Suchbegriffe: RECEPTOR, NOTCH1 - GENETICS , . Treffer: 4
Larose, H; Prokoph, N; Matthews, JD; Schlederer, M; Högler, S; Alsulami, AF; Ducray, SP; Nuglozeh, E; Fazaludeen, FMS; Elmouna, A; Ceccon, M; Mologni, L; Gambacorti-Passerini, C; Hoefler, G; Lobello, C; Pospisilova, S; Janikova, A; Woessmann, W; Damm-Welk, C; Zimmermann, M; Federova, A; Malone, A; Smith, O; Wasik, M; Inghirami, G; Lamant, L; Blundell, TL; Klapper, W; Merkel, O; Burke, AGA; Mian, S; Ashankyty, I; Kenner, L; Turner, SD
Whole Exome Sequencing reveals NOTCH1 mutations in anaplastic large cell lymphoma and points to Notch both as a key pathway and a potential therapeutic target.
HAEMATOLOGICA. 2021; 106(6): 1693-1704.
Doi: 10.3324/haematol.2019.238766
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Ortega, M; Bhatnagar, H; Lin, AP; Wang, L; Aster, JC; Sill, H; Aguiar, RC
A microRNA-mediated regulatory loop modulates NOTCH and MYC oncogenic signals in B- and T-cell malignancies.
Leukemia. 2015; 29(4):968-976
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Neumann, M; Heesch, S; Schlee, C; Schwartz, S; Gökbuget, N; Hoelzer, D; Konstandin, NP; Ksienzyk, B; Vosberg, S; Graf, A; Krebs, S; Blum, H; Raff, T; Brüggemann, M; Hofmann, WK; Hecht, J; Bohlander, SK; Greif, PA; Baldus, CD
Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations.
Blood. 2013; 121(23): 4749-4752.
Doi: 10.1182/blood-2012-11-465138
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Strehl, S; Nebral, K; König, M; Harbott, J; Strobl, H; Ratei, R; Struski, S; Bielorai, B; Lessard, M; Zimmermann, M; Haas, OA; Izraeli, S
ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.
Clin Cancer Res. 2008; 14(4):977-983
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