Mahadevan MS - Search Results

1

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.

2

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

3

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

4

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

5

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 Free article.

6

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

7

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

8

Analysis of trinucleotide repeats in myotonic dystrophy.

Surh LC, Mahadevan M, Korneluk RG. Surh LC, et al. Curr Protoc Hum Genet. 2001 May;Chapter 9:Unit 9.6. doi: 10.1002/0471142905.hg0906s01. Curr Protoc Hum Genet. 2001. PMID: 18428318

9

The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy.

Hunter A, Tsilfidis C, Mettler G, Jacob P, Mahadevan M, Surh L, Korneluk R. Hunter A, et al. J Med Genet. 1992 Nov;29(11):774-9. doi: 10.1136/jmg.29.11.774. J Med Genet. 1992. PMID: 1453425 Free PMC article.

10

Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy.

Mahadevan MS, Foitzik MA, Surh LC, Korneluk RG. Mahadevan MS, et al. Genomics. 1993 Feb;15(2):446-8. doi: 10.1006/geno.1993.1087. Genomics. 1993. PMID: 8449517

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