Complex Karyotype with PH¹ Chromosome in Myelodysplasia: Cytogenetic and Molecular Studies

References

• Rowley J. D. A new consistent chromosomal abnormality in chronic myelogenous leukemia identifies by quinacrine fluorescence and Giemsa staining. Nature 1973; 243: 290–291
   PubMed Web of Science ®Google Scholar
• Bernstein R. Cytogenetics of chronic myelogenous leukemia. Sem. Hematol. 1988; 25: 20–34
   PubMed Web of Science ®Google Scholar
• Rowley J. D. Chromosome abnormalities in human leukemia. Annu. Rev. Genet. 1980; 14: 17–39
   PubMed Web of Science ®Google Scholar
• Look A. T. The emerging genetics of acute lymphoblastic leukemia: clinical and biologic implications. Semin. Oncol. 1985; 12: 92–104
   PubMed Web of Science ®Google Scholar
• Whang-Peng J., Henderson R. S., Knutsen T., Freireich E. J., Gart J. J. Cytogenetic studies in acute myelocytic leukemia with special emphasis on the occurrence of the Ph1 chromosome. Blood 1970; 36: 448–457
   PubMed Web of Science ®Google Scholar
• Van den Berghe H., Louwagie A., Broeckaert-Van Orshoven A., David G., Verwilghen R., Michaux J. L., Sokal G. Philadelphia chromosome in multiple myeloma. J. Natl. Cancer Inst. 1979; 63: 11–16
   PubMed Web of Science ®Google Scholar
• Karpas A., Fisher P., Swirsky D. Human myeloma cell line carrying a Philadelphia chromosome. Science 1982; 216: 997–999
   PubMed Web of Science ®Google Scholar
• Ghosh M. L. Primary haemorrhagic thrombocythemia with Philadelphia chromosome. Postgrad Med. J. 1972; 48: 686–688
   PubMed Web of Science ®Google Scholar
• Rajendra B. R., Lee M., Nissemblatt M. J., Gartenberg G., Rose D. V., Sciorra L. J. The occurrence of the Philadelphia chromosome in essential thrombocythemia. Hum. Genet. 1981; 56: 287–291
   PubMed Web of Science ®Google Scholar
• Canellos G. P., Whang-Peng J. Philadelphia-chromosome positive preleukaemia state. Lancet 1972; 2: 1227–1229
   PubMed Web of Science ®Google Scholar
• Shiraishi Y., Yamamoto K., Taguchi H., Ueda N., Shiomi F. Philadelphia chromosome in pure red cell aplasia: A preleukemia state. Cancer. Genet. Cytogenet. 1980; 2: 1–5
   Web of Science ®Google Scholar
• Roth D. G., Richman C. M., Rowley J. D. Chronic myelodysplastic syndrome (preleukemia) with the Philadelphia chromosome. Blood 1980; 56: 262–264
   PubMed Web of Science ®Google Scholar
• Michalski K. A., Miles J. H., Perry M. C. Unusual Ph1 translocation in a preleukemia. Cancer Genet. Cytogenet. 1982; 6: 89–90
   PubMed Web of Science ®Google Scholar
• Berrebi A., Bruck R., Shtalrid M., Chemke J. Philadelphia chromosome in idiopathic acquired sideroblastic anemia. Acta Haemat. 1984; 72: 343–345
   PubMed Web of Science ®Google Scholar
• Ohyashiki K., Ohyashiki J. H., Raza A., Preisler H. D., Sandberg A. A. Phenylbutazone-induced myelodysplastic syndrome with Philadelphia translocation. Cancer Genet. Cytogenet. 1987; 26: 213–216
   PubMed Web of Science ®Google Scholar
• Smadja N., Krulik M., Hagemeijer A., van der Plas D. C., Gonzalez Canalli G., de Gramont A. Cytogenetic and molecular studies of the Philadelphia translocation t(9;22) observed in a patient with myelodysplastic syndrome. Leukemia 1989; 3: 236–238
   PubMed Web of Science ®Google Scholar
• Groffen J., Stephenson J. R., Heisterkamp N., de Klein A., Bartram C. R., Grosveld G. Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22. Cell 1984; 36: 93–99
   PubMed Web of Science ®Google Scholar
• de Klein A., Geurts Van Kessel A., Grosveld G., Bartram C. R., Hagameijer A., Bootsma D., Spurr N. K., Heisterkamp N., Groffen J., Stephenson J. R. A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukemia. Nature 1982; 300: 756–787
   Google Scholar
• Collins S. J., Kubonishi I., Miyoshi 1., Groudine M. T. Altered transcription of c-abl oncogenes in K562 and other chronic myelogenous leukemia cells. Science 1984; 225: 72–74
   PubMed Web of Science ®Google Scholar
• Konopka J. B., Watanabe S. M., Witte O. N. An alteration of the human c-abl protein in K562 leukemia cells, unmasks associated thyrosine kinase activity. Cell 1984; 37: 1035–1042
   PubMed Web of Science ®Google Scholar
• Ben-Neriah Y., Daley G. Q., Mes-Messon A. M., Witte O. N., Baltimore D. The chronic myelogenous leukemia specific P 210 protein is the product of the bcr/abl hybrid gene. Science 1986; 233: 212–214
