- BAUCHINGER, M., SCHMID, E., ZITZELSBERGER, H., BRASELMANN, H. and NAHRSTBDT, U., 1993, Radiation-induced chromosome aberrations analysed by two-colour fluorescence in situ hybridization with composite whole chromosome-specific DNA probes and a pancentromeric DNA probe. International Journal of Radiation Biology, 64, 179-184.
- BOEI, J. J. W. A. and NATARAIAN, A. T., 1996, Classification of X-ray-induced Robertsonian fusion-like configurations in mouse Splenocytes. International Journal of Radiation Biology. 69, 421-427.
- BOEI, J. J. W. A., BALAIEE, A.S., DE BOER, P., RENS, W., ATEN, J. A., MULLENDERS, L. H. F. and NATARAIAN, A. T., 1994, Construction of mouse chromosome-specific DNA libraries and their use for the detection of X-ray-induced aberrations. International Journal of Radiation Biology, 65, 583-590.
- BOEI, J. J. W. A., VERMEULEN, S. and NATARAIAN, A. T., 1996, Detection of chromosomal aberrations by fluorescence in situ hybridization in the first three postirradiation divisions of human lymphocytes. Mutation Research, 349, 127-135.
- BOBI, J. J. W. A., VERMEULEN, S. and NATARAIAN, A. T., 1997, Differential involvement of chromosomes 1 and 4 in the formation of chromosomal aberrations in human lymphocytes after X-irradiation. International Journal of Radiation Biology, 72, 139-145.
- BOUFFLER, S., SILVER, A., PAPWORTH, D., COATES, J. and Cox, R., 1993, Murine radiation myeloid leukaemogenesis: relationship between interstitial telomere-like sequences and chromosome 2 fragile sites. Genes, Chromosomes & Cancer, 6, 98-106.
- BROCCOLI, D., MILLER, O. J. and MILLER, D. A., 1990, Relationship of mouse minor satellite DNA to centromere activity. Cytogenelics and Cell Genetics, 54, 182-186.
- CREMER, T., KURZ, A., ZIRBEL, R., DIBTZEL, S., RINKE, B., SCHROCK, E., SPEICHER, M. R., MATHIEU, U., JAUCH, A., EMMERICH, P., SCHERTAN, H., RIED, T., CREMER, C. and LICHTER, P., 1993, Role of chromosome territories in the functional compartimentalization of the cell nucleus. Cold Spring Harbor Symposia on Quantitative Biology (New York, Cold Spring Harbor), 58, 777-792.
- DIETRICH, W. F., MILLER, J., STEBN, R., MERCHANT, M. A., DAMRON-BOLES, D., HUSAIN, Z., DREDGE, R., DALY, M. J., INGALLS, K. A., O'CONNOR, T. J., EVANS, C. A. et al. 1996, A comprehensive genetic map of the mouse genome. Nature, 380, 149-152.
- DOMINGUEZ, I., BOBI, J. J. W. A., BALAIBE, A. S. and NATARAIAN, A. T., 1996, Analysis of radiation-induced chromosome aberrations in Chinese hamster cells by FISH using Chromosome-Specific DNA libraries. International Journal of Radiation Biology, 70, 199-208.
- FINNON, P., LLOYD, D. C. and EDWARDS, A. A., 1995, Fluorescence in situ hybridization detection of chromosomal aberrations in human lymphocytes: applicability to biological dosimetry. International Journal of Radiation Biology, 68, 429-435.
- GRIGOROVA, M., BRAND, R. and NATARAIAN, A. T., 1997, Analysis of radiation-induced chromosomal aberrations in Chinese hamster splenocytes by FISH using chromosome Specific DNA libraries. International Journal of Radiation Biology (submitted).
- HANDE, M. P., BOEI, J. J. W. A., GRANATH, F. and NATARAIAN, A. T., 1996, Induction and persistence of cytogenetic damage in mouse splenocytes following whole-body X-irradiation analysed by fluorescence in situ hybridization. I. DicentriCS and translocations. International Journal of Radiation Biology, 69, 437-446.
- IJDO, J. W., WELLS, R. A., BALDINI, A. and REEDERS, S. T., 1991, Improved telomere detection using a telomere repeat probe (TTAGGG)n generated by PCR. Nucleic Acids Research, 19, 4780.
- KIPLING, D., ACKFORD, H. E., TAYLOR, B. A. and COOKE, H. J., 1991, Mouse minor satellite DNA genetically maps to the centromere and is physically linked to the proximal telomere. Genomics, 11, 235-241.
- KIPLING, D. and COOKE, H. J., 1990, Hypervariable ultra-long telomeres in mice. Nature, 347, 400-402.
- KNEHR, S., ZITZELSBERGER, H., BRASELMANN, H. and BAUCHINGER, M., 1994, Analysis for DNA-proportional distribution of radiation-induced chromosome aberrations in various triple combinations of human chromosomes Using fluorescence in situ hybridization. International Journal of Radiation Biology, 65, 683-690.
