AbstractIntroductionFusions of the anaplastic lymphoma receptor tyrosine kinase gene (ALK), ret proto-oncogene (RET), ROS proto-oncogene 1, receptor tyrosine kinase gene (ROS1), B-Raf proto-oncogene, serine/threonine kinase gene (BRAF), and neuregulin 1 gene (NRG1) and intronic MMNG HOS Transforming gene (MET) mutations are druggable oncogene alterations in lung adenocarcinoma that cause expression of aberrant transcripts. Because these aberrant transcripts are both infrequent (incidence <5%) and mutually exclusive, multiplex assays are required to detect them in tumor samples.MethodsAberrant transcripts of the six aforementioned oncogenes (36 transcripts in total) were examined in a molecular counting (MC) assay, which counts RNA molecules...
Adenocarcinoma of the lung is the leading cause of cancer death worldwide. Here we report molecular ...
Precision medicine requires accurate multi-gene clinical diagnostics. We describe the implementation...
Context.-Next-generation sequencing is a high-throughput method for detecting genetic abnormalities ...
AbstractIntroductionFusions of the anaplastic lymphoma receptor tyrosine kinase gene (ALK), ret prot...
Abstract Background Gene fusion events resulting from chromosomal rearrangements play an important r...
Simple Summary Treatment of patients diagnosed with advanced pulmonary adenocarcinoma depends on the...
Background: Gene fusion events resulting from chromosomal rearrangements play an important role in i...
BACKGROUND: Anaplastic lymphoma receptor tyrosine kinase (ALK), ROS proto-oncogene 1, receptor tyros...
International audienceTheranostic translocations may be difficult to detect by routine techniques, e...
Introduction. In this study, we attempted to detect selected abnormalities in the MET gene using var...
Adenocarcinoma of the lung is the leading cause of cancer death worldwide. Here we report molecular ...
Identification of driver mutations in lung adenocarcinoma has led to development of targeted agents ...
Identification of driver mutations in lung adenocarcinoma has led to development of targeted agents ...
Adenocarcinoma of the lung is the leading cause of cancer death worldwide. Here we report molecular ...
Liquid biopsy to access the circulating tumor DNA is a promising surrogate for invasive tumor genoty...
Adenocarcinoma of the lung is the leading cause of cancer death worldwide. Here we report molecular ...
Precision medicine requires accurate multi-gene clinical diagnostics. We describe the implementation...
Context.-Next-generation sequencing is a high-throughput method for detecting genetic abnormalities ...
AbstractIntroductionFusions of the anaplastic lymphoma receptor tyrosine kinase gene (ALK), ret prot...
Abstract Background Gene fusion events resulting from chromosomal rearrangements play an important r...
Simple Summary Treatment of patients diagnosed with advanced pulmonary adenocarcinoma depends on the...
Background: Gene fusion events resulting from chromosomal rearrangements play an important role in i...
BACKGROUND: Anaplastic lymphoma receptor tyrosine kinase (ALK), ROS proto-oncogene 1, receptor tyros...
International audienceTheranostic translocations may be difficult to detect by routine techniques, e...
Introduction. In this study, we attempted to detect selected abnormalities in the MET gene using var...
Adenocarcinoma of the lung is the leading cause of cancer death worldwide. Here we report molecular ...
Identification of driver mutations in lung adenocarcinoma has led to development of targeted agents ...
Identification of driver mutations in lung adenocarcinoma has led to development of targeted agents ...
Adenocarcinoma of the lung is the leading cause of cancer death worldwide. Here we report molecular ...
Liquid biopsy to access the circulating tumor DNA is a promising surrogate for invasive tumor genoty...
Adenocarcinoma of the lung is the leading cause of cancer death worldwide. Here we report molecular ...
Precision medicine requires accurate multi-gene clinical diagnostics. We describe the implementation...
Context.-Next-generation sequencing is a high-throughput method for detecting genetic abnormalities ...