Cytogenetic instability in ovarian epithelial cells from women at risk of ovarian cancer.
暂无分享,去创建一个
Philippe Thuillier | Abdellatif Errami | J. Cain | N. Ameziane | F. Cappuccini | S. Olson | P. Thuillier | L. Hays | A. Bale | Allen E Bale | Tanja Pejovic | Jane E Yates | Hong Y Liu | Laura E Hays | Yassmine Akkari | Yumi Torimaru | Winifred Keeble | R Keaney Rathbun | William H Rodgers | Najim Ameziane | C Michael Zwaan | Fabio Cappuccini | Susan B Olson | Joanna M Cain | Grover C Bagby | A. Errami | W. Rodgers | J. Yates | G. Bagby | W. Keeble | R. Rathbun | Yassmine Akkari | Y. Torimaru | T. Pejovic | C. Zwaan | H. Y. Liu | Yumi Torimaru
[1] H. Nelson,et al. Genetic Risk Assessment and BRCA Mutation Testing for Breast and Ovarian Cancer Susceptibility: Recommendation Statement , 2005 .
[2] H. Katabuchi,et al. Pathophysiological dynamics of human ovarian surface epithelial cells in epithelial ovarian carcinogenesis. , 2005, International review of cytology.
[3] G. Bagby. Genetic basis of Fanconi anemia , 2003, Current opinion in hematology.
[4] M. Lensch,et al. Selective pressure as an essential force in molecular evolution of myeloid leukemic clones: a view from the window of Fanconi anemia , 1999, Leukemia.
[5] K. Offit. Clinical Cancer Genetics: Risk Counseling and Management , 1998 .
[6] G. Pals,et al. X-linked inheritance of Fanconi anemia complementation group B , 2004, Nature Genetics.
[7] K.-L Xu,et al. Loss of heterozygosity at chromosome 3p in epithelial ovarian cancer in China , 2001, International Journal of Gynecologic Cancer.
[8] R. Moses,et al. Hypersensitivity to oxygen is a uniform and secondary defect in Fanconi anemia cells. , 1993, Mutation research.
[9] C. Roskelley,et al. The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancer , 2003, Reproductive biology and endocrinology : RB&E.
[10] M. Walton,et al. Characterisation of the P53 status, BCL‐2 expression and radiation and platinum drug sensitivity of a panel of human ovarian cancer cell lines , 1998, International journal of cancer.
[11] M. Grompe,et al. Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice. , 2003, Genes & development.
[12] G. Woude,et al. Abnormal Centrosome Amplification in the Absence of p53 , 1996, Science.
[13] S. Olson,et al. Cisplatin and the sensitive cell , 2003, Nature Medicine.
[14] J. Grill,et al. Conditionally replicative adenovirus expressing p53 exhibits enhanced oncolytic potency. , 2002, Cancer research.
[15] B. Johansson,et al. Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders , 2005, Genes, chromosomes & cancer.
[16] C. Mathew,et al. Disruption of the Fanconi anemia–BRCA pathway in cisplatin-sensitive ovarian tumors , 2003, Nature Medicine.
[17] J. Cheng,et al. Molecular alterations of the AKT2 oncogene in ovarian and breast carcinomas , 1995, International journal of cancer.
[18] A. D’Andrea,et al. A novel diagnostic screen for defects in the Fanconi anemia pathway. , 2002, Blood.
[19] R. Berkowitz,et al. Genetic alterations of the WT1 gene in papillary serous carcinoma of the peritoneum. , 2000, Gynecologic oncology.
[20] C. Mathew,et al. The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J , 2005, Nature Genetics.
[21] G. Bagby,et al. FANCC interacts with Hsp70 to protect hematopoietic cells from IFN-gamma/TNF-alpha-mediated cytotoxicity. , 2001, The EMBO journal.
[22] W. B. Smith,et al. A Role for Endothelial NO Synthase in LTP Revealed by Adenovirus-Mediated Inhibition and Rescue , 1996, Science.
[23] M. Inoue,et al. K-ras activation occurs frequently in mucinous adenocarcinomas and rarely in other common epithelial tumors of the human ovary. , 1991, The American journal of pathology.
[24] T. Richmond,et al. Analysis of chromosome breakpoints in neuroblastoma at sub‐kilobase resolution using fine‐tiling oligonucleotide array CGH , 2005, Genes, chromosomes & cancer.
[25] S. Ganesan,et al. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. , 2001, Molecular cell.
[26] Joe W. Gray,et al. PIK3CA is implicated as an oncogene in ovarian cancer , 1999, Nature Genetics.
[27] Tracy A Wolff,et al. Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility. , 2006, American family physician.
[28] G. Chenevix-Trench,et al. Frequent PTEN/MMAC mutations in endometrioid but not serous or mucinous epithelial ovarian tumors. , 1998, Cancer research.
[29] D. Beier,et al. Generation of murine stromal cell lines supporting hematopoietic stem cell proliferation by use of recombinant retrovirus vectors encoding simian virus 40 large T antigen , 1988, Molecular and cellular biology.
[30] W Godolphin,et al. Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer. , 1989, Science.
[31] D. Zwijnenburg,et al. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification. , 2002, Nucleic acids research.
[32] Christopher G Mathew,et al. Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways. , 2004, Human molecular genetics.
[33] D. Näf,et al. Functional Activity of the Fanconi Anemia Protein FAA Requires FAC Binding and Nuclear Localization , 1998, Molecular and Cellular Biology.
[34] M. Wigler,et al. Circular binary segmentation for the analysis of array-based DNA copy number data. , 2004, Biostatistics.
[35] J. Ott,et al. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia , 2005, Nature Genetics.
[36] A. D’Andrea,et al. S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51. , 2002, Blood.
[37] Thomas D. Schmittgen,et al. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.
[38] A. D’Andrea,et al. Carboxy terminal region of the Fanconi anemia protein, FANCG/XRCC9, is required for functional activity. , 2000, Blood.
[39] J. Schouten,et al. Methylation-Specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences , 2005, Nucleic acids research.
[40] J W Gray,et al. NOEY2 (ARHI), an imprinted putative tumor suppressor gene in ovarian and breast carcinomas. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[41] H. Tashiro,et al. c‐myc over‐expression in human primary ovarian tumours: Its relevance to tumour progression , 1992, International journal of cancer.
[42] Hans Joenje,et al. Biallelic Inactivation of BRCA2 in Fanconi Anemia , 2002, Science.