scholarly article | Q13442814 |
P356 | DOI | 10.3390/IJMS20061483 |
P953 | full work available at URL | https://www.mdpi.com/1422-0067/20/6/1483 |
P932 | PMC publication ID | 6472057 |
P698 | PubMed publication ID | 30934534 |
P50 | author | Filippo Casoni | Q55447475 |
Paolo Fava | Q61079668 | ||
Ottavio Cremona | Q88958887 | ||
Paola Savoia | Q91122223 | ||
P2093 | author name string | Ottavio Cremona | |
Paola Savoia | |||
Paolo Fava | |||
Filippo Casoni | |||
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Tipifarnib Inhibits HRAS-Driven Dedifferentiated Thyroid Cancers | Q88669750 | ||
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The Role of the PI3K-AKT Pathway in Melanoma | Q37997546 | ||
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Dragging ras back in the ring | Q38197825 | ||
Update on primary mucosal melanoma. | Q38210789 | ||
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Profile of selumetinib and its potential in the treatment of melanoma | Q38256348 | ||
GNAQ and GNA11 mutations in uveal melanoma. | Q38258992 | ||
The melanoma revolution: from UV carcinogenesis to a new era in therapeutics. | Q38270141 | ||
BRAF and MEK inhibition in melanoma. | Q38342905 | ||
Compromised MAPK signaling in human diseases: an update | Q38359194 | ||
A compendium of ERK targets | Q38373402 | ||
Treatment of NRAS-mutant melanoma. | Q38386344 | ||
Patient perception of the benefit of a BRAF inhibitor in metastatic melanoma: quality-of-life analyses of the BREAK-3 study comparing dabrafenib with dacarbazine | Q38431409 | ||
Pilot study of PD-0325901 in previously treated patients with advanced melanoma, breast cancer, and colon cancer | Q38491964 | ||
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Signaling pathway of MAPK/ERK in cell proliferation, differentiation, migration, senescence and apoptosis | Q38533700 | ||
MEK1 and MEK2 inhibitors and cancer therapy: the long and winding road | Q38591835 | ||
NRAS-mutant melanoma: current challenges and future prospect | Q38598958 | ||
Mutations in the promoter of the telomerase gene TERT contribute to tumorigenesis by a two-step mechanism | Q38619216 | ||
Combinatorial Therapies in Melanoma: MAPK Inhibitors and Beyond | Q38634557 | ||
Binimetinib for the treatment of NRAS-mutant melanoma. | Q38636033 | ||
Targeting the Ras palmitoylation/depalmitoylation cycle in cancer | Q38669156 | ||
A review of binimetinib for the treatment of mutant cutaneous melanoma | Q38674107 | ||
MEK Inhibitors in the Treatment of Metastatic Melanoma and Solid Tumors | Q38679954 | ||
Selumetinib Inhibits Melanoma Metastasis to Mouse Liver via Suppression of EMT-targeted Genes | Q38717224 | ||
Oncogenic NRAS has multiple effects on the malignant phenotype of human melanoma cells cultured in vitro | Q39936278 | ||
Mutually exclusive NRASQ61R and BRAFV600E mutations at the single-cell level in the same human melanoma | Q40319765 | ||
Genomic Characterization of Dysplastic Nevi Unveils Implications for Diagnosis of Melanoma. | Q40455273 | ||
Dabrafenib and trametinib versus dabrafenib and placebo for Val600 BRAF-mutant melanoma: a multicentre, double-blind, phase 3 randomised controlled trial | Q40875359 | ||
Paradoxical activation of Raf by a novel Raf inhibitor | Q40939473 | ||
DUSP5 and DUSP6, two ERK specific phosphatases, are markers of a higher MAPK signaling activation in BRAF mutated thyroid cancers. | Q41070178 | ||
Primary HPV test screening in cervical cancer: a two-year experience of a single screening center in Latina (Italy). | Q41171788 | ||
A first-in-human phase I, multicenter, open-label, dose-escalation study of the oral RAF/VEGFR-2 inhibitor (RAF265) in locally advanced or metastatic melanoma independent from BRAF mutation status | Q41311583 | ||
Basal and treatment-induced activation of AKT mediates resistance to cell death by AZD6244 (ARRY-142886) in Braf-mutant human cutaneous melanoma cells | Q42478581 | ||
Transforming ras genes from human melanoma: a manifestation of tumour heterogeneity? | Q42819175 | ||
Discovery of RAF265: A Potent mut-B-RAF Inhibitor for the Treatment of Metastatic Melanoma | Q43242901 | ||
Dabrafenib in patients with Val600Glu or Val600Lys BRAF-mutant melanoma metastatic to the brain (BREAK-MB): a multicentre, open-label, phase 2 trial | Q44442912 | ||
