Expression of C-terminal ALK, RET, or ROS1 in lung cancer cells with or without fusion
Background Genetic alterations, including mutation of epidermal growth factor receptor or v-Ki-ras2 kirsten rat sarcoma viral oncogene homolog and fusion of anaplastic lymphoma kinase (ALK), RET proto-oncogene (RET), or v-ros UR2 sarcoma virus oncogene ...
Koh Furugaki +5 more
doaj +1 more source
A biologia molecular no prognóstico do carcinoma da tireóide
This overview examines some selected genetic mechanisms of cancer development. Strong evidence has been accumulated suggesting that alteration in either the struture or activity of proto-oncogene contributes to the development and for the maintenance of ...
Aluizio Soares de Souza Rodrigues
doaj +1 more source
Mutation of rearranged during transfection (RET) is associated with enhanced tumor immunogenicity and favorable outcomes in pan-cancer immunotherapy. [PDF]
Cai J +7 more
europepmc +1 more source
Medullary thyroid carcinoma exclusively associated with a homozygous RET V778I pathogenic variant: a case report with review of literature. [PDF]
Kihara M, Miyauchi A, Akamizu T.
europepmc +1 more source
Precision management of medullary thyroid carcinoma: a dynamic framework integrating biomarkers, genotyping, and risk stratification. [PDF]
Jia C +7 more
europepmc +1 more source
Protein kinase-related tumors in the pediatric population : Updated review on an emerging group with emphasis on the more rarely involved kinases. [PDF]
Flucke U +5 more
europepmc +1 more source
Discovery of a Proteolysis Targeting Chimera for TRKA and RET-derived oncoproteins. [PDF]
Moccia M +7 more
europepmc +1 more source
Accurate <i>RET</i> Fusion Detection in Solid Tumors Using RNA Sequencing Coverage Imbalance Analysis. [PDF]
Gaziev I +12 more
europepmc +1 more source
Sporadic medullary thyroid carcinoma with a rare RET transmembrane domain mutation (A641R) that responds to selpercatinib. [PDF]
Fukuda N +17 more
europepmc +1 more source
Rare cases in two Chinese MEN2A families with RET C634Y germline mutation-a homozygous female patient and heterozygous identical twins: a systematic review of literature. [PDF]
Qi XP +11 more
europepmc +1 more source

