Associated Papers
Molecular analysis of the evolutionary history of endometrial and ovarian carcinoma in Lynch syndrome.
Kauppinen AK et al.
International Journal of Cancer, 2025
40772756 (PubMed )
Supplement: IJC-157-2294-s002.xlsx › B_Tissue_as_normal
A base editing platform for the correction of cancer driver mutations unmasks conserved p53 transcription programs.
Wang P et al.
Genome Biology, 2025
40696461 (PubMed )
Supplement: 13059_2025_3667_MOESM1_ESM.xlsx › Overlap_between_lines
LncRNA SLNCR phenocopies the E2F1 DNA binding site to promote melanoma progression.
Shah K et al.
Cell Reports, 2025
Arginine methylation expands the regulatory mechanisms and extends the genomic landscape under E2F control.
Roworth AP et al.
Science Advances, 2019
Integrated clinical, whole-genome, and transcriptome analysis of multisampled lethal metastatic prostate cancer.
Bova GS et al.
Cold Spring Harbor Molecular Case Studies, 2016
27148588 (PubMed )
Supplement: supp_mcs.a000752_SuppTable2.xls › Sheet_1
Heterozygous loss of NF2 is an early molecular alteration in well-differentiated papillary mesothelioma of the peritoneum.
Nemoto H et al.
Cancer Genetics, 2012
First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneum.
Yu W et al.
Genome Biology, 2011
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