Antitumor activity of the selective pan-RAF inhibitor TAK-632 in BRAF inhibitor-resistant melanoma | Q45124043 | ||
Farnesyltransferase-Mediated Delivery of a Covalent Inhibitor Overcomes Alternative Prenylation to Mislocalize K-Ras. | Q46078887 | ||
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The PI3K Pathway in Human Disease | Q46546002 | ||
Combination of vemurafenib and cobimetinib in patients with advanced BRAF(V600)-mutated melanoma: a phase 1b study | Q46570875 | ||
Ral signaling pathway in health and cancer. | Q47124416 | ||
RAL GTPases: Biology and Potential as Therapeutic Targets in Cancer | Q47340259 | ||
Advanced Melanoma: Current Treatment Options, Biomarkers, and Future Perspectives. | Q47375181 | ||
Molecular testing for BRAF mutations to inform melanoma treatment decisions: a move toward precision medicine | Q47392574 | ||
Trajectories of premalignancy during the journey from melanocyte to melanoma. | Q47605767 | ||
New perspectives for targeting RAF kinase in human cancer. | Q47688064 | ||
Adjuvant Dabrafenib plus Trametinib in Stage III BRAF-Mutated Melanoma. | Q47824495 | ||
New Drug Combination Strategies in Melanoma: Current Status and Future Directions. | Q47881317 | ||
Melanocytic nevi and non-neoplastic hyperpigmentations | Q48614143 | ||
Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group | Q48771295 | ||
Role of the HGF/c-MET tyrosine kinase inhibitors in metastasic melanoma. | Q49887930 | ||
Targeting the MAPK Signaling Pathway in Cancer: Promising Preclinical Activity with the Novel Selective ERK1/2 Inhibitor BVD-523 (Ulixertinib). | Q49912368 | ||
Epigenetics of malignant melanoma. | Q50091675 | ||
Roads to melanoma: Key pathways and emerging players in melanoma progression and oncogenic signaling | Q38722722 | ||
Phase I Dose-Escalation and -Expansion Study of the BRAF Inhibitor Encorafenib (LGX818) in Metastatic BRAF-Mutant Melanoma | Q38727030 | ||
An Integrated Model of RAF Inhibitor Action Predicts Inhibitor Activity against Oncogenic BRAF Signaling | Q38752000 | ||
Next-Generation Sequencing to Guide Treatment of Advanced Melanoma | Q38754313 | ||
Somatic driver mutations in melanoma. | Q38764368 | ||
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 | Q38802138 | ||
Incidence, course, and management of toxicities associated with cobimetinib in combination with vemurafenib in the coBRIM study | Q38819416 | ||
Resistance to combination BRAF and MEK inhibition in metastatic melanoma: Where to next? | Q38845962 | ||
Preexisting MEK1P124 mutations diminish response to BRAF inhibitors in metastatic melanoma patients. | Q38942785 | ||
Mutation-specific RAS oncogenicity explains NRAS codon 61 selection in melanoma | Q38953667 | ||
Antitumor activity of the ERK inhibitor SCH772984 [corrected] against BRAF mutant, NRAS mutant and wild-type melanoma | Q38964277 | ||
Vemurafenib in metastatic melanoma patients with brain metastases: an open-label, single-arm, phase 2, multicentre study. | Q39043736 | ||
Whole-genome landscapes of major melanoma subtypes. | Q39060449 | ||
KRAS, NRAS and BRAF mutations in colorectal cancer and melanoma | Q39078976 | ||
A mini-review of c-Met as a potential therapeutic target in melanoma | Q39096746 | ||
MAPK pathway in melanoma part II-secondary and adaptive resistance mechanisms to BRAF inhibition. | Q39120374 | ||
The mitogen-activated protein kinase pathway in melanoma part I - Activation and primary resistance mechanisms to BRAF inhibition. | Q39124064 | ||
Clinicopathological features and clinical outcomes associated with TP53 and BRAFNon-V600 mutations in cutaneous melanoma patients | Q39135886 | ||
Melanocytic naevi with globular and reticular dermoscopic patterns display distinct BRAF V600E expression profiles and histopathological patterns | Q39157527 | ||
Clinical Pharmacokinetics of Vemurafenib | Q39159365 | ||
Discovery of a Novel ERK Inhibitor with Activity in Models of Acquired Resistance to BRAF and MEK Inhibitors | Q39161270 | ||
Mechanisms of Drug Resistance in Melanoma | Q39169776 | ||
Strategies for Overcoming Resistance in Tumours Harboring BRAF Mutations | Q39173195 | ||
Post translational modifications of Rab GTPases | Q39252084 | ||
