Genome-Wide Survey of Human Alternative Pre-mRNA Splicing with Exon Junction Microarrays

Jason M. Johnson, John C. Castle, Philip W. Garrett-Engele, +7

Science

GeneticsRna SplicingMolecular BiologyGenomicsExon-exon Junction +15

Large-Scale Proteomic Analysis of the Human Spliceosome

Juri Rappsilber, Ursula Ryder, Angus I. Lamond, +1

Genome Research

Proteomic TechnologySpliceosome-associated FactorsHuman SpliceosomeFunctional GenomicsHuman Spliceosome-associated Factors +11

A Muscleblind Knockout Model for Myotonic Dystrophy

Rahul Kanadia, Karen A. Johnstone, Ami Mankodi, +6

Science

Muscle FunctionGeneticsMutant RnaMolecular GeneticsDisease Gene Identification +15

Utrophin-Dystrophin-Deficient Mice as a Model for Duchenne Muscular Dystrophy

Anne E. Deconinck, Jill A. Rafael, Judith A. Skinner, +7

Cell

Skeletal MuscleDuchenne Muscular DystrophyPhysiologyDegenerative DiseaseCell Biology +1

A Gene Expression Map for <i>Caenorhabditis elegans</i>

Stuart K. Kim, Jim Lund, Moni Kiraly, +6

Science

BioinformaticsTranscriptional RegulationSystems BiologyDevelopmental BiologyEngineering +13

Skeletal and Cardiac Myopathies in Mice Lacking Utrophin and Dystrophin: A Model for Duchenne Muscular Dystrophy

R. Mark Grady, Haibing Teng, Mia C. Nichol, +3

Cell

Mitochondrial MyopathyMice Lacking UtrophinSkeletal MuscleDuchenne Muscular DystrophyPhysiology +3

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

Judith C. T. van Deutekom, Cisca Wljmenga, Esther A.E.Van Tlenhoven, +6

Human Molecular Genetics

Inappropriate Gene Activation in FSHD

Davide Gabellini, Michael R. Green, Rossella Tupler

Cell

Inappropriate Gene ActivationGenetic DisorderGeneticsGenomic MechanismMolecular Genetics +4

Force and power output of fast and slow skeletal muscles from <i>mdx</i> mice 6‐28 months old

Gordon S. Lynch, Richard T. Hinkle, Jeffrey S. Chamberlain, +2

The Journal of Physiology

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype

Enzo Ricci, Giuliana Galluzzi, Giancarlo Deidda, +12

Annals of Neurology

Ecori Fragment SizeRare DiseasesFacioscapulohumeral Muscular DystrophyEcori FragmentMendelian Disorder +13