Cargando…
The Clinical and Molecular Features in the VHL Renal Cancers; Close or Distant Relatives with Sporadic Clear Cell Renal Cell Carcinoma?
SIMPLE SUMMARY: VHL syndrome is an autosomal dominant hereditary cancer syndrome and one of the leading causes of death is ccRCC. Current target therapies may lead to stable disease or partial remission, as best response and scant evidence supports the therapeutic decision-making in metastatic ccRCC...
Autores principales: | Cinque, Alessandra, Minnei, Roberto, Floris, Matteo, Trevisani, Francesco |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657498/ https://www.ncbi.nlm.nih.gov/pubmed/36358771 http://dx.doi.org/10.3390/cancers14215352 |
Ejemplares similares
-
Renal Oncocytoma: The Diagnostic Challenge to Unmask the Double of Renal Cancer
por: Trevisani, Francesco, et al.
Publicado: (2022) -
Long Non-Coding RNAs as Novel Biomarkers in the Clinical Management of Papillary Renal Cell Carcinoma Patients: A Promise or a Pledge?
por: Trevisani, Francesco, et al.
Publicado: (2022) -
Von Hippel-Lindau (VHL) Inactivation in Sporadic Clear Cell Renal Cancer: Associations with Germline VHL Polymorphisms and Etiologic Risk Factors
por: Moore, Lee E., et al.
Publicado: (2011) -
Characterization of VHL missense mutations in sporadic clear cell renal cell carcinoma: hotspots, affected binding domains, functional impact on pVHL and therapeutic relevance
por: Razafinjatovo, Caroline, et al.
Publicado: (2016) -
MicroRNA Signatures in the Upper Urinary Tract Urothelial Carcinoma Scenario: Ready for the Game Changer?
por: Cinque, Alessandra, et al.
Publicado: (2022)