Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 21 December 1990:
Vol. 250. no. 4988, pp. 1684 - 1689
DOI: 10.1126/science.2270482

Articles

Science, Vol 250, Issue 4988, 1684-1689
Copyright © 1990 by American Association for the Advancement of Science


articles

Linkage of early-onset familial breast cancer to chromosome 17q21

JM Hall, MK Lee, B Newman, JE Morrow, LA Anderson, B Huey, and MC King

School of Public Health, University of California, Berkeley 94720.

Human breast cancer is usually caused by genetic alterations of somatic cells of the breast, but occasionally, susceptibility to the disease is inherited. Mapping the genes responsible for inherited breast cancer may also allow the identification of early lesions that are critical for the development of breast cancer in the general population. Chromosome 17q21 appears to be the locale of a gene for inherited susceptibility to breast cancer in families with early-onset disease. Genetic analysis yields a lod score (logarithm of the likelihood ratio for linkage) of 5.98 for linkage of breast cancer susceptibility to D17S74 in early-onset families and negative lod scores in families with late-onset disease. Likelihood ratios in favor of linkage heterogeneity among families ranged between 2000:1 and greater than 10(6):1 on the basis of multipoint analysis of four loci in the region.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Polymorphic Variants in Hereditary Pancreatic Cancer Genes Are Not Associated with Pancreatic Cancer Risk.
R. R. McWilliams, W. R. Bamlet, M. de Andrade, D. N. Rider, F. J. Couch, J. M. Cunningham, M. E. Matsumoto, K. G. Rabe, T. J. Hammer, and G. M. Petersen (2009)
Cancer Epidemiol. Biomarkers Prev. 18, 2549-2552
   Abstract »    Full Text »    PDF »
Cancer Prevention: From 1727 to Milestones of the Past 100 Years.
S. M. Lippman and E. T. Hawk (2009)
Cancer Res. 69, 5269-5284
   Abstract »    Full Text »    PDF »
Cancer Prevention Research: Back to the Future.
S. M. Lippman (2009)
Cancer Prevention Research 2, 503-513
   Full Text »    PDF »
Evidence for an Inherited Predisposition Contributing to the Risk for Rotator Cuff Disease.
R. Z. Tashjian, J. M. Farnham, F. S. Albright, C. C. Teerlink, and L. A. Cannon-Albright (2009)
J. Bone Joint Surg. Am. 91, 1136-1142
   Abstract »    Full Text »    PDF »
Two mutations of BRCA2 gene at exon and splicing site in a woman who underwent oncogenetic counseling.
M. Pensabene, I. Spagnoletti, I. Capuano, C. Condello, S. Pepe, A. Contegiacomo, G. Lombardi, G. Bevilacqua, and M. A. Caligo (2009)
Ann. Onc. 20, 874-878
   Abstract »    Full Text »    PDF »
Age-dependent penetrance of different germline mutations in the BRCA1 gene.
F Al-Mulla, J M Bland, D Serratt, J Miller, C Chu, and G T Taylor (2009)
J. Clin. Pathol. 62, 350-356
   Abstract »    Full Text »    PDF »
How Is a Statistical Link Established Between a Human Outcome and a Genetic Variant?.
Guang Guo and D. E. Adkins (2008)
Sociological Methods Research 37, 201-226
   Abstract »    PDF »
BRCA1 Is Required for Meiotic Spindle Assembly and Spindle Assembly Checkpoint Activation in Mouse Oocytes.
B. Xiong, S. Li, J.-S. Ai, S. Yin, Y.-C. OuYang, S.-C. Sun, D.-Y. Chen, and Q.-Y. Sun (2008)
Biol Reprod 79, 718-726
   Abstract »    Full Text »    PDF »
Hereditary breast cancer: from molecular pathology to tailored therapies.
D S P Tan, C Marchio, and J S Reis-Filho (2008)
J. Clin. Pathol. 61, 1073-1082
   Abstract »    Full Text »    PDF »
Genetic and Genomic Discovery Using Family Studies.
