Publications by authors named "Terence Partridge"

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Skeletal muscle: a biologists' adventure playground.
Terence Partridge

J Muscle Res Cell Motil· December 2025

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Correction: Skeletal muscle: a biologists' adventure playground.
Terence Partridge

J Muscle Res Cell Motil· December 2025

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Altered muscle niche contributes to myogenic deficit in the D2-mdx model of severe DMD.
Davi A G Mázala, Ravi Hindupur, Young Jae Moon, Fatima Shaikh, Iteoluwakishi H Gamu, Terence A Partridge

Cell Death Discov· July 2023

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Altered muscle niche contributes to myogenic deficit in the D2- model of severe DMD.
Davi A G Mázala, Ravi Hindupur, Young Jae Moon, Fatima Shaikh, Iteoluwakishi H Gamu, Terence A Partridge

bioRxiv· March 2023

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Enhancing Interrogation of Skeletal Muscle Samples for Informative Quantitative Data.
Terence A Partridge

J Neuromuscul Dis· January 2022

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Interrogation of Dystrophin and Dystroglycan Complex Protein Turnover After Exon Skipping Therapy.
James S Novak, Rita Spathis, Utkarsh J Dang, Alyson A Fiorillo, Ravi Hindupur, Terence A Partridge

J Neuromuscul Dis· December 2021

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Effects of Chronic, Maximal Phosphorodiamidate Morpholino Oligomer (PMO) Dosing on Muscle Function and Dystrophin Restoration in a Mouse Model of Duchenne Muscular Dystrophy.
Margaret E Benny Klimek, Maria Candida Vila, Katie Edwards, Jessica Boehler, James Novak, Terence A Partridge

J Neuromuscul Dis· December 2021

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A Exon-52 Deleted Miniature Pig Model of Duchenne Muscular Dystrophy and Evaluation of Exon Skipping.
Yusuke Echigoya, Nhu Trieu, William Duddy, Hong M Moulton, HaiFang Yin, Terence A Partridge

Int J Mol Sci· December 2021

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Human muscle stem cells are refractory to aging.
James S Novak, Davi A G Mázala, Marie Nearing, Ravi Hindupur, Prech Uapinyoying, Terence A Partridge

Aging Cell· July 2021

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A long-read RNA-seq approach to identify novel transcripts of very large genes.
Prech Uapinyoying, Jeremy Goecks, Susan M Knoblach, Karuna Panchapakesan, Carsten G Bonnemann, Terence A Partridge

Genome Res· June 2020

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TGF-β-driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model.
Davi Ag Mázala, James S Novak, Marshall W Hogarth, Marie Nearing, Prabhat Adusumalli, Terence A Partridge

JCI Insight· March 2020

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Skeletal muscle in health and disease.
Jennifer Morgan, Terence Partridge

Dis Model Mech· February 2020

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Vamorolone, a dissociative steroidal compound, reduces collagen antibody-induced joint damage and inflammation when administered after disease onset.
Jesse M Damsker, Michaelyn R Cornish, Priya Kanneboyina, Ila Kanneboyina, Qing Yu, Terence Partridge

Inflamm Res· November 2019

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Morpholino-induced exon skipping stimulates cell-mediated and humoral responses to dystrophin in mdx mice.
Maria C Vila, James S Novak, Margaret Benny Klimek, Ning Li, Melissa Morales, Terence A Partridge

J Pathol· July 2019

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Fibroadipogenic progenitors are responsible for muscle loss in limb girdle muscular dystrophy 2B.
Marshall W Hogarth, Aurelia Defour, Christopher Lazarski, Eduard Gallardo, Jordi Diaz Manera, Terence A Partridge

Nat Commun· June 2019

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Efficacy of Multi-exon Skipping Treatment in Duchenne Muscular Dystrophy Dog Model Neonates.
Kenji Rowel Q Lim, Yusuke Echigoya, Tetsuya Nagata, Mutsuki Kuraoka, Masanori Kobayashi, Terence Partridge

Mol Ther· January 2019

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Shorter Phosphorodiamidate Morpholino Splice-Switching Oligonucleotides May Increase Exon-Skipping Efficacy in DMD.
Ugur Akpulat, Haicui Wang, Kerstin Becker, Adriana Contreras, Terence A Partridge

Mol Ther Nucleic Acids· December 2018

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The macrophage as a Trojan horse for antisense oligonucleotide delivery.
James S Novak, Jyoti K Jaiswal, Terence A Partridge

Expert Opin Ther Targets· June 2018

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Greater Colo-Rectal Activation Phenotype in Exercised mdx Mice.
Marie Nearing, James Novak, Terence Partridge

PLoS Curr· May 2018

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Author Correction: Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle.
James S Novak, Marshall W Hogarth, Jessica F Boehler, Marie Nearing, Maria C Vila, Terence A Partridge

Nat Commun· March 2018

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Author Correction: Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle.
James S Novak, Marshall W Hogarth, Jessica F Boehler, Marie Nearing, Maria C Vila, Terence A Partridge

Nat Commun· January 2018

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Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle.
James S Novak, Marshall W Hogarth, Jessica F Boehler, Marie Nearing, Maria C Vila, Terence A Partridge

Nat Commun· October 2017

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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, Terence A Partridge

Hum Mol Genet· January 2016

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Elusive sources of variability of dystrophin rescue by exon skipping.
Maria Candida Vila, Margaret Benny Klimek, James S Novak, Sree Rayavarapu, Kitipong Uaesoontrachoon, Terence A Partridge

Skelet Muscle· December 2015

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TNF-α-Induced microRNAs Control Dystrophin Expression in Becker Muscular Dystrophy.
Alyson A Fiorillo, Christopher R Heier, James S Novak, Christopher B Tully, Kristy J Brown, Terence A Partridge

Cell Rep· September 2015

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