(Q34253580)

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Cancer genetics.

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scholarly article

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Europe PubMed Central

Cancer genetics. (English)

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Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Ponder BA

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Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

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publication date

1 May 2001

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Europe PubMed Central

PubMed publication ID

31 July 2017

411

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Europe PubMed Central

PubMed publication ID

31 July 2017

6835

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Europe PubMed Central

PubMed publication ID

31 July 2017

336-341

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

The clonal evolution of tumor cell populations

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The Hallmarks of Cancer

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Molecular profiling of human cancer

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DNA hypermethylation in tumorigenesis: epigenetics joins genetics

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Environmental health and genomics: visions and implications

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Know thy neighbor: stromal cells can contribute oncogenic signals

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Hormonal etiology of epithelial ovarian cancer, with a hypothesis concerning the role of androgens and progesterone

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Role of the insulin-like growth factor family in cancer development and progression

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Modifier genes in mice and humans

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Mutation and cancer: statistical study of retinoblastoma

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Enemies within: the genesis of retrovirus oncogenes.

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Human EJ bladder carcinoma oncogene is homologue of Harvey sarcoma virus ras gene

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Chromosomal translocations in human cancer.

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A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

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Genome changes and gene expression in human solid tumors

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Integration of cytogenetic landmarks into the draft sequence of the human genome

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The age of cancer

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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Tumor suppressor genes

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Tumour-suppressor genes: evolving definitions in the genomic age

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Cancer-susceptibility genes. Gatekeepers and caretakers

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The murine gene p27Kip1 is haplo-insufficient for tumour suppression

1 reference

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Relaxation of imprinted genes in human cancer.

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Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability

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DNA hypomethylation leads to elevated mutation rates

1 reference

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Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation

1 reference

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Methylation of the oestrogen receptor CpG island links ageing and neoplasia in human colon

1 reference

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Methylation meets genomics

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Genome imprinting, cellular mosaicism and carcinogenesis.

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A strain-specific modifier on mouse chromosome 4 controls the methylation of independent transgene loci

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Inheritance of allelic blueprints for methylation patterns.

1 reference

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How many mutations are required for tumorigenesis? Implications from human cancer data

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Interleukin-1 polymorphisms associated with increased risk of gastric cancer

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Single nucleotide polymorphisms, metabolic activation and environmental carcinogenesis: why molecular epidemiologists should think about enzyme expression

1 reference

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Too many rodent carcinogens: mitogenesis increases mutagenesis

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At the crossroads of inflammation and tumorigenesis

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Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group

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The stromal proteinase MMP3/stromelysin-1 promotes mammary carcinogenesis

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MMP-9 supplied by bone marrow-derived cells contributes to skin carcinogenesis

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A prospective study of endogenous serum hormone concentrations and breast cancer risk in post-menopausal women on the island of Guernsey

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Inherited predisposition to cancer

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Studying cancer in the mouse

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Genetic testing for cancer risk

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Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype

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The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

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Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group

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. . .to a future of genetic medicine

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Association study designs for complex diseases

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

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Cancer resistance genes in mice: models for the study of tumour modifiers

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Quantitative trait loci in Drosophila

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The new genetics in clinical practice

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Will Genetics Revolutionize Medicine?

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Identifiers

10.1038/35077207

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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