Found: 40
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Polymorphisms in DNA repair genes and epithelial ovarian cancer risk.
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- International Journal of Cancer, 2005, v. 117, n. 4, p. 611, doi. 10.1002/ijc.21047
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- Article
BRCA2 arg372hispolymorphism and epithelial ovarian cancer risk.
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- International Journal of Cancer, 2003, v. 103, n. 3, p. 427, doi. 10.1002/ijc.10814
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- Article
Frequent loss of BRCA1 mRNA and protein expression in sporadic ovarian cancers.
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- International Journal of Cancer, 2000, v. 87, n. 3, p. 317, doi. 10.1002/1097-0215(20000801)87:3<317::AID-IJC2>3.0.CO;2-B
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- Article
Ovarian and breast cancer risks to women in families with two or more cases of ovarian cancer.
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- International Journal of Cancer, 2000, v. 87, n. 1, p. 110, doi. 10.1002/1097-0215(20000701)87:1<110::AID-IJC16>3.0.CO;2-6
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- Article
Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study.
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- Genetic Epidemiology, 2001, v. 21, n. 1, p. 1, doi. 10.1002/gepi.1014
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- Article
Risk models for familial ovarian and breast cancer.
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- Genetic Epidemiology, 2000, v. 18, n. 2, p. 173, doi. 10.1002/(SICI)1098-2272(200002)18:2<173::AID-GEPI6>3.0.CO;2-R
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- Article
Minisatellite DNA Profiles: Rapid Sample Identification in Linkage Analysis.
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- Human Heredity, 1990, v. 40, n. 2, p. 77, doi. 10.1159/000153909
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- Article
Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population.
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- Carcinogenesis, 2008, v. 29, n. 2, p. 333, doi. 10.1093/carcin/bgm284
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- Article
Common variants in mismatch repair genes and risk of invasive ovarian cancer.
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- Carcinogenesis, 2006, v. 27, n. 11, p. 2235, doi. 10.1093/carcin/bgl089
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- Article
Polymorphisms in CYP1A1 and smoking: no association with breast cancer risk.
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- Carcinogenesis, 2001, v. 22, n. 11, p. 1797, doi. 10.1093/carcin/22.11.1797
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- Article
Polymorphisms in the human aromatase cytochrome P450 gene (CYP19) and breast cancer risk.
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- Carcinogenesis, 2000, v. 21, n. 2, p. 189, doi. 10.1093/carcin/21.2.189
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- Publication type:
- Article
Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.
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- Human Molecular Genetics, 2010, v. 19, n. 14, p. 2886, doi. 10.1093/hmg/ddq174
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- Article
Association of ESR1 gene tagging SNPs with breast cancer risk.
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- Human Molecular Genetics, 2009, v. 18, n. 6, p. 1131, doi. 10.1093/hmg/ddn429
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- Publication type:
- Article
IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancer.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 1, doi. 10.1093/hmg/ddi398
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- Article
Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2349, doi. 10.1093/hmg/ddi237
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- Article
Mutation screening of the CDKN2A promoter in melanoma families.
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- Genes, Chromosomes & Cancer, 2000, v. 28, n. 1, p. 45, doi. 10.1002/(SICI)1098-2264(200005)28:1<45::AID-GCC6>3.0.CO;2-F
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- Article
Determination of the frequency of the common 657Del5 Nnijmegen breakage syndrome mutation in the German population: No association with risk of breast cancer.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 4, p. 393, doi. 10.1002/(SICI)1098-2264(199908)25:4<393::AID-GCC12>3.0.CO;2-8
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- Publication type:
- Article
Increased frequency of TP53 mutations in BRCA1 and BRCA2 ovarian tumours.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 2, p. 91, doi. 10.1002/(SICI)1098-2264(199906)25:2<91::AID-GCC3>3.0.CO;2-5
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- Publication type:
- Article
Family history and the risk of breast cancer: A systematic review and meta-analysis.
