A kinase-deficient NTRK2 splice variant predominates in glioma and amplifies several oncogenic signaling pathways
Tropomyosin receptor kinase B (TrkB), encoded by the neurotrophic tyrosine receptor kinase 2 (NTRK2) gene, exhibits intricate splicing patterns and post-translational modifications. Here, the authors perform whole gene and transcript-level analyses and report the TrkB.T1 splice variant enhances PDGF...
Guardado en:
Autores principales: | Siobhan S. Pattwell, Sonali Arora, Patrick J. Cimino, Tatsuya Ozawa, Frank Szulzewsky, Pia Hoellerbauer, Tobias Bonifert, Benjamin G. Hoffstrom, Norman E. Boiani, Hamid Bolouri, Colin E. Correnti, Barbara Oldrini, John R. Silber, Massimo Squatrito, Patrick J. Paddison, Eric C. Holland |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2020
|
Materias: | |
Acceso en línea: | https://doaj.org/article/e76b737ec4c34d949cb32dc9395b4f44 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
NTRK fusion in Japanese colorectal adenocarcinomas
por: Yuya Yamashiro, et al.
Publicado: (2021) -
NTRK Gene Fusion Detection in Atypical Spitz Tumors
por: Rocco Cappellesso, et al.
Publicado: (2021) -
Dermoscopic Features of Spitz Tumor With LMNA-NTRK1 Fusion
por: Ben J. Friedman, et al.
Publicado: (2020) -
Applicability of pan-TRK immunohistochemistry for identification of NTRK fusions in lung carcinoma
por: Simon Strohmeier, et al.
Publicado: (2021) -
Clinical and radiographic response following targeting of BCAN-NTRK1 fusion in glioneuronal tumor
por: Christopher Alvarez-Breckenridge, et al.
Publicado: (2017)