Publications by authors named "Gregory A Cox"

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Efficient Cas9 nuclease-based editing in skeletal muscle via lipid nanoparticle delivery.
Sukanya Iyer, Katelyn Daman, Yehui Sun, Amanda Tutto, Sarah E Holbrook, Gregory A Cox

bioRxiv· May 2025

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Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1.
Sarah E Holbrook, Amy N Hicks, Paige B Martin, Timothy J Hines, Harold P Castro, Gregory A Cox

Hum Mol Genet· October 2024

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Poly-alanine-tailing is a modifier of neurodegeneration caused by Listerin mutation.
Hao-Chih Hung, Carlos Costas-Insua, Sarah E Holbrook, Jennifer E Stauffer, Paige B Martin, Gregory A Cox

bioRxiv· August 2024

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Clinically relevant mouse models of Charcot-Marie-Tooth type 2S.
Paige B Martin, Sarah E Holbrook, Amy N Hicks, Timothy J Hines, Laurent P Bogdanik, Gregory A Cox

Hum Mol Genet· April 2023

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Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease.
Guillermo M Alexander, Terry D Heiman-Patterson, Frank Bearoff, Roger B Sher, Laura Hennessy, Gregory A Cox

PLoS One· September 2022

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A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin.
Phaneendra Chennampally, Ambreen Sayed-Zahid, Prabakaran Soundararajan, Jocelyn Sharp, Gregory A Cox

Sci Rep· September 2021

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Author Correction: A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin.
Phaneendra Chennampally, Ambreen Sayed-Zahid, Prabakaran Soundararajan, Jocelyn Sharp, Gregory A Cox

Sci Rep· September 2021

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Convergence of mammalian RQC and C-end rule proteolytic pathways via alanine tailing.
Anna Thrun, Aitor Garzia, Yu Kigoshi-Tansho, Pratik R Patil, Charles S Umbaugh, Gregory A Cox

Mol Cell· May 2021

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Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn mouse model of spinal muscular atrophy.
Emily J Reedich, Martin Kalski, Nicholas Armijo, Gregory A Cox, Christine J DiDonato

Exp Neurol· March 2021

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Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
Paige B Martin, Yu Kigoshi-Tansho, Roger B Sher, Gianina Ravenscroft, Jennifer E Stauffer, Gregory A Cox

Nat Commun· October 2020

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NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
Paige B Martin, Yu Kigoshi-Tansho, Roger B Sher, Gianina Ravenscroft, Jennifer E Stauffer, Gregory A Cox

Nat Commun· September 2020

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Overlapping spectrums: The clinicogenetic commonalities between Charcot-Marie-Tooth and other neurodegenerative diseases.
Paige B Martin, Amy N Hicks, Sarah E Holbrook, Gregory A Cox

Brain Res· January 2020

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Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy.
Ambreen A Sayed-Zahid, Roger B Sher, Stacey J Sukoff Rizzo, Laura C Anderson, Kathryn E Patenaude, Gregory A Cox

Hum Mol Genet· August 2019

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Neuromuscular Disease Models and Analysis.
Robert W Burgess, Gregory A Cox, Kevin L Seburn

Methods Mol Biol· December 2017

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Analysis of BMAA enantiomers in cycads, cyanobacteria, and mammals: in vivo formation and toxicity of D-BMAA.
J S Metcalf, Doug Lobner, Sandra Anne Banack, Gregory A Cox, Peter B Nunn, Paul Alan Cox

Amino Acids· August 2017

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Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes.
Kathryn H Morelli, Kevin L Seburn, David G Schroeder, Emily L Spaulding, Loiuse A Dionne, Gregory A Cox

Cell Rep· March 2017

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Development-on-chip: in vitro neural tube patterning with a microfluidic device.
Christopher J Demers, Prabakaran Soundararajan, Phaneendra Chennampally, Gregory A Cox, James Briscoe

Development· June 2016

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Absence of UCHL 1 function leads to selective motor neuropathy.
Barış Genç, Javier H Jara, Megan C Schultz, Marin Manuel, Macdonell J Stanford, Gregory A Cox

Ann Clin Transl Neurol· May 2016

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Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders.
Wen Zhang, Lifeng Zhang, Bo Liang, David Schroeder, Zhong-Wei Zhang, Gregory A Cox

Nat Neurosci· April 2016

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Effect of genetic background on the dystrophic phenotype in mdx mice.
William D Coley, Laurent Bogdanik, Maria Candida Vila, Qing Yu, Jack H Van Der Meulen, Gregory A Cox

Hum Mol Genet· January 2016

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Corticospinal Motor Neurons Are Susceptible to Increased ER Stress and Display Profound Degeneration in the Absence of UCHL1 Function.
Javier H Jara, Barış Genç, Gregory A Cox, Martha C Bohn, Raymond P Roos

Cereb Cortex· November 2015

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Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease.
Terry D Heiman-Patterson, Elizabeth P Blankenhorn, Roger B Sher, Juliann Jiang, Priscilla Welsh, Gregory A Cox

PLoS One· November 2015

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Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders.
Heather Fairfield, Anuj Srivastava, Guruprasad Ananda, Rangjiao Liu, Martin Kircher, Gregory A Cox

Genome Res· July 2015

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A major QTL on mouse chromosome 17 resulting in lifespan variability in SOD1-G93A transgenic mouse models of amyotrophic lateral sclerosis.
Roger B Sher, Terry D Heiman-Patterson, Elizabeth A Blankenhorn, Juliann Jiang, Guillermo Alexander, Gregory A Cox

Amyotroph Lateral Scler Frontotemporal Degener· December 2014

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Choline kinase beta is required for normal endochondral bone formation.
Zhuo Li, Gengshu Wu, Roger B Sher, Zohreh Khavandgar, Martin Hermansson, Gregory A Cox

Biochim Biophys Acta· July 2014

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