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SMA genes: deleted and duplicated.
Mahadevan MS, Korneluk RG, Roy N, MacKenzie A, Ikeda J. Mahadevan MS, et al. Among authors: ikeda j. 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: ikeda je. Cytogenet Cell Genet. 1996;75(4):243-7. doi: 10.1159/000134493. Cytogenet Cell Genet. 1996. PMID: 9067434
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: ikeda je. Nature. 1996 Jan 25;379(6563):349-53. doi: 10.1038/379349a0. Nature. 1996. PMID: 8552191
Elevation of neuronal expression of NAIP reduces ischemic damage in the rat hippocampus.
Xu DG, Crocker SJ, Doucet JP, St-Jean M, Tamai K, Hakim AM, Ikeda JE, Liston P, Thompson CS, Korneluk RG, MacKenzie A, Robertson GS. Xu DG, et al. Among authors: ikeda je. Nat Med. 1997 Sep;3(9):997-1004. doi: 10.1038/nm0997-997. Nat Med. 1997. PMID: 9288726
Functional human NAIP promoter transcription regulatory elements for the NAIP and PsiNAIP genes.
Xu M, Okada T, Sakai H, Miyamoto N, Yanagisawa Y, MacKenzie AE, Hadano S, Ikeda JE. Xu M, et al. Biochim Biophys Acta. 2002 Feb 20;1574(1):35-50. doi: 10.1016/s0167-4781(01)00343-8. Biochim Biophys Acta. 2002. PMID: 11955612
Dinucleotide repeat polymorphism at the human PDGF RB gene.
Yaraghi Z, Kang X, Ikeda JE, MacKenzie A. Yaraghi Z, et al. Among authors: ikeda je. Hum Mol Genet. 1994 Nov;3(11):2082. Hum Mol Genet. 1994. PMID: 7874139 No abstract available.
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: ikeda je. Hum Mol Genet. 1994 Nov;3(11):1951-6. doi: 10.1093/hmg/3.11.1951. Hum Mol Genet. 1994. PMID: 7874111
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: ikeda je. Hum Genet. 1995 Sep;96(3):330-4. doi: 10.1007/BF00210417. Hum Genet. 1995. PMID: 7649551
Characterization of myotonic dystrophy kinase (DMK) protein in human and rodent muscle and central nervous tissue.
Whiting EJ, Waring JD, Tamai K, Somerville MJ, Hincke M, Staines WA, Ikeda JE, Korneluk RG. Whiting EJ, et al. Among authors: ikeda je. Hum Mol Genet. 1995 Jun;4(6):1063-72. doi: 10.1093/hmg/4.6.1063. Hum Mol Genet. 1995. PMID: 7655460
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: ikeda je. Genomics. 1998 Feb 15;48(1):121-7. doi: 10.1006/geno.1997.5141. Genomics. 1998. PMID: 9503025
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