Associated Papers
Co-occurrence of BAP1 and SF3B1 mutations in uveal melanoma induces cellular senescence.
Yu L et al.
Molecular Oncology, 2022
34706158 (PubMed )
Supplement: MOL2-16-607-s006.xls › UM_BNLM_PLMT
Integrated Genomic Classification of Melanocytic Tumors of the Central Nervous System Using Mutation Analysis, Copy Number Alterations, and DNA Methylation Profiling.
Griewank KG et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2018
29891723 (PubMed )
Supplement: 10780432ccr180763-sup-198200_3_supp_4796636_p9nkv7.docx
Computational analysis of the mutations in BAP1, PBRM1 and SETD2 genes reveals the impaired molecular processes in renal cell carcinoma.
Piva F et al.
Oncotarget, 2015
26452128 (PubMed )
Supplement: oncotarget-06-32161-s002.xls › Predictions
The Importance of Multidisciplinary Approach in Early Detection of BAP1 Tumor Predisposition Syndrome: Clinical Management and Risk Assessment.
Battaglia A
Clinical Medicine Insights. Oncology, 2014
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