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1996 Journal Article +P5(D1S3309E), a novel target binding site for the Wilms' tumour suppressor 1 (WT1) gene, maps to human chromosome 1q21->q22Negus, K, Holmes, GH, Wicking, C, Wainwright, BJ and Little, MH (1996). +P5(D1S3309E), a novel target binding site for the Wilms' tumour suppressor 1 (WT1) gene, maps to human chromosome 1q21->q22. Cytogenetics and Cell Genetics, 72 (4), 306-309. doi: 10.1159/000134210 |
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1995 Journal Article Methylation and P16 - Suppressing the SuppressorLittle, M and Wainwright, B (1995). Methylation and P16 - Suppressing the Suppressor. Nature Medicine, 1 (7), 633-634. doi: 10.1038/nm0795-633 |
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1995 Journal Article Murine Wnt-11 and Wnt-12 have temporally and spatially restricted expression patterns during embryonic developmentChristiansen, Jeffrey H., Dennis, Carina L., Wicking, Carol A., Monkley, Susan J., Wilkinson, David G. and Wainwright, Brandon J. (1995). Murine Wnt-11 and Wnt-12 have temporally and spatially restricted expression patterns during embryonic development. Mechanisms of Development, 51 (2-3), 341-350. doi: 10.1016/0925-4773(95)00383-5 |
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1995 Journal Article Dna-Binding Capacity of the Wt1 Protein Is Abolished by Denys-Drash Syndrome Wt1 Point MutationsLittle, M, Holmes, G, Bickmore, W, Vanheyningen, V, Hastie, N and Wainwright, B (1995). Dna-Binding Capacity of the Wt1 Protein Is Abolished by Denys-Drash Syndrome Wt1 Point Mutations. Human Molecular Genetics, 4 (3), 351-358. doi: 10.1093/hmg/4.3.351 |
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1995 Journal Article Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomasM.shanley, Susan, Dawkins, Hugh, J.wainwright, Brandon, Wicking, Carol, Heenan, Peter, Eldon, Michael, Searle, Jeffrey and Chenevlx-trench, Georgia (1995). Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas. Human Molecular Genetics, 4 (1), 129-133. doi: 10.1093/hmg/4.1.129 |
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1995 Journal Article The human growth-arrest-specific gene gas 1 maps outside the candidate region of the gene for nevoid basal-cell carcinoma syndromeWicking, C., Breen, M., Negus, K., Berkman, J., Evdokiou, A., Cowled, P., Chenevix-Trench, G. and Wainwright, B. (1995). The human growth-arrest-specific gene gas 1 maps outside the candidate region of the gene for nevoid basal-cell carcinoma syndrome. Cytogenetics and Cell Genetics, 68 (1-2), 119-121. doi: 10.1159/000133904 |
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1995 Journal Article Detection of c-fms protooncogene in early mouse embryos by whole mount in situ hybridization indicates roles for macrophages in tissue remodellingHume, D. A., Monkley, S. J. and Wainwright, B. J. (1995). Detection of c-fms protooncogene in early mouse embryos by whole mount in situ hybridization indicates roles for macrophages in tissue remodelling. British Journal of Haematology, 90 (4), 939-942. doi: 10.1111/j.1365-2141.1995.tb05220.x |
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1994 Journal Article Alternative splicing of the first nucleotide binding fold of CFTR in mouse testes is associated with specific stages of spermatogenesisDelaney, Stephen J., Koopman, Peter, Lovelock, Paul K. and Wainwright, Brandon J. (1994). Alternative splicing of the first nucleotide binding fold of CFTR in mouse testes is associated with specific stages of spermatogenesis. Genomics, 20 (3), 517-518. doi: 10.1006/geno.1994.1214 |
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1994 Journal Article Fine genetic mapping of the gene for nevoid basal cell carcinoma syndromeWicking C., Berkman J., Wainwright B. and Chenevix-Trench G. (1994). Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome. Genomics, 22 (3), 505-511. doi: 10.1006/geno.1994.1423 |
