Risultati della ricerca - Cheryl Wall
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1
Gentamicin‐induced readthrough of stop codons in duchenne muscular dystrophy di Vinod Malik, Louise R. Rodino‐Klapac, Laurence Viollet, Cheryl Wall, Wendy King, Roula Al‐Dahhak, Sarah Lewis, Christopher Shilling, Janaiah Kota, Carmen Serrano, John R. Hayes, John D. Mahan, Katherine J. Campbell, Brenda Banwell, Majed Dasouki, Victoria Watts, Kumaraswamy Sivakumar, Ricardo Bien‐Willner, Kevin M. Flanigan, Zarife Sahenk, Richard J. Barohn, Christopher M. Walker, Jerry R. Mendell
Pubblicazione 2010Artigo -
2
Limb-Girdle Muscular Dystrophy in the United States di Steven A. Moore, Christopher Shilling, Steven Westra, Cheryl Wall, Matthew Wicklund, Catherine A. Stolle, Charlotte A. Brown, Daniel E. Michele, F. Piccolo, Thomas Winder, Aaron A. Stence, Rita Barresi, Nick King, Wendy King, Julaine Florence, Kevin P. Campbell, Gerald M. Fenichel, Hansell H. Stedman, John T. Kissel, Robert C. Griggs, Shree Pandya, Katherine D. Mathews, Alan Pestronk, Carmen Serrano, Daniel Darvish, Jerry R. Mendell
Pubblicazione 2006Artigo -
3
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort di Kevin M. Flanigan, Diane M. Dunn, Andrew von Niederhausern, Payam Soltanzadeh, Eduard Gappmaier, Michael Howard, Jacinda B. Sampson, Jerry R. Mendell, Cheryl Wall, Wendy King, Alan Pestronk, Julaine Florence, Anne M. Connolly, Katherine D. Mathews, Carrie Stephan, Karla S. Laubenthal, Brenda Wong, P. Morehart, Amy Meyer, Richard S. Finkel, Carsten G. Bönnemann, Līvija Medne, John Day, Joline Dalton, Marcia K. Margolis, Veronica J. Hinton, Robert B. Weiss
Pubblicazione 2009Artigo
Strumenti per la ricerca:
Soggetti correlati
Biology
Gene
Genetics
Mutation
Duchenne muscular dystrophy
Dystrophin
Medicine
Muscular dystrophy
Alternative splicing
Antibiotics
Bioinformatics
Biopsy
Cohort
Creatine kinase
Environmental health
Exon
Exon skipping
Frameshift mutation
Genotype
Gentamicin
Histopathology
Internal medicine
Limb-girdle muscular dystrophy
Missense mutation
Muscle biopsy
Nonsense mutation
Pathology
Point mutation
Population
Stop codon