Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 80 checked references that resolve
resolves10.1016/j.ejca.2016.05.005Diagnosis and treatment of melanoma. European consensus-based interdisciplinary guideline – Update 2016
resolves10.3892/ol.2013.1345Efficacy of combined axitinib with dacarbazine in a B16F1 melanoma xenograft model
resolves10.1200/JCO.1999.17.9.2745Phase III Multicenter Randomized Trial of the Dartmouth Regimen Versus Dacarbazine in Patients With Metastatic Melanoma
resolves10.1200/JCO.2004.04.165Fotemustine Compared With Dacarbazine in Patients With Disseminated Malignant Melanoma: A Phase III Study
resolves10.1200/JCO.1996.14.1.7Interferon alfa-2b adjuvant therapy of high-risk resected cutaneous melanoma: the Eastern Cooperative Oncology Group Trial EST 1684.
resolves10.1016/S0305-7372(03)00074-4Does adjuvant interferon-α for high-risk melanoma provide a worthwhile benefit? A meta-analysis of the randomised trials
resolves10.1007/s00262-013-1428-4Analysis of surrogate gene expression markers in peripheral blood of melanoma patients to predict treatment outcome of adjuvant pegylated interferon alpha 2b (EORTC 18991 side study)
resolves10.1016/j.ejca.2011.09.028Ulceration and stage are predictive of interferon efficacy in melanoma: Results of the phase III adjuvant trials EORTC 18952 and EORTC 18991
resolves10.1038/sj.bjc.6601320Phase II trial of intralesional therapy with interleukin-2 in soft-tissue melanoma metastases
resolves10.1158/0008-5472.CAN-08-1430BRAF V600E Disrupts AZD6244-Induced Abrogation of Negative Feedback Pathways between Extracellular Signal-Regulated Kinase and Raf Proteins
resolves10.1038/nature08902RAF inhibitors transactivate RAF dimers and ERK signalling in cells with wild-type BRAF
resolves10.1016/S1470-2045(14)70012-9Safety and efficacy of vemurafenib in BRAFV600E and BRAFV600K mutation-positive melanoma (BRIM-3): extended follow-up of a phase 3, randomised, open-label study
resolves10.1016/S1470-2045(12)70431-XDabrafenib in patients with Val600Glu or Val600Lys BRAF-mutant melanoma metastatic to the brain (BREAK-MB): a multicentre, open-label, phase 2 trial
resolves10.1200/JCO.2013.49.8691Phase II Trial (BREAK-2) of the BRAF Inhibitor Dabrafenib (GSK2118436) in Patients With Metastatic Melanoma
resolves10.1016/S0140-6736(12)60398-5Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial
resolves10.2146/ajhp140045Trametinib: A novel signal transduction inhibitor for the treatment of metastatic cutaneous melanoma
resolves10.1038/sj.onc.1210422Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer
resolves10.1016/S0140-6736(12)60868-XDabrafenib in BRAF-mutated metastatic melanoma: a multicentre, open-label, phase 3 randomised controlled trial
resolves10.1158/1535-7163.MCT-12-0530Intratumoral Molecular Heterogeneity in a <i>BRAF</i>-Mutant, BRAF Inhibitor-Resistant Melanoma: A Case Illustrating the Challenges for Personalized Medicine
resolves10.1200/JCO.2012.44.7888Pharmacodynamic Effects and Mechanisms of Resistance to Vemurafenib in Patients With Metastatic Melanoma
resolves10.1038/bjc.2014.139Mechanism and consequences of RAF kinase activation by small-molecule inhibitors
resolves10.1016/j.ccr.2012.10.009Relief of Profound Feedback Inhibition of Mitogenic Signaling by RAF Inhibitors Attenuates Their Activity in BRAFV600E Melanomas
resolves10.1073/pnas.0900780106<sup>V600E</sup>
BRAF is associated with disabled feedback inhibition of RAF–MEK signaling and elevated transcriptional output of the pathway
resolves10.1038/nature08833RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth
resolves10.1007/s00262-012-1227-3Assessment of association between BRAF-V600E mutation status in melanomas and clinical response to ipilimumab
resolves10.1093/annonc/mdt161Four-year survival rates for patients with metastatic melanoma who received ipilimumab in phase II clinical trials
resolves10.1200/JCO.2012.47.7836Imatinib for Melanomas Harboring Mutationally Activated or Amplified <i>KIT</i> Arising on Mucosal, Acral, and Chronically Sun-Damaged Skin
resolves10.1200/JCO.2010.33.9275Phase II, Open-Label, Single-Arm Trial of Imatinib Mesylate in Patients With Metastatic Melanoma Harboring
<i>c-Kit</i>
Mutation or Amplification
resolves10.1002/cncr.26724<i>NRAS</i> mutation status is an independent prognostic factor in metastatic melanoma
resolves10.1016/S1470-2045(13)70024-XMEK162 for patients with advanced melanoma harbouring NRAS or Val600 BRAF mutations: a non-randomised, open-label phase 2 study
resolves10.1038/nm.2941Oncogenic NRAS signaling differentially regulates survival and proliferation in melanoma
resolves10.1371/journal.pone.0038364Clinical Efficacy and Safety of Bevacizumab Monotherapy in Patients with Metastatic Melanoma: Predictive Importance of Induced Early Hypertension
resolves10.2174/138920012802850074Nanoparticles Improve Biological Functions of Phthalocyanine Photosensitizers Used for Photodynamic Therapy
resolves10.1039/c2cs15344kTargeted polymeric therapeutic nanoparticles: design, development and clinical translation
resolves10.1248/bpb.b12-00817Systemic Delivery of Small Interfering RNA by Use of Targeted Polycation Liposomes for Cancer Therapy
resolves10.1021/bc2005945Lysosomal Delivery of a Lipophilic Gemcitabine Prodrug Using Novel Acid-Sensitive Micelles Improved Its Antitumor Activity
resolves10.3402/nano.v5.24381Perspectives on the application of nanotechnology in photodynamic therapy for the treatment of melanoma
resolves10.1016/S1011-1344(98)00071-2Photoinactivation of amelanotic and melanotic melanoma cells sensitized by axially substituted Si-naphthalocyanines
resolves10.1038/nm.2933In vivo photodynamic therapy using upconversion nanoparticles as remote-controlled nanotransducers
resolves10.1016/j.cell.2010.04.020A Temporarily Distinct Subpopulation of Slow-Cycling Melanoma Cells Is Required for Continuous Tumor Growth
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