Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gesk, S"'
Autor:
Hasselblatt, M., Frühwald, Michael C., Schneppenheim, R., Oyen, F., Kordes, U., Gesk, S., Siebert, R., Paulus, W.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3341::56c5a16116fc9a4aea173f100d8beba2
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/73635
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/73635
Autor:
Weniger, MA, Pulford, K, Gesk, S, Ehrlich, S, Banham, AH, Lyne, L, Martin-Subero, JI, Siebert, R, Dyer, MJS, Moeller, P, Barth, TFE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::adb5bcb92c436c254149811357267579
https://ora.ox.ac.uk/objects/uuid:1ad86d8e-36dd-4d3e-b1e2-851d0bb2603b
https://ora.ox.ac.uk/objects/uuid:1ad86d8e-36dd-4d3e-b1e2-851d0bb2603b
Autor:
Wesemann, M, Nagel, I, Fischer, S, Stahn, V, Gesk, S, Oyen, F, Schneppenheim, R, Siebert, R, Paulus, W, Harder, A
Publikováno v:
57th Annual Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN); 20120912-20120915; Erlangen; DOC12dgnnPP3.21 /20120911/
Common benign peripheral nerve sheath tumors such as schwannomas and neurofibromas arise both sporadically and in the setting of neurofibromatosis. They differ not only by histologic features but also by distinct molecular genetic events, leading to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3cc0f2aecc62440f5e19e6a41c52959
Autor:
Marafioti, T., Pozzobon, M., Hansmann, M. -L., Ventura, R., Pileri, S. A., Roberton, H., Gesk, S., Gaulard, P., Earth, T. F. E., M. Q., Du, Leoncini, L., Moller, P., Natkunam, Y., Siebert, R., Mason, D. Y.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1820::158238003472e1a42c39fa63da017e93
http://hdl.handle.net/11365/1076547
http://hdl.handle.net/11365/1076547
Autor:
Ma Z, Jan Cools, Marynen P, Cui X, Siebert R, Gesk S, Schlegelberger B, Peeters B, De Wolf-Peeters C, Wlodarska I, Sw, Morris
Publikováno v:
Europe PubMed Central
The non-Hodgkin lymphoma (NHL) subtype anaplastic large-cell lymphoma (ALCL) is frequently associated with a t(2;5)(p23;q35) that results in the fusion of the ubiquitously expressed nucleophosmin (NPM) gene at 5q35 to the anaplastic lymphoma kinase (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d8861f3d1eb021a5ed3854d8635b015f
http://europepmc.org/abstract/med/10706887
http://europepmc.org/abstract/med/10706887
Autor:
Martinez-Climent, J. A., Siebert, R., Harder, S., Gesk, S., Alessandro Gozzetti, Price, H. P., Hernandez-Rivas, H., Dyer, M. J. S., Le Beau, M. M., Schlgelberger, B., Garcia-Conde, J.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::09ff9fc0829b56eff63254a5d92162da
http://www.scopus.com/inward/record.url?eid=2-s2.0-33748648827&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-33748648827&partnerID=MN8TOARS
Autor:
Stefanie Bug, Ralf Küppers, Sylvia Hartmann, Martin-Leo Hansmann, Anna Porwit, René Scholtysik, Sergio Cogliatti, Stefan Gesk, Marie Parrens, Markus Kreuz, Claudia Döring, Anna Kwiecinska, Reiner Siebert, Gerald Hoefler, Jean-Philippe Merlio, Inga Vater, Pier Paolo Piccaluga, Stefano Pileri
Publikováno v:
British journal of haematology. 148(3)
Little is known about genomic aberrations in peripheral T cell lymphoma, not otherwise specified (PTCL NOS). We studied 47 PTCL NOS by 250k GeneChip single nucleotide polymorphism arrays and detected genomic imbalances in 22 of the cases. Recurrent g
Autor:
Teresa, Marafioti, Teresa, Marafiot, Michela, Pozzobon, Martin-Leo, Hansmann, Roland, Ventura, Stefano A, Pileri, Helen, Roberton, Stefan, Gesk, Philippe, Gaulard, Thomas F E, Barth, Ming Q, Du, Lorenzo, Leoncini, Peter, Möller, Yasodha, Natkunam, Reiner, Siebert, David Y, Mason
Stimulation of lymphoid cells via their surface receptors triggers signalling pathways that terminate in the nucleus, where they induce alterations in gene transcription. Nuclear factor of activated T cells (NFAT) transcription factors, involved in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef188def80519951a6616fccffe8d4d1
http://hdl.handle.net/11365/9790
http://hdl.handle.net/11365/9790