I. B. Borecki and M. A. Province (2008)
Circulation 118, 1057-1063
   Full Text »    PDF »
Tilting at Quixotic Trait Loci (QTL): An Evolutionary Perspective on Genetic Causation.
K. M. Weiss (2008)
Genetics 179, 1741-1756
   Abstract »    Full Text »    PDF »
LOT: a tool for linkage analysis of ordinal traits for pedigree data.
M. Zhang, R. Feng, X. Chen, B. Hu, and H. Zhang (2008)
Bioinformatics 24, 1737-1739
   Abstract »    Full Text »    PDF »
Functional Analysis of the Transcription Repressor PLU-1/JARID1B.
A. G. Scibetta, S. Santangelo, J. Coleman, D. Hall, T. Chaplin, J. Copier, S. Catchpole, J. Burchell, and J. Taylor-Papadimitriou (2007)
Mol. Cell. Biol. 27, 7220-7235
   Abstract »    Full Text »    PDF »
Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening.
A Smith, A Moran, M C Boyd, M Bulman, A Shenton, L Smith, R Iddenden, E R Woodward, F Lalloo, E R Maher, et al. (2007)
J. Med. Genet. 44, 10-15
   Abstract »    Full Text »    PDF »
Ashkenazi Jews and Breast Cancer: The Consequences of Linking Ethnic Identity to Genetic Disease.
S. I. Brandt-Rauf, V. H. Raveis, N. F. Drummond, J. A. Conte, and S. M. Rothman (2006)
Am J Public Health 96, 1979-1988
   Abstract »    Full Text »    PDF »
ASCO/SSO Review of Current Role of Risk-Reducing Surgery in Common Hereditary Cancer Syndromes.
J. G. Guillem, W. C. Wood, J. F. Moley, A. Berchuck, B. Y. Karlan, D. G. Mutch, R. F. Gagel, J. Weitzel, M. Morrow, B. L. Weber, et al. (2006)
J. Clin. Oncol. 24, 4642-4660
   Abstract »    Full Text »    PDF »
Familial Aggregation of Illness Chronicity in Recurrent, Early-Onset Major Depression Pedigrees.
F. M. Mondimore, P. P. Zandi, D. F. MacKinnon, M. G. McInnis, E. B. Miller, R. P. Crowe, W. A. Scheftner, D. H. Marta, M. M. Weissman, D. F. Levinson, et al. (2006)
Am J Psychiatry 163, 1554-1560
   Abstract »    Full Text »    PDF »
Genetic Dissection of Complex Traits.
E. S. Lander and N. J. Schork (2006)
Focus 4, 442
   Abstract »    Full Text »    PDF »
Genetic Analysis of Chromosome Pairing, Recombination, and Cell Cycle Control during First Meiotic Prophase in Mammals.
P. E. Cohen, S. E. Pollack, and J. W. Pollard (2006)
Endocr. Rev. 27, 398-426
   Abstract »    Full Text »    PDF »
Deliberate Deceit of Family Members: A Challenge to Providers of Clinical Genetics Services.
J. T. Loud, N. E. Weissman, J. A. Peters, R. M. Giusti, B. S. Wilfond, W. Burke, and M. H. Greene (2006)
J. Clin. Oncol. 24, 1643-1646
   Full Text »    PDF »
BRCA1: cell cycle checkpoint, genetic instability, DNA damage response and cancer evolution.
C.-X. Deng (2006)
Nucleic Acids Res. 34, 1416-1426
   Abstract »    Full Text »    PDF »
Lymphocytes of BRCA1 and BRCA2 germ-line mutation carriers, with or without breast cancer, are not abnormally sensitive to the chromosome damaging effect of moderate folate deficiency.
S. Beetstra, C. Salisbury, J. Turner, M. Altree, R. McKinnon, G. Suthers, and M. Fenech (2006)
Carcinogenesis 27, 517-524
   Abstract »    Full Text »    PDF »
Clinical Correlates and Familial Aggregation of Age at Onset in Bipolar Disorder.
