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Activation of the mas oncogene involves coupling to human alphoid sequences

Autor: L J, van 't Veer, M J, van der Feltz, C A, van den Berg-Bakker, N C, Cheng, R P, Hermens, D A, van Oorschot, T, Kievits, P I, Schrier

Publikováno v: Oncogene. 8(10)

We have shown previously that mouse NIH3T3 cells transfected with DNA from a human ovarian carcinoma were rendered tumourigenic by an activated mas oncogene in four independent transfection experiments. In all cases the 5'-noncoding region was rearra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::256a7fcc2e75fe1fe4ddd198fb84a3c5
https://pubmed.ncbi.nlm.nih.gov/8378079

Eleventh International Chromosome Conference

Autor: P. Meera Khan, G.C. Beverstock, P. Charmley, R.F. Wintle, T. Knutsen, J. Nguyen, D. Bérubé, S.J. Palmer, M.F. Croquette, C. Petit, V.T.H.B.M. Smit, A. Sánchez, J C de la Torre, C. Bouza, R. Gagné, V. Goyanes, J. Couturier, P. Mollevanger, T. Trautmann, P.I. Schrier, D.F.C.M. Smeets, H. Winking, J. Levilliers, G.E. Séralini, P. Sillekens, I.N.M. Day, A.G. Geurts van Kessel, A.K. Raap, H.A. Bixenman, A.M.V. Duncan, D. Noonan, J. Kemp, J. Gellin, T.C. Willcocks, W. van Venrooij, E. Takahashi, G.H. Moore, A.Y. Sakaguchi, R. Berger, M. Goodman, M.-Y. Yip, Y. Rumpler, I.A. Stewart-Scott, U. Eichenlaub-Ritter, H.F. Willard, B.J. Morris, M. Dalens, W.W. Grody, J. Gosálvez, G.F.M. Merkx, E. Wimmer, M.-C. King, F. Libert, R.A. Gatti, S.L. Naylor, E. Passage, D.A. Tagle, P.F. Fennessy, M. Atger, P.L. Pearson, S.D. Cederbaum, G.R. Sutherland, M. Fredholm, G.L. Hammond, O. Galman, G.J.B. van Ommen, M. Misrahi, R. Kisilevsky, G. Vassart, T. Hori, M.F. Seldin, R. Jiménez, A. Viñas, H. Loosfelt, S.P. Craig, C.J. Cornelisse, D.A. Miller, M. Burgos, M.C. Wapenaar, J. Trapman, I.W. Craig, J.W. Wessels, A.H.N. Hopman, B. Wieringa, P.K. Martin, A.C.M. Akkermans-Scholten, C. Holm, K. Christensen, H. Qin, P. Martínez, R. Díaz de la Guardia, M.F. Rousseau-Merck, S.K. Mahadevaiah, H. Lawce, M. Schwerin, D. Schonk, P. Shier, P.S. Burgoyne, M. Yerle, L. Martinez, M.-G. Mattei, P. Riegmann, A. Lefort, A. Latos-Bielenska, E. Milgrom, V.M. Watt, R.J. Thompson, C. Ratomponirina, H.-H. Ropers, P.D. Pearce, T. Kievits, O. Gabriel-Robez, W. Vogel, L. Sánchez, J.F.Y. Hoh, P.D. Thomsen, P. van Dijk, T.A. Howard, P.R.L. Lam-Po-Tang

Publikováno v: Cytogenetic and Genome Research. 54:5-5

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::136273de5ca4c34a8549335d893cad80
https://doi.org/10.1159/000132943

der(1)t(1;9): a specific chromosome abnormality in polycythemia vera? Cytogenetic and in situ hybridization studies

Autor: J I, den Nijs van Weert, G C, Beverstock, T, Kievits, H L, Haak, F C, Havik-Bogaard, C H, Leeksma

Publikováno v: Cancer genetics and cytogenetics. 40(1)

Two patients with polycythemia vera and an extra der(1)t(1;9) chromosome are reported. In one patient this was found as the sole abnormality. The other patient originally presented with trisomy 9 but later developed an extra der(1) during the further

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bd539ddc205004984a49a0fa75fd9259
https://pubmed.ncbi.nlm.nih.gov/2758394

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