- KNEHR, S., ZITZELSBERGER, H., BRASELMANN, H., NAHRSTEDT, U. and BAUCHINGER, M., 1996, Chromosome analysis by fluorescence in situ hybridization: further indications for a non-DNA-proportional involvement of single chromosomes in radiation-induced structural aberrations. International Journal of Radiation Biology, 70, 385-392.
- KODAMA, Y., NAKANO, M., OHTAKI, K., DELONGCHAMP, R., AWA, A. A. and NAKAMURA, N., 1997, Estimation of minimal size of translocated chromosome segments detectable by fluorescence in situ hybridization, international Journal of Radiation Biology, 71, 35-39.
- LUCAS, J. N., TENJIN, T., STRAUME, T., PINKEL, D., MOORE, II D., LITT, M. and GRAY, J. W., 1989, Rapid human chromosome aberration analysis using fluorescence in situ hybridization. International Journal of Radiation Biology, 56, 35-44.
- MASUMOTO, H., MASUKATA, H., MURO, Y., NOZAKI, N. and OKAZAKI, T., 1989, A human centromere antigen (CENP-B) interacts with a short specific sequence in alphoid DNA, a human centromeric satellite. Journal of Cell Biology, 109, 1963-1973.
- NATARAJAN, A. T., BALAJEE, A. S., BOEI, J. J. W. A., CHATTERJEE, S., DARROUDI, F., GRIGOROVA, M., NODITI, M., OH, H. J., SLIJEPCEVIC, P. and VERMEULEN, S., 1994, Recent developments in the assessment of Chromosomal damage. International Journal of Radiation Biology, 66, 615-623.
- NATARAIAN, A. T., BOEI, J. J. W. A., VERMEULEN, S. and BALAIEE, A. S., 1996, Frequencies of X-ray induced pericentric inversions and centric rings in human blood lymphocytes detected by FISH using chromosome armSpecific DNA libraries. Mutation Research, 372, 1-7.
- NATARAJAN, A. T., VYAS, R. C., DARROUDI, F. and VERMEULEN,S., 1992, Frequencies of X-ray-induced chromosome translocations in human peripheral lymphocytes as detected by in situ hybridization using chromosome-specific DNA libraries. International Journal of Radiation Biology, 61, 199-203.
- PIETRAS, D. F., BENNETT, K. L., SIRACUSA, L. D., WOODWORTH-GUTAI, M., CHAPMAN, V. M., GROSS, K. W., KANE-HAAS, C. and HASTIB, N. D., 1983, Construction of a small M us musculus repetitive DNA library: identification of a new satellite sequence in MUS musculus. Nucleic Acids Research, 11, 6965-6983.
- SAVAGE, J. R. K. and SIMPSON, P. J., 1994, FISH 'painting' patterns resulting from complex exchanges. Mutation Research, 312, 51-60.
- SCHMID, E., ZITZELSBERGER, H., BRASELMANN, H., GRAY, J. W. and BAUCHINGER, M., 1992, Radiation-induced chromosome aberrations analysed by fluorescence in situ hybridization with a triple combination of composite whole Chromosome-Specific DNA probes. International Journal of Radiation Biology, 62, 673-678.
- SPRUILL, M. D., RAMSEY, M. J., SWIGER, R. R., NATH, J. and TUCKER, J. D., 1996, The persistence of aberrations in mice induced by gamma radiation as measured by chromosome painting. Mutation Research, 356, 135-145.
- STRAUMB, T. and LUCAS, J. N., 1993, A comparison of the yields of translocations and dicentrics measured using fluorescence in situ hybridization. International Journal of Radiation Biology, 64, 185-187.
- TUCKER, J. D., LEE, D. A. and MOORE, II D. H., 1995a, Validation of chromosome painting. II. A detailed analysis of aberrations following high doses of ionizing radiation in vitro. International Journal of Radiation Biology, 67, 19-28.
- TUCKER, J. D., MORGAN, W. F., AWA, A. A., BAUCHINGER, M., BLAKEY, D., CORNFORTH, M. N., LITTLEFIELD, L. G., NATARAJAN, A. T. and SHASSERRE, C., 1995b, A proposed system for scoring structural aberrations detected by Chromosome painting. Cytogenetics and Cell Genetics, 68, 211-221.
- TUCKER, J. D., RAMSEY, M. J., LEE, D. A. and MINKLER, J. L., 1993, Validation of chromosome painting as a biodosimeter in human peripheral lymphocytes following acute exposure to ionizing radiation in vitro. International Journal of Radiation Biology, 64, 27-37.
- WEIER, H-U. G., LUCAS, J. N., POGGENSEE, M., SEGRAVES, R., PINKEL, D. and GRAY, J. W., 1991, Two-color hybridization with high complexity chromosome-specific probes and a degenerate alpha satellite probe DNA allows unambiguous discrimination between symmetrical and asymmetrical translocations, chromosoma, 100, 371-376.
- WONG, A. K. C. and RATTNER, J. B., 1988, Sequence organization and cytological localization of the minor satellite of mouse. Nucleic Acids Research, 16, 11645-11661.
Combined use of chromosome painting and telomere detection to analyse radiation-induced chromosomal aberrations in mouse splenocytes
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