Jordan T. Gladman

Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype

Christopher R. Pierson, Ashley N. Dulin-Smith, Ashley N. Durban et al. · Human Molecular Genetics · 2011 · 63 citations · Full text

TWEAK/Fn14, a pathway and novel therapeutic target in myotonic dystrophy

Ramesh S. Yadava, Erin P. Foff, Qing Yu et al. · Human Molecular Genetics · 2014 · 41 citations · Full text

Immunology, Cell Death, Therapeutics +24

A humanized Smn gene containing the SMN2 nucleotide alteration in exon 7 mimics SMN2 splicing and the SMA disease phenotype

Jordan T. Gladman, Thomas W. Bebee, Chris Edwards et al. · Human Molecular Genetics · 2010 · 31 citations · Full text

Genetics, Molecular Biology, Gene Characterization +18

Stress-Induced Isoforms of MDM2 and MDM4 Correlate with High-Grade Disease and an Altered Splicing Network in Pediatric Rhabdomyosarcoma

Aishwarya G. Jacob, Dennis O'Brien, Ravi K. Singh et al. · Neoplasia · 2013 · 25 citations · Full text

Age of Onset of RNA Toxicity Influences Phenotypic Severity: Evidence from an Inducible Mouse Model of Myotonic Dystrophy (DM1)

Jordan T. Gladman, Mahua Mandal, Varadamurthy Srinivasan et al. · PLoS ONE · 2013 · 21 citations · Full text