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• W2080632007 abstract "Annals of the New York Academy of SciencesVolume 677, Issue 1 p. 194-198 Molecular Cytogenetic Analysis of Human Tumors a JOE W. GRAY, JOE W. GRAY Department of Laboratory Medicine Division of Molecular Cytometry University of California, San Francisco San Francisco, California 94143-0808Search for more papers by this author JOE W. GRAY, JOE W. GRAY Department of Laboratory Medicine Division of Molecular Cytometry University of California, San Francisco San Francisco, California 94143-0808Search for more papers by this author First published: March 1993 https://doi.org/10.1111/j.1749-6632.1993.tb38777.xCitations: 4 a This work was supported by the Office of Health and Environmental Research under Contract No. DE-AC-3-76SF00098 and by Imagenetics. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL References 1 Trask, B. & D. Pinkel.1990. Fluorescence in situ hybridization with DNA probes. Methods Cell Biol. 33: 383– 400. 2 Trask. B., G. Van Den Engh, D. Pinkel, J. Mullikin, F. Waldman, H. Van Dekken & J. Gray.1988. Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization. Hum. Genet. 78: 251– 259. 3 Harper, M. & G. Saunders.1981. Localization of a single copy DNA sequence to G-banded human chromosomes by in situ hybridization. Chromosoma 83: 431– 439. 4 Van Dekken, H., D. Pinkel, J. Mullikin & J. W. Gray.1988. Enzymatic production of single-stranded DNA as a target for fluorescence in situ hybridization. Chromosoma 97: 1– 5. 5 Pinkel. D., J. Landegent, C. Collins, J. Fuscoe, R. Segraves, J. Lucas & J. Gray.1988. Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. Proc. Natl. Acad. Sci. U.S.A. 85: 9138– 9142. 6 Lighter, P., T. Cremer, J. Borden, L. Manuelidis & D. C. Ward.1988. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum. Genet. 80: 224– 234. 7 Langer, P., A. Waldorp & D. Ward.1981. Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes. Proc. Natl. Acad. Sci. U.S.A. 78: 6633– 6637. 8 Zhang, F. R., R. Heilig, G. Thomas & A. Aurias.1990. A one-step efficient and specific non-radioactive non-fluorescent method for in situ hybridization of banded chromosomes. Chromosoma 99: 436– 439. 9 Landegent, J., N. Jansen in de Wal, R. Baan, J. Hoeijmakers & M. Van Der Ploeg.1984. 2-Acetylaminofluorene-modified probes for the indirect hybridocytochemical detection of specific nucleic acid sequences. Exp. Cell Res. 153: 61– 72. 10 Pinkel, D., T. Straume & J. Gray.1986. Cytogenetic analysis using quantitative, high sensitivity fluorescence in situ hybridization. Proc. Natl. Acad. Sci. U.S.A. 83: 2934– 2938. 11 Eastmond, D. A. & D. Pinkel.1989. Aneuploidy detection by analysis of interphase nuclei using fluorescence in situ hybridization with chromosome-specific probes. Prog. Clin. Biol. Res. 318: 277– 284. 12 Willard, H. F.1990. Centromeres of mammalian chromosomes. Trends Genet. 6: 410– 416. 13 Balazs, M., B. H. Mayali. & F. M. Waldman.1991. Interphase cytogenetics of a male breast cancer. Cancer Genet. Cytogenet. 55: 243– 247. 14 Bauman, J., D. Pinkel, M. Van Der Ploeg & B. Trask.1989. Flow cytometric measurement of specific DNA and RNA sequences. In Flow Cytogenetics. J. Gray, Ed. : 276– 303. Academic Press. New York/London . 15 Van Dekken, H., D. Pinkel, J. Mullikin, B. Trask, G. Van Den Engh & J. Gray.1989. Three-dimensional reconstruction of human chromosomes in hybrid and human cell line nuclei using fluorescence in situ hybridization. Acta Histochem. Suppl. 37: 91– 94. 16 Collins, C, W. L. Kuo, R. Segraves, J. Fuscoe, D. Pinkel & J. W. Gray.1991. Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes. Genomics 11: 997– 1006. 17 Gray, J. W., J. Lucas, O. Kallioniemi, A. Kallioniemi, W. L. Kuo, T. Straume, D. Tkachuk, T. Tenjin, H. U. Weier & D. Pinkel.1991. Applications of fluorescence in situ hybridization in biological dosimetry and detection of disease-specific chromosome aberrations. Prog. Clin. Biol. Res. 372: 399– 411. 18 Matsumura, K., A. Kallioniemi, O. Kallioniemi, L. Chen, H. S. Smith, D. Pinkel, J. Gray & F. M. Waldman.1992. Deletion of chromosome 17p loci in breast cancer cells detected by fluorescence in situ hybridization. Cancer Res. 52: 3474– 3477. 19 Gray, J., A. Kallioniemi, O. Kallioniemi, M. Pallavicini, F. Waldman & D. Pinkel.1992. Molecular Cytogenetics: Diagnosis and Prognostic Assessment. GATA. In press. 20 Tkachuk, D. C, C. A. Westbrook, M. Andreeff, T. A. Donlon, M. L. Cleary, K. Suryanarayan, M. Homge, A. Redner, J. Gray & D. Pinkel.1990. Detection of bcr-ab) fusion in chronic myelogeneous leukemia by in situ hybridization. Science 250: 559– 562. 21 Kallioniemi, O., A. Kallioniemi, W. Kurisu, A. Thor, L. Chen, H. Smith, F. Waldman, D. Pinkel & J. Gray.1992. ERBB2 amplification in breast cancer analyzed by fluorescence in situ hybridization. Proc. Natl. Acad. Sci. U.S.A. 89: 5321– 5325. 22 Ried, T., A. Baldini, T. C. Rand & D. C. Ward.1992. Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy. Proc. Natl. Acad. Sci. U.S.A. 89: 1388– 1392. 23 Nederlof, P. M., D. Robinson, R. Abuknesha, J. Wiegant, A. H. Hopman, H. J. Tanke & A. K. Raap.1989. Three-color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequences. Cytometry 10: 20– 27. 24 Lichter, P., C. J. Tang, K. Call, G. Hermanson, G. A. Evans, D. Housman & D. C. Ward.1990. High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science 247: 64– 69. 25 White, R.1992. Inherited cancer genes. Curr. Opin. Genet. Dev. 2: 53– 57. 26 Kallioniemi, A., O. Kallioniemi, F. Waldman, L-C. Chen, L-C. Yu, Y. Fung, H. S. Smith, D. Pinkel & J. Gray.1992. Detection of retinoblastoma gene copy number in metaphase chromosomes in interphase nuclei by fluorescence in situ hybridization. Cytogenet. Cell Genet. 60: 190– 193. 27 Arnoldus, E. P., J. Wiegant, I. A. Noordermeer, J. W. Wessels, G. C. Beverstock, G. C. Grosveld, M. Van Der Ploeg & A. K. Raap.1990. Detection of the Philadelphia chromosome in interphase nuclei. Cytogenet. Cell Genet. 54: 108– 111. Citing Literature Volume677, Issue1Clinical Flow CytometryMarch 1993Pages 194-198 ReferencesRelatedInformation" @default.
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