Davies KE - Search Results

1

Characterization of Ngef, a novel member of the Dbl family of genes expressed predominantly in the caudate nucleus.

Rodrigues NR, Theodosiou AM, Nesbit MA, Campbell L, Tandle AT, Saranath D, Davies KE. Rodrigues NR, et al. Among authors: davies ke. Genomics. 2000 Apr 1;65(1):53-61. doi: 10.1006/geno.2000.6138. Genomics. 2000. PMID: 10777665

2

Mapping of retrotransposon sequences in the unstable region surrounding the spinal muscular atrophy locus in 5q13.

Francis MJ, Nesbit MA, Theodosiou AM, Rodrigues NR, Campbell L, Christodoulou Z, Qureshi SJ, Porteous DJ, Brookes AJ, Davies KE. Francis MJ, et al. Among authors: davies ke. Genomics. 1995 May 20;27(2):366-9. doi: 10.1006/geno.1995.1059. Genomics. 1995. PMID: 7558009

3

A member of the MAP kinase phosphatase gene family in mouse containing a complex trinucleotide repeat in the coding region.

Theodosiou AM, Rodrigues NR, Nesbit MA, Ambrose HJ, Paterson H, McLellan-Arnold E, Boyd Y, Leversha MA, Owen N, Blake DJ, Ashworth A, Davies KE. Theodosiou AM, et al. Among authors: davies ke. Hum Mol Genet. 1996 May;5(5):675-84. doi: 10.1093/hmg/5.5.675. Hum Mol Genet. 1996. PMID: 8733137

4

Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2.

Nesbit MA, Hodges MD, Campbell L, de Meulemeester TM, Alders M, Rodrigues NR, Talbot K, Theodosiou AM, Mannens MA, Nakamura Y, Little PF, Davies KE. Nesbit MA, et al. Among authors: davies ke. Genomics. 1997 Jun 1;42(2):284-94. doi: 10.1006/geno.1997.4737. Genomics. 1997. PMID: 9192849

5

A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy.

Burton EA, Tinsley JM, Holzfeind PJ, Rodrigues NR, Davies KE. Burton EA, et al. Among authors: davies ke. Proc Natl Acad Sci U S A. 1999 Nov 23;96(24):14025-30. doi: 10.1073/pnas.96.24.14025. Proc Natl Acad Sci U S A. 1999. PMID: 10570192 Free PMC article.

6

Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?

Campbell L, Hunter KM, Mohaghegh P, Tinsley JM, Brasch MA, Davies KE. Campbell L, et al. Among authors: davies ke. Hum Mol Genet. 2000 Apr 12;9(7):1093-100. doi: 10.1093/hmg/9.7.1093. Hum Mol Genet. 2000. PMID: 10767334

7

Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13.

Theodosiou AM, Morrison KE, Nesbit AM, Daniels RJ, Campbell L, Francis MJ, Christodoulou Z, Davies KE. Theodosiou AM, et al. Among authors: davies ke. Am J Hum Genet. 1994 Dec;55(6):1209-17. Am J Hum Genet. 1994. PMID: 7977382 Free PMC article.

8

A 1.8-Mb YAC contig in Xp11.23: identification of CpG islands and physical mapping of CA repeats in a region of high gene density.

Coleman MP, Németh AH, Campbell L, Raut CP, Weissenbach J, Davies KE. Coleman MP, et al. Among authors: davies ke. Genomics. 1994 May 15;21(2):337-43. doi: 10.1006/geno.1994.1274. Genomics. 1994. PMID: 8088827

9

Molecular genetics of autosomal recessive spinal muscular atrophy.

Rodrigues NR, Talbot K, Davies KE. Rodrigues NR, et al. Among authors: davies ke. Mol Med. 1996 Jul;2(4):400-4. Mol Med. 1996. PMID: 8827710 Free PMC article. Review. No abstract available.

10

Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?

Talbot K, Ponting CP, Theodosiou AM, Rodrigues NR, Surtees R, Mountford R, Davies KE. Talbot K, et al. Among authors: davies ke. Hum Mol Genet. 1997 Mar;6(3):497-500. doi: 10.1093/hmg/6.3.497. Hum Mol Genet. 1997. PMID: 9147655

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