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S D Wilton

Showing results (41-50 of 52) with videos related to

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Neuroscience|June 27, 2012
Co-regulation of survival of motor neuron and Bcl-xL expression: implications for neuroprotection in spinal muscular atrophyR S Anderton, L L Price, B J Turner, et al.
Nature Genetics|June 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1N G Laing, S D Wilton, P A Akkari, et al.
Nature Genetics|January 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyN G Laing, S D Wilton, P A Akkari, et al.
American Journal of Human Genetics|February 1, 1995
Autosomal dominant distal myopathy: linkage to chromosome 14N G Laing, B A Laing, C Meredith, et al.
Neuromuscular Disorders : NMD|March 14, 2000
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletionK J Nowak, P Walsh, R L Jacob, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisationC C Hunt, H J Eyre, P A Akkari, et al.
Biochemical Society Transactions|July 20, 2007
Cell-penetrating peptide-morpholino conjugates alter pre-mRNA splicing of DMD (Duchenne muscular dystrophy) and inhibit murine coronavirus replication in vivoH M Moulton, S Fletcher, B W Neuman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 17, 1999
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathyF L Mastaglia, K J Nowak, R Stell, et al.
Human Gene Therapy|September 5, 2007
Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin pre-mRNA splicing in human muscleV Arechavala-Gomeza, I R Graham, L J Popplewell, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Molecular analysis of a spontaneous dystrophin 'knockout' dogS J Schatzberg, N J Olby, M Breen, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Neuroscience|June 27, 2012
Co-regulation of survival of motor neuron and Bcl-xL expression: implications for neuroprotection in spinal muscular atrophyR S Anderton, L L Price, B J Turner, et al.
Nature Genetics|June 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1N G Laing, S D Wilton, P A Akkari, et al.
Nature Genetics|January 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyN G Laing, S D Wilton, P A Akkari, et al.
American Journal of Human Genetics|February 1, 1995
Autosomal dominant distal myopathy: linkage to chromosome 14N G Laing, B A Laing, C Meredith, et al.
Neuromuscular Disorders : NMD|March 14, 2000
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletionK J Nowak, P Walsh, R L Jacob, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisationC C Hunt, H J Eyre, P A Akkari, et al.
Biochemical Society Transactions|July 20, 2007
Cell-penetrating peptide-morpholino conjugates alter pre-mRNA splicing of DMD (Duchenne muscular dystrophy) and inhibit murine coronavirus replication in vivoH M Moulton, S Fletcher, B W Neuman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 17, 1999
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathyF L Mastaglia, K J Nowak, R Stell, et al.
Human Gene Therapy|September 5, 2007
Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin pre-mRNA splicing in human muscleV Arechavala-Gomeza, I R Graham, L J Popplewell, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Molecular analysis of a spontaneous dystrophin 'knockout' dogS J Schatzberg, N J Olby, M Breen, et al.
Pageof 6