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SMA genes: deleted and duplicated.
Mahadevan MS, Korneluk RG, Roy N, MacKenzie A, Ikeda J. Mahadevan MS, et al. Nat Genet. 1995 Feb;9(2):112-3. doi: 10.1038/ng0295-112. Nat Genet. 1995. PMID: 7719336 No abstract available.
FISH detection of chromosome polymorphism and deletions in the spinal muscular atrophy (SMA) region of 5q13.
Rajcan-Separovic E, Mahadevan MS, Lefebvre C, Besner-Johnston A, Ikeda JE, Korneluk RG, MacKenzie A. Rajcan-Separovic E, et al. Among authors: mahadevan ms. Cytogenet Cell Genet. 1996;75(4):243-7. doi: 10.1159/000134493. Cytogenet Cell Genet. 1996. PMID: 9067434
The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy.
Roy N, Mahadevan MS, McLean M, Shutler G, Yaraghi Z, Farahani R, Baird S, Besner-Johnston A, Lefebvre C, Kang X, et al. Roy N, et al. Among authors: mahadevan ms. Cell. 1995 Jan 13;80(1):167-78. doi: 10.1016/0092-8674(95)90461-1. Cell. 1995. PMID: 7813013
Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene.
Sabouri LA, Mahadevan MS, Narang M, Lee DS, Surh LC, Korneluk RG. Sabouri LA, et al. Among authors: mahadevan ms. Nat Genet. 1993 Jul;4(3):233-8. doi: 10.1038/ng0793-233. Nat Genet. 1993. PMID: 8358430
The RNA-binding protein Staufen1 is increased in DM1 skeletal muscle and promotes alternative pre-mRNA splicing.
Ravel-Chapuis A, Bélanger G, Yadava RS, Mahadevan MS, DesGroseillers L, Côté J, Jasmin BJ. Ravel-Chapuis A, et al. Among authors: mahadevan ms. J Cell Biol. 2012 Mar 19;196(6):699-712. doi: 10.1083/jcb.201108113. J Cell Biol. 2012. PMID: 22431750 Free PMC article.
Mutant DMPK 3'-UTR transcripts disrupt C2C12 myogenic differentiation by compromising MyoD.
Amack JD, Reagan SR, Mahadevan MS. Amack JD, et al. Among authors: mahadevan ms. J Cell Biol. 2002 Nov 11;159(3):419-29. doi: 10.1083/jcb.200206020. Epub 2002 Nov 11. J Cell Biol. 2002. PMID: 12427866 Free PMC article.
Intergenerational stability of the myotonic dystrophy protomutation.
Barceló JM, Mahadevan MS, Tsilfidis C, MacKenzie AE, Korneluk RG. Barceló JM, et al. Among authors: mahadevan ms. Hum Mol Genet. 1993 Jun;2(6):705-9. doi: 10.1093/hmg/2.6.705. Hum Mol Genet. 1993. PMID: 8353489
High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation.
Neville CE, Mahadevan MS, Barceló JM, Korneluk RG. Neville CE, et al. Among authors: mahadevan ms. Hum Mol Genet. 1994 Jan;3(1):45-51. doi: 10.1093/hmg/3.1.45. Hum Mol Genet. 1994. PMID: 7909252
Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission.
O'Hoy KL, Tsilfidis C, Mahadevan MS, Neville CE, Barceló J, Hunter AG, Korneluk RG. O'Hoy KL, et al. Among authors: mahadevan ms. Science. 1993 Feb 5;259(5096):809-12. doi: 10.1126/science.8094260. Science. 1993. PMID: 8094260
Sequence of a 131-kb region of 5q13.1 containing the spinal muscular atrophy candidate genes SMN and NAIP.
Chen Q, Baird SD, Mahadevan M, Besner-Johnston A, Farahani R, Xuan J, Kang X, Lefebvre C, Ikeda JE, Korneluk RG, MacKenzie AE. Chen Q, et al. Genomics. 1998 Feb 15;48(1):121-7. doi: 10.1006/geno.1997.5141. Genomics. 1998. PMID: 9503025
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