Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Doorn, R. van"'
Autor:
Ipenburg, N.A., Sharouni, M.A. el, Doorn, R. van, Diest, P.J. van, Leerdam, M.E. van, Rhee, J.I. van der, Goeman, J., Kukutsch, N.A., Netherlands Fdn Detection
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::436509a40fe3dcdaf94eb04958d290c5
http://hdl.handle.net/1887/3562846
http://hdl.handle.net/1887/3562846
Autor:
Dalmasso, B., Pastorino, L., Nathan, V., Shah, N.N., Palmer, J.M., Howlie, M., Johansson, P.A., Freedman, N.D., Carter, B.D., Beane-Freeman, L., Hicks, B., Molven, A., Helgadottir, H., Sankar, A., Tsao, H., Stratigos, A.J., Helsing, P., Doorn, R. van, Gruis, N.A., Visser, M., Wadt, K.A.W., Mann, G., Holland, E.A., Nagore, E., Potrony, M., Puig, S., Menin, C., Peris, K., Fargnoli, M.C., Calista, D., Soufir, N., Harland, M., Bishop, T., Kanetsky, P.A., Elder, D.E., Andreotti, V., Vanni, I., Bruno, W., Hoiom, V., Tucker, M.A., Yang, X.R., Andresen, P.A., Adams, D.J., Landi, M.T., Hayward, N.K., Goldstein, A.M., Ghiorzo, P., GenoMEL, MelaNostrum Consortia
Publikováno v:
Genetics in Medicine, 23(11), 2087-2095. SPRINGERNATURE
Genetics in Medicine
Genetics in medicine : official journal of the American College of Medical Genetics, vol 23, iss 11
Genetics in Medicine
Genetics in medicine : official journal of the American College of Medical Genetics, vol 23, iss 11
Purpose Ataxia–Telangiectasia Mutated (ATM) has been implicated in the risk of several cancers, but establishing a causal relationship is often challenging. Although ATM single-nucleotide polymorphisms have been linked to melanoma, few functional a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51b0ef9606b12f87dff498e2a2603490
http://hdl.handle.net/1887/3280197
http://hdl.handle.net/1887/3280197
Autor:
Potjer, T.P., Bollen, S., Grimbergen, A.J.E.M., Doorn, R. van, Gruis, N.A., Asperen, C.J. van, Hes, F.J., Stoep, N. van der, Dutch Working Grp Clinical Oncogen
Publikováno v:
International Journal of Cancer, 144(10), 2453-2464. WILEY
International Journal of Cancer
International Journal of Cancer, 144(10):31984. Wiley
International Journal of Cancer
International Journal of Cancer, 144(10):31984. Wiley
Germline mutations in the major melanoma susceptibility gene CDKN2A explain genetic predisposition in only 10–40% of melanoma‐prone families. In our study we comprehensively characterized 488 melanoma cases from 451 non‐CDKN2A/CDK4 families for
Autor:
Scheeren, F.A., Doorn, R. van
Publikováno v:
Journal of Investigative Dermatology, 141(2), 252-254. ELSEVIER SCIENCE INC
BRD4 acts as an epigenetic reader to regulate gene transcription. It represents a valid therapeutic target in cancer, and several selective and potent small molecule inhibitors have been discovered. A study by Le et al. (2020) published in Journal of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d8d0f9e7c85d3ee54357b183a2c7fb98
https://hdl.handle.net/1887/3209079
https://hdl.handle.net/1887/3209079
Publikováno v:
Genes, Chromosomes and Cancer, 59(6), 366-374. Wiley
Melanoma demonstrates altered patterns of DNA methylation that are associated with genetic instability and transcriptional repression of numerous genes. Active DNA demethylation is mediated by TET enzymes that catalyze conversion of 5-methylcytosine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a5c2a3d89e9c307d81a9db7ca2b7990b
https://hdl.handle.net/1887/3181526
https://hdl.handle.net/1887/3181526
Autor:
