X chromosome inactivation in a female carrier of a 1.28 Mb deletion encompassing the human X inactivation centre

Autor: de Hoon, B., Splinter, Erik, Eussen, B., Douben, J. C. W., Rentmeester, E., van de Heijning, M., Laven, J. S. E., de Klein, J. E. M. M., Liebelt, J., Gribnau, J.

Publikováno v: Philosophical Transactions: Biological Sciences, 2017 Nov 01. 372(1733), 1-8.

Externí odkaz: https://www.jstor.org/stable/44679439

Multi-Modality Analysis Improves Survival Prediction in Enucleated Uveal Melanoma Patients

Autor: Drabarek, W., Yavuzyigitoglu, S., Obulkasim, A., Riet, J., Smit, K.N., Poppelen, N.M., Vaarwater, J., Brands, T., Eussen, B., Verdijk, R.M., Naus, N.C., Mensink, H.W., Paridaens, D., Boersma, E., Werken, H.J.G. van de, Kilic, E., Klein, A. de, Keizer, R.O.B. de, Beek, J. van, Rij, C.M. van, Brosens, E., Ipenburg, J.A. van, Bruyn, D.P. de, Rotterdam Ocular Melanoma Study

Publikováno v: Investigative Ophthalmology & Visual Science, 60(10), 3595-3605. Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science, 60(10), 3595-3605. ASSOC RESEARCH VISION OPHTHALMOLOGY INC

PURPOSE. Uveal melanoma (UM) is characterized by multiple chromosomal rearrangements and recurrent mutated genes. The aim of this study was to investigate if copy number variations (CNV) alone and in combination with other genetic and clinico-histopa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3178465fd83e69da1578f7d4c156cd0
https://pubmed.ncbi.nlm.nih.gov/31425584

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Next-generation sequencing reveals novel rare fusion events with functional implication in prostate cancer.

Autor: Teles Alves, I, Hartjes, T, McClellan, E, Hiltemann, S, Böttcher, R, Dits, N, Temanni, M R, Janssen, B, van Workum, W, van der Spek, P, Stubbs, A, de Klein, A, Eussen, B, Trapman, J, Jenster, G

Publikováno v: Oncogene; 1/29/2015, Vol. 34 Issue 5, p568-577, 10p