Dysferlin associates with the developing T‐tubule system in rodent and human skeletal muscle

Lars Klinge, John B. Harris, Caroline A. Sewry, +9

Muscle & Nerve

Metazoan Scc4 Homologs Link Sister Chromatid Cohesion to Cell and Axon Migration Guidance

Vlad C. Seitan, Peter Banks, Steve Laval, +13

PLoS Biology

Molecular RegulationGeneticsMolecular GeneticsCellular PhysiologyTranscriptional Regulation +17

From T‐tubule to sarcolemma: damage‐induced dysferlin translocation in early myogenesis

Lars Klinge, Steve Laval, Sharon Keers, +4

The FASEB Journal

Mature Skeletal MuscleEngineeringMuscle FunctionCytoskeletonMechanotransduction +15

Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display

Yanchao Huang, Peter Verheesen, Andreas Roussis, +11

European Journal of Human Genetics

Autoimmune DiseaseLlama-derived Antibody FragmentsDiagnostic TestImmunologySerologic Testing +8

Long-Term Blocking of Calcium Channels in mdx Mice Results in Differential Effects on Heart and Skeletal Muscle

Louise Helskov Jørgensen, A. Blain, Elizabeth Greally, +9

American Journal Of Pathology

Reverse Engineering Gene Network Identifies New Dysferlin-interacting Proteins

Mafalda Cacciottolo, Vincenzo Belcastro, Steve Laval, +3

Journal of Biological Chemistry

Miyoshi MyopathyFunctional GenomicsInteractomicsMedicineGenetics +13

Neural crest cell‐specific inactivation of <i>Nipbl</i> or <i>Mau2</i> during mouse development results in a late onset of craniofacial defects

Terence G. Smith, Steve Laval, Fangli Chen, +3

genesis

Neural Crest CellsGeneticsNeural Stem CellLate OnsetTissue Development +18

Beta-Blockers, Left and Right Ventricular Function, and In-Vivo Calcium Influx in Muscular Dystrophy Cardiomyopathy

A. Blain, Elizabeth Greally, Steve Laval, +3

PLoS ONE

Cardiac MuscleCardiomyopathyHeart FailureMdx MiceCardiovascular Disease +13

Heterogeneous abnormalities of in-vivo left ventricular calcium influx and function in mouse models of muscular dystrophy cardiomyopathy

Elizabeth Greally, Benjamin Davison, A. Blain, +4

Journal of Cardiovascular Magnetic Resonance

Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb

Ramakrishna Kurapati, Caoimhe McKenna, Johan Lindqvist, +11

Human Molecular Genetics