P.-I Lin, M. G. McInnis, J. B. Potash, V. Willour, D. F. MacKinnon, J. R. DePaulo, and P. P. Zandi (2006)
Am J Psychiatry 163, 240-246
   Abstract »    Full Text »    PDF »
Detection of Genes for Ordinal Traits in Nuclear Families and a Unified Approach for Association Studies.
H. Zhang, X. Wang, and Y. Ye (2006)
Genetics 172, 693-699
   Abstract »    Full Text »    PDF »
Tumor suppressor genetics.
S. R. Payne and C. J. Kemp (2005)
Carcinogenesis 26, 2031-2045
   Abstract »    Full Text »    PDF »
Relationship Between a High-Risk Haplotype in the DTNBP1 (Dysbindin) Gene and Clinical Features of Schizophrenia.
A. H. Fanous, E. J. van den Oord, B. P. Riley, S. H. Aggen, M. C. Neale, F. A. O'Neill, D. Walsh, and K. S. Kendler (2005)
Am J Psychiatry 162, 1824-1832
   Abstract »    Full Text »    PDF »
The Role of the BRCA1 Tumor Suppressor in DNA Double-Strand Break Repair.
J. Zhang and S. N. Powell (2005)
Mol. Cancer Res. 3, 531-539
   Abstract »    Full Text »    PDF »
A Haplotype-Based Case-Control Study of BRCA1 and Sporadic Breast Cancer Risk.
M. L. Freedman, K. L. Penney, D. O. Stram, S. Riley, R. McKean-Cowdin, L. Le Marchand, D. Altshuler, and C. A. Haiman (2005)
Cancer Res. 65, 7516-7522
   Abstract »    Full Text »    PDF »
Critical Junctures in Genetic Medicine: The Transformation of DNA Lab Science to Commercial Pharmacogenomics.
S. S. Turner (2005)
Journal of Business and Technical Communication 19, 328-352
   Abstract »    PDF »
Early Adult-Onset POAG Linked to 15q11-13 Using Ordered Subset Analysis.
R. R. Allingham, J. L. Wiggs, E. R. Hauser, K. R. Larocque-Abramson, C. Santiago-Turla, B. Broomer, E. A. Del Bono, F. L. Graham, J. L. Haines, M. A. Pericak-Vance, et al. (2005)
Invest. Ophthalmol. Vis. Sci. 46, 2002-2005
   Abstract »    Full Text »    PDF »
Neurogenetics II: complex disorders.
A F Wright (2005)
J. Neurol. Neurosurg. Psychiatry 76, 623-631
   Abstract »    Full Text »    PDF »
A novel BRCA2 mutation in an Indonesian family found with a new, rapid, and sensitive mutation detection method based on pooled denaturing gradient gel electrophoresis and targeted sequencing.
D Purnomosari, D K Paramita, T Aryandono, G Pals, and P J van Diest (2005)
J. Clin. Pathol. 58, 493-499
   Abstract »    Full Text »    PDF »
N-(4-Hydroxyphenyl)retinamide is more potent than other phenylretinamides in inhibiting the growth of BRCA1-mutated breast cancer cells.
A.-M. Simeone, C.-X. Deng, G. J. Kelloff, V. E. Steele, M. M. Johnson, and A. M. Tari (2005)
Carcinogenesis 26, 1000-1007
   Abstract »    Full Text »    PDF »
An Autosome-Wide Scan for Linkage Disequilibrium-Based Association in Sporadic Breast Cancer Cases in Eastern Finland: Three Candidate Regions Found.
J. M. Hartikainen, H. Tuhkanen, V. Kataja, A. M. Dunning, A. Antoniou, P. Smith, A. Arffman, M. Pirskanen, D. F. Easton, M. Eskelinen, et al. (2005)
Cancer Epidemiol. Biomarkers Prev. 14, 75-80
   Abstract »    Full Text »    PDF »
Haplotype-Based Localization of an Alcohol Dependence Gene to the 5q34 {gamma}-Aminobutyric Acid Type A Gene Cluster.
