Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Geena Skaria"'
Publikováno v:
JMIR Research Protocols, Vol 13, p e50732 (2024)
BackgroundType 2 diabetes mellitus (T2DM) is one of the leading noncommunicable diseases that require diabetes self-management (DSM) practices. This study proposes to develop a customized mobile health (mHealth) app integrated with a hospital informa
Externí odkaz:
https://doaj.org/article/bc7605835ee04095820562482a47dc8c
Autor:
Geena Skaria
Publikováno v:
Journal of Mobile Technology in Medicine. 2:26-29
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-17 (2019)
Abstract CGG repeat expansions in FMR1 cause the neurodegenerative disorder Fragile X-associated Tremor/Ataxia Syndrome (FXTAS). Ubiquitinated neuronal intranuclear inclusions (NIIs) are the neuropathological hallmark of FXTAS. Both sense strand deri
Externí odkaz:
https://doaj.org/article/25002b7b607e4fef9510a020e6041f5a
Autor:
Geena Skariah, Joseph Seimetz, Miles Norsworthy, Monica C. Lannom, Phillip J. Kenny, Mohamed Elrakhawy, Craig Forsthoefel, Jenny Drnevich, Auinash Kalsotra, Stephanie Ceman
Publikováno v:
BMC Biology, Vol 15, Iss 1, Pp 1-19 (2017)
Abstract Background Moloney leukemia virus 10 (Mov10) is an RNA helicase that mediates access of the RNA-induced silencing complex to messenger RNAs (mRNAs). Until now, its role as an RNA helicase and as a regulator of retrotransposons has been chara
Externí odkaz:
https://doaj.org/article/2378c5d379f844ebb71dd0031d7ee75d
Autor:
Jill M. Haenfler, Geena Skariah, Caitlin M. Rodriguez, Andre Monteiro da Rocha, Jack M. Parent, Gary D. Smith, Peter K. Todd
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 11 (2018)
Fragile X Syndrome (FXS) is the most common inherited cause of intellectual disability and autism. It results from expansion of a CGG nucleotide repeat in the 5′ untranslated region (UTR) of FMR1. Large expansions elicit repeat and promoter hyper-m
Externí odkaz:
https://doaj.org/article/51d2a59766964b4fb80cf15d790eed9c
Autor:
Phillip J. Kenny, Hongjun Zhou, Miri Kim, Geena Skariah, Radhika S. Khetani, Jenny Drnevich, Mary Luz Arcila, Kenneth S. Kosik, Stephanie Ceman
Publikováno v:
Cell Reports, Vol 9, Iss 5, Pp 1729-1741 (2014)
Summary: The fragile X mental retardation protein FMRP regulates translation of its bound mRNAs through incompletely defined mechanisms. FMRP has been linked to the microRNA pathway, and we show here that it associates with the RNA helicase MOV10, al
Externí odkaz:
https://doaj.org/article/ec4584b53408443fb65003d588eb89c0