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John Ravits

Showing results (51-60 of 102) with videos related to

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Acta Neuropathologica|December 3, 2017
Sense-encoded poly-GR dipeptide repeat proteins correlate to neurodegeneration and uniquely co-localize with TDP-43 in dendrites of repeat-expanded C9orf72 amyotrophic lateral sclerosisShahram Saberi, Jennifer E Stauffer, Jie Jiang, et al.
Acta Neuropathologica|July 1, 2022
Aberrant NOVA1 function disrupts alternative splicing in early stages of amyotrophic lateral sclerosisFlorian Krach, Emily C Wheeler, Martin Regensburger, et al.
Cell Reports|October 31, 2019
Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated GliaOliver H Tam, Nikolay V Rozhkov, Regina Shaw, et al.
Nature Cell Biology|November 1, 2025
TDP-43 skein-like inclusions are formed by BAG3- and HSP70-guided co-aggregation with actin-binding proteinsShan Lu, Sitao Zhang, Spencer Oung, et al.
Nature Cell Biology|September 8, 2022
Heat-shock chaperone HSPB1 regulates cytoplasmic TDP-43 phase separation and liquid-to-gel transitionShan Lu, Jiaojiao Hu, Olubankole Aladesuyi Arogundade, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 26, 2003
Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputesPeter M Andersen, Katherine B Sims, Winnie W Xin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 2014
Direct conversion of patient fibroblasts demonstrates non-cell autonomous toxicity of astrocytes to motor neurons in familial and sporadic ALSKathrin Meyer, Laura Ferraiuolo, Carlos J Miranda, et al.
JAMA Neurology|February 19, 2014
TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosisJanet Cady, Erica D Koval, Bruno A Benitez, et al.
The Journal of Clinical Investigation|May 22, 2019
Membralin deficiency dysregulates astrocytic glutamate homeostasis leading to ALS-like impairmentLu-Lin Jiang, Bing Zhu, Yingjun Zhao, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 18, 2013
Deciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesisJohn Ravits, Stanley Appel, Robert H Baloh, et al.
Pageof 11

Showing results (51-60 of 102) with videos related to

Sort By:
Pageof 11
Acta Neuropathologica|December 3, 2017
Sense-encoded poly-GR dipeptide repeat proteins correlate to neurodegeneration and uniquely co-localize with TDP-43 in dendrites of repeat-expanded C9orf72 amyotrophic lateral sclerosisShahram Saberi, Jennifer E Stauffer, Jie Jiang, et al.
Acta Neuropathologica|July 1, 2022
Aberrant NOVA1 function disrupts alternative splicing in early stages of amyotrophic lateral sclerosisFlorian Krach, Emily C Wheeler, Martin Regensburger, et al.
Cell Reports|October 31, 2019
Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated GliaOliver H Tam, Nikolay V Rozhkov, Regina Shaw, et al.
Nature Cell Biology|November 1, 2025
TDP-43 skein-like inclusions are formed by BAG3- and HSP70-guided co-aggregation with actin-binding proteinsShan Lu, Sitao Zhang, Spencer Oung, et al.
Nature Cell Biology|September 8, 2022
Heat-shock chaperone HSPB1 regulates cytoplasmic TDP-43 phase separation and liquid-to-gel transitionShan Lu, Jiaojiao Hu, Olubankole Aladesuyi Arogundade, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 26, 2003
Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputesPeter M Andersen, Katherine B Sims, Winnie W Xin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 2014
Direct conversion of patient fibroblasts demonstrates non-cell autonomous toxicity of astrocytes to motor neurons in familial and sporadic ALSKathrin Meyer, Laura Ferraiuolo, Carlos J Miranda, et al.
JAMA Neurology|February 19, 2014
TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosisJanet Cady, Erica D Koval, Bruno A Benitez, et al.
The Journal of Clinical Investigation|May 22, 2019
Membralin deficiency dysregulates astrocytic glutamate homeostasis leading to ALS-like impairmentLu-Lin Jiang, Bing Zhu, Yingjun Zhao, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 18, 2013
Deciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesisJohn Ravits, Stanley Appel, Robert H Baloh, et al.
Pageof 11