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- International Journal of Cancer, 1997, v. 71, n. 5, p. 800, doi. 10.1002/(SICI)1097-0215(19970529)71:5<800::AID-IJC18>3.0.CO;2-B
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- Publication type:
- Article
Identification of Stk6/STK15 as a candidate low-penetrance tumor-susceptibility gene in mouse and human.
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- Nature Genetics, 2003, v. 34, n. 4, p. 403, doi. 10.1038/ng1220
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- Article
310. Discovered Peptide Mediates Specific Binding to Primary Medullary Thyroid Carcinoma after Systemic Injection
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- 2005
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- Abstract
Polygenic susceptibility to breast cancer and implications for prevention.
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- Nature Genetics, 2002, v. 31, n. 1, p. 33, doi. 10.1038/ng853
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- Publication type:
- Article
A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability.
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- Nature Genetics, 2000, v. 26, n. 3, p. 362, doi. 10.1038/81691
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- Article
Mutations truncating the EP300 acetylase in human cancers.
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- Nature Genetics, 2000, v. 24, n. 3, p. 300, doi. 10.1038/73536
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- Publication type:
- Article
Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma.
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- Clinical Endocrinology, 1995, v. 43, n. 1, p. 123, doi. 10.1111/j.1365-2265.1995.tb01903.x
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- Article
Contribution of BRCA1 and BRCA2 mutations to inherited ovarian cancer.
- Published in:
- Human Mutation, 2007, v. 28, n. 12, p. 1207, doi. 10.1002/humu.20599
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- Article
BRCA1 and BRCA2 mutations in Russian familial breast cancer.
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- Human Mutation, 2002, v. 19, n. 2, p. 184, doi. 10.1002/humu.9008
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- Article
Clues to the Function of the Tumour Susceptibility Gene BRCA2.
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- Disease Markers, 1998, v. 14, n. 1, p. 1, doi. 10.1155/1998/613765
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- Article
Variants in DNA double-strand break repair genes and breast cancer susceptibility.
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- Human Molecular Genetics, 2002, v. 11, n. 12, p. 1399, doi. 10.1093/hmg/11.12.1399
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- Publication type:
- Article
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.
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- Human Molecular Genetics, 1995, v. 4, n. 8, p. 1381
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- Article
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.
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- Human Molecular Genetics, 1994, v. 3, n. 12, p. 2163
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- Article
Haplotype analysis of MEN 2 mutations.
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- Human Molecular Genetics, 1994, v. 3, n. 10, p. 1771
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- Publication type:
- Article
A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung‘s disease.
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- Human Molecular Genetics, 1994, v. 3, n. 8, p. 1439
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- Publication type:
- Article
A de novo mutation of the RET proto-oncogene in a patient with MEN 2A.
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- Human Molecular Genetics, 1994, v. 3, n. 6, p. 1007
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- Publication type:
- Article
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.
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- Human Molecular Genetics, 1994, v. 3, n. 2, p. 237
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- Article
Localisation of the gene for multiple endocrine neoplasia type 2A to a 480 kb region in chromosome band 10q11.2.
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- Human Molecular Genetics, 1993, v. 2, n. 3, p. 247
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- Article
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2.
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- Human Molecular Genetics, 1993, v. 2, n. 3, p. 241
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- Article
The JmjC domain-containing histone demethylase KDM3A is a positive regulator of the G<sub>1</sub>/S transition in cancer cells via transcriptional regulation of the HOXA1 gene.
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- International Journal of Cancer, 2012, v. 131, n. 3, p. E179, doi. 10.1002/ijc.26501
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- Article
Dysregulation of PRMT1 and PRMT6, Type I arginine methyltransferases, is involved in various types of human cancers.
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- International Journal of Cancer, 2011, v. 128, n. 3, p. 562, doi. 10.1002/ijc.25366
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- Publication type:
- Article
Overexpression of LSD1 contributes to human carcinogenesis through chromatin regulation in various cancers.
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- International Journal of Cancer, 2011, v. 128, n. 3, p. 574, doi. 10.1002/ijc.25349
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- Article