An improved high throughput heteroduplex mutation detection system for screening BRCA2 mutations—fluorescent mutation detection (F‐MD)
暂无分享,去创建一个
R. Eeles | Z. Kote-Jarai | S. Edwards | R. Eeles | R. Hamoudi | R A Eeles | S M Edwards | Z Kote-Jarai | R Hamoudi
[1] M. Stratton,et al. The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer. The Cancer Research Campaign/British Prostate Group United Kingdom Familial Prostate Cancer Study Collaborators. , 2000, Cancer research.
[2] J. Mendell,et al. A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient , 1993, Nature Genetics.
[3] E. Gross,et al. A highly sensitive, fast, and economical technique for mutation analysis in hereditary breast and ovarian cancers , 1999, Human mutation.
[4] B. Ponder,et al. Rapid detection of regionally clustered germ-line BRCA1 mutations by multiplex heteroduplex analysis. UKCCCR Familial Ovarian Cancer Study Group. , 1996, American journal of human genetics.
[5] H. Olsson. Cancer risks in BRCA2 mutation carriers. , 1999, Journal of the National Cancer Institute.
[6] Sheila Seal,et al. BRCA2 mutations in primary breast and ovarian cancers , 1996, Nature Genetics.
[7] I. Verma,et al. Transcriptional activation by BRCA1 , 1996, Nature.
[8] D. Bentley,et al. Identification of the breast cancer susceptibility gene BRCA2 , 1995, Nature.
[9] D. Schaid,et al. Genetic heterogeneity in Peutz‐Jeghers syndrome , 2000, Human mutation.
[10] D. Bentley,et al. Mutation detection by fluorescent chemical cleavage: application to hemophilia B. , 1994, PCR methods and applications.
[11] Hui Tian,et al. BRCA1 physically associates with p53 and stimulates its transcriptional activity , 1998, Oncogene.
[12] J. Klijn,et al. Rapid detection of BRCA1 mutations by the protein truncation test , 1995, Nature Genetics.
[13] A. Ashworth,et al. A missense mutation in the BRCA2 gene in three siblings with ovarian cancer. , 1998, British Journal of Cancer.
[14] T. Sekiya,et al. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[15] E. Gross,et al. A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC , 1999, Human Genetics.
[16] D. Livingston,et al. Genetic analysis of BRCA1 function in a defined tumor cell line. , 1999, Molecular cell.
[17] J. Uitto,et al. Cloning of the human type XVII collagen gene (COL17A1), and detection of novel mutations in generalized atrophic benign epidermolysis bullosa. , 1997, American journal of human genetics.
[18] P. Underhill,et al. Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations. , 1999, Human molecular genetics.
[19] D J Prockop,et al. Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[20] Julian Peto,et al. Identification of the breast cancer susceptibility gene BRCA2 , 1996, Nature.
[21] A. Ashworth,et al. Identification of the familial cylindromatosis tumour-suppressor gene , 2000, Nature Genetics.
[22] R. Eeles,et al. No germline mutations in the dimerization domain of MXI1 in prostate cancer clusters. The CRC/BPG UK Familial Prostate Cancer Study Collaborators. Cancer Research Campaign/British Prostate Group. , 1997, British Journal of Cancer.
[23] A. Ganguly,et al. High throughput fluorescence-based conformation-sensitive gel electrophoresis (F-CSGE) identifies six unique BRCA2 mutations and an overall low incidence of BRCA2 mutations in high-risk BRCA1-negative breast cancer families , 1998, Human Genetics.
[24] J. D. den Dunnen,et al. Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test. , 1994, Genomics.
[25] Phang-lang Chen,et al. Expression of BRC Repeats in Breast Cancer Cells Disrupts the BRCA2-Rad51 Complex and Leads to Radiation Hypersensitivity and Loss of G2/M Checkpoint Control* , 1999, The Journal of Biological Chemistry.
[26] B. Weber,et al. Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing. , 2000, American journal of human genetics.
[27] F. Collins,et al. Human BRCA1 inhibits growth in yeast: potential use in diagnostic testing. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[28] J Chang-Claude,et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. , 1998, American journal of human genetics.
[29] M. Stratton,et al. Screening for BRCA2 mutations in 81 Dutch breast–ovarian cancer families , 1999, British Journal of Cancer.
[30] F. Couch,et al. Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells. , 1998, Molecular cell.
[31] R. Cotton. Mutation detection by chemical cleavage. , 1999, Genetic analysis : biomolecular engineering.