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EMBO Molecular Medicine|March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expressionEleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature|July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier geneDwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Environmental Health Perspectives|August 17, 2012
The Head-off Environmental Asthma in Louisiana (HEAL) study--methods and study populationPatricia C Chulada, Suzanne Kennedy, Mosanda M Mvula, et al.
Pediatrics|July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylationRonald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Plos One|November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrelsEva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
Environmental Health Perspectives|August 17, 2012
Implementation of evidence-based asthma interventions in post-Katrina New Orleans: the Head-off Environmental Asthma in Louisiana (HEAL) studyHerman Mitchell, Richard D Cohn, Jeremy Wildfire, et al.
Nature Medicine|July 18, 2017
Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanismDwi U Kemaladewi, Eleonora Maino, Elzbieta Hyatt, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Nature Medicine|January 24, 2007
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic statesRonald D Cohn, Christel van Erp, Jennifer P Habashi, et al.
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