The importance of BRCA1 and BRCA2 genes mutations in breast cancer development
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[1] D. West,et al. A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer , 2011, Familial Cancer.
[2] Seyed Mohsen Mousavi,et al. Cancer incidence and mortality in Iran. , 2009, Annals of oncology : official journal of the European Society for Medical Oncology.
[3] L. Cortesi,et al. A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region. , 2009, Clinica chimica acta; international journal of clinical chemistry.
[4] Valerie Beral,et al. Breast cancer and hormone-replacement therapy in the Million Women Study , 2003, The Lancet.
[5] Katri Pylkäs,et al. Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families , 2008, BMC Cancer.
[6] B. Strom,et al. Breast Cancer Risk and Hormone Receptor Status in Older Women by Parity, Age of First Birth, and Breastfeeding: A Case-Control Study , 2008, Cancer Epidemiology Biomarkers & Prevention.
[7] K. Phillips. Immunophenotypic and pathologic differences between BRCA1 and BRCA2 hereditary breast cancers. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[8] Yuntao Xie,et al. BRCA1 germline mutations and tumor characteristics in Chinese women with familial or early-onset breast cancer , 2009, Breast Cancer Research and Treatment.
[9] U. Nöthlings,et al. Identification of a dietary pattern characterized by high-fat food choices associated with increased risk of breast cancer: the European Prospective Investigation into Cancer and Nutrition (EPIC)-Potsdam Study. , 2008, The British journal of nutrition.
[10] T. Walsh,et al. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. , 2006, JAMA.
[11] J. Biswas,et al. Influence of dietary habits, physical activity and affluence factors on breast cancer in East India: a case-control study. , 2009, Asian Pacific journal of cancer prevention : APJCP.
[12] U. Hamann,et al. Similar contributions of BRCA1 and BRCA2 germline mutations to early-onset breast cancer in Germany , 2003, European Journal of Human Genetics.
[13] J. Ferlay,et al. Global Cancer Statistics, 2002 , 2005, CA: a cancer journal for clinicians.
[14] Å. Borg,et al. Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer. , 2001, Journal of the National Cancer Institute.
[15] G. Di,et al. [Mutational analysis of BRCA1 and BRCA2 genes in early-onset breast cancer patients in Shanghai]. , 2005, Zhonghua yi xue za zhi.
[16] S. Teo,et al. BRCA1 and BRCA2 Germline Mutations in Malaysian Women with Early-Onset Breast Cancer without a Family History , 2008, PloS one.
[17] D. Noh,et al. Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation , 2009, Clinical genetics.
[18] Giovanni Parmigiani,et al. Meta-analysis of BRCA1 and BRCA2 penetrance. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[19] Tom L. Blundell,et al. Insights into DNA recombination from the structure of a RAD51–BRCA2 complex , 2002, Nature.
[20] L. Volpi,et al. Mutation analysis of the BRCA1 gene in Malaysian breast cancer patients. , 2002, Singapore medical journal.
[21] G. Lüleci,et al. Genomic Large Rearrangement Screening of BRCA1 and BRCA2 Genes in High-Risk Turkish Breast/Ovarian Cancer Patients by Using Multiplex Ligation-Dependent Probe Amplification Assay , 2011, Cancer investigation.
[22] C. Adebamowo,et al. Parity and breastfeeding are protective against breast cancer in Nigerian women , 2008, British Journal of Cancer.
[23] T. Ozcelik,et al. Germ line BRCA1 and BRCA2 gene mutations in Turkish breast cancer patients. , 2000, European journal of cancer.
[24] A. Musolino,et al. A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes , 2005, Breast Cancer Research and Treatment.
[25] S. Hodgson,et al. Low Prevalence of BRCA1 Exon Rearrangements in Familial and Young Sporadic Breast Cancer Patients , 2006, Familial Cancer.
[26] Norman Boyd,et al. The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer , 2004, Breast Cancer Research.
[27] H. Park,et al. Characteristics and Survival of Breast Cancer Patients with Multiple Synchronous or Metachronous Primary Cancers , 2015, Yonsei medical journal.
[28] M. C. Leske,et al. Alcohol, tobacco and breast cancer – collaborative reanalysis of individual data from 53 epidemiological studies, including 58 515 women with breast cancer and 95 067 women without the disease , 2002, British Journal of Cancer.
[29] Michael J Thun,et al. Overweight, obesity, and mortality from cancer in a prospectively studied cohort of U.S. adults. , 2003, The New England journal of medicine.
[30] C. Szabo,et al. High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area , 2005, Breast Cancer Research.
[31] J. Garcia-conde,et al. Mutational analysis of BRCA1 and BRCA2 in Mediterranean Spanish women with early‐onset breast cancer: Identification of three novel pathogenic mutations , 2003, Human mutation.
[32] H. Barrera-Saldana,et al. Clinical follow up of mexican women with early onset of breast cancer and mutations in the BRCA1 and BRCA2 genes. , 2005, Salud publica de Mexico.
[33] O. Olopade,et al. Advances in Breast Cancer: Pathways to Personalized Medicine , 2008, Clinical Cancer Research.
[34] F. Bray,et al. The changing global patterns of female breast cancer incidence and mortality , 2004, Breast Cancer Research.
[35] S. Fox,et al. Contribution of large genomic BRCA1 alterations to early-onset breast cancer selected for family history and tumour morphology: a report from The Breast Cancer Family Registry , 2011, Breast Cancer Research.
