McLean MD - Search Results

1

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: mclean md. Hum Genet. 1995 Sep;96(3):330-4. doi: 10.1007/BF00210417. Hum Genet. 1995. PMID: 7649551

2

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. Cell. 1995 Jan 13;80(1):167-78. doi: 10.1016/0092-8674(95)90461-1. Cell. 1995. PMID: 7813013 Free article.

3

A multicopy dinucleotide marker that maps close to the spinal muscular atrophy gene.

Burghes AH, Ingraham SE, McLean M, Thompson TG, McPherson JD, Kote-Jarai Z, Carpten JD, DiDonato CJ, Ikeda JE, Surh L, et al. Burghes AH, et al. Genomics. 1994 May 15;21(2):394-402. doi: 10.1006/geno.1994.1282. Genomics. 1994. PMID: 8088834

4

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: mclean md. Genomics. 1995 Apr 10;26(3):451-60. doi: 10.1016/0888-7543(95)80162-f. Genomics. 1995. PMID: 7607667

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. Hum Mol Genet. 1994 Nov;3(11):1951-6. doi: 10.1093/hmg/3.11.1951. Hum Mol Genet. 1994. PMID: 7874111

6

Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele.

Daniels RJ, Campbell L, Rodrigues NR, Francis MJ, Morrison KE, McLean M, MacKenzie A, Ignatius J, Dubowitz V, Davies KE. Daniels RJ, et al. J Med Genet. 1995 Feb;32(2):93-6. doi: 10.1136/jmg.32.2.93. J Med Genet. 1995. PMID: 7760328 Free PMC article.

7

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. Nature. 1996 Jan 25;379(6563):349-53. doi: 10.1038/379349a0. Nature. 1996. PMID: 8552191

8

Severe phenytoin hypersensitivity with myopathy: a case report.

Barclay CL, McLean M, Hagen N, Brownell AK, MacRae ME. Barclay CL, et al. Neurology. 1992 Dec;42(12):2303. doi: 10.1212/wnl.42.12.2303. Neurology. 1992. PMID: 1461384 No abstract available.

9

Incidence of Guillain-Barré syndrome in Ontario and Quebec, 1983-1989, using hospital service databases.

McLean M, Duclos P, Jacob P, Humphreys P. McLean M, et al. Epidemiology. 1994 Jul;5(4):443-8. doi: 10.1097/00001648-199407000-00011. Epidemiology. 1994. PMID: 7918815

10

Organization of the Saccharomyces cerevisiae actin gene UAS: functional significance of reiterated REB1 binding sites and AT-rich elements.

McLean M, Hubberstey AV, Bouman DJ, Pece N, Mastrangelo P, Wildeman AG. McLean M, et al. Mol Microbiol. 1995 Nov;18(4):605-14. doi: 10.1111/j.1365-2958.1995.mmi_18040605.x. Mol Microbiol. 1995. PMID: 8817483

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