Combination Small Molecule MEK and PI3K Inhibition Enhances Uveal Melanoma Cell Death in a Mutant GNAQ- and GNA11-Dependent Manner | Q39325158 | ||
Mechanisms and strategies to overcome resistance to molecularly targeted therapy for melanoma | Q39329582 | ||
MEK inhibitors in oncology: a patent review (2015-Present). | Q39359514 | ||
Combinations of BRAF, MEK, and PI3K/mTOR Inhibitors Overcome Acquired Resistance to the BRAF Inhibitor GSK2118436 Dabrafenib, Mediated byNRASorMEKMutations | Q39385617 | ||
RAS Proteins and Their Regulators in Human Disease | Q39407402 | ||
Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma. | Q39422587 | ||
Role Played by Signalling Pathways in Overcoming BRAF Inhibitor Resistance in Melanoma | Q39434922 | ||
Discovery of a Highly Potent and Selective MEK Inhibitor: GSK1120212 (JTP-74057 DMSO Solvate). | Q39514463 | ||
Cobimetinib combined with vemurafenib in advanced BRAF(V600)-mutant melanoma (coBRIM): updated efficacy results from a randomised, double-blind, phase 3 trial | Q39537308 | ||
RG7204 (PLX4032), a selective BRAFV600E inhibitor, displays potent antitumor activity in preclinical melanoma models | Q39692674 | ||
Differential sensitivity of melanoma cell lines with BRAFV600E mutation to the specific Raf inhibitor PLX4032. | Q39712781 | ||
Both nuclear-cytoplasmic shuttling of the dual specificity phosphatase MKP-3 and its ability to anchor MAP kinase in the cytoplasm are mediated by a conserved nuclear export signal | Q28273355 | ||
Guilty as charged: B-RAF is a human oncogene | Q28288202 | ||
Discovery and saturation analysis of cancer genes across 21 tumour types | Q28305204 | ||
Regulation and role of Raf-1/B-Raf heterodimerization | Q28580581 | ||
Registered report: RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth | Q28603655 | ||
Routine multiplex mutational profiling of melanomas enables enrollment in genotype-driven therapeutic trials | Q28730438 | ||
BRAF mutation predicts sensitivity to MEK inhibition | Q29614281 | ||
Dabrafenib in BRAF-mutated metastatic melanoma: a multicentre, open-label, phase 3 randomised controlled trial | Q29614756 | ||
Highly Recurrent TERT Promoter Mutations in Human Melanoma | Q29614798 | ||
Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion | Q29616531 | ||
RAF inhibitors transactivate RAF dimers and ERK signalling in cells with wild-type BRAF | Q29616828 | ||
Rational design of inhibitors that bind to inactive kinase conformations | Q29617558 | ||
Improved survival with MEK inhibition in BRAF-mutated melanoma | Q29620663 | ||
Uveal melanoma: epidemiology, etiology, and treatment of primary disease | Q30235934 | ||
Towards Personalized Medicine in Melanoma: Implementation of a Clinical Next-Generation Sequencing Panel | Q33674041 | ||
Prognostic and Clinicopathologic Associations of BRAF Mutation in Primary Acral Lentiginous Melanoma in Korean Patients: A Preliminary Study | Q33682137 | ||
A highly recurrent RPS27 5'UTR mutation in melanoma | Q33917519 | ||
Enhanced Inhibition of ERK Signaling by a Novel Allosteric MEK Inhibitor, CH5126766, That Suppresses Feedback Reactivation of RAF Activity | Q33971120 | ||
Somatic mutation of GRIN2A in malignant melanoma results in loss of tumor suppressor activity via aberrant NMDAR complex formation | Q34051230 | ||
Ral activation promotes melanomagenesis | Q34086528 | ||
High frequency of BRAF mutations in nevi | Q34160519 | ||
Landscape of genomic alterations in cervical carcinomas | Q34169464 | ||
Identification of Unique MEK-Dependent Genes in GNAQ Mutant Uveal Melanoma Involved in Cell Growth, Tumor Cell Invasion, and MEK Resistance | Q34272199 | ||
Mutations induced by ultraviolet light | Q34400112 | ||
Updates of reactive oxygen species in melanoma etiology and progression | Q34403921 | ||
K- and N-Ras are geranylgeranylated in cells treated with farnesyl protein transferase inhibitors | Q34427029 | ||
The MAPK pathway across different malignancies: a new perspective | Q34459097 | ||
Absorption, Metabolism, Excretion, and the Contribution of Intestinal Metabolism to the Oral Disposition of [14C]Cobimetinib, a MEK Inhibitor, in Humans | Q34497490 | ||
Clinical Correlates of NRAS and BRAF Mutations in Primary Human Melanoma | Q34500495 | ||