   PubMed Web of Science ®Google Scholar
• de Klein A., Hagemeijer A., Bartram C. T., Houwen T., Hoefsloot L., Carbonell F., Chan L., Greaves M., Kleihauer E., Heisterkamp N., Groffen J., Grosveld G. bcr Rearrangement and translocation of the c-abl oncogen in Philadelphia positive acute lymphoblastic leukemia. Blood 1986; 68: 1369–1375
   PubMed Web of Science ®Google Scholar
• Kurzrock R., Shtalrid M., Talpaz M., Kloetzer W. S., Gutterman J. U. Expression of c-abl in Philadelphia-positive acute myelogenous leukemia. Blood 1987; 70: 1584–1588
   PubMed Web of Science ®Google Scholar
• Bennett J. M., Catovsky D., Daniel M. T., Flandrin G., Galton D. A. G., Gralnick H. R., Sultan C. Proposal for the classification of the myelodysplastic syndromes. Br. J. Haematol 1986; 51: 189–199
   Web of Science ®Google Scholar
• Seabright M. A rapid banding technique for human chromosomes. Lancet 1971; 2: 971–972
   PubMed Web of Science ®Google Scholar
• ISCN. An International System for Human Cytogenetic Nomenclature. Cytogenet. Cell Genet., 21: 309–404
   PubMedGoogle Scholar
• Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J. Mol. Biol. 1975; 98: 503–517
   PubMed Web of Science ®Google Scholar
• Sambrook J., Fritsch E. F., Maniatis T. Molecular cloning: A laboratory manual, Second Edition. Cold Spring Harbour Laboratory, Cold Spring Harbour, New York 1989
   Google Scholar
• Heim S., Mitelman F. Myelodysplastic syndromes. Cancer Cytogenetics. Alan R. Liss, Inc., New York 1987; 111–128
   Google Scholar
• Morris C. M., Fitzgerald P. H., Hollings P. E., Archer S. A., Rosman I., Beard M. E. J., Heaton D. C., Newhook C. J. Essential thrombocythaemia and the Philadelphia chromosome. Br. J. Haematol. 1988; 70: 13–19
   PubMed Web of Science ®Google Scholar
• Martiat P., Ifrah N., Rassol F., Morgan G., Giles F., Gow J., Goldman J. M. Molecular analysis of Philadelphia positive essential thrombocythemia. Leukemia 1989; 3: 563–565
   PubMed Web of Science ®Google Scholar
• Rodenhuis S., Smets L. A., Slater R. M., Behrendt H., Veerman A. J. P. Distinguishing the Philadelphia chromosome of acute lymphoblastic leukemia from its counterpart in chronic myelogenous leukemia. N. Engl. J. Med. 1985; 313: 51–52
   PubMed Web of Science ®Google Scholar
• Erikson J., Griffin C. A., Ar-Rushdi A., Valtieri M., Hoxied J., Finana J., Emanual B. S., Rover G., Nowell P. C., Croce C. M. Heterogeneity of chromosome 22 breakpoint in Philadelphia (Ph +) acute lymphoblastic leukemia. Proc. Natl. Acad. Sci. USA 1986; 83: 1807–1811
   PubMed Web of Science ®Google Scholar
• Martiat P., Mecucci C., Nizet Y., Stul M., Philippe M., Cassiman J. J., Michaux J. L., Van den Berghe H., Sokal G. P190 BCR/ABL Transcript in a case of Philadelphia-positive multiple myeloma. Leukemia 1990; 4: 751–754
   PubMed Web of Science ®Google Scholar
• Yunis J. J., Rydell R. E., Oken M. M., Arnesen M. A., Mayer M. G., Lobell M. Refined chromosomes analysis as an independent prognostic indicator in de novo myelodysplastic syndromes. Blood 1986; 67: 1721–1730
   PubMed Web of Science ®Google Scholar
• Larripa I., Labal de Vinuesa M., Bengió R., Slavutsky I. Chromosomes studied in human hematologic diseases: II Myelodysplastic syndromes. Haematoloaica 1987; 72: 399–403
   PubMedGoogle Scholar
• Pierre R. V., Catosvky D., Mufti G. J., Swansbury G. J., Mecucci C., Dewald G. W., Ruutu T., Van Den Berghe H., Rowley J. D., Mitelman F., Reeves B. R., Alimena G., Garson O. M., Lawler S. D., de la Chapelle A. Clinical-Cytogenetic correlations in myelodysplasia (Preleukemia). Cancer Genet. Cytogenet. 1989; 40: 149–161
   PubMed Web of Science ®Google Scholar
• Larpipa I., Acevedo S., Slavutsky I. Chromosome abnormalities of 12q in myelodysplastic syndromes. Biol Clin. Hematol. 1991; 13: 23–26
   Google Scholar
• Sutherland G. R., Ledbetter D. H. Human Gene Mapping 10. Report of the committee on cytogenetic markers. Cytogenet. Cell. Genet. 1989; 51: 452–458
   PubMedGoogle Scholar
• Trent J. M., Kaneko Y., Mitelman F. Human Gene Mapping 10. Report of the committee on structural chromosome changes in neoplasia. Cytogenet. Cell Genet. 1989; 51: 533–562
   PubMedGoogle Scholar