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The Journal of Biological Chemistry|August 11, 2012
Cathepsin G-regulated release of formyl peptide receptor agonists modulate neutrophil effector functionsJosh C Woloszynek, Ying Hu, Christine T N Pham
The Journal of Biological Chemistry|October 4, 2007
Lysosomal dysfunction results in altered energy balanceJosh C Woloszynek, Trey Coleman, Clay F Semenkovich, et al.
The Journal of Biological Chemistry|August 25, 2009
Metabolic adaptations to interrupted glycosaminoglycan recyclingJosh C Woloszynek, Atilla Kovacs, Kevin K Ohlemiller, et al.
The Biochemical Journal|January 7, 2004
Numerous transcriptional alterations in liver persist after short-term enzyme-replacement therapy in a murine model of mucopolysaccharidosis type VIIJosh C Woloszynek, Marie Roberts, Trey Coleman, et al.
Nucleic Acid Therapeutics|February 7, 2025
Targeting a Novel Site in Exon 51 with Antisense Oligonucleotides Induces Enhanced Exon Skipping in a Mouse Model of Duchenne Muscular DystrophyTodd Oppeneer, Yulan Qi, Joshua Henshaw, et al.
Scientific Reports|July 15, 2021
Substrate reduction therapy for Krabbe disease and metachromatic leukodystrophy using a novel ceramide galactosyltransferase inhibitorMichael C Babcock, Christina R Mikulka, Bing Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 19, 2019
Genetic ablation of acid ceramidase in Krabbe disease confirms the psychosine hypothesis and identifies a new therapeutic targetYedda Li, Yue Xu, Bruno A Benitez, et al.
The Journal of Biological Chemistry|October 28, 2022
Intracerebroventricular dosing of N-sulfoglucosamine sulfohydrolase in mucopolysaccharidosis IIIA mice reduces markers of brain lysosomal dysfunctionJenna Magat, Samantha Jones, Brian Baridon, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 2014
Delivery of an enzyme-IGFII fusion protein to the mouse brain is therapeutic for mucopolysaccharidosis type IIIBShih-Hsin Kan, Mika Aoyagi-Scharber, Steven Q Le, et al.
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