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Human Molecular Genetics|April 16, 2019
Rare variants in MYH15 modify amyotrophic lateral sclerosis riskHyerim Kim, Junghwa Lim, Han Bao, et al.Molecular Cell|August 7, 2018
Active N<sup>6</sup>-Methyladenine Demethylation by DMAD Regulates Gene Expression by Coordinating with Polycomb Protein in NeuronsBing Yao, Yujing Li, Zhiqin Wang, et al.Cell Reports|April 30, 2015
Increased expression of the PI3K enhancer PIKE mediates deficits in synaptic plasticity and behavior in fragile X syndromeChristina Gross, Chia-Wei Chang, Seth M Kelly, et al.Cell Reports|August 10, 2017
The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila NeuronsRick S Bienkowski, Ayan Banerjee, J Christopher Rounds, et al.Plos Genetics|July 10, 2020
A Drosophila model of Pontocerebellar Hypoplasia reveals a critical role for the RNA exosome in neuronsDerrick J Morton, Binta Jalloh, Lily Kim, et al.Human Molecular Genetics|July 2, 2017
The RNA-binding protein, ZC3H14, is required for proper poly(A) tail length control, expression of synaptic proteins, and brain function in miceJennifer Rha, Stephanie K Jones, Jonathan Fidler, et al.Proceedings of the National Academy of Sciences of the United States of America|July 8, 2011
Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humansChanghui Pak, Masoud Garshasbi, Kimia Kahrizi, et al.Pageof 5