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1994 Journal Article Isolation and genetic mapping of two novel members of the murine Wnt gene family, Wnt11 and Wnt12, and the mapping of Wnt5a and Wnt7aAdamson M.C., Dennis C., Delaney S., Christiansen J., Monkley S., Kozak C.A. and Wainwright B. (1994). Isolation and genetic mapping of two novel members of the murine Wnt gene family, Wnt11 and Wnt12, and the mapping of Wnt5a and Wnt7a. Genomics, 24 (1), 9-13. doi: 10.1006/geno.1994.1575 |
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1994 Journal Article Familial melanoma and p16 — A hung juryWainwright B. (1994). Familial melanoma and p16 — A hung jury. Nature Genetics, 8 (1), 3-5. doi: 10.1038/ng0994-3 |
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1994 Journal Article Simple repeat polymorphism at the D9S151 locusBerkman, Jenny, Armour, John A.L., Chenevix-trench, Georgia, Wicking, Carol and Wainwright, Brandon (1994). Simple repeat polymorphism at the D9S151 locus. Human Molecular Genetics, 3 (1), 211-211. doi: 10.1093/hmg/3.1.211 |
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1993 Journal Article Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channelsDelaney, Stephen J., Rich, Devra P., Thomson, Scott A., Hargrave, Murray R., Lovelock, Paul K., Welsh, Michael J. and Wainwright, Brandon J. (1993). Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels. Nature Genetics, 4 (4), 426-430. doi: 10.1038/ng0893-426 |
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1993 Journal Article The isolation of disease genes by positional cloningWainwright, B. J. (1993). The isolation of disease genes by positional cloning. Medical Journal of Australia, 159 (3), 170-174. doi: 10.5694/j.1326-5377.1993.tb137781.x |
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1992 Journal Article Localization of the cystic fibrosis transmembrane conductance regulator (Cftr) to mouse chromosome 6Siegel, D., Irving, N. G., Friedman, J. M. and Wainwright, B. J. (1992). Localization of the cystic fibrosis transmembrane conductance regulator (Cftr) to mouse chromosome 6. Cytogenetic and Genome Research, 61 (3), 184-185. doi: 10.1159/000133404 |
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1991 Journal Article 'Touchdown' PCR to circumvent spurious priming during gene amplificationDon R.H., Cox P.T., Wainwright B.J., Baker K. and Mattick J.S. (1991). 'Touchdown' PCR to circumvent spurious priming during gene amplification. Nucleic Acids Research, 19 (14), 4008. doi: 10.1093/nar/19.14.4008 |
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1991 Journal Article The molecular pathology of cystic fibrosisWainwright, B. (1991). The molecular pathology of cystic fibrosis. Current Biology, 1 (2), 80-82. doi: 10.1016/0960-9822(91)90283-3 |
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1990 Journal Article A NEW POLYMORPHIC LOCUS, D7S411, ISOLATED BY CLONING FROM PREPARATIVE PULSE-FIELD GELS IS CLOSE TO THE MUTATION CAUSING CYSTIC-FIBROSISRAMSAY, M, WAINWRIGHT, BJ, FARRALL, M, ESTIVILL, , SUTHERLAND, H, HO, MF, DAVIES, R, HALFORD, S, TATA, F, WICKING, C, LENCH, N, BAUER, , FEREC, C, FARNDON, P, KRUYER, H, STANIER, P, WILLIAMSON, R and SCAMBLER, PJ (1990). A NEW POLYMORPHIC LOCUS, D7S411, ISOLATED BY CLONING FROM PREPARATIVE PULSE-FIELD GELS IS CLOSE TO THE MUTATION CAUSING CYSTIC-FIBROSIS. Genomics, 6 (1), 39-47. doi: 10.1016/0888-7543(90)90446-2 |
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1988 Journal Article RECOMBINATIONS BETWEEN IRP AND CYSTIC-FIBROSISFARRALL, M, WAINWRIGHT, BJ, FELDMAN, GL, BEAUDET, A, SRETENOVIC, Z, HALLEY, D, SIMON, M, DICKERMAN, L, DEVOTO, M, ROMEO, G, KAPLAN, JC, KITZIS, A and WILLIAMSON, R (1988). RECOMBINATIONS BETWEEN IRP AND CYSTIC-FIBROSIS. American Journal of Human Genetics, 43 (4), 471-475. |
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1988 Journal Article ISOLATION OF A HUMAN-GENE WITH PROTEIN-SEQUENCE SIMILARITY TO HUMAN AND MURINE INT-1 AND THE DROSOPHILA SEGMENT POLARITY MUTANT WINGLESSWAINWRIGHT, BJ, SCAMBLER, PJ, STANIER, P, WATSON, EK, BELL, G, WICKING, C, ESTIVILL, , COURTNEY, M, BOUE, A, PEDERSEN, PS, WILLIAMSON, R and FARRALL, M (1988). ISOLATION OF A HUMAN-GENE WITH PROTEIN-SEQUENCE SIMILARITY TO HUMAN AND MURINE INT-1 AND THE DROSOPHILA SEGMENT POLARITY MUTANT WINGLESS. Embo Journal, 7 (6), 1743-1748. doi: 10.1002/j.1460-2075.1988.tb03003.x |