M. Radel, R. L. Vallejo, N. Iwata, R. Aragon, J. C. Long, M. Virkkunen, and D. Goldman (2005)
Arch Gen Psychiatry 62, 47-55
   Abstract »    Full Text »    PDF »
Linkage analysis of ordinal traits for pedigree data.
R. Feng, J. F. Leckman, and H. Zhang (2004)
PNAS 101, 16739-16744
   Abstract »    Full Text »    PDF »
Functional Phe31Ile polymorphism in Aurora A and risk of breast carcinoma.
T. Sun, X. Miao, J. Wang, W. Tan, Y. Zhou, C. Yu, and D. Lin (2004)
Carcinogenesis 25, 2225-2230
   Abstract »    Full Text »    PDF »
Age at onset in mesial temporal lobe epilepsy with a history of febrile seizures.
J. Janszky, I. Janszky, and A. Ebner (2004)
Neurology 63, 1296-1298
   Abstract »    Full Text »    PDF »
Low-Density Lipoprotein Particle Size Loci in Familial Combined Hyperlipidemia: Evidence for Multiple Loci From a Genome Scan.
M. D. Badzioch, R. P. Igo Jr, F. Gagnon, J. D. Brunzell, R. M. Krauss, A. G. Motulsky, E. M. Wijsman, and G. P. Jarvik (2004)
Arterioscler Thromb Vasc Biol 24, 1942-1950
   Abstract »    Full Text »    PDF »
Truncating BRCA1 Mutations Are Uncommon in a Cohort of Hereditary Prostate Cancer Families with Evidence of Linkage to 17q Markers.
K. A. Zuhlke, J. J. Madeoy, J. Beebe-Dimmer, K. A. White, A. Griffin, E. M. Lange, S. B. Gruber, E. A. Ostrander, and K. A. Cooney (2004)
Clin. Cancer Res. 10, 5975-5980
   Abstract »    Full Text »    PDF »
Oncogenes and Tumor Suppressor Genes in Breast Cancer: Potential Diagnostic and Therapeutic Applications.
C. Osborne, P. Wilson, and D. Tripathy (2004)
Oncologist 9, 361-377
   Abstract »    Full Text »    PDF »
Substantial reduction in risk of breast cancer associated with genetic polymorphisms in the promoters of the matrix metalloproteinase-2 and tissue inhibitor of metalloproteinase-2 genes.
Y. Zhou, C. Yu, X. Miao, W. Tan, G. Liang, P. Xiong, T. Sun, and D. Lin (2004)
Carcinogenesis 25, 399-404
   Abstract »    Full Text »    PDF »
Functional Dissection of Transcription Factor ZBRK1 Reveals Zinc Fingers with Dual Roles in DNA-binding and BRCA1-dependent Transcriptional Repression.
W. Tan, L. Zheng, W.-H. Lee, and T. G. Boyer (2004)
J. Biol. Chem. 279, 6576-6587
   Abstract »    Full Text »    PDF »
BRCA1 c.2845insA is a recurring mutation with a founder effect in Singapore Malay women with early onset breast/ovarian cancer.
J-H Sng, A B Ali, S C Lee, D Zahar, J E L Wong, V Blake, A Sharif, G Cross, and P T C Iau (2003)
J. Med. Genet. 40, e117-117
   Full Text »    PDF »
Stroma Adjacent to Metastatic Mature Teratoma after Chemotherapy for Testicular Germ Cell Tumors Is Derived from the Same Progenitor Cells as the Teratoma.
D. W. Brandli, T. M. Ulbright, R. S. Foster, O. W. Cummings, S. Zhang, C. J. Sweeney, J. N. Eble, and L. Cheng (2003)
Cancer Res. 63, 6063-6068
   Abstract »    Full Text »    PDF »
Genetic loading in familial migraine with aura.
