Wainwright B - Search Results

1

The effects of splice site mutations in patients with naevoid basal cell carcinoma syndrome.

Smyth I, Wicking C, Wainwright B, Chenevix-Trench G. Smyth I, et al. Among authors: wainwright b. Hum Genet. 1998 May;102(5):598-601. doi: 10.1007/s004390050747. Hum Genet. 1998. PMID: 9654212

2

A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis.

Ramsay M, Wainwright BJ, Farrall M, Estivill X, Sutherland H, Ho MF, Davies R, Halford S, Tata F, Wicking C, et al. Ramsay M, et al. Among authors: wainwright bj. Genomics. 1990 Jan;6(1):39-47. doi: 10.1016/0888-7543(90)90446-2. Genomics. 1990. PMID: 1968045

3

Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless.

Wainwright BJ, Scambler PJ, Stanier P, Watson EK, Bell G, Wicking C, Estivill X, Courtney M, Boue A, Pedersen PS, et al. Wainwright BJ, et al. EMBO J. 1988 Jun;7(6):1743-8. doi: 10.1002/j.1460-2075.1988.tb03003.x. EMBO J. 1988. PMID: 2971536 Free PMC article.

4

Murine Wnt-11 and Wnt-12 have temporally and spatially restricted expression patterns during embryonic development.

Christiansen JH, Dennis CL, Wicking CA, Monkley SJ, Wilkinson DG, Wainwright BJ. Christiansen JH, et al. Among authors: wainwright bj. Mech Dev. 1995 Jun;51(2-3):341-50. doi: 10.1016/0925-4773(95)00383-5. Mech Dev. 1995. PMID: 7547479 Free article.

5

Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels.

Delaney SJ, Rich DP, Thomson SA, Hargrave MR, Lovelock PK, Welsh MJ, Wainwright BJ. Delaney SJ, et al. Among authors: wainwright bj. Nat Genet. 1993 Aug;4(4):426-31. doi: 10.1038/ng0893-426. Nat Genet. 1993. PMID: 7691356

6

Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas.

Shanley SM, Dawkins H, Wainwright BJ, Wicking C, Heenan P, Eldon M, Searle J, Chenevix-Trench G. Shanley SM, et al. Among authors: wainwright bj. Hum Mol Genet. 1995 Jan;4(1):129-33. doi: 10.1093/hmg/4.1.129. Hum Mol Genet. 1995. PMID: 7711724

7

DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutations.

Little M, Holmes G, Bickmore W, van Heyningen V, Hastie N, Wainwright B. Little M, et al. Among authors: wainwright b. Hum Mol Genet. 1995 Mar;4(3):351-8. doi: 10.1093/hmg/4.3.351. Hum Mol Genet. 1995. PMID: 7795587

8

The human growth-arrest-specific gene GAS1 maps outside the candidate region of the gene for nevoid basal cell carcinoma syndrome.

Wicking C, Breen M, Negus K, Berkman J, Evdokiou A, Cowled P, Chenevix-Trench G, Wainwright B. Wicking C, et al. Among authors: wainwright b. Cytogenet Cell Genet. 1995;68(1-2):119-21. doi: 10.1159/000133904. Cytogenet Cell Genet. 1995. PMID: 7956349

9

Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome.

Wicking C, Berkman J, Wainwright B, Chenevix-Trench G. Wicking C, et al. Among authors: wainwright b. Genomics. 1994 Aug;22(3):505-11. doi: 10.1006/geno.1994.1423. Genomics. 1994. PMID: 8001963

10

Simple repeat polymorphism at the D9S151 locus.

Berkman J, Armour JA, Chenevix-Trench G, Wicking C, Wainwright B. Berkman J, et al. Among authors: wainwright b. Hum Mol Genet. 1994 Jan;3(1):211. doi: 10.1093/hmg/3.1.211. Hum Mol Genet. 1994. PMID: 8162036 No abstract available.

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