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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 25, 2006
Antisense oligonucleotides, exon skipping and the dystrophin gene transcript
S D Wilton, S Fletcher
Current Opinion in Neurology
|
November 10, 2000
Gene therapy and molecular approaches to the treatment of hereditary muscular disorders
S Fletcher, S D Wilton, J M Howell
Trends in Molecular Medicine
|
June 9, 2015
The emperor's new dystrophin: finding sense in the noise
S D Wilton, R N Veedu, S Fletcher
Prenatal Diagnosis
|
August 1, 1993
Verification of carrier status for Becker muscular dystrophy from analysis of a blighted ovum
S D Wilton, J Goldblatt, N G Laing
DNA Sequence : the Journal of DNA Sequencing and Mapping
|
January 1, 1996
Characterisation of the chicken Cu,Zn superoxide dismutase gene
J L Stanton, S D Wilton, N G Laing
Muscle & Nerve
|
June 1, 1997
Dystrophin gene transcripts skipping the mdx mutation
S D Wilton, D E Dye, N G Laing
Veterinary Microbiology
|
April 1, 1991
Use of DNA amplification for the rapid identification of Mycobacterium bovis
D V Cousins, S D Wilton, B R Francis
Biotechniques
|
April 1, 1997
Bandstab: a PCR-based alternative to cloning PCR products
S D Wilton, L Lim, D Dye, et al.
Biochimica Et Biophysica Acta
|
March 20, 1985
Isolation and characterisation of keratin mRNA from the scale epidermis of the embryonic chick
S D Wilton, L A Crocker, G E Rogers
Human Mutation
|
April 1, 1998
Snapback SSCP analysis: engineered conformation changes for the rapid typing of known mutations
S D Wilton, K Honeyman, S Fletcher, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 52) with videos related to
Sort By:
Page
of 6
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 25, 2006
Antisense oligonucleotides, exon skipping and the dystrophin gene transcript
S D Wilton, S Fletcher
Current Opinion in Neurology
|
November 10, 2000
Gene therapy and molecular approaches to the treatment of hereditary muscular disorders
S Fletcher, S D Wilton, J M Howell
Trends in Molecular Medicine
|
June 9, 2015
The emperor's new dystrophin: finding sense in the noise
S D Wilton, R N Veedu, S Fletcher
Prenatal Diagnosis
|
August 1, 1993
Verification of carrier status for Becker muscular dystrophy from analysis of a blighted ovum
S D Wilton, J Goldblatt, N G Laing
DNA Sequence : the Journal of DNA Sequencing and Mapping
|
January 1, 1996
Characterisation of the chicken Cu,Zn superoxide dismutase gene
J L Stanton, S D Wilton, N G Laing
Muscle & Nerve
|
June 1, 1997
Dystrophin gene transcripts skipping the mdx mutation
S D Wilton, D E Dye, N G Laing
Veterinary Microbiology
|
April 1, 1991
Use of DNA amplification for the rapid identification of Mycobacterium bovis
D V Cousins, S D Wilton, B R Francis
Biotechniques
|
April 1, 1997
Bandstab: a PCR-based alternative to cloning PCR products
S D Wilton, L Lim, D Dye, et al.
Biochimica Et Biophysica Acta
|
March 20, 1985
Isolation and characterisation of keratin mRNA from the scale epidermis of the embryonic chick
S D Wilton, L A Crocker, G E Rogers
Human Mutation
|
April 1, 1998
Snapback SSCP analysis: engineered conformation changes for the rapid typing of known mutations
S D Wilton, K Honeyman, S Fletcher, et al.
Page
of 6