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Annals of the New York Academy of Sciences
|
July 16, 2015
Developing therapies for spinal muscular atrophy
Mary H Wertz, Mustafa Sahin
Molecular Neurodegeneration
|
May 26, 2020
Interleukin-6 deficiency exacerbates Huntington's disease model phenotypes
Mary 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 atrophy
Mary 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 cells
Doo 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 sclerosis
Sek 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 ULK1
Alessia 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 deficits
Bikem Akten, Min Jeong Kye, Le T Hao, et al.
Nature Cell Biology
|
June 20, 2007
BACE1 regulates voltage-gated sodium channels and neuronal activity
Doo Yeon Kim, Bryce W Carey, Haibin Wang, et al.
Human Molecular Genetics
|
July 25, 2014
SMN regulates axonal local translation via miR-183/mTOR pathway
Min 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 Toxicity
Mary H Wertz, Mollie R Mitchem, S Sebastian Pineda, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Annals of the New York Academy of Sciences
|
July 16, 2015
Developing therapies for spinal muscular atrophy
Mary H Wertz, Mustafa Sahin
Molecular Neurodegeneration
|
May 26, 2020
Interleukin-6 deficiency exacerbates Huntington's disease model phenotypes
Mary 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 atrophy
Mary 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 cells
Doo 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 sclerosis
Sek 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 ULK1
Alessia 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 deficits
Bikem Akten, Min Jeong Kye, Le T Hao, et al.
Nature Cell Biology
|
June 20, 2007
BACE1 regulates voltage-gated sodium channels and neuronal activity
Doo Yeon Kim, Bryce W Carey, Haibin Wang, et al.
Human Molecular Genetics
|
July 25, 2014
SMN regulates axonal local translation via miR-183/mTOR pathway
Min 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 Toxicity
Mary H Wertz, Mollie R Mitchem, S Sebastian Pineda, et al.
Page
of 1