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Kathryn R Moss

Showing results (1-10 of 15) with videos related to

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Cells|January 10, 2025
Schwann Cells in Neuromuscular Disorders: A Spotlight on Amyotrophic Lateral SclerosisKathryn R Moss, Smita Saxena
Neurologic Clinics|October 29, 2025
Inherited Peripheral NeuropathiesRyan Castoro, Kathryn R Moss
Brain Research|November 6, 2019
Targeting the programmed axon degeneration pathway as a potential therapeutic for Charcot-Marie-Tooth diseaseKathryn R Moss, Ahmet Höke
Neuroscience Letters|December 28, 2020
New evidence for secondary axonal degeneration in demyelinating neuropathiesKathryn R Moss, Taylor S Bopp, Anna E Johnson, et al.
Glia|December 16, 2025
Aberrant Molecular Myelin Architecture in Charcot-Marie-Tooth Disease Type 1A and Hereditary Neuropathy With Liability to Pressure PalsiesKathryn R Moss, Marvis A Arowolo, Dave R Gutierrez, et al.
Journal of the Peripheral Nervous System : JPNS|February 9, 2022
SARM1 knockout does not rescue neuromuscular phenotypes in a Charcot-Marie-Tooth disease Type 1A mouse modelKathryn R Moss, Anna E Johnson, Taylor S Bopp, et al.
Plos One|May 22, 2019
FMRP - G-quadruplex mRNA - miR-125a interactions: Implications for miR-125a mediated translation regulation of PSD-95 mRNABrett DeMarco, Snezana Stefanovic, Allison Williams, et al.
Molecular Biosystems|June 15, 2017
Fragile X mental retardation protein recognizes a G quadruplex structure within the survival motor neuron domain containing 1 mRNA 5'-UTRDamian S McAninch, Ashley M Heinaman, Cara N Lang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 3, 2016
Dysregulation of mRNA Localization and Translation in Genetic DiseaseEric T Wang, J Matthew Taliaferro, Ji-Ann Lee, et al.
Iscience|May 21, 2024
hESC- and hiPSC-derived Schwann cells are molecularly comparable and functionally equivalentKathryn R Moss, Ruifa Mi, Riki Kawaguchi, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Cells|January 10, 2025
Schwann Cells in Neuromuscular Disorders: A Spotlight on Amyotrophic Lateral SclerosisKathryn R Moss, Smita Saxena
Neurologic Clinics|October 29, 2025
Inherited Peripheral NeuropathiesRyan Castoro, Kathryn R Moss
Brain Research|November 6, 2019
Targeting the programmed axon degeneration pathway as a potential therapeutic for Charcot-Marie-Tooth diseaseKathryn R Moss, Ahmet Höke
Neuroscience Letters|December 28, 2020
New evidence for secondary axonal degeneration in demyelinating neuropathiesKathryn R Moss, Taylor S Bopp, Anna E Johnson, et al.
Glia|December 16, 2025
Aberrant Molecular Myelin Architecture in Charcot-Marie-Tooth Disease Type 1A and Hereditary Neuropathy With Liability to Pressure PalsiesKathryn R Moss, Marvis A Arowolo, Dave R Gutierrez, et al.
Journal of the Peripheral Nervous System : JPNS|February 9, 2022
SARM1 knockout does not rescue neuromuscular phenotypes in a Charcot-Marie-Tooth disease Type 1A mouse modelKathryn R Moss, Anna E Johnson, Taylor S Bopp, et al.
Plos One|May 22, 2019
FMRP - G-quadruplex mRNA - miR-125a interactions: Implications for miR-125a mediated translation regulation of PSD-95 mRNABrett DeMarco, Snezana Stefanovic, Allison Williams, et al.
Molecular Biosystems|June 15, 2017
Fragile X mental retardation protein recognizes a G quadruplex structure within the survival motor neuron domain containing 1 mRNA 5'-UTRDamian S McAninch, Ashley M Heinaman, Cara N Lang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 3, 2016
Dysregulation of mRNA Localization and Translation in Genetic DiseaseEric T Wang, J Matthew Taliaferro, Ji-Ann Lee, et al.
Iscience|May 21, 2024
hESC- and hiPSC-derived Schwann cells are molecularly comparable and functionally equivalentKathryn R Moss, Ruifa Mi, Riki Kawaguchi, et al.
Pageof 2