A CENSUS OF HUMAN CANCER GENES
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Summary
A 'census' of cancer genes is conducted that indicates that mutations in more than 1% of genes contribute to human cancer.
- Type
- review
- Published
- 2004-03-01
- Cited by
- 3,194
- References
- 42
- OpenAlex
- https://openalex.org/W2102140136
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:5594451
Keywords
Gene, Carcinogenesis, Biology, Cancer, Genetics
References
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- Altered methylation patterns in cancer cell genomes: cause or consequence?
- Structural alterations of the epidermal growth factor receptor gene in human gliomas.
- The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer.
- A cell cycle regulator potentially involved in genesis of many tumor types.
- Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk.
- A point mutation is responsible for the acquisition of transforming properties by the T24 human bladder carcinoma oncogene
- Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations
- Mechanism of activation of a human oncogene
- Transforming activity of human tumor DNAs.
- Mutations of the RET proto‐oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease
- BRCA1 mutations in primary breast and ovarian carcinomas.
- Expression of the ETV6-NTRK3 gene fusion as a primary event in human secretory breast carcinoma.
- Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC
- Passage of phenotypes of chemically transformed cells via transfection of DNA and chromatin.
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- Modelling chromosome missegregation in tumour evolution
- Introduction: the rationale for the development of targeted drugs in cancer therapy.
- On ubiquitin ligases and cancer
- Allele-Specific Amplification in Cancer Revealed by SNP Array Analysis
- Structure-based prediction of insertion-site preferences of transposons into chromosomes
- Molecular cytogenetics in translational oncology: when chromosomes meet genomics
- Integrative approach for prioritizing cancer genes in sporadic colon cancer
- ChimerDB 2.0—a knowledgebase for fusion genes updated
- Disparate Companions: Tissue Engineering Meets Cancer Research
- Human variation databases
- Mutational Profiling of Kinases in Human Tumours of Pancreatic Origin Identifies Candidate Cancer Genes in Ductal and Ampulla of Vater Carcinomas
- Innovative technology for cancer risk analysis.
- Remarkable difference of somatic mutation patterns between oncogenes and tumor suppressor genes.
- Single-cell exome sequencing and monoclonal evolution of a JAK2-negative myeloproliferative neoplasm.
- Epithelial-Mesenchymal Transition in Oral Squamous Cell Carcinoma
- omniBiomarker: A Web-Based Application for Knowledge-Driven Biomarker Identification
- Exome Sequencing on Malignant Meningiomas Identified Mutations in Neurofibromatosis Type 2 (NF2) and Meningioma 1 (MN1) Genes
- Genome wide proteomics of ERBB2 and EGFR and other oncogenic pathways in inflammatory breast cancer
- Research and applications: An integrated approach to identify causal network modules of complex diseases with application to colorectal cancer
- The transcription factor FOXM1 (Forkhead box M1): proliferation-specific expression, transcription factor function, target genes, mouse models, and normal biological roles.
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