Novel variants of the ATRX gene identified in MYCN non-amplified Neuroblastoma in Brazilian patients
Open Access
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Identification of MYCN non-amplified neuroblastoma subgroups points towards molecular signatures for precision prognosis and therapy stratificationBritish Journal of Cancer, 2024
- Therapeutic vulnerabilities in the DNA damage response for the treatment of ATRX mutant neuroblastomaEBioMedicine, 2020
- MYCN amplification and ATRX mutations are incompatible in neuroblastomaNature Communications, 2020
- Clinical significance of MYCN amplification in patients with high‐risk neuroblastomaPediatric Blood & Cancer, 2018
- Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitriesNature Genetics, 2017
- Adult infiltrating gliomas with WHO 2016 integrated diagnosis: additional prognostic roles of ATRX and TERTActa Neuropathologica, 2017
- NeuroblastomaNature Reviews Disease Primers, 2016
- Association of Age at Diagnosis and Genetic Mutations in Patients With NeuroblastomaJAMA, 2012
- Functional significance of mutations in the Snf2 domain of ATRXHuman Molecular Genetics, 2011
- Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardationProceedings of the National Academy of Sciences, 2007