Associated Papers
Prospective clinical sequencing of 1016 Chinese prostate cancer patients: uncovering genomic characterization and race disparity.
Wei Y et al.
Molecular Oncology, 2023
37584393 (PubMed )
Supplement: MOL2-17-2183-s002.xlsx › Table_S6
ConVarT: a search engine for matching human genetic variants with variants from non-human species.
Pir MS et al.
Nucleic Acids Research, 2022
34718716 (PubMed )
Supplement: gkab939_supplemental_files.zip › Table_S14.xls › human_pat_mouse_unk_orthovar_14
Analyzing aggregation propensities of clinically relevant PTEN mutants: a new culprit in pathogenesis of cancer and other PTENopathies.
Palumbo E et al.
Journal of Biomolecular Structure & Dynamics, 2020
31232187 (PubMed )
Supplement: supplement_1.zip › Supplement_S6_decrease_aggreg_analysis.xlsx › Intrinsic_Disorder_all
Mismatch repair deficiency endows tumors with a unique mutation signature and sensitivity to DNA double-strand breaks.
Zhao H et al.
Elife, 2014
25085081 (PubMed )
Supplement: elife02725s004.xlsx › Validation_results
Genetic and clonal dissection of murine small cell lung carcinoma progression by genome sequencing.
McFadden DG et al.
Cell, 2014
Exploiting the mutanome for tumor vaccination.
Castle JC et al.
Cancer Research, 2012
Methylation of the PTEN promoter defines low-grade gliomas and secondary glioblastoma.
Wiencke JK et al.
Neuro-oncology, 2007
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