Folate and breast cancer: the role of polymorphisms in methylenetetrahydrofolate reductase (MTHFR) by Sharp, L, Little, J, Schofield, A.C, Pavlidou, E, Cotton, S.C, Miedzybrodzka, Z, Baird, J.O.C, Haites, N.E, Heys, S.D, Grubb, D.A

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Epidermal growth factor (EGF) Increases the in vitro invasion, motility and adhesion interactions of the primary renal carcinoma cell line, A704 by Price, J.T., Wilson, H.M., Haites, N.E.

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Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene, intakes of folate and related B vitamins and colorectal cancer: a case–control study in a population with rel... by Sharp, Linda, Little, Julian, Brockton, Nigel T., Cotton, Seonaidh C., Masson, Lindsey F., Haites, Neva E., Cassidy, Jim

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Germ line BRCA1 & BRCA2 mutations in Greek breast/ovarian cancer families: 5382insC is the most frequent mutation observed by Ladopoulou, A., Kroupis, C., Konstantopoulou, I., Ioannidou-Mouzaka, L., Schofield, A.C., Pantazidis, A., Armaou, S., Tsiagas, I., Lianidou, E., Efstathiou, E., Tsionou, C., Panopoulos, C., Mihalatos, M., Nasioulas, G., Skarlos, D., Haites, N.E., Fountzilas, G., Pandis, N., Yannoukakos, D.

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Current policies for surveillance and management in women at risk of breast and ovarian cancer: a survey among 16 European family cancer clinics by Vasen, H.F.A, Haites, N.E, Evans, D.G.R, Steel, C.M, Møller, P, Hodgson, S, Eccles, D, Morrison, P, Stoppa Lyonet, D, Chang-Claude, J, Caligo, M

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The ethical management of genetic testing by Haites, N.E.

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Multifocal transitional cell carcinoma in a patient with hereditary nonpolyposis colon cancer by Ong, E., Joseph, J.V., Bramwell, S.P., Haites, N.E.

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Breast cancer in two sisters with Friedreich's ataxia by Kidd, A., Coleman, R., Whiteford, M., Barron, L.H., Simpson, S.A., Haites, N.E.

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Immunohistochemical detection of a germline BRCA1 mutation in a breast and ovarian cancer family by Schofied, A.C., Payne, S., Ross, V.G., Miller, I.D., Heys, S.D., Haites, N.E.

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A study of familial paget's disease in the U.K by aslam, S., Thomson, J.M.G., Haites, N.E., Ralston, S.H.

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Polymorphisms in P21CIP1/WAF1 are not correlated with TP53 status in sporadic ovarian tumours by MILNER, B. J, HOSKING, L, SUN, S, HAITES, N. E, FOULKES, W. D

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Polymorphisms in P21 CIP1/ WAF1 are not correlated with TP53 status in sporadic ovarian tumours by Milner, B.J., Hosking, L., Sun, S., Haites, N.E., Foulkes, W.D.

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Mutations in the connexin 32 gene in X-linked dominant Charcot—Marie—Tooth disease (CMTX1) by Fairweather, N., Bell, C., Cochrane, S., Chelly, J., Wang, S., Mostacciuolo, M.L., Monaco, A.P., Haites, N.E.

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The p21WAF1 gene is infrequently mutated in human ovarian tumours and p21WAF1 protein levels appear to be regulated independently of p53 status by Milner, B.J., Miller, I.D., Brown, I., Kitchener, H.C., Parkin, D., Haites, N.E.

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The p21 WAF1 gene is infrequently mutated in human ovarian tumours and p21 WAF1 protein levels appear to be regulated independently of p53 status by Milner, B.J., Miller, I.D., Brown, I., Kitchener, H.C., Parkin, D., Haites, N.E.

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