S E Noble-Topham, M Z Cader, D A Dyment, G P A Rice, J D Brown, and G C Ebers (2003)
J. Neurol. Neurosurg. Psychiatry 74, 1128-1130
   Abstract »    Full Text »    PDF »
Breast and Ovarian Cancer.
R. Wooster and B. L. Weber (2003)
N. Engl. J. Med. 348, 2339-2347
   Full Text »    PDF »
Roles of BRCA1 in DNA damage repair: a link between development and cancer.
C.-X. Deng and R.-H. Wang (2003)
Hum. Mol. Genet. 12, R113-123
   Abstract »    Full Text »    PDF »
Clinical challenges posed by new biotechnology.
D Castle (2003)
Postgrad. Med. J. 79, 65-66
   Full Text »    PDF »
Finding genetic contributions to sporadic disease: A recessive locus at 12q24 commonly contributes to patent ductus arteriosus.
A. Mani, S.-M. Meraji, R. Houshyar, J. Radhakrishnan, A. Mani, M. Ahangar, T. M. Rezaie, M.-A. Taghavinejad, B. Broumand, H. Zhao, et al. (2002)
PNAS 99, 15054-15059
   Abstract »    Full Text »    PDF »
Cancer Incidence in BRCA1 Mutation Carriers.
D. Thompson, D. F. Easton, and the Breast Cancer Linkage Consortium (2002)
J Natl Cancer Inst 94, 1358-1365
   Abstract »    Full Text »    PDF »
Cancer Risk Estimates for BRCA1 Mutation Carriers Identified in a Risk Evaluation Program.
M. S. Brose, T. R. Rebbeck, K. A. Calzone, J. E. Stopfer, K. L. Nathanson, and B. L. Weber (2002)
J Natl Cancer Inst 94, 1365-1372
   Abstract »    Full Text »    PDF »
Sex hormone-binding globulin polymorphisms in familial and sporadic breast cancer.
A. Forsti, Q. Jin, E. Grzybowska, M. Soderberg, H. Zientek, M. Sieminska, J. Rogozinska-Szczepka, E. Chmielik, B. Utracka-Hutka, and K. Hemminki (2002)
Carcinogenesis 23, 1315-1320
   Abstract »    Full Text »    PDF »
A multigenerational family with multiple sclerosis.
D. A. Dyment, M. Z. Cader, C. J. Willer, N. Risch, A. D. Sadovnick, and G. C. Ebers (2002)
Brain 125, 1474-1482
   Abstract »    Full Text »    PDF »
BRCA1 transcriptionally regulates genes involved in breast tumorigenesis.
P. L. Welcsh, M. K. Lee, R. M. Gonzalez-Hernandez, D. J. Black, M. Mahadevappa, E. M. Swisher, J. A. Warrington, and M.-C. King (2002)
PNAS 99, 7560-7565
   Abstract »    Full Text »    PDF »
Variation in BRCA1 Cancer Risks by Mutation Position.
D. Thompson and D. Easton (2002)
Cancer Epidemiol. Biomarkers Prev. 11, 329-336
   Abstract »    Full Text »    PDF »
Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility.
M M de Jong, I M Nolte, G J te Meerman, W T A van der Graaf, J C Oosterwijk, J H Kleibeuker, M Schaapveld, and E G E de Vries (2002)
J. Med. Genet. 39, 225-242
   Abstract »    Full Text »    PDF »
Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.
E. K. Silverman, J. D. Mosley, L. J. Palmer, M. Barth, J. M. Senter, A. Brown, J. M. Drazen, D. J. Kwiatkowski, H. A. Chapman, E. J. Campbell, et al. (2002)
Hum. Mol. Genet. 11, 623-632
   Abstract »    Full Text »    PDF »
BRCA1 and BRCA2 Mutation Frequency in Women Evaluated in a Breast Cancer Risk Evaluation Clinic.
H. A. Shih, F. J. Couch, K. L. Nathanson, M. A. Blackwood, T. R. Rebbeck, K. A. Armstrong, K. Calzone, J. Stopfer, S. Seal, M. R. Stratton, et al. (2002)
J. Clin. Oncol. 20, 994-999
   Abstract »    Full Text »    PDF »
Comorbid Bipolar Disorder and Panic Disorder in Families With a High Prevalence of Bipolar Disorder.
