Analysis of rare fusions in NSCLC: Genomic architecture and clinical implications-Reference-Cited by-同舟云学术

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Analysis of rare fusions in NSCLC: Genomic architecture and clinical implications

Published:2023-10 Issue: Volume:184 Page:107317
ISSN:0169-5002
Container-title:Lung Cancer
language:en
Short-container-title:Lung Cancer

Author:

Seker-Cin Huriye,Tay Timothy Kwang Yong,Kazdal Daniel,Kluck Klaus,Ball Markus,Neumann Olaf,Winter Hauke,Herth Felix,Heußel Claus-Peter,Savai Rajkumar,Schirmacher Peter,Thomas Michael,Budczies Jan,Allgäuer Michael,Christopoulos Petros,Stenzinger Albrecht,Volckmar Anna-Lena

Publisher

Elsevier BV

Subject

Cancer Research,Pulmonary and Respiratory Medicine,Oncology

Reference65 articles.

1. Lung cancer;Herbst;N. Engl. J. Med.,2008

2. Combined targeted DNA and RNA sequencing of advanced NSCLC in routine molecular diagnostics: Analysis of the first 3,000 Heidelberg cases;Volckmar;Int. J. Cancer,2019

3. Capmatinib in MET Exon 14-mutated or MET-amplified non-small-cell lung cancer;Wolf;N. Engl. J. Med.,2020

4. Fusion-positive non-small cell lung carcinoma: Biological principles, clinical practice, and diagnostic implications;Kazdal;Genes Chromosom. Cancer,2022

5. K. Lucken, L. O'Regan, J. Choi, J. Sampson, S.L. Pashley, R. Bayliss, S. Khan, A.M. Fry, EML4-ALK variant 3 promotes mitotic errors and spindle assembly checkpoint deficiency leading to increased microtubule poison sensitivity. Mol. Cancer Res, 20(6) (2022) 854-866.

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