Showing results (111-120 of 152) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|February 9, 2011
The COPI vesicle complex binds and moves with survival motor neuron within axonsCyril Jayakumar Peter, Matthew Evans, Venugopal Thayanithy, et al.
The Journal of Cell Biology|September 6, 2007
Extracellular stimuli specifically regulate localized levels of individual neuronal mRNAsDianna E Willis, Erna A van Niekerk, Yukio Sasaki, et al.
Neuron|October 8, 2013
Experience-induced Arc/Arg3.1 primes CA1 pyramidal neurons for metabotropic glutamate receptor-dependent long-term synaptic depressionVikram Jakkamsetti, Nien-Pei Tsai, Christina Gross, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Muscleblind-like proteins dimerize by forming disulfide bonds to regulate alternative splicing and pathogenic RNA foci formationLuke A Knudson, Adam Kosti, Kathryn R Moss, et al.
Plos One|July 5, 2012
Coaggregation of RNA-binding proteins in a model of TDP-43 proteinopathy with selective RGG motif methylation and a role for RRM1 ubiquitinationEric B Dammer, Claudia Fallini, Yair M Gozal, et al.
Nature Communications|June 9, 2023
Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranesRyan P Hildebrandt, Kathryn R Moss, Aleksandra Janusz-Kaminska, et al.
Nucleic Acids Research|June 2, 2026
Muscleblind-like proteins dimerize by forming disulfide bonds to regulate alternative splicing and pathogenic RNA foci formationLuke A Knudson, Adam Kosti, Ryan P Hildebrandt, et al.
Molecular Neurodegeneration|June 26, 2016
Trehalose upregulates progranulin expression in human and mouse models of GRN haploinsufficiency: a novel therapeutic lead to treat frontotemporal dementiaChristopher J Holler, Georgia Taylor, Zachary T McEachin, et al.
The Journal of Biological Chemistry|May 9, 2021
TBK1 interacts with tau and enhances neurodegeneration in tauopathyMeasho H Abreha, Shamsideen Ojelade, Eric B Dammer, et al.
Human Molecular Genetics|February 11, 2005
SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMNThanh T Le, Lan T Pham, Matthew E R Butchbach, et al.
Pageof 16