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Showing results (441-450 of 499) with videos related to

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The Journal of Clinical Investigation|August 1, 2006
Antisense oligonucleotide therapy for neurodegenerative diseaseRichard A Smith, Timothy M Miller, Koji Yamanaka, et al.
Acta Neuropathologica Communications|June 26, 2015
Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALSJacqueline C Mitchell, Remy Constable, Eva So, et al.
Neuron|June 26, 2012
Sustained therapeutic reversal of Huntington's disease by transient repression of huntingtin synthesisHolly B Kordasiewicz, Lisa M Stanek, Edward V Wancewicz, et al.
Science (New York, N.Y.)|December 18, 2020
HSP70 chaperones RNA-free TDP-43 into anisotropic intranuclear liquid spherical shellsHaiyang Yu, Shan Lu, Kelsey Gasior, et al.
Cancer Cell|July 16, 2015
MYC Is a Major Determinant of Mitotic Cell FateCaroline Topham, Anthony Tighe, Peter Ly, et al.
Molecular Neurodegeneration|September 7, 2021
Wild-type FUS corrects ALS-like disease induced by cytoplasmic mutant FUS through autoregulationInmaculada Sanjuan-Ruiz, Noé Govea-Perez, Melissa McAlonis-Downes, 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.
Neurobiology of Disease|August 14, 1998
Axonal transport of mutant superoxide dismutase 1 and focal axonal abnormalities in the proximal axons of transgenic miceD R Borchelt, P C Wong, M W Becher, et al.
Free Radical Biology & Medicine|May 24, 2016
Evaluation of NADPH oxidases as drug targets in a mouse model of familial amyotrophic lateral sclerosisTamara Seredenina, Zeynab Nayernia, Silvia Sorce, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Mutant SOD1 expressed by oligodendrocytes aggregates in myelinic nanochannels and accelerates disease progression in familial ALS miceAlexandra I Mot, Ying Li, Payam Dibaj, et al.
Pageof 50

Showing results (441-450 of 499) with videos related to

Sort By:
Pageof 50
The Journal of Clinical Investigation|August 1, 2006
Antisense oligonucleotide therapy for neurodegenerative diseaseRichard A Smith, Timothy M Miller, Koji Yamanaka, et al.
Acta Neuropathologica Communications|June 26, 2015
Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALSJacqueline C Mitchell, Remy Constable, Eva So, et al.
Neuron|June 26, 2012
Sustained therapeutic reversal of Huntington's disease by transient repression of huntingtin synthesisHolly B Kordasiewicz, Lisa M Stanek, Edward V Wancewicz, et al.
Science (New York, N.Y.)|December 18, 2020
HSP70 chaperones RNA-free TDP-43 into anisotropic intranuclear liquid spherical shellsHaiyang Yu, Shan Lu, Kelsey Gasior, et al.
Cancer Cell|July 16, 2015
MYC Is a Major Determinant of Mitotic Cell FateCaroline Topham, Anthony Tighe, Peter Ly, et al.
Molecular Neurodegeneration|September 7, 2021
Wild-type FUS corrects ALS-like disease induced by cytoplasmic mutant FUS through autoregulationInmaculada Sanjuan-Ruiz, Noé Govea-Perez, Melissa McAlonis-Downes, 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.
Neurobiology of Disease|August 14, 1998
Axonal transport of mutant superoxide dismutase 1 and focal axonal abnormalities in the proximal axons of transgenic miceD R Borchelt, P C Wong, M W Becher, et al.
Free Radical Biology & Medicine|May 24, 2016
Evaluation of NADPH oxidases as drug targets in a mouse model of familial amyotrophic lateral sclerosisTamara Seredenina, Zeynab Nayernia, Silvia Sorce, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Mutant SOD1 expressed by oligodendrocytes aggregates in myelinic nanochannels and accelerates disease progression in familial ALS miceAlexandra I Mot, Ying Li, Payam Dibaj, et al.
Pageof 50