Inhibition of SHP2-mediated dephosphorylation of Ras suppresses oncogenesis | Q34503441 | ||
The transformation rate of moles (melanocytic nevi) into cutaneous melanoma: a population-based estimate | Q34531909 | ||
MAP kinases in the immune response | Q34542231 | ||
Effect of dabrafenib on melanoma cell lines harbouring the BRAF(V600D/R) mutations | Q34547540 | ||
Meta-analysis of risk factors for cutaneous melanoma: II. Sun exposure | Q34553701 | ||
The dual RAF/MEK inhibitor CH5126766/RO5126766 may be a potential therapy for RAS-mutated tumor cells | Q34572036 | ||
Src promotes GTPase activity of Ras via tyrosine 32 phosphorylation. | Q34583708 | ||
Combined BRAF and MEK inhibition versus BRAF inhibition alone in melanoma | Q34664981 | ||
Genomic Classification of Cutaneous Melanoma | Q34670776 | ||
A study of tumor progression: the precursor lesions of superficial spreading and nodular melanoma | Q34710725 | ||
Paradox-breaking RAF inhibitors that also target SRC are effective in drug-resistant BRAF mutant melanoma | Q34978580 | ||
Transformation by Hras(G12V) is consistently associated with mutant allele copy gains and is reversed by farnesyl transferase inhibition. | Q35044902 | ||
A single-dose mass balance and metabolite-profiling study of vemurafenib in patients with metastatic melanoma | Q35073752 | ||
Low mutational burden of eight genes involved in the MAPK/ERK, PI3K/AKT, and GNAQ/11 pathways in female genital tract primary melanomas. | Q35073876 | ||
Exome sequencing identifies GRIN2A as frequently mutated in melanoma | Q35179796 | ||
Incidence and relevance of QTc-interval prolongation caused by tyrosine kinase inhibitors. | Q35198387 | ||
PI3K in cancer: divergent roles of isoforms, modes of activation and therapeutic targeting | Q35260766 | ||
Dissection of RAS downstream pathways in melanomagenesis: a role for Ral in transformation. | Q35779541 | ||
Impact of P-Glycoprotein (ABCB1) and Breast Cancer Resistance Protein (ABCG2) on the Brain Distribution of a Novel BRAF Inhibitor: Vemurafenib (PLX4032) | Q36057973 | ||
The MAPK signalling pathways and colorectal cancer | Q36111490 | ||
Could BRAF mutations in melanocytic lesions arise from DNA damage induced by ultraviolet radiation? | Q36538084 | ||
Mechanisms Limiting Distribution of the Threonine-Protein Kinase B-RaFV600E Inhibitor Dabrafenib to the Brain: Implications for the Treatment of Melanoma Brain Metastases | Q36642420 | ||
Preexisting MEK1 exon 3 mutations in V600E/KBRAF melanomas do not confer resistance to BRAF inhibitors | Q36676466 | ||
NMR-based functional profiling of RASopathies and oncogenic RAS mutations. | Q36712670 | ||
The dysplastic nevus: from historical perspective to management in the modern era: part II. Molecular aspects and clinical management | Q36752192 | ||
The dysplastic nevus: from historical perspective to management in the modern era: part I. Historical, histologic, and clinical aspects | Q36762792 | ||
Targeting mutant NRAS signaling pathways in melanoma | Q36902066 | ||
Phase II study of the MEK1/MEK2 inhibitor Trametinib in patients with metastatic BRAF-mutant cutaneous melanoma previously treated with or without a BRAF inhibitor | Q36929804 | ||
RAF265 inhibits the growth of advanced human melanoma tumors | Q37047974 | ||
Oncogenic NRAS signaling differentially regulates survival and proliferation in melanoma | Q37183820 | ||
Growth-inhibitory and antiangiogenic activity of the MEK inhibitor PD0325901 in malignant melanoma with or without BRAF mutations | Q37269341 | ||
Synchronous BRAF(V600E) and MEK inhibition leads to superior control of murine melanoma by limiting MEK inhibitor induced skin toxicity | Q37360534 | ||
COSMIC: somatic cancer genetics at high-resolution | Q37556877 | ||
P275 | copyright license | Creative Commons Attribution | Q6905323 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | BRAF inhibitors [cytosol] | Q50256226 |
MAP kinase signaling system | Q71130435 | ||
P304 | page(s) | 1483 | |
P577 | publication date | 2019-01-01 | |
2019-03-25 | |||
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | International Journal of Molecular Sciences | Q3153277 |
P1476 | title | Targeting the ERK Signaling Pathway in Melanoma | |
P478 | volume | 20 |
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