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Mani Mahadevan
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Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene
M Mahadevan, C Tsilfidis, L Sabourin, G Shutler, C Amemiya, G Jansen, ...
Science 255 (5049), 1253-1255, 1992
20061992
The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy
N Roy, MS Mahadevan, M McLean, G Shutter, Z Yaraghi, R Farahani, ...
Cell 80 (1), 167-178, 1995
12521995
Cloning of the essential myotonic dystrophy region and mapping of the putative defect
C Aslanidis, G Jansen, C Amemiya, G Shutler, M Mahadevan, C Tsilfidis, ...
Nature 355 (6360), 548-551, 1992
6511992
The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy.
A Hunter, C Tsilfidis, G Mettler, P Jacob, M Mahadevan, L Surh, ...
Journal of medical genetics 29 (11), 774-779, 1992
3021992
Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy
MS Mahadevan, RS Yadava, Q Yu, S Balijepalli, CD Frenzel-McCardell, ...
Nature genetics 38 (9), 1066-1070, 2006
2092006
Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene
LA Sabouri, MS Mahadevan, M Narang, DSC Lee, LC Surh, RG Korneluk
Nature genetics 4 (3), 233-238, 1993
1911993
Structure and genomic sequence of the myotonic dystrophy (DM kinase) gene
MS Mahadevan, C Amemiya, G Jansen, L Sabourin, S Baird, CE Neville, ...
Human molecular genetics 2 (3), 299-304, 1993
1851993
Characterization of the myotonic dystrophy region predicts multiple protein isoform–encoding mRNAs
G Jansen, M Mahadevan, C Amemiya, N Wormskamp, B Segers, ...
Nature genetics 1 (4), 261-266, 1992
1791992
Cis and Trans Effects of the Myotonic Dystrophy (DM) Mutation in a Cell Culture Model
JD Amack, AP Paguio, MS Mahadevan
Human molecular genetics 8 (11), 1975-1984, 1999
1651999
Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission
KL O'Hoy, C Tsilfidis, MS Mahadevan, CE Neville, J Barceló, AGW Hunter, ...
Science 259 (5096), 809-812, 1993
1551993
The RNA-binding protein Staufen1 is increased in DM1 skeletal muscle and promotes alternative pre-mRNA splicing
A Ravel-Chapuis, G Bélanger, RS Yadava, MS Mahadevan, ...
The Journal of cell biology 196 (6), 699, 2012
1412012
The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiation
JD Amack, MS Mahadevan
Human molecular genetics 10 (18), 1879-1887, 2001
1202001
RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression
RS Yadava, CD Frenzel-McCardell, Q Yu, V Srinivasan, AL Tucker, ...
Nature genetics 40 (1), 61-68, 2008
1072008
Intergenerational stability of the myotonic dystrophy protomutation
JM Barceló, MS Mahadevan, C Tsilfidis, AE MacKenzie, RG Korneluk
Human Molecular Genetics 2 (6), 705-709, 1993
1051993
Sequence of a 131-kb region of 5q13. 1 containing the spinal muscular atrophy candidate genes SMN and NAIP
Q Chen, SD Baird, M Mahadevan, A Besner-Johnston, R Farahani, ...
Genomics 48 (1), 121-127, 1998
991998
Myotonic dystrophy: the role of the CUG triplet repeats in splicing of a novel DMPK exon and altered cytoplasmic DMPK mRNA isoform ratios
G Tiscornia, MS Mahadevan
Molecular cell 5 (6), 959-967, 2000
812000
Therapeutics development in myotonic dystrophy type 1
EP Foff, MS Mahadevan
Muscle & nerve 44 (2), 160-169, 2011
762011
Myogenic defects in myotonic dystrophy
JD Amack, MS Mahadevan
Developmental biology 265 (2), 294-301, 2004
752004
Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy
MS Mahadevan, MA Foitzik, LC Surh, RG Korneluk
Genomics 15 (2), 446-448, 1993
731993
Overexpression of MBNL1 fetal isoforms and modified splicing of Tau in the DM1 brain: two individual consequences of CUG trinucleotide repeats
CM Dhaenens, S Schraen-Maschke, H Tran, V Vingtdeux, D Ghanem, ...
Experimental neurology 210 (2), 467-478, 2008
722008
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