay eyeblink conditioning (EBC), which involves integration of sensory signals in the cerebellu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c5064392c4ad866f2dca7ea4f8e6ecd
https://doi.org/10.1016/j.bpsgos.2021.09.004
https://doi.org/10.1016/j.bpsgos.2021.09.004
Publikováno v:
The Cerebellum.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bb85b3ed72bb7edd5ceda0177e376ea
https://doi.org/10.1007/s12311-023-01567-9
https://doi.org/10.1007/s12311-023-01567-9
Publikováno v:
The Cerebellum.
MicroRNAs, a class of small RNA regulators, function throughout neurodevelopment, from neural stem cell neurogenesis to neuronal maturation, synaptic formation, and plasticity. α1ACT, a transcription factor (TF), plays a critical role in neonatal ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a6fe423dba6fb297b0470ac60f7c0d8
https://doi.org/10.1007/s12311-022-01431-2
https://doi.org/10.1007/s12311-022-01431-2
Autor:
Xiaofei Du, João L. Carvalho-de-Souza, Natalie Petrossian, Ramon Latorre, Timothy C. Hain, Julia Staisch, Willy Carrasquel-Ursulaez, Christopher M. Gomez, Francisco Bezanilla, Yenisleidy Lorenzo, Michael Xu, Tomoya Kubota, Naileth Gonzalez, Cenfu Wei
Publikováno v:
Proc Natl Acad Sci U S A
Despite a growing number of ion channel genes implicated in hereditary ataxia, it remains unclear how ion channel mutations lead to loss-of-function or death of cerebellar neurons. Mutations in the gene KCNMA1 , encoding the α-subunit of the BK chan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e4334845fe91b59649ed951ee18ec74
https://doi.org/10.1073/pnas.1920008117
https://doi.org/10.1073/pnas.1920008117
Autor:
Yan Li, Ann C. Palmenberg, Jack Godfrey, Xiaofei Du, Daniel Parviz Hejazi Pastor, Christian Hansel, Jorge Andrade, Giorgio Grasselli, Eshaan R. Rao, Christopher M. Gomez, Cenfu Wei
Publikováno v:
Neuron. 102:770-785.e7
Summary Postnatal cerebellar development is a precisely regulated process involving well-orchestrated expression of neural genes. Neurological phenotypes associated with CACNA1A gene defects have been increasingly recognized, yet the molecular princi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff832685f16a90d6bd7666a2eacb6fd2
https://doi.org/10.1016/j.neuron.2019.02.036
https://doi.org/10.1016/j.neuron.2019.02.036