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Human Mutation|February 12, 2009
DMD exon 1 truncating point mutations: amelioration of phenotype by alternative translation initiation in exon 6Olga L Gurvich, Baijayanta Maiti, Robert B Weiss, et al.
Plos One|December 16, 2017
Transcriptome profiling identifies regulators of pathogenesis in collagen VI related muscular dystrophyRussell J Butterfield, Diane M Dunn, Ying Hu, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|November 7, 2015
CYP2A6 Effects on Subjective Reactions to Initial Smoking AttemptDale S Cannon, Robin J Mermelstein, Tait R Medina, et al.
Muscle & Nerve|October 19, 2011
Becker muscular dystrophy due to an inversion of exons 23 and 24 of the DMD geneKevin M Flanigan, Diane Dunn, C Aaron Larsen, et al.
Immunology|July 14, 2006
Altered localization of CXCL13 expressing cells in mice deficient in Pactolus following an inflammatory stimulusAndrias Hojgaard, Rebecca Close, Dianne M Dunn, et al.
American Journal of Human Genetics|March 13, 2003
Rapid direct sequence analysis of the dystrophin geneKevin M Flanigan, Andrew von Niederhausern, Diane M Dunn, et al.
Neuromuscular Disorders : NMD|January 7, 2018
Low-level dystrophin expression attenuating the dystrophinopathy phenotypeMegan A Waldrop, Felecia Gumienny, Saleh El Husayni, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Low-level expression of EPG5 leads to an attenuated Vici syndrome phenotypeMegan A Waldrop, Felecia Gumienny, Daniel Boue, et al.
Immunogenetics|October 1, 2018
A genome-wide association study for mastitis resistance in phenotypically well-characterized Holstein dairy cattle using a selective genotyping approachJacqueline P Kurz, Zhou Yang, Robert B Weiss, et al.
Alcoholism, Clinical and Experimental Research|January 17, 2014
Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adultsHilary Coon, Thomas M Piasecki, Edwin H Cook, et al.
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