Detection of gene mutations and gene–gene fusions in circulating cell‐free DNA of glioblastoma patients: an avenue for clinically relevant diagnostic analysis

Glioblastoma (GBM) is the most common type of glioma and is uniformly fatal. Currently, tumour heterogeneity and mutation acquisition are major impedances for tailoring personalized therapy. We collected blood and tumour tissue samples from 25 GBM patients and 25 blood samples from healthy controls....

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Detalles Bibliográficos
Autores principales: Palande, Vikrant, Siegal, Tali, Detroja, Rajesh, Gorohovski, Alessandro, Glass, Rainer, Flueh, Charlotte, Kanner, Andrew A., Laviv, Yoseph, Har‐Nof, Sagi, Levy‐Barda, Adva, Viviana Karpuj, Marcela, Kurtz, Marina, Perez, Shira, Raviv Shay, Dorith, Frenkel‐Morgenstern, Milana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120899/
https://www.ncbi.nlm.nih.gov/pubmed/34875133
http://dx.doi.org/10.1002/1878-0261.13157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120899/
https://www.ncbi.nlm.nih.gov/pubmed/34875133
http://dx.doi.org/10.1002/1878-0261.13157

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