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Steve H Laval

Showing results (1-10 of 5) with videos related to

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Human Gene Therapy Methods|August 2, 2016
Optimization of Internally Deleted Dystrophin ConstructsMojgan Reza, Steve H Laval, Andreas Roos, et al.
Biomolecules|October 27, 2015
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, et al.
Human Molecular Genetics|September 20, 2011
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiencyAlasdair J Wood, Juliane S Müller, Catherine D Jepson, et al.
The American Journal of Pathology|January 13, 2011
Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscleLouise H Jørgensen, Alison Blain, Elizabeth Greally, et al.
Human Mutation|April 23, 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 mutationAnna Sarkozy, Debbie Hicks, Judith Hudson, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Human Gene Therapy Methods|August 2, 2016
Optimization of Internally Deleted Dystrophin ConstructsMojgan Reza, Steve H Laval, Andreas Roos, et al.
Biomolecules|October 27, 2015
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, et al.
Human Molecular Genetics|September 20, 2011
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiencyAlasdair J Wood, Juliane S Müller, Catherine D Jepson, et al.
The American Journal of Pathology|January 13, 2011
Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscleLouise H Jørgensen, Alison Blain, Elizabeth Greally, et al.
Human Mutation|April 23, 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 mutationAnna Sarkozy, Debbie Hicks, Judith Hudson, et al.
Pageof 1