M S Mahadevan
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Explore the profile of M S Mahadevan including associated specialties, affiliations and a list of published articles.
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16
Citations
510
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Recent Articles
1.
Dhaenens C, Schraen-Maschke S, Tran H, Vingtdeux V, Ghanem D, Leroy O, et al.
Exp Neurol
. 2008 Jan;
210(2):467-78.
PMID: 18177861
Neurofibrillary degeneration is often observed in the brain of patients with type 1 myotonic dystrophy (DM1). It consists principally of the aggregation of Tau isoforms that lack exon 2/3 encoded...
2.
Amack J, Mahadevan M
Hum Mol Genet
. 2001 Sep;
10(18):1879-87.
PMID: 11555624
Myotonic dystrophy type 1 (DM1) is a dominant neuromuscular disorder caused by a trinucleotide (CTG) repeat expansion. Mutant DMPK 3'-untranslated region (3'-UTR) transcripts aggregate in nuclear foci and are thought...
3.
Tiscornia G, Mahadevan M
Mol Cell
. 2000 Jul;
5(6):959-67.
PMID: 10911990
The mechanism by which (CTG)n expansion in the 3' UTR of the DMPK gene causes myotonic dystrophy (DM) is unknown. We identified four RNA splicing factors--hnRNP C, U2AF (U2 auxiliary...
4.
Amack J, Paguio A, Mahadevan M
Hum Mol Genet
. 1999 Sep;
8(11):1975-84.
PMID: 10484765
The mutation causing myotonic dystrophy (DM) has been identified as a CTG expansion in the 3'-untranslated region (3'-UTR) of the DM protein kinase gene ( DMPK ), but the mechanism(s)...
5.
Rajcan-Separovic E, Mahadevan M, Lefebvre C, Ikeda J, Korneluk R, MacKenzie A
Cytogenet Cell Genet
. 1996 Jan;
75(4):243-7.
PMID: 9067434
The search for the SMA defect has culminated in the identification of two candidate 5q13.1 SMA genes, NAIP and SMN both of which are deleted in individuals with SMA. It...
6.
Mahadevan M, Baird S, Bailly J, Shutler G, Sabourin L, Tsilfidis C, et al.
Genomics
. 1995 Nov;
30(1):84-8.
PMID: 8595909
We present the cloning and sequencing of the human gene for a novel G-protein coupled receptor (GPR4), from the critical myotonic dystrophy (DM) region on chromosome 19q13.3. The homologous porcine...
7.
Mahadevan M, Korneluk R, Roy N, MacKenzie A, Ikeda J
Nat Genet
. 1995 Feb;
9(2):112-3.
PMID: 7719336
No abstract available.
8.
Roy N, Mahadevan M, McLean M, Shutler G, Yaraghi Z, Farahani R, et al.
Cell
. 1995 Jan;
80(1):167-78.
PMID: 7813013
The spinal muscular atrophies (SMAs), characterized by spinal cord motor neuron depletion, are among the most common autosomal recessive disorders. One model of SMA pathogenesis invokes an inappropriate persistence of...
9.
Neville C, Mahadevan M, Barcelo J, Korneluk R
Hum Mol Genet
. 1994 Jan;
3(1):45-51.
PMID: 7909252
The mutation causing myotonic dystrophy (DM) has been identified as an amplification of an unstable trinucleotide (CTG)n repeat in over 99% of the global DM population. It is in complete...
10.
Sabouri L, Mahadevan M, Narang M, Lee D, Surh L, Korneluk R
Nat Genet
. 1993 Jul;
4(3):233-8.
PMID: 8358430
Myotonic dystrophy (DM) results from the amplification of an unstable CTG repeat in the 3' untranslated region of a transcript encoding a putative serine/threonine kinase. We have analysed the amplification...