D. F. MacKinnon, P. P. Zandi, J. Cooper, J. B. Potash, S. G. Simpson, E. Gershon, J. Nurnberger, T. Reich, and J. R. DePaulo (2002)
Am J Psychiatry 159, 30-35
   Abstract »    Full Text »    PDF »
Tamoxifen and Breast Cancer Incidence Among Women With Inherited Mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial.
M.-C. King, S. Wieand, K. Hale, M. Lee, T. Walsh, K. Owens, J. Tait, L. Ford, B. K. Dunn, J. Costantino, et al. (2001)
JAMA 286, 2251-2256
   Abstract »    Full Text »    PDF »
Clinical Characteristics of Prostate Cancer in an Analysis of Linkage to Four Putative Susceptibility Loci.
E. L. Goode, J. L. Stanford, M. A. Peters, M. Janer, M. Gibbs, S. Kolb, M. D. Badzioch, L. Hood, E. A. Ostrander, and G. P. Jarvik (2001)
Clin. Cancer Res. 7, 2739-2749
   Abstract »    Full Text »    PDF »
The Genetic Epidemiology of Cancer: Interpreting Family and Twin Studies and Their Implications for Molecular Genetic Approaches.
N. Risch (2001)
Cancer Epidemiol. Biomarkers Prev. 10, 733-741
   Abstract »    Full Text »    PDF »
Pathological Features and BRCA1 Mutation Screening in Premenopausal Breast Cancer Patients.
J. Chang, S. G. Hilsenbeck, J. H. Sng, J. Wong, and G. C. Ragu (2001)
Clin. Cancer Res. 7, 1739-1742
   Abstract »    Full Text »    PDF »
Admixture Analysis of Age at Onset in Bipolar I Affective Disorder.
F. Bellivier, J.-L. Golmard, C. Henry, M. Leboyer, and F. Schurhoff (2001)
Arch Gen Psychiatry 58, 510-512
   Full Text »    PDF »
BRCA1 and BRCA2 and the genetics of breast and ovarian cancer.
P. L. Welcsh and M.-C. King (2001)
Hum. Mol. Genet. 10, 705-713
   Abstract »    Full Text »    PDF »
Allele-sharing among affected relatives: non-parametric methods for identifying genes.
M.-C. Shih and A. S Whittemore (2001)
Statistical Methods in Medical Research 10, 27-55
   Abstract »    PDF »
Genetic Disease, Genetic Testing, and the Clinician.
K. C. Smith (2001)
JAMA 285, 91
   Full Text »    PDF »
Allelic imbalance on chromosomes 13 and 17 and mutation analysis of BRCA1 and BRCA2 genes in monozygotic twins concordant for breast cancer.
A. Forsti, L. Luo, I. Vorechovsky, M. Soderberg, P. Lichtenstein, and K. Hemminki (2001)
Carcinogenesis 22, 27-33
   Abstract »    Full Text »    PDF »
Familial Breast and Ovarian Cancer: A Swedish Population-based Register Study.
H. Anderson, A. Bladstrom, H. Olsson, and T. R. Moller (2000)
Am. J. Epidemiol. 152, 1154-1163
   Abstract »    Full Text »    PDF »
Statistical designs for familial aggregation.
K.-Y. Liang and T. H Beaty (2000)
Statistical Methods in Medical Research 9, 543-562
   Abstract »    PDF »
Effect of Radiotherapy After Breast-Conserving Treatment in Women With Breast Cancer and Germline BRCA1/2 Mutations.
L. J. Pierce, M. Strawderman, S. A. Narod, I. Oliviotto, A. Eisen, L. Dawson, D. Gaffney, L. J. Solin, A. Nixon, J. Garber, et al. (2000)
J. Clin. Oncol. 18, 3360-3369
   Abstract »    Full Text »    PDF »
Randomized Trial of a Specialist Genetic Assessment Service for Familial Breast Cancer.
