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M S Mahadevan

Showing results (1-10 of 16) with videos related to

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Molecular Cell|July 27, 2000
Myotonic dystrophy: the role of the CUG triplet repeats in splicing of a novel DMPK exon and altered cytoplasmic DMPK mRNA isoform ratiosG Tiscornia, M S Mahadevan
Human Molecular Genetics|September 14, 2001
The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiationJ D Amack, M S Mahadevan
Clinical Chemistry|May 1, 1988
Changes in free thyroxin (FT4) values of Clinical Assays Gammacoat two-step assayM S Mahadevan, D S Ooi
Human Molecular Genetics|September 15, 1999
Cis and trans effects of the myotonic dystrophy (DM) mutation in a cell culture modelJ D Amack, A P Paguio, M S Mahadevan
Genomics|February 1, 1993
Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophyM S Mahadevan, M A Foitzik, L C Surh, et al.
Human Molecular Genetics|January 1, 1994
High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutationC E Neville, M S Mahadevan, J M Barceló, et al.
Clinical Chemistry|November 1, 1988
Evaluation of four commercially available assays for free thyroxinD S Ooi, M S Mahadevan, D C Greenway, et al.
Nature Genetics|February 1, 1995
SMA genes: deleted and duplicatedM S Mahadevan, R G Korneluk, N Roy, et al.
Human Molecular Genetics|June 1, 1993
Intergenerational stability of the myotonic dystrophy protomutationJ M Barceló, M S Mahadevan, C Tsilfidis, et al.
Nature Genetics|July 1, 1993
Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM geneL A Sabouri, M S Mahadevan, M Narang, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Molecular Cell|July 27, 2000
Myotonic dystrophy: the role of the CUG triplet repeats in splicing of a novel DMPK exon and altered cytoplasmic DMPK mRNA isoform ratiosG Tiscornia, M S Mahadevan
Human Molecular Genetics|September 14, 2001
The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiationJ D Amack, M S Mahadevan
Clinical Chemistry|May 1, 1988
Changes in free thyroxin (FT4) values of Clinical Assays Gammacoat two-step assayM S Mahadevan, D S Ooi
Human Molecular Genetics|September 15, 1999
Cis and trans effects of the myotonic dystrophy (DM) mutation in a cell culture modelJ D Amack, A P Paguio, M S Mahadevan
Genomics|February 1, 1993
Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophyM S Mahadevan, M A Foitzik, L C Surh, et al.
Human Molecular Genetics|January 1, 1994
High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutationC E Neville, M S Mahadevan, J M Barceló, et al.
Clinical Chemistry|November 1, 1988
Evaluation of four commercially available assays for free thyroxinD S Ooi, M S Mahadevan, D C Greenway, et al.
Nature Genetics|February 1, 1995
SMA genes: deleted and duplicatedM S Mahadevan, R G Korneluk, N Roy, et al.
Human Molecular Genetics|June 1, 1993
Intergenerational stability of the myotonic dystrophy protomutationJ M Barceló, M S Mahadevan, C Tsilfidis, et al.
Nature Genetics|July 1, 1993
Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM geneL A Sabouri, M S Mahadevan, M Narang, et al.
Pageof 2