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JCI Insight|April 10, 2019
ERK1/2 signaling induces skeletal muscle slow fiber-type switching and reduces muscular dystrophy disease severityJustin G Boyer, Vikram Prasad, Taejeong Song, et al.
Human Molecular Genetics|May 31, 2014
P38α MAPK underlies muscular dystrophy and myofiber death through a Bax-dependent mechanismErin R Wissing, Justin G Boyer, Jennifer Q Kwong, et al.
Molecular and Cellular Biology|May 2, 2018
Defective Flux of Thrombospondin-4 through the Secretory Pathway Impairs Cardiomyocyte Membrane Stability and Causes CardiomyopathyMatthew J Brody, Davy Vanhoutte, Tobias G Schips, et al.
The Journal of Clinical Investigation|April 18, 2018
Specialized fibroblast differentiated states underlie scar formation in the infarcted mouse heartXing Fu, Hadi Khalil, Onur Kanisicak, et al.
Nature Communications|May 26, 2022
Depletion of skeletal muscle satellite cells attenuates pathology in muscular dystrophyJustin G Boyer, Jiuzhou Huo, Sarah Han, et al.
JCI Insight|November 16, 2018
The mitochondrial calcium uniporter underlies metabolic fuel preference in skeletal muscleJennifer Q Kwong, Jiuzhou Huo, Michael J Bround, et al.
JCI Insight|August 9, 2019
Cell-specific ablation of Hsp47 defines the collagen-producing cells in the injured heartHadi Khalil, Onur Kanisicak, Ronald J. Vagnozzi, et al.
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