First application of the Automated QUantitative Analysis (AQUA) technique to quantify PTEN protein expression in ovarian cancer: A correlative study of NCIC CTG OV.16 von Weberpals, J.I, Amin, M.S, Chen, B.E, Tu, D, Spaans, J.N, Squire, J.A, Eisenhauer, E.A, Virk, S, Ma, D, Duciaume, M, Hoskins, P, LeBrun, D.P

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Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas von Veiga-Castelli, L C, Silva, J C Rosa E, Meola, J, Ferriani, R A, Yoshimoto, M, Santos, S A, Squire, J A, Martelli, L

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Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer von Sadikovic, B, Al-Romaih, K, Squire, J A, Zielenska, M

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High-resolution cDNA microarray CGH mapping of genomic imbalances in osteosarcoma using formalin-fixed paraffin-embedded tissue von Zielenska, M., Marrano, P., Thorner, P., Pei, J., Beheshti, B., Ho, M., Bayani, J., Liu, Y., Sun, B.C., Squire, J.A., Hao, X.-S.

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MP-17.17: FISH analysis of 107 prostate cancers shows that PTEN genomic deletion is associated with poor clinical outcome von Yoshimoto, M, Cunha, I.W, Coudry, R.A, Fonseca, F.P, Torres, C.H, Soares, F.A, Squire, J.A

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The Role of RUNX2 in Osteosarcoma Oncogenesis von van Wijnen, A. J., Zielenska, Maria, Stein, Gary S., Squire, Jeremy A., Martin, Jeff W.

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Breast cancer 1 (BRCA1) protein expression as a prognostic marker in sporadic epithelial ovarian carcinoma: an NCIC CTG OV.16 correlative study von Weberpals, J.I., Tu, D., Squire, J.A., Amin, M.S., Islam, S., Pelletier, L.B., O'Brien, A.M., Hoskins, P.J., Eisenhauer, E.A.

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PTEN deletion detected using dual-color FISH in esophageal squamous cell carcinoma correlates with poor prognosis von Sato-Kuwabara, Y, Yoshimoto, M, Neves, J.I, Squire, J.A, Soares, F.A

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Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH von Selvarajah, S., Yoshimoto, M., Ludkovski, O., Park, P.C., Bayani, J., Thorner, P., Maire, G., Squire, J.A., Zielenska, M.

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Topographical analysis of telomere length and correlation with genomic instability in whole mount prostatectomies von Joshua, A.M., Shen, E., Yoshimoto, M., Marrano, P., Zielenska, M., Evans, A.J., Van der Kwast, T., Squire, J.A.

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Prostatic preneoplasia and beyond von Joshua, A.M., Evans, A., Van der Kwast, T., Zielenska, M., Meeker, A.K., Chinnaiyan, A., Squire, J.A.

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Correlating breakage-fusion-bridge events with the overall chromosomal instability and in vitro karyotype evolution in prostate cancer von Vukovic, B., Beheshti, B., Park, P., Lim, G., Bayani, J., Zielenska, M., Squire, J.A.

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Integrated Cytogenetic and High-Resolution Array CGH Analysis of Genomic Alterations Associated with MYCN Amplification von Pandita, A., Bayani, J., Paderova, J., Marrano, P., Graham, C., Barrett, M., Prasad, M., Zielenska, M., Squire, J.A.

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Analysis of Segmental Duplications, Mouse Genome Synteny and Recurrent Cancer-Associated Amplicons in Human Chromosome 6p21–p12 von Martin, J.W., Yoshimoto, M., Ludkovski, O., Thorner, P.S., Zielenska, M., Squire, J.A., Nuin, P.A.S.

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Supplement Material for: Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH von karger, figshare admin, Squire, J.A.

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The use of cytogenetics in understanding ovarian cancer von Bernardini, M., Weberpals, J., Squire, J.A.

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Use of whole genome amplification and comparative genomic hybridisation to detect chromosomal copy number alterations in cell line material and tumour tissue von Hughes, S., Lim, G., Beheshti, B., Bayani, J., Marrano, P., Huang, A., Squire, J.A.

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Assignment of the Human Prostaglandin-Endoperoxide Synthase 2 (PTGS2) Gene to 1q25 by Fluorescence in Situ Hybridization von Tay, A., Squire, J.A., Goldberg, H., Skorecki, K.

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Identification of a high frequency of chromosomal rearrangements in the centromeric regions of prostate cancer cell lines by sequential Giemsa banding and spectral karyotyping von Beheshti, B., Karaskova, J., Park, P.C., Squire, J.A., Beatty, B.G.

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Supplementary Material for: Analysis of Segmental Duplications, Mouse Genome Synteny and Recurrent Cancer-Associated Amplicons in Human Chromosome 6p21–p12 von Martin, J.W., Yoshimoto, M., Ludkovski, O., Thorner, P.S., Zielenska, M., Squire, J.A., Nuin P.A.S.

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