Shaw J - Search Results

1

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. Among authors: shaw j. Am J Hum Genet. 1993 Jan;52(1):99-109. Am J Hum Genet. 1993. PMID: 8434613 Free PMC article.

2

Identification of CpG islands in a physical map encompassing the Friedreich's ataxia locus.

Wilkes D, Shaw J, Anand R, Riley J, Winter P, Wallis J, Driesel AG, Williamson R, Chamberlain S. Wilkes D, et al. Among authors: shaw j. Genomics. 1991 Jan;9(1):90-5. doi: 10.1016/0888-7543(91)90224-3. Genomics. 1991. PMID: 2004770

3

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

4

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. Among authors: shaw j. Am J Med Genet. 1989 Nov;34(3):458-61. doi: 10.1002/ajmg.1320340327. Am J Med Genet. 1989. PMID: 2574535

5

"Acadian" and "classical" forms of Friedreich ataxia are most probably caused by mutations at the same locus.

Keats BJ, Ward LJ, Shaw J, Wickremasinghe A, Chamberlain S. Keats BJ, et al. Among authors: shaw j. Am J Med Genet. 1989 Jun;33(2):266-8. doi: 10.1002/ajmg.1320330224. Am J Med Genet. 1989. PMID: 2764036

6

Mapping of mutation causing Friedreich's ataxia to human chromosome 9.

Chamberlain S, Shaw J, Rowland A, Wallis J, South S, Nakamura Y, von Gabain A, Farrall M, Williamson R. Chamberlain S, et al. Among authors: shaw j. Nature. 1988 Jul 21;334(6179):248-50. doi: 10.1038/334248a0. Nature. 1988. PMID: 2899844

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. Among authors: shaw j. Am J Hum Genet. 1989 Apr;44(4):518-21. Am J Hum Genet. 1989. PMID: 2929596 Free PMC article.

8

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. Among authors: shaw j. Hum Genet. 1987 Jun;76(2):186-90. doi: 10.1007/BF00284919. Hum Genet. 1987. PMID: 3475247

9

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

10

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. 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

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