Shaw JM - Search Results

1

Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene.

Langan JE, Cole CG, Huckle EJ, Byrne S, McRonald FE, Rowbottom L, Ellis A, Shaw JM, Leigh IM, Kelsell DP, Dunham I, Field JK, Risk JM. Langan JE, et al. Among authors: shaw jm. Hum Genet. 2004 May;114(6):534-40. doi: 10.1007/s00439-004-1100-3. Epub 2004 Mar 9. Hum Genet. 2004. PMID: 15007728

2

Characterization of a 500 kb region on 17q25 and the exclusion of candidate genes as the familial Tylosis Oesophageal Cancer (TOC) locus.

Risk JM, Evans KE, Jones J, Langan JE, Rowbottom L, McRonald FE, Mills HS, Ellis A, Shaw JM, Leigh IM, Kelsell DP, Field JK. Risk JM, et al. Among authors: shaw jm. Oncogene. 2002 Sep 12;21(41):6395-402. doi: 10.1038/sj.onc.1205768. Oncogene. 2002. PMID: 12214281

3

Down-regulation of the cytoglobin gene, located on 17q25, in tylosis with oesophageal cancer (TOC): evidence for trans-allele repression.

McRonald FE, Liloglou T, Xinarianos G, Hill L, Rowbottom L, Langan JE, Ellis A, Shaw JM, Field JK, Risk JM. McRonald FE, et al. Among authors: shaw jm. Hum Mol Genet. 2006 Apr 15;15(8):1271-7. doi: 10.1093/hmg/ddl042. Epub 2006 Mar 1. Hum Mol Genet. 2006. PMID: 16510494

4

Tylosis oesophageal cancer mapped.

Risk JM, Field EA, Field JK, Whittaker J, Fryer A, Ellis A, Shaw JM, Friedmann PS, Bishop DT, Bodmer J, et al. Risk JM, et al. Among authors: shaw jm. Nat Genet. 1994 Dec;8(4):319-21. doi: 10.1038/ng1294-319. Nat Genet. 1994. PMID: 7534553 No abstract available.

5

Tylosis associated with carcinoma of the oesophagus and oral leukoplakia in a large Liverpool family--a review of six generations.

Ellis A, Field JK, Field EA, Friedmann PS, Fryer A, Howard P, Leigh IM, Risk J, Shaw JM, Whittaker J. Ellis A, et al. Among authors: shaw jm. Eur J Cancer B Oral Oncol. 1994;30B(2):102-12. doi: 10.1016/0964-1955(94)90061-2. Eur J Cancer B Oral Oncol. 1994. PMID: 8032299 No abstract available.

6

Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q.

Chamberlain S, Farrall M, Shaw J, Wilkes D, Carvajal J, Hillerman R, Doudney K, Harding AE, Williamson R, Sirugo G, et al. Chamberlain S, et al. Am J Hum Genet. 1993 Jan;52(1):99-109. Am J Hum Genet. 1993. PMID: 8434613 Free PMC article.

7

Genetic homogeneity at the Friedreich ataxia locus on chromosome 9.

Chamberlain S, Shaw J, Wallis J, Rowland A, Chow L, Farrall M, Keats B, Richter A, Roy M, Melancon S, et al. Chamberlain S, et al. Am J Hum Genet. 1989 Apr;44(4):518-21. Am J Hum Genet. 1989. PMID: 2929596 Free PMC article.

8

Regional localisation of the Friedreich ataxia locus to human chromosome 9q13----q21.1.

Shaw J, Lichter P, Driesel AJ, Williamson R, Chamberlain S. Shaw J, et al. Cytogenet Cell Genet. 1990;53(4):221-4. doi: 10.1159/000132936. Cytogenet Cell Genet. 1990. PMID: 2209091

9

Exclusion of the Friedreich ataxia gene from chromosome 19.

Chamberlain S, Worrall CS, South S, Shaw J, Farrall M, Williamson R. Chamberlain S, et al. Hum Genet. 1987 Jun;76(2):186-90. doi: 10.1007/BF00284919. Hum Genet. 1987. PMID: 3475247

10

Prenatal diagnosis of Friedreich ataxia.

Wallis J, Shaw J, Wilkes D, Farrall M, Williamson R, Chamberlain S, Skare JC, Milunsky A. Wallis J, et al. Am J Med Genet. 1989 Nov;34(3):458-61. doi: 10.1002/ajmg.1320340327. Am J Med Genet. 1989. PMID: 2574535

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