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Disease Models & Mechanisms|September 29, 2020
A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai Ying Wong, Abdalla Ahmed, Grace Yang, et al.Journal of Genetic Counseling|October 21, 2021
Genome sequencing among children with medical complexity: What constitutes value from parents' perspective?Whiwon Lee, Stephanie Luca, Gregory Costain, et al.NPJ Genomic Medicine|December 22, 2017
Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort studyIris Cohn, Tara A Paton, Christian R Marshall, et al.Nature Medicine|June 9, 2004
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophiesRita Barresi, Daniel E Michele, Motoi Kanagawa, et al.Cell|September 17, 2002
Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regenerationRonald D Cohn, Michael D Henry, Daniel E Michele, et al.The Journal of Allergy and Clinical Immunology. in Practice|February 7, 2018
Clinician Agreement, Self-Efficacy, and Adherence with the Guidelines for the Diagnosis and Management of AsthmaMichelle M Cloutier, Paivi M Salo, Lara J Akinbami, et al.Gut|June 22, 2000
Neoplastic progression occurs through mutator pathways in hyperplastic polyposis of the colorectumJ R Jass, H Iino, A Ruszkiewicz, et al.Environmental Health Perspectives|August 17, 2012
Indoor environmental exposures for children with asthma enrolled in the HEAL study, post-Katrina New OrleansL Faye Grimsley, Patricia C Chulada, Suzanne Kennedy, et al.Nature|July 26, 2002
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophiesDaniel E Michele, Rita Barresi, Motoi Kanagawa, et al.Disease Models & Mechanisms|June 17, 2024
An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndromeEleonora Maino, Ori Scott, Samar Z Rizvi, et al.Pageof 38