Korneluk RG - Search Results

1

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: korneluk rg. Hum Mol Genet. 1995 Jun;4(6):1063-72. doi: 10.1093/hmg/4.6.1063. Hum Mol Genet. 1995. PMID: 7655460

2

Inhibition of myogenesis in transgenic mice expressing the human DMPK 3'-UTR.

Storbeck CJ, Drmanic S, Daniel K, Waring JD, Jirik FR, Parry DJ, Ahmed N, Sabourin LA, Ikeda JE, Korneluk RG. Storbeck CJ, et al. Among authors: korneluk rg. Hum Mol Genet. 2004 Mar 15;13(6):589-600. doi: 10.1093/hmg/ddh064. Epub 2004 Jan 20. Hum Mol Genet. 2004. PMID: 14734627

3

Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localization.

Whiting EJ, Tsilfidis C, Surh L, MacKenzie AE, Korneluk RG. Whiting EJ, et al. Among authors: korneluk rg. Eur J Hum Genet. 1995;3(3):195-202. doi: 10.1159/000472295. Eur J Hum Genet. 1995. PMID: 7583045

4

Investigation of myotonic dystrophy kinase isoform translocation and membrane association.

Waring JD, Haq R, Tamai K, Sabourin LA, Ikeda JE, Korneluk RG. Waring JD, et al. Among authors: korneluk rg. J Biol Chem. 1996 Jun 21;271(25):15187-93. doi: 10.1074/jbc.271.25.15187. J Biol Chem. 1996. PMID: 8663097 Free article.

5

Definition of regulatory sequence elements in the promoter region and the first intron of the myotonic dystrophy protein kinase gene.

Storbeck CJ, Sabourin LA, Waring JD, Korneluk RG. Storbeck CJ, et al. Among authors: korneluk rg. J Biol Chem. 1998 Apr 10;273(15):9139-47. doi: 10.1074/jbc.273.15.9139. J Biol Chem. 1998. PMID: 9535904 Free article.

6

Myotonic dystrophy (DM) protein kinase levels in congenital and adult DM patients.

Narang MA, Waring JD, Sabourin LA, Korneluk RG. Narang MA, et al. Among authors: korneluk rg. Eur J Hum Genet. 2000 Jul;8(7):507-12. doi: 10.1038/sj.ejhg.5200490. Eur J Hum Genet. 2000. PMID: 10909850

7

Identification of the origin of double minutes in normal human cells by laser-based chromosome microdissection approach.

Rajcan-Separovic E, Wang HS, Speevak MD, Janes L, Korneluk RG, Wakasa K, Ikeda JE. Rajcan-Separovic E, et al. Among authors: korneluk rg. Hum Genet. 1995 Jul;96(1):39-43. doi: 10.1007/BF00214184. Hum Genet. 1995. PMID: 7607652

8

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

9

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

10

Overexpression of 3'-untranslated region of the myotonic dystrophy kinase cDNA inhibits myoblast differentiation in vitro.

Sabourin LA, Tamai K, Narang MA, Korneluk RG. Sabourin LA, et al. Among authors: korneluk rg. J Biol Chem. 1997 Nov 21;272(47):29626-35. doi: 10.1074/jbc.272.47.29626. J Biol Chem. 1997. PMID: 9368029 Free article.

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