Publications by authors named "Steve Laval"

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Optimization of Internally Deleted Dystrophin Constructs.
Mojgan Reza, Steve H Laval, Andreas Roos, Stephanie Carr, Hanns Lochmüller

Hum Gene Ther Methods· October 2016

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Global N-linked Glycosylation is Not Significantly Impaired in Myoblasts in Congenital Myasthenic Syndromes Caused by Defective Glutamine-Fructose-6-Phosphate Transaminase 1 (GFPT1).
Qiushi Chen, Juliane S Müller, Poh-Choo Pang, Steve H Laval, Stuart M Haslam

Biomolecules· October 2015

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Neural crest cell-specific inactivation of Nipbl or Mau2 during mouse development results in a late onset of craniofacial defects.
Terence Gordon Smith, Steve Laval, Fangli Chen, Matthew James Rock, Tom Strachan

Genesis· July 2014

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Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy.
Alison Blain, Elizabeth Greally, Steve Laval, Andrew Blamire, Volker Straub

PLoS One· August 2013

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ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation.
Anna Sarkozy, Debbie Hicks, Judith Hudson, Steve H Laval, Rita Barresi

Hum Mutat· August 2013

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Exon skipping and gene transfer restore dystrophin expression in hiPSC-cardiomyocytes harbouring DMD mutations.
Emily Dick, Spandan Kalra, David Anderson, Vinoj George, Morten Ritson, Steve Laval

Stem Cells Dev· June 2013

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Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis.
Elizabeth Harris, Steve Laval, Judith Hudson, Rita Barresi, Liesbeth De Waele

PLoS Curr· May 2013

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Heterogeneous abnormalities of in-vivo left ventricular calcium influx and function in mouse models of muscular dystrophy cardiomyopathy.
Elizabeth Greally, Benjamin J Davison, Alison Blain, Steve Laval, Andrew Blamire

J Cardiovasc Magn Reson· January 2013

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Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb.
Ramakrishna Kurapati, Caoimhe McKenna, Johan Lindqvist, Debbie Williams, Michelle Simon, Steve Laval

Hum Mol Genet· April 2012

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Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency.
Alasdair J Wood, Juliane S Müller, Catherine D Jepson, Steve H Laval, Hanns Lochmüller

Hum Mol Genet· December 2011

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Reverse engineering gene network identifies new dysferlin-interacting proteins.
Mafalda Cacciottolo, Vincenzo Belcastro, Steve Laval, Kate Bushby, Diego di Bernardo

J Biol Chem· February 2011

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Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscle.
Louise H Jørgensen, Alison Blain, Elizabeth Greally, Steve H Laval, Andrew M Blamire

Am J Pathol· January 2011

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Intolerance to ß-blockade in a mouse model of δ-sarcoglycan-deficient muscular dystrophy cardiomyopathy.
Ralf Bauer, Alison Blain, Elizabeth Greally, Kate Bushby, Hanns Lochmüller, Steve Laval

Eur J Heart Fail· November 2010

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Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle.
Lars Klinge, John Harris, Caroline Sewry, Richard Charlton, Louise Anderson, Steve Laval

Muscle Nerve· February 2010

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From T-tubule to sarcolemma: damage-induced dysferlin translocation in early myogenesis.
Lars Klinge, Steve Laval, Sharon Keers, Faye Haldane, Volker Straub

FASEB J· June 2007

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Metazoan Scc4 homologs link sister chromatid cohesion to cell and axon migration guidance.
Vlad C Seitan, Peter Banks, Steve Laval, Nazia A Majid, Dale Dorsett

PLoS Biol· July 2006

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Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display.
Yanchao Huang, Peter Verheesen, Andreas Roussis, Wendy Frankhuizen, Ieke Ginjaar, Steve Laval

Eur J Hum Genet· June 2005

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Confirmatory evidence for linkage of relative hand skill to 2p12-q11.
Clyde Francks, Lynn E DeLisi, Simon E Fisher, Steve H Laval, Judith E Rue

Am J Hum Genet· February 2003

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