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Rob Moccia

Showing results (1-10 of 10) with videos related to

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Bioinformatics (Oxford, England)|May 23, 2025
Simple controls exceed best deep learning algorithms and reveal foundation model effectiveness for predicting genetic perturbationsDaniel R Wong, Abby S Hill, Rob Moccia
HGG Advances|May 24, 2025
Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variantsSamantha J Klasfeld, Katherine A Knutson, Melissa R Miller, et al.
Nature Neuroscience|November 5, 2013
The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTDNaoki Suzuki, Asif M Maroof, Florian T Merkle, et al.
American Journal of Medicine Open|July 22, 2024
Prevalence and Clinical Burden of Idiopathic Dilated Cardiomyopathy in the United StatesYaa Ababio, Scott P Kelly, Franca S Angeli, et al.
Acta Neuropathologica Communications|July 6, 2018
Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patientsDaniel A Mordes, Mercedes Prudencio, Lindsey D Goodman, et al.
Science Translational Medicine|July 15, 2016
Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune diseaseAaron Burberry, Naoki Suzuki, Jin-Yuan Wang, et al.
Nature Neuroscience|January 16, 2019
ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repairJoseph R Klim, Luis A Williams, Francesco Limone, et al.
Brain Communications|June 30, 2025
Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of <i>HTT</i> associated with an early disease onset in <i>C9orf72</i> carriersMathieu Barbier, Thomas Gareau, Agnès Camuzat, et al.
Ebiomedicine|April 21, 2018
Activation of Liver AMPK with PF-06409577 Corrects NAFLD and Lowers Cholesterol in Rodent and Primate Preclinical ModelsRyan M Esquejo, Christopher T Salatto, Jake Delmore, et al.
Cell Stem Cell|April 8, 2014
Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1Evangelos Kiskinis, Jackson Sandoe, Luis A Williams, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|May 23, 2025
Simple controls exceed best deep learning algorithms and reveal foundation model effectiveness for predicting genetic perturbationsDaniel R Wong, Abby S Hill, Rob Moccia
HGG Advances|May 24, 2025
Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variantsSamantha J Klasfeld, Katherine A Knutson, Melissa R Miller, et al.
Nature Neuroscience|November 5, 2013
The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTDNaoki Suzuki, Asif M Maroof, Florian T Merkle, et al.
American Journal of Medicine Open|July 22, 2024
Prevalence and Clinical Burden of Idiopathic Dilated Cardiomyopathy in the United StatesYaa Ababio, Scott P Kelly, Franca S Angeli, et al.
Acta Neuropathologica Communications|July 6, 2018
Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patientsDaniel A Mordes, Mercedes Prudencio, Lindsey D Goodman, et al.
Science Translational Medicine|July 15, 2016
Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune diseaseAaron Burberry, Naoki Suzuki, Jin-Yuan Wang, et al.
Nature Neuroscience|January 16, 2019
ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repairJoseph R Klim, Luis A Williams, Francesco Limone, et al.
Brain Communications|June 30, 2025
Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of <i>HTT</i> associated with an early disease onset in <i>C9orf72</i> carriersMathieu Barbier, Thomas Gareau, Agnès Camuzat, et al.
Ebiomedicine|April 21, 2018
Activation of Liver AMPK with PF-06409577 Corrects NAFLD and Lowers Cholesterol in Rodent and Primate Preclinical ModelsRyan M Esquejo, Christopher T Salatto, Jake Delmore, et al.
Cell Stem Cell|April 8, 2014
Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1Evangelos Kiskinis, Jackson Sandoe, Luis A Williams, et al.
Pageof 1