Chromosome 17 Aneusomy is Associated with Poor Prognostic Factors in Invasive Breast Carcinoma
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J. Bartlett | T. Cooke | J. Going | A. Watters | Timothy G. Cooke | James J. Going | J. M. S. Bartlett
[1] J. R. Reeves,et al. Evaluating HER2 amplification and overexpression in breast cancer , 2001, The Journal of pathology.
[2] A. Cochran,et al. The role of practising pathologists in the generation of novel and original observations , 2001, The Journal of pathology.
[3] J. Inazawa,et al. Detection of chromosomal aneusomy by fluorescence in situ hybridization in fine‐needle aspirates from breast tumors , 2000, Cancer.
[4] J. Eyfjörd,et al. p53 abnormality and chromosomal instability in the same breast tumor cells. , 2000, Cancer genetics and cytogenetics.
[5] M. Mottolese,et al. Incidence of chromosomes 1 and 17 aneusomy in breast cancer and adjacent tissue: an interphase cytogenetic study. , 2000, Journal of the American College of Surgeons.
[6] K. Grigor,et al. Aneusomy of chromosomes 7 and 17 predicts the recurrence of transitional cell carcinoma of the urinary bladder , 2000, BJU international.
[7] Written on behalf of the Biomarkers Ad-hoc Group of the Un Research. Can biological markers improve the management of breast cancer patients? , 2000 .
[8] M. Dowsett,et al. Assessment of HER2 status in breast cancer: why, when and how? , 2000, European journal of cancer.
[9] E. Schröck,et al. Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: A phenotype/genotype correlation , 1999, Genes, chromosomes & cancer.
[10] F. Mertens,et al. Multiple polysomies in breast carcinomas: preferential gain of chromosomes 1, 5, 6, 7, 12, 16, 17, 18, and 19. , 1999, Cancer genetics and cytogenetics.
[11] P. Maxwell,et al. Interphase cytogenetics of chromosomes 11 and 17 in fine needle aspirates of breast cancer. , 1999, Human pathology.
[12] K. Grigor,et al. Is Chromosome 9 Loss a Marker of Disease Recurrence in Transitional Cell Carcinoma of the Urinary Bladder , 1999 .
[13] A. Børresen-Dale,et al. Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters. , 1998, Cancer research.
[14] 市川 大輔. Analysis of numerical aberrations in specific chromosomes by fluorescent in situ hybridization as a diagnostic tool in breast cancer , 1998 .
[15] D. Dillon,et al. The molecular biology of breast cancer: accelerating clinical applications. , 1998, Critical reviews in oncogenesis.
[16] J. R. Reeves,et al. Quantitative radioimmunohistochemical measurements of p185(erbB-2) in frozen tissue sections. , 1996, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[17] D. Slamon,et al. Detection and quantitation of HER-2/neu gene amplification in human breast cancer archival material using fluorescence in situ hybridization. , 1996, Oncogene.
[18] I. Ellis,et al. Prognostic factors in primary breast carcinoma. , 1995, Journal of clinical pathology.
[19] C. Herrington,et al. Correlation of numerical chromosome 11 and 17 imbalance with metastasis of primary breast cancer to lymph nodes , 1995, The Journal of pathology.
[20] E. Mallon,et al. Interphase cytogenetic analysis of erbB2 and topollα co‐amplification in invasive breast cancer and polysomy of chromosome 17 in ductal carcinoma in situ , 1995, International journal of cancer.
[21] S. Wolman. Fluorescence in situ hybridization: a new tool for the pathologist. , 1994, Human pathology.
[22] D. Visscher,et al. Chromosomal aneuploidy in proliferative breast disease. , 1994, Human pathology.