Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Valentina Dal Pozzo"'
Publikováno v:
Biomolecules, Vol 10, Iss 7, p 975 (2020)
Traumatic brain injury (TBI) is a relatively common occurrence following accidents or violence, and often results in long-term cognitive or motor disability. Despite the high health cost associated with this type of injury, presently there are no eff
Externí odkaz:
https://doaj.org/article/a00cdc2639744c4a94dfa0c0a9651c3b
Autor:
Valerie Baubet, Sharmistha Pal, Noah Alexander, Ramana V. Davuluri, Nadia Dahmane, Yingtao Bi, Karla K Frietze, Christopher E. Mason, Yanwen Li, Valentina Dal Pozzo, Victoria D'Acunto, Chaomei Xiang
Publikováno v:
Mol Cell Biol
How mammalian neuronal identity is progressively acquired and reinforced during development is not understood. We have previously shown that loss of RP58 (ZNF238 or ZBTB18), a BTB/POZ-zinc finger-containing transcription factor, in the mouse brain le
Autor:
Huijuan Cui, Nicole L. Volk, Xiaobing Luo, Gabriella D'Arcangelo, Alfonso Roque, Ronald P. Hart, Ishan Khosla, Mladen-Roko Rasin, Geeta Palsule, Shawn Tucai, Iva Salamon, Wendy Liu, Megerditch Kiledjian, Xinfu Jiao, Valentina Dal Pozzo, Petronio Zalamea
Publikováno v:
Cereb Cortex
Homozygous mutations in the gene encoding the scavenger mRNA-decapping enzyme, DcpS, have been shown to underlie developmental delay and intellectual disability. Intellectual disability is associated with both abnormal neocortical development and mRN
Autor:
Muyuan Chen, Kevin Huynh, Michael J. Currie, Daniel Mitchell, Liam S. Turk, Renwick C. J. Dobson, Valentina Dal Pozzo, Gabriella D'Arcangelo, Xuyuan Kuang, Davide Comoletti, Khush Patel, Wei Dai
Publikováno v:
Structure (London, England : 1993). 29(10)
Reelin operates through canonical and non-canonical pathways that mediate several aspects of brain development and function. Reelin's dimeric central fragment (CF), generated through proteolytic cleavage, is required for the lipoprotein-receptor-depe
Publikováno v:
Biomolecules, Vol 10, Iss 975, p 975 (2020)
Biomolecules
Volume 10
Issue 7
Biomolecules
Volume 10
Issue 7
Traumatic brain injury (TBI) is a relatively common occurrence following accidents or violence, and often results in long-term cognitive or motor disability. Despite the high health cost associated with this type of injury, presently there are no eff
Autor:
Alina Afinogenova, Avery J. Zucco, Orrin Devinsky, Ronald P. Hart, Gabriella D'Arcangelo, Valentina Dal Pozzo
Tuberous Sclerosis Complex (TSC) is a disease caused by autosomal dominant mutations in the TSC1 or TSC2 genes, and is characterized by tumor susceptibility, brain lesions, seizures and behavioral impairments. The TSC1 and TSC2 genes encode proteins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d10a397dc7c099c3e67ab6d011eb4f7
https://europepmc.org/articles/PMC6250058/
https://europepmc.org/articles/PMC6250058/
Publikováno v:
eNeuro
Mutations in the TSC1 and TSC2 genes cause tuberous sclerosis complex (TSC), a genetic disease often associated with epilepsy, intellectual disability, and autism, and characterized by the presence of anatomical malformations in the brain as well as
Publikováno v:
eneuro. 2:ENEURO.0046-15.2015
Mutations in theTSC1andTSC2genes cause tuberous sclerosis complex (TSC), a genetic disease often associated with epilepsy, intellectual disability, and autism, and characterized by the presence of anatomical malformations in the brain as well as tumo