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Daniela C Zarnescu

Showing results (31-40 of 46) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 28, 2014
Futsch/MAP1B mRNA is a translational target of TDP-43 and is neuroprotective in a Drosophila model of amyotrophic lateral sclerosisAlyssa N Coyne, Bhavani Bagevalu Siddegowda, Patricia S Estes, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
<i>C9orf72</i> -associated G4C2 hexanucleotide repeat expression in <i>Drosophila</i> mushroom bodies causes age dependent TDP-43 pathology and dementia relevant phenotypes mediated in part by the glypican Dlp/GPC6Brijesh S Chauhan, Megan A Brennan, Peter C Forstmeier, et al.
Circulation|November 5, 2017
Increased Cardiac Arrhythmogenesis Associated With Gap Junction Remodeling With Upregulation of RNA-Binding Protein FXR1Miensheng Chu, Stefanie Mares Novak, Cathleen Cover, et al.
ACS Chemical Biology|June 27, 2019
Small Molecule Targeting TDP-43's RNA Recognition Motifs Reduces Locomotor Defects in a <i>Drosophila</i> Model of Amyotrophic Lateral Sclerosis (ALS)Liberty François-Moutal, Razaz Felemban, David D Scott, et al.
Biology Open|January 24, 2018
<i>miR-9a</i> mediates the role of Lethal giant larvae as an epithelial growth inhibitor in <i>Drosophila</i>Scott G Daniel, Atlantis D Russ, Kathryn M Guthridge, et al.
Developmental Cell|December 29, 2004
Fragile X protein functions with lgl and the par complex in flies and miceDaniela C Zarnescu, Peng Jin, Joerg Betschinger, et al.
Cell Reports|October 6, 2017
Post-transcriptional Inhibition of Hsc70-4/HSPA8 Expression Leads to Synaptic Vesicle Cycling Defects in Multiple Models of ALSAlyssa N Coyne, Ileana Lorenzini, Ching-Chieh Chou, et al.
Elife|June 11, 2019
Glycolysis upregulation is neuroprotective as a compensatory mechanism in ALSErnesto Manzo, Ileana Lorenzini, Dianne Barrameda, et al.
Acta Neuropathologica Communications|October 20, 2023
Modelling TDP-43 proteinopathy in Drosophila uncovers shared and neuron-specific targets across ALS and FTD relevant circuitsR Keating Godfrey, Eric Alsop, Reed T Bjork, et al.
Acta Neuropathologica Communications|March 25, 2021
TDP-43 proteinopathy alters the ribosome association of multiple mRNAs including the glypican Dally-like protein (Dlp)/GPC6Erik M Lehmkuhl, Suvithanandhini Loganathan, Eric Alsop, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 28, 2014
Futsch/MAP1B mRNA is a translational target of TDP-43 and is neuroprotective in a Drosophila model of amyotrophic lateral sclerosisAlyssa N Coyne, Bhavani Bagevalu Siddegowda, Patricia S Estes, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
<i>C9orf72</i> -associated G4C2 hexanucleotide repeat expression in <i>Drosophila</i> mushroom bodies causes age dependent TDP-43 pathology and dementia relevant phenotypes mediated in part by the glypican Dlp/GPC6Brijesh S Chauhan, Megan A Brennan, Peter C Forstmeier, et al.
Circulation|November 5, 2017
Increased Cardiac Arrhythmogenesis Associated With Gap Junction Remodeling With Upregulation of RNA-Binding Protein FXR1Miensheng Chu, Stefanie Mares Novak, Cathleen Cover, et al.
ACS Chemical Biology|June 27, 2019
Small Molecule Targeting TDP-43's RNA Recognition Motifs Reduces Locomotor Defects in a <i>Drosophila</i> Model of Amyotrophic Lateral Sclerosis (ALS)Liberty François-Moutal, Razaz Felemban, David D Scott, et al.
Biology Open|January 24, 2018
<i>miR-9a</i> mediates the role of Lethal giant larvae as an epithelial growth inhibitor in <i>Drosophila</i>Scott G Daniel, Atlantis D Russ, Kathryn M Guthridge, et al.
Developmental Cell|December 29, 2004
Fragile X protein functions with lgl and the par complex in flies and miceDaniela C Zarnescu, Peng Jin, Joerg Betschinger, et al.
Cell Reports|October 6, 2017
Post-transcriptional Inhibition of Hsc70-4/HSPA8 Expression Leads to Synaptic Vesicle Cycling Defects in Multiple Models of ALSAlyssa N Coyne, Ileana Lorenzini, Ching-Chieh Chou, et al.
Elife|June 11, 2019
Glycolysis upregulation is neuroprotective as a compensatory mechanism in ALSErnesto Manzo, Ileana Lorenzini, Dianne Barrameda, et al.
Acta Neuropathologica Communications|October 20, 2023
Modelling TDP-43 proteinopathy in Drosophila uncovers shared and neuron-specific targets across ALS and FTD relevant circuitsR Keating Godfrey, Eric Alsop, Reed T Bjork, et al.
Acta Neuropathologica Communications|March 25, 2021
TDP-43 proteinopathy alters the ribosome association of multiple mRNAs including the glypican Dally-like protein (Dlp)/GPC6Erik M Lehmkuhl, Suvithanandhini Loganathan, Eric Alsop, et al.
Pageof 5