Steve H. Laval

Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 9 publications

Optimization of Internally Deleted Dystrophin Constructs.

Optimization of Internally Deleted Dystrophin Constructs.

Journal: Human gene therapy methods
Published: August 02, 2016

Global N-linked Glycosylation is Not Significantly Impaired in Myoblasts in Congenital Myasthenic Syndromes Caused by Defective Glutamine-Fructose-6-Phosphate Transaminase 1 (GFPT1).

Global N-linked Glycosylation is Not Significantly Impaired in Myoblasts in Congenital Myasthenic Syndromes Caused by Defective Glutamine-Fructose-6-Phosphate Transaminase 1 (GFPT1).

Journal: Biomolecules
Published: June 16, 2015

Neural crest cell-specific inactivation of Nipbl or Mau2 during mouse development results in a late onset of craniofacial defects.

Neural crest cell-specific inactivation of Nipbl or Mau2 during mouse development results in a late onset of craniofacial defects.

Journal: Genesis (New York, N.Y. : 2000)
Published: January 24, 2014

Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis.

Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis.

Journal: PLoS currents
Published: June 22, 2013

Exon skipping and gene transfer restore dystrophin expression in hiPSC-cardiomyocytes harbouring DMD mutations.

Exon skipping and gene transfer restore dystrophin expression in hiPSC-cardiomyocytes harbouring DMD mutations.

Journal: Stem cells and development
Published: June 22, 2013

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.

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.

Journal: Human mutation
Published: February 13, 2013

Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy.

Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy.

Journal: PloS one
Published: October 04, 2012

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

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

Journal: Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
Published: June 15, 2012

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

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

Journal: Human molecular genetics
Published: December 27, 2011
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Last Updated: 09/26/2026