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S D Wilton

Showing results (21-30 of 52) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2006
The influence of antisense oligonucleotide length on dystrophin exon skippingP L Harding, A M Fall, K Honeyman, et al.
Gene Therapy|May 26, 2006
Antisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMDG McClorey, H M Moulton, P L Iversen, et al.
FEBS Letters|October 7, 2003
Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscleK E Wells, S Fletcher, C J Mann, et al.
Experimental Neurology|June 26, 2001
The regrowth of axons within tissue defects in the CNS is promoted by implanted hydrogel matrices that contain BDNF and CNTF producing fibroblastsN K Loh, S Woerly, S M Bunt, et al.
American Journal of Veterinary Research|January 5, 2002
Evaluation of a short interspersed nucleotide element in the 3' untranslated region of the defective dystrophin gene of dogs with muscular dystrophyS Fletcher, K S Carville, J M Howell, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotidesS D Wilton, F Lloyd, K Carville, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human skeletal muscle alpha-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridizationH Eyre, P A Akkari, S D Wilton, et al.
Neuromuscular Disorders : NMD|July 1, 1997
A splice-site mutation causing ovine McArdle's diseaseP Tan, J G Allen, S D Wilton, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human a-tropomyosin gene TPM3 to 1q22-->q23 by fluorescence in situ hybridisationS D Wilton, H Eyre, P A Akkari, et al.
The Journal of Cell Biology|March 8, 2000
Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansionQ L Lu, G E Morris, S D Wilton, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2006
The influence of antisense oligonucleotide length on dystrophin exon skippingP L Harding, A M Fall, K Honeyman, et al.
Gene Therapy|May 26, 2006
Antisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMDG McClorey, H M Moulton, P L Iversen, et al.
FEBS Letters|October 7, 2003
Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscleK E Wells, S Fletcher, C J Mann, et al.
Experimental Neurology|June 26, 2001
The regrowth of axons within tissue defects in the CNS is promoted by implanted hydrogel matrices that contain BDNF and CNTF producing fibroblastsN K Loh, S Woerly, S M Bunt, et al.
American Journal of Veterinary Research|January 5, 2002
Evaluation of a short interspersed nucleotide element in the 3' untranslated region of the defective dystrophin gene of dogs with muscular dystrophyS Fletcher, K S Carville, J M Howell, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotidesS D Wilton, F Lloyd, K Carville, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human skeletal muscle alpha-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridizationH Eyre, P A Akkari, S D Wilton, et al.
Neuromuscular Disorders : NMD|July 1, 1997
A splice-site mutation causing ovine McArdle's diseaseP Tan, J G Allen, S D Wilton, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human a-tropomyosin gene TPM3 to 1q22-->q23 by fluorescence in situ hybridisationS D Wilton, H Eyre, P A Akkari, et al.
The Journal of Cell Biology|March 8, 2000
Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansionQ L Lu, G E Morris, S D Wilton, et al.
Pageof 6