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Mary H Wertz

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

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Annals of the New York Academy of Sciences|July 16, 2015
Developing therapies for spinal muscular atrophyMary H Wertz, Mustafa Sahin
Molecular Neurodegeneration|May 26, 2020
Interleukin-6 deficiency exacerbates Huntington's disease model phenotypesMary H Wertz, S Sebastian Pineda, Hyeseung Lee, et al.
Human Molecular Genetics|March 24, 2016
Cell-type-specific miR-431 dysregulation in a motor neuron model of spinal muscular atrophyMary H Wertz, Kellen Winden, Pierre Neveu, et al.
Neuro-Degenerative Diseases|November 13, 2013
The E280A presenilin mutation reduces voltage-gated sodium channel levels in neuronal cellsDoo Yeon Kim, Mary H Wertz, Vivek Gautam, et al.
Molecular Autism|February 26, 2014
Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosisSek Won Kong, Mustafa Sahin, Christin D Collins, et al.
Human Molecular Genetics|March 7, 2014
Neuronal Tsc1/2 complex controls autophagy through AMPK-dependent regulation of ULK1Alessia Di Nardo, Mary H Wertz, Erica Kwiatkowski, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2011
Interaction of survival of motor neuron (SMN) and HuD proteins with mRNA cpg15 rescues motor neuron axonal deficitsBikem Akten, Min Jeong Kye, Le T Hao, et al.
Nature Cell Biology|June 20, 2007
BACE1 regulates voltage-gated sodium channels and neuronal activityDoo Yeon Kim, Bryce W Carey, Haibin Wang, et al.
Human Molecular Genetics|July 25, 2014
SMN regulates axonal local translation via miR-183/mTOR pathwayMin Jeong Kye, Emily D Niederst, Mary H Wertz, et al.
Neuron|February 1, 2020
Genome-wide In Vivo CNS Screening Identifies Genes that Modify CNS Neuronal Survival and mHTT ToxicityMary H Wertz, Mollie R Mitchem, S Sebastian Pineda, et al.
Pageof 1

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

Sort By:
Pageof 1
Annals of the New York Academy of Sciences|July 16, 2015
Developing therapies for spinal muscular atrophyMary H Wertz, Mustafa Sahin
Molecular Neurodegeneration|May 26, 2020
Interleukin-6 deficiency exacerbates Huntington's disease model phenotypesMary H Wertz, S Sebastian Pineda, Hyeseung Lee, et al.
Human Molecular Genetics|March 24, 2016
Cell-type-specific miR-431 dysregulation in a motor neuron model of spinal muscular atrophyMary H Wertz, Kellen Winden, Pierre Neveu, et al.
Neuro-Degenerative Diseases|November 13, 2013
The E280A presenilin mutation reduces voltage-gated sodium channel levels in neuronal cellsDoo Yeon Kim, Mary H Wertz, Vivek Gautam, et al.
Molecular Autism|February 26, 2014
Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosisSek Won Kong, Mustafa Sahin, Christin D Collins, et al.
Human Molecular Genetics|March 7, 2014
Neuronal Tsc1/2 complex controls autophagy through AMPK-dependent regulation of ULK1Alessia Di Nardo, Mary H Wertz, Erica Kwiatkowski, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2011
Interaction of survival of motor neuron (SMN) and HuD proteins with mRNA cpg15 rescues motor neuron axonal deficitsBikem Akten, Min Jeong Kye, Le T Hao, et al.
Nature Cell Biology|June 20, 2007
BACE1 regulates voltage-gated sodium channels and neuronal activityDoo Yeon Kim, Bryce W Carey, Haibin Wang, et al.
Human Molecular Genetics|July 25, 2014
SMN regulates axonal local translation via miR-183/mTOR pathwayMin Jeong Kye, Emily D Niederst, Mary H Wertz, et al.
Neuron|February 1, 2020
Genome-wide In Vivo CNS Screening Identifies Genes that Modify CNS Neuronal Survival and mHTT ToxicityMary H Wertz, Mollie R Mitchem, S Sebastian Pineda, et al.
Pageof 1