K. Brain, J. Gray, P. Norman, E. France, C. Anglim, G. Barton, E. Parsons, A. Clarke, H. Sweetland, M. Tischkowitz, et al. (2000)
J Natl Cancer Inst 92, 1345-1351
   Abstract »    Full Text »    PDF »
Why Are the Majority of Hereditary Cases of Early-Onset Breast Cancer Sporadic? A Simulation Study.
J. Cui and J. L. Hopper (2000)
Cancer Epidemiol. Biomarkers Prev. 9, 805-812
   Abstract »    Full Text »
Familial Aggregation: Sorting Susceptibility From Shared Environment.
G. M. Petersen (2000)
J Natl Cancer Inst 92, 1114-1115
   Full Text »    PDF »
Genetic and Hormonal Risk Factors in Breast Cancer.
A.-M. Martin and B. L. Weber (2000)
J Natl Cancer Inst 92, 1126-1135
   Abstract »    Full Text »    PDF »
Intention to Undergo Prophylactic Bilateral Mastectomy in Women at Increased Risk of Developing Hereditary Breast Cancer.
B. Meiser, P. Butow, M. Friedlander, V. Schnieden, M. Gattas, J. Kirk, G. Suthers, E. Haan, and K. Tucker (2000)
J. Clin. Oncol. 18, 2250-2257
   Abstract »    Full Text »    PDF »
Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancer.
B. MEISER, P. BUTOW, A. BARRATT, G. SUTHERS, M. SMITH, A. COLLEY, E. THOMPSON, and K. TUCKER (2000)
J. Med. Genet. 37, 472-476
   Full Text »
Functional Assay for BRCA1: Mutagenesis of the COOH-Terminal Region Reveals Critical Residues for Transcription Activation.
F. Hayes, C. Cayanan, D. Barillà, and A. N. A. Monteiro (2000)
Cancer Res. 60, 2411-2418
   Abstract »    Full Text »
BRCA1 and E-Cadherin Promoter Hypermethylation and Gene Inactivation in Cancer--Association or Mechanism?.
E. R. Fearon (2000)
J Natl Cancer Inst 92, 515-517
   Full Text »    PDF »
Promoter Hypermethylation and BRCA1 Inactivation in Sporadic Breast and Ovarian Tumors.
M. Esteller, J. M. Silva, G. Dominguez, F. Bonilla, X. Matias-Guiu, E. Lerma, E. Bussaglia, J. Prat, I. C. Harkes, E. A. Repasky, et al. (2000)
J Natl Cancer Inst 92, 564-569
   Abstract »    Full Text »    PDF »
Risk assessment in first degree female relatives of breast cancer patients using the alkaline Comet assay.
N. Rajeswari, Y.R. Ahuja, U. Malini, S. Chandrashekar, N. Balakrishna, K.V. Rao, and A. Khar (2000)
Carcinogenesis 21, 557-561
   Abstract »    Full Text »    PDF »
Establishment of a radiation- and estrogen-induced breast cancer model.
G. M. Calaf and T. K. Hei (2000)
Carcinogenesis 21, 769-776
   Abstract »    Full Text »    PDF »
Communicating Genetic Risk: Pros, Cons, and Counsel.
R. T. Penson, M. V. Seiden, K. M. Shannon, M. L. Lubratovich, M. Roche, B. A. Chabner, and T. J. Lynch Jr. (2000)
Oncologist 5, 152-161
   Abstract »    Full Text »
Age and sex based genetic locus heterogeneity in type 1 diabetes.
A. D Paterson and A. Petronis (2000)
J. Med. Genet. 37, 186-191
   Abstract »    Full Text »
A model protocol evaluating the introduction of genetic assessment for women with a family history of breast cancer.
J. Gray, K. Brain, P. Norman, C. Anglim, L. France, G. Barton, L. Branston, E. Parsons, A. Clarke, J. Sampson, et al. (2000)
J. Med. Genet. 37, 192-196
   Abstract »    Full Text »
Why do women attend familial breast cancer clinics?.
