Associated Papers
Genomic alterations in ovarian endometriosis and subsequently diagnosed ovarian carcinoma.
Linder A et al.
Human Reproduction (oxford, England), 2024
38459814 (PubMed )
Supplement: deae043_supplementary_table_s3.xlsx › Endometriosis
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
39021676 (PubMed )
Supplement: DataSheet1.ZIP › Somatic › 18R12365.xls › SNVIndel
FPGS relapse-specific mutations in relapsed childhood acute lymphoblastic leukemia.
Yu SL et al.
Scientific Reports, 2020
32694622 (PubMed )
Supplement: 41598_2020_69059_MOESM2_ESM.xlsx › PuiBALL_with_purity_4_pp
Genetic evaluation of BRCA1 associated a complex genes with triple-negative breast cancer susceptibility in Chinese women.
Ling H et al.
Oncotarget, 2016
Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.
Szeto CY et al.
Febs Open Bio, 2014
24490137 (PubMed )
Supplement: mmc5.xlsx › all_info
Loss of BRCA1-A complex function in RAP80 null tumor cells.
Bian C et al.
Plos One, 2012
Familial breast cancer screening reveals an alteration in the RAP80 UIM domain that impairs DNA damage response function.
Nikkilä J et al.
Oncogene, 2009
Germline RAP80 mutations and susceptibility to breast cancer.
Akbari MR et al.
Breast Cancer Research and Treatment, 2009
[Familial breast cancer-susceptibility genes].
Ma Y et al.
Zhonghua Bing Li Xue Za Zhi = Chinese Journal of Pathology, 1997
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