MUTANT MELANOMA
<em>NRAS</em>-mutant melanoma: current challenges and future prospect
7
Dabrafenib plus trametinib versus dabrafenib monotherapy in patients with metastatic BRAF V600E/K-mutant melanoma: long-term survival and safety analysis of a phase 3 study.
26
MNK1/2 inhibition limits oncogenicity and metastasis of KIT mutant melanoma
15
Inhibition of mitochondrial respiration prevents BRAF-mutant melanoma brain metastasis
19
MEK inhibitors for the treatment of NRAS mutant melanoma
13
The c-Jun/RHOB/AKT pathway confers resistance of BRAF -mutant melanoma cells to MAPK inhibitors
15
Synergistic cytotoxicity of radiation and oncolytic Lister strain vaccinia in V600D/E BRAF mutant melanoma depends on JNK and TNF-α signaling
39
BRAF-mutant melanoma: treatment approaches, resistance mechanisms, and diagnostic strategies
12
Dabrafenib for treatment of<em> BRAF</em>-mutant melanoma
9
Mitochondrial oxidative phosphorylation controls cancer cell’s life and death decisions upon exposure to MAPK inhibitors
13
Metformin and trametinib have synergistic effects on cell viability and tumor growth in NRAS mutant cancer
10
Potential Therapeutic Strategies to Overcome Acquired Resistance to BRAF or MEK Inhibitors in BRAF Mutant Cancers
11
Mutational analysis of the role of glycoprotein I in varicella-zoster virus replication and its effects on glycoprotein E conformation and trafficking.
10
Variation of mutant allele frequency in NRAS Q61 mutated melanomas
10
Vemurafenib resistance reprograms melanoma cells towards glutamine dependence
11
Disulfiram anti-cancer efficacy without copper overload is enhanced by extracellular H
11
<p>Treatment of Advanced/Metastatic Melanoma in the United States and Western Europe: Results of the CancerMPact Survey</p>
7
Encorafenib/binimetinib for the treatment of BRAF-mutant advanced, unresectable, or metastatic melanoma: design, development, and potential place in therapy
9
PIM kinases as therapeutic targets against advanced melanoma
16
Differentiation of Varicella-Zoster Virus ORF47 Protein Kinase and IE62 Protein Binding Domains and Their Contributions to Replication in Human Skin Xenografts in the SCID-hu Mouse
11