Davies A - Search Results

1

A comparison of the genetic pathways involved in the pathogenesis of three types of colorectal cancer.

Tomlinson I, Ilyas M, Johnson V, Davies A, Clark G, Talbot I, Bodmer W. Tomlinson I, et al. Among authors: davies a. J Pathol. 1998 Feb;184(2):148-52. doi: 10.1002/(SICI)1096-9896(199802)184:2<148::AID-PATH986>3.0.CO;2-M. J Pathol. 1998. PMID: 9602705

2

A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map.

Markie D, Huson S, Maher E, Davies A, Tomlinson I, Bodmer WF. Markie D, et al. Among authors: davies a. Hum Genet. 1996 Aug;98(2):125-8. doi: 10.1007/s004390050173. Hum Genet. 1996. PMID: 8698325

3

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.

Vetrie D, Vorechovský I, Sideras P, Holland J, Davies A, Flinter F, Hammarström L, Kinnon C, Levinsky R, Bobrow M, et al. Vetrie D, et al. Among authors: davies a. Nature. 1993 Jan 21;361(6409):226-33. doi: 10.1038/361226a0. Nature. 1993. PMID: 8380905

4

Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region.

Male A, Davies A, Bergbaum A, Keeling J, FitzPatrick D, Mackie Ogilvie C, Berg J. Male A, et al. Among authors: davies a. Eur J Hum Genet. 2002 Dec;10(12):807-12. doi: 10.1038/sj.ejhg.5200890. Eur J Hum Genet. 2002. PMID: 12461687

5

A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome.

Davies AF, Olavesen MG, Stephens RJ, Davidson R, Delneste D, Van Regemorter N, Vamos E, Flinter F, Abusaad I, Ragoussis J. Davies AF, et al. Hum Genet. 1996 Oct;98(4):454-9. doi: 10.1007/s004390050239. Hum Genet. 1996. PMID: 8792822

6

An integrated map of human chromosome 6p23.

Olavesen MG, Davies AF, Broxholme SJ, Wixon JL, Senger G, Nizetic D, Campbell RD, Ragoussis J. Olavesen MG, et al. Among authors: davies af. Genome Res. 1995 Nov;5(4):342-58. doi: 10.1101/gr.5.4.342. Genome Res. 1995. PMID: 8750194 Free article.

7

An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development.

Davies AF, Mirza G, Flinter F, Ragoussis J. Davies AF, et al. J Med Genet. 1999 Sep;36(9):708-10. J Med Genet. 1999. PMID: 10507730 Free PMC article.

8

Delineation of two distinct 6p deletion syndromes.

Davies AF, Mirza G, Sekhon G, Turnpenny P, Leroy F, Speleman F, Law C, van Regemorter N, Vamos E, Flinter F, Ragoussis J. Davies AF, et al. Hum Genet. 1999 Jan;104(1):64-72. doi: 10.1007/s004390050911. Hum Genet. 1999. PMID: 10071194

9

Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting.

Davies AF, Imaizumi K, Mirza G, Stephens RS, Kuroki Y, Matsuno M, Ragoussis J. Davies AF, et al. J Med Genet. 1998 Oct;35(10):857-61. doi: 10.1136/jmg.35.10.857. J Med Genet. 1998. PMID: 9783713 Free PMC article.

10

Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications.

Brachmann CB, Davies A, Cost GJ, Caputo E, Li J, Hieter P, Boeke JD. Brachmann CB, et al. Among authors: davies a. Yeast. 1998 Jan 30;14(2):115-32. doi: 10.1002/(SICI)1097-0061(19980130)14:2<115::AID-YEA204>3.0.CO;2-2. Yeast. 1998. PMID: 9483801

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