Clinical characteristics of patients with lung adenocarcinomas harboring BRAF mutations.
By P. Paik, M. Arcila, Michael Fara, C. Sima, Vincent A. Miller, M. Kris, Marc Ladanyi, Gregory Riely. Journal of Clinical Oncology, 2011
679 citations recorded by the source corpus.
Subfields: Molecular Biology, Pathology and Forensic Medicine, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/f09788c6330bdac1ea0591aab0ce705f50770b56
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In Molecular Biology
Citations in the corpus
- MET Exon 14 Mutations in Non-Small-Cell Lung Cancer Are Associated With Advanced Age and Stage-Dependent MET Genomic Amplification and c-Met Overexpression. (2016, neutral): “5 (59-84) 61 (30-93) 65 (42-93) Sex Male 9 (32) 30 (30) 62 (37) Female 19 (68) 69 (70) 107 (63) Smoking history, pack-years* Never-smoker 10 (36) 57 (58) 6 (4) # 10 3 (11) 10 (10) 11 (7) .”
- Using Multiplexed Assays of Oncogenic Drivers in Lung Cancers to Select Targeted Drugs (2014, neutral): “EGFR (sensitizing)e 175 (17) [15-20] 122 (17) [14-20] 146 (83)”
- Non-small cell lung cancer: current treatment and future advances. (2016, background): “com present in 18 (3%), of which the BRAF mutations identified were V600E (50%), G469A (39%) and D594G (11%) (69).”
- ERK/MAPK signalling pathway and tumorigenesis (2020, background): “Among the three subtypes, B-Raf has the highest mutation rate, which is 90% in melanoma (Table I) (51-73).”