Potjer, T.P., Helgadottir, H., Leenheer, M., Stoep, N. van der, Gruis, N.A., Hoiom, V., Olsson, H., Doorn, R. van, Vasen, H.F.A., Asperen, C.J. van, Dekkers, O.M., Hes, F.J., Dutch Working Grp Clinical Onc
Publikováno v:
Journal of Medical Genetics, 55(10), 661-668
Journal of Medical Genetics, 55, 10, pp. 661-668
Journal of Medical Genetics, 55, 661-668
Journal of Medical Genetics, 55, 10, pp. 661-668
Journal of Medical Genetics, 55, 661-668
BackgroundSeveral factors have been reported that influence the probability of a germline CDKN2A mutation in a melanoma family. Our goal was to create a scoring system to estimate this probability, based on a set of clinical features present in the p
Autor:
Sluijs, P.J. van der, Aten, E., Barge-Schaapveld, D.Q.C.M., Bijlsma, E.K., Bokenkamp-Gramann, R., Kaat, L.D., Doorn, R. van, Putte, D.F. van de, Haeringen, A. van, Harkel, A.D.J. ten, Hilhorst-Hofstee, Y., Hoffer, M.J.V., Hollander, N.S. den, Ierland, Y. van, Koopmans, M., Kriek, M., Moghadasi, S., Nibbeling, E.A.R., Peeters-Scholte, C.M.P.C.D., Potjer, T.P., Rij, M. van, Ruivenkamp, C.A.L., Rutten, J.W., Steggerda, S.J., Suerink, M., Tan, R.N.G.B., Tuin, K. van der, Visser, R., Werf-'t Lam, A.S. van der, Williams, M., Witlox, R., Santen, G.W.E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d12b5da8a07bddc55f5c510107503594
https://doi.org/10.1038/s41436-018-0363-3
https://doi.org/10.1038/s41436-018-0363-3
Autor:
Duffy, D.L., Zhu, G., Li, X., Sanna, M., Iles, M.M., Jacobs, L.C., Evans, D.M., Yazar, S., Beesley, J., Law, M.H., Kraft, P., Visconti, A., Taylor, J.C., Liu, F., Wright, M.J., Henders, A.K., Bowdler, L., Glass, D., Ikram, M.A., Uitterlinden, A.G., Madden, P.A., Heath, A.C., Nelson, E.C., Green, A.C., Chanock, S., Barrett, J.H., Brown, M.A., Hayward, N.K., MacGregor, S., Sturm, R.A., Hewitt, A.W., Kayser, M., Hunter, D.J., Bishop, J.A.N., Spector, T.D., Montgomery, G.W., Mackey, D.A., Smith, G.D., Nijsten, T.E., Bishop, D.T., Bataille, V., Falchi, M., Han, J., Martin, N.G., Lee, J.E., Brossard, M., Moses, E.K., Song, F., Kumar, R., Easton, D.F., Pharoah, P.D.P., Swerdlow, A.J., Kypreou, K.P., Harland, M., Randerson-Moor, J., Akslen, L.A., Andresen, P.A., Avril, M.F., Azizi, E., Scarra, G.B., Brown, K.M., Debniak, T., Elder, D.E., Fang, S.Y., Friedman, E., Galan, P., Ghiorzo, P., Gillanders, E.M., Goldstein, A.M., Gruis, N.A., Hansson, J., Helsing, P., Hocevar, M., Hoiom, V., Ingvar, C., Kanetsky, P.A., Chen, W.V., Landi, M.T., Lang, J., Lathrop, G.M., Lubinski, J., Mackie, R.M., Mann, G.J., Molven, A., Novakovic, S., Olsson, H., Puig, S., Puig-Butille, J.A., Radford-Smith, G.L., Stoep, N. van der, Doorn, R. van, Whiteman, D.C., Craig, J.E., Schadendorf, D., Simms, L.A., Burdon, K.P., Nyholt, D.R., Pooley, K.A., Orr, N., Stratigos, A.J., Cust, A.E., Ward, S.V., Schulze, H.J., Dunning, A.M., Demenais, F., Amos, C.I., Melanoma GWAS Consortium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::087cbd4595fb9475c25021ce2436fbba
https://hdl.handle.net/1887/119454
https://hdl.handle.net/1887/119454
Publikováno v:
Netherlands Journal of Medicine, 75(6), 258-259
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0f7075b36d89ea3060b96476efe4fa2d
https://hdl.handle.net/1887/115963
https://hdl.handle.net/1887/115963
Autor:
Santos, I.P., Lee, A. van der, Gu, X., Caspers, P.J., Schut, T.C.B., Doorn, R. van, Hegt, V.N., Koljenovic, S., Puppels, G.J.
Publikováno v:
Journal of Raman Spectroscopy, 48(6), 872-877
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f5e00117a87611ba5af243065b64e332
https://doi.org/10.1002/jrs.5124
https://doi.org/10.1002/jrs.5124