Korneluk RG - Search Results

1

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. Among authors: korneluk rg. Genomics. 1998 Feb 15;48(1):121-7. doi: 10.1006/geno.1997.5141. Genomics. 1998. PMID: 9503025

2

A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus.

Korneluk RG, MacKenzie AE, Nakamura Y, Dubé I, Jacob P, Hunter AG. Korneluk RG, et al. Genomics. 1989 Oct;5(3):596-604. doi: 10.1016/0888-7543(89)90028-1. Genomics. 1989. PMID: 2613241

3

Refined physical map of the spinal muscular atrophy gene (SMA) region at 5q13 based on YAC and cosmid contiguous arrays.

Roy N, McLean MD, Besner-Johnston A, Lefebvre C, Salih M, Carpten JD, Burghes AH, Yaraghi Z, Ikeda JE, Korneluk RG, et al. Roy N, et al. Among authors: korneluk rg. Genomics. 1995 Apr 10;26(3):451-60. doi: 10.1016/0888-7543(95)80162-f. Genomics. 1995. PMID: 7607667

4

A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy.

Yaraghi Z, McLean MD, Roy N, Surh L, Ikeda JE, Korneluk RG, MacKenzie A. Yaraghi Z, et al. Among authors: korneluk rg. Hum Genet. 1995 Sep;96(3):330-4. doi: 10.1007/BF00210417. Hum Genet. 1995. PMID: 7649551

5

Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type 1 spinal muscular atrophy.

McLean MD, Roy N, MacKenzie AE, Salih M, Burghes AH, Simard L, Korneluk RG, Ikeda JE, Surh L. McLean MD, et al. Among authors: korneluk rg. Hum Mol Genet. 1994 Nov;3(11):1951-6. doi: 10.1093/hmg/3.11.1951. Hum Mol Genet. 1994. PMID: 7874111

6

Suppression of apoptosis in mammalian cells by NAIP and a related family of IAP genes.

Liston P, Roy N, Tamai K, Lefebvre C, Baird S, Cherton-Horvat G, Farahani R, McLean M, Ikeda JE, MacKenzie A, Korneluk RG. Liston P, et al. Among authors: korneluk rg. Nature. 1996 Jan 25;379(6563):349-53. doi: 10.1038/379349a0. Nature. 1996. PMID: 8552191

7

Isolation of a novel G protein-coupled receptor (GPR4) localized to chromosome 19q13.3.

Mahadevan MS, Baird S, Bailly JE, Shutler GG, Sabourin LA, Tsilfidis C, Neville CE, Narang M, Korneluk RG. Mahadevan MS, et al. Among authors: korneluk rg. Genomics. 1995 Nov 1;30(1):84-8. doi: 10.1006/geno.1995.0013. Genomics. 1995. PMID: 8595909

8

Assignment of human inhibitor of apoptosis protein (IAP) genes xiap, hiap-1, and hiap-2 to chromosomes Xq25 and 11q22-q23 by fluorescence in situ hybridization.

Rajcan-Separovic E, Liston P, Lefebvre C, Korneluk RG. Rajcan-Separovic E, et al. Among authors: korneluk rg. Genomics. 1996 Nov 1;37(3):404-6. doi: 10.1006/geno.1996.0579. Genomics. 1996. PMID: 8938457 No abstract available.

9

Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genes.

Somerville MJ, Hunter AG, Aubry HL, Korneluk RG, MacKenzie AE, Surh LC. Somerville MJ, et al. Among authors: korneluk rg. Am J Med Genet. 1997 Mar 17;69(2):159-65. Am J Med Genet. 1997. PMID: 9056553

10

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: korneluk rg. Cytogenet Cell Genet. 1996;75(4):243-7. doi: 10.1159/000134493. Cytogenet Cell Genet. 1996. PMID: 9067434

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