[36] S. Vadaparampil,et al. BRCA1/2 in high-risk African American women with breast cancer: providing genetic testing through various recruitment strategies. , 2008, Genetic testing.
[37] E. Ostrander,et al. Frequency of BRCA1/BRCA2 mutations in a population‐based sample of young breast carcinoma cases , 2000, Cancer.
[38] Douglas F Easton,et al. Cancer Incidence in BRCA1 mutation carriers. , 2002, Journal of the National Cancer Institute.
[39] A. Benider,et al. BRCA1 and BRCA2 germline mutations in Moroccan breast/ovarian cancer families: novel mutations and unclassified variants. , 2012, Gynecologic oncology.
[40] D. Yannoukakos,et al. BRCA2 gene mutations in Greek patients with familial breast cancer , 2002, Human mutation.
[41] N E Day,et al. A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes , 2002, British Journal of Cancer.
[42] V. Poole,et al. Iodide transport and breast cancer. , 2015, The Journal of endocrinology.
[43] G. Lenoir,et al. Analysis of breast cancer susceptibility genes BRCA1 and BRCA2 in Thai familial and isolated early‐onset breast and ovarian cancer , 2002, Human mutation.
[44] M. J. van de Vijver,et al. The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[45] P. Pharoah,et al. BRCA1 and BRCA2 mutations in Russian familial breast cancer , 2002, Human mutation.
[46] Tom Walsh,et al. Ten genes for inherited breast cancer. , 2007, Cancer cell.
[47] L. Esserman,et al. Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry. , 2005, JAMA.
[48] T. Rebbeck,et al. Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program. , 2002, Journal of the National Cancer Institute.
[49] A. Jemal,et al. Global cancer statistics , 2011, CA: a cancer journal for clinicians.
[50] D. Easton,et al. Risk models for familial ovarian and breast cancer , 2000, Genetic epidemiology.
[51] W. Han,et al. BRCA1 and BRCA2 germline mutations in Korean breast cancer patients at high risk of carrying mutations. , 2007, Cancer letters.
[52] Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases , 2009, British Journal of Cancer.
[53] Ilir Agalliu,et al. Familial clustering of breast and prostate cancer and risk of postmenopausal breast cancer in the Women's Health Initiative Study , 2015, Cancer.
[54] D. Saranath,et al. BRCA1/BRCA2 gene mutations/SNPs and BRCA1 haplotypes in early-onset breast cancer patients of Indian ethnicity , 2012, Medical Oncology.
[55] H. Senn,et al. BRCA1/2 mutations in Swiss patients with familial or early-onset breast and ovarian cancer. , 2001, Swiss medical weekly.
[56] M. Jasin,et al. BRCA2 is required for homology-directed repair of chromosomal breaks. , 2001, Molecular cell.
[57] G. Abdulrahman,et al. Epidemiology of Breast Cancer in Europe and Africa , 2012, Journal of cancer epidemiology.
[58] R. Eeles. Future possibilities in the prevention of breast cancer: Intervention strategies in BRCA1 and BRCA2 mutation carriers , 2000, Breast Cancer Research.
[59] H. Neamatzadeh,et al. BRCA1 and BRCA2 mutations in Iranian breast cancer patients: A systematic review , 2015, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.
[60] D. Baralle,et al. Identification of a de novo BRCA1 mutation in a woman with early onset bilateral breast cancer , 2009, Familial Cancer.
[61] B. Kingham,et al. BRCA1 E1644X: a deleterious mutation in an African American individual with early onset breast cancer , 2008, Breast Cancer Research and Treatment.
[62] Qiang Li,et al. Neogenin expression is inversely associated with breast cancer grade in ex vivo , 2014, World Journal of Surgical Oncology.
[63] S. Narod,et al. A low frequency of non‐founder BRCA1 mutations in Ashkenazi Jewish breast–ovarian cancer families , 2002, Human mutation.
[64] R. Dumitrescu,et al. Understanding breast cancer risk ‐ where do we stand in 2005? , 2005, Journal of cellular and molecular medicine.
[65] P. Pharoah,et al. Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases , 2000, British Journal of Cancer.
[66] K. Wani,et al. Mutational analysis of the BRCA2 gene in breast carcinoma patients of Kashmiri descent. , 2014, Molecular medicine reports.
[67] J. Ranstam,et al. Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50 302 women with breast cancer and 96 973 women without the disease , 2002, The Lancet.
[68] K. Kyriacou,et al. Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early‐onset breast cancer in Cyprus , 2007, Clinical genetics.
[69] D. Parkin. International variation , 2004, Oncogene.
[70] R. Sutphen,et al. Identification of the prevalent BRCA1 and BRCA2 mutations in the female population of Puerto Rico. , 2012, Cancer genetics.
[71] J.,et al. The New England Journal of Medicine , 2012 .
[72] Giske Ursin,et al. Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years. , 2006, Cancer research.
[73] G. Ricca,et al. BRCA1 and BRCA2 genetic test in high risk patients and families: counselling and management. , 2010, Oncology reports.
[74] S. Merajver,et al. Factors related to incomplete treatment of breast cancer in Kumasi, Ghana. , 2014, Breast.
[75] S C West,et al. Role of BRCA2 in control of the RAD51 recombination and DNA repair protein. , 2001, Molecular cell.