K. Brain, J. Gray, P. Norman, E. Parsons, A. Clarke, C. Rogers, R. Mansel, and P. Harper (2000)
J. Med. Genet. 37, 197-202
   Abstract »    Full Text »
Cancer Risk Estimates for Family Members of a Population-based Family Registry for Breast and Ovarian Cancer.
A. Ziogas, M. Gildea, P. Cohen, D. Bringman, T. H. Taylor, D. Seminara, D. Barker, G. Casey, R. Haile, S.-Y. Liao, et al. (2000)
Cancer Epidemiol. Biomarkers Prev. 9, 103-111
   Abstract »    Full Text »
Interactions of the Nijmegen Breakage Syndrome Protein with ATM and BRCA1.
X. WU, G. RATHBUN, W.S. LANE, D.T. WEAVER, and D.M. LIVINGSTON (2000)
Cold Spring Harb Symp Quant Biol 65, 535-546
   Abstract »    PDF »
Chromosomal Instability and Cancer Predisposition: Insights from Studies on the Breast Cancer Susceptibility Gene, BRCA2.
A.R. VENKITARAMAN (2000)
Cold Spring Harb Symp Quant Biol 65, 567-572
   Abstract »    PDF »
Genetic Polymorphisms and Risk of Breast Cancer.
S. S. Coughlin and M. Piper (1999)
Cancer Epidemiol. Biomarkers Prev. 8, 1023-1032
   Full Text »
Survival in Hereditary Breast Cancer Associated With Germline Mutations of BRCA2.
L. C. Verhoog, C.T.M. Brekelmans, C. Seynaeve, G. Dahmen, A. N. van Geel, C.C.M. Bartels, M.M.A. Tilanus-Linthorst, A. Wagner, P. Devilee, D.J.J. Halley, et al. (1999)
J. Clin. Oncol. 17, 3396-3402
   Abstract »    Full Text »    PDF »
BRCA1/BRCA2 Germline Mutations in Locally Recurrent Breast Cancer Patients After Lumpectomy and Radiation Therapy: Implications for Breast-Conserving Management in Patients With BRCA1/BRCA2 Mutations.
B. C. Turner, E. Harrold, E. Matloff, T. Smith, A. A. Gumbs, M. Beinfield, B. Ward, M. Skolnick, P. M. Glazer, A. Thomas, et al. (1999)
J. Clin. Oncol. 17, 3017-3024
   Abstract »    Full Text »    PDF »
Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancer.
Y. Y. SHUGART, C. COUR, H. RENARD, G. LENOIR, D. GOLDGAR, D. TEARE, D. EASTON, N. RAHMAN, R. GUSTERTON, S. SEAL, et al. (1999)
J. Med. Genet. 36, 720-721
   Full Text »
Association of BRCA1 with the hRad50-hMre11-p95 Complex and the DNA Damage Response.
Q. Zhong, C. Chen, S. Li, Y. Chen, C. Wang, J. Xiao, P. Chen, Z. D. Sharp, and W. Lee (1999)
Science 285, 747-750
   Abstract »    Full Text »
Prevalence of BRCA1 and BRCA2 Gene Mutations in Patients With Early-Onset Breast Cancer.
J. Peto, N. Collins, R. Barfoot, S. Seal, W. Warren, N. Rahman, D. F. Easton, C. Evans, J. Deacon, and M. R. Stratton (1999)
J Natl Cancer Inst 91, 943-949
   Abstract »    Full Text »    PDF »
Positive Regulation of the BRCA1 Promoter.
S. Thakur and C. M. Croce (1999)
J. Biol. Chem. 274, 8837-8843
   Abstract »    Full Text »    PDF »
Hereditary Factors in Gynecologic Cancer.
H. T. Lynch, M. J. Casey, T. G. Shaw, and J. F. Lynch (1998)
Oncologist 3, 319-338
   Abstract »    Full Text »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)