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pigment cell and melanoma research
  
سال:2018 - دوره:31 - شماره:1
  
 
2018, forward, going online and all that..
- صفحه:6-
  
 
dual mek/akt inhibition with trametinib and gsk2141795 does not yield clinical benefit in metastatic nras-mutant and wild-type melanoma
- صفحه:110-114
  
 
feasibility of monitoring advanced melanoma patients using cell-free dna from plasma
- صفحه:73-81
  
 
genetic variation in irf4 expression modulates growth characteristics, tyrosinase expression and interferon-gamma response in melanocytic cells
- صفحه:51-63
  
 
in vivo knockdown of antisense non-coding mitochondrial rnas by a lentiviral-encoded shrna inhibits melanoma tumor growth and lung colonization
- صفحه:64-72
  
 
leptomeningeal melanoma—a case series in the era of modern systemic therapy
- صفحه:120-124
  
 
melanin quantification by in vitro and in vivo analysis of near-infrared fluorescence
- صفحه:31-38
  
 
melanocortin 1 receptor (mc1r) polymorphisms’ influence on size and dermoscopic features of nevi
- صفحه:39-50
  
 
melanoma-associated grm3 variants dysregulate melanosome trafficking and camp signaling
- صفحه:115-119
  
 
metabolic strategies of melanoma cells: mechanisms, interactions with the tumor microenvironment, and therapeutic implications
- صفحه:11-30
  
 
rare, yet relevant tumor cells – a new twist to melanoma cell plasticity
- صفحه:7-9
  
 
the avidity of tumor-specific t cells amplified by a plasmacytoid dendritic cell-based assay can predict the clinical evolution of melanoma patients
- صفحه:82-94
  
 
the patterns of birthmarks suggest a novel population of melanocyte precursors arising around the time of gastrulation
- صفحه:95-109
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