메뉴 건너뛰기




Volumn 186, Issue 1, 2008, Pages 12-18

Pattern of trisomy 1q in hematological malignancies: a single institution experience

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; ADULT; AGED; ARTICLE; CHROMOSOME 14; CHROMOSOME 15; CHROMOSOME 16; CHROMOSOME 19; CHROMOSOME 1Q; CHROMOSOME 7; CHROMOSOME TRANSLOCATION 1; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; LEUKEMOGENESIS; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; TRISOMY; Y CHROMOSOME;

EID: 51249121800     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2008.05.003     Document Type: Article
Times cited : (15)

References (33)
  • 1
    • 2542423217 scopus 로고
    • Chromosomal changes in primary and metastatic tumors and in lymphomas: their nonrandomness and significance
    • Arrighi F.F., Rao P.N., and Stublefield E. (Eds), Raven, New York
    • Sandberg A.A., and Wake N. Chromosomal changes in primary and metastatic tumors and in lymphomas: their nonrandomness and significance. In: Arrighi F.F., Rao P.N., and Stublefield E. (Eds). Genes, Chromosomes and Neoplasia (1981), Raven, New York 297
    • (1981) Genes, Chromosomes and Neoplasia , pp. 297
    • Sandberg, A.A.1    Wake, N.2
  • 2
    • 0023008771 scopus 로고
    • Trisomy 1q in polycythemia vera and its relation to disease transition
    • Swolin B., Weinfeild A., and Westin J. Trisomy 1q in polycythemia vera and its relation to disease transition. Am J Hematol 22 (1986) 155-167
    • (1986) Am J Hematol , vol.22 , pp. 155-167
    • Swolin, B.1    Weinfeild, A.2    Westin, J.3
  • 3
    • 0021925745 scopus 로고
    • The pattern and clinical significance of karyotypic abnormalities in patients with idiopathic and postpolycythemic myelofibrosis
    • Miler J.B., Testa J.R., Lindgren V., and Rowley J.D. The pattern and clinical significance of karyotypic abnormalities in patients with idiopathic and postpolycythemic myelofibrosis. Cancer 55 (1985) 582-591
    • (1985) Cancer , vol.55 , pp. 582-591
    • Miler, J.B.1    Testa, J.R.2    Lindgren, V.3    Rowley, J.D.4
  • 4
    • 0026356617 scopus 로고
    • Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes
    • Fonatsch C., Haase D., Freund M., Bartles H., and Tesch M. Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes. Cancer Genet Cytogenet 56 (1991) 243-253
    • (1991) Cancer Genet Cytogenet , vol.56 , pp. 243-253
    • Fonatsch, C.1    Haase, D.2    Freund, M.3    Bartles, H.4    Tesch, M.5
  • 6
    • 0032030675 scopus 로고    scopus 로고
    • Jumping translocations of chromosome 1q in multiple myeloma: evidence for a mechanism involving decondensation of pericentromeric heterochromatin
    • Sawyer J.R., Tricot G., Mattox S., Jugannath S., and Barlogie B. Jumping translocations of chromosome 1q in multiple myeloma: evidence for a mechanism involving decondensation of pericentromeric heterochromatin. Blood 9 (1998) 1732-1741
    • (1998) Blood , vol.9 , pp. 1732-1741
    • Sawyer, J.R.1    Tricot, G.2    Mattox, S.3    Jugannath, S.4    Barlogie, B.5
  • 7
    • 0024801447 scopus 로고
    • Abnormalities of chromosome 1 in relation to human malignant diseases
    • Olah E., Balogh E., Kovacs I., and Kiss A. Abnormalities of chromosome 1 in relation to human malignant diseases. Cancer Genet Cytogenet 43 (1989) 179-194
    • (1989) Cancer Genet Cytogenet , vol.43 , pp. 179-194
    • Olah, E.1    Balogh, E.2    Kovacs, I.3    Kiss, A.4
  • 8
    • 0029010609 scopus 로고
    • Der(16)t(1;16)(q11;q11) in myelodysplastic syndromes: a new non-random abnormality characterized by cytogenetic and fluorescence in situ hybridization studies
    • Mugneret F., Dastugue N., Favre B., Sidaner I., Salles B., Huguet-Rigal F., and Solary E. Der(16)t(1;16)(q11;q11) in myelodysplastic syndromes: a new non-random abnormality characterized by cytogenetic and fluorescence in situ hybridization studies. Br J Haematol 90 (1995) 119-124
    • (1995) Br J Haematol , vol.90 , pp. 119-124
    • Mugneret, F.1    Dastugue, N.2    Favre, B.3    Sidaner, I.4    Salles, B.5    Huguet-Rigal, F.6    Solary, E.7
  • 9
    • 0027184450 scopus 로고
    • Partial trisomy 1q, an uncommon chromosomal aberration in erythroleukemia
    • Baumgarten E., Wagner R.D., Fengler R., Koch H., and Hanze G. Partial trisomy 1q, an uncommon chromosomal aberration in erythroleukemia. Leuk Lymphoma 10 (1993) 237-240
    • (1993) Leuk Lymphoma , vol.10 , pp. 237-240
    • Baumgarten, E.1    Wagner, R.D.2    Fengler, R.3    Koch, H.4    Hanze, G.5
  • 13
    • 0034177695 scopus 로고    scopus 로고
    • Jumping translocations of 11q in acute myeloid leukemia and 1q in follicular lymphoma
    • Fan Y.-S., Rizkalla K., William B.F., and Engel C.J. Jumping translocations of 11q in acute myeloid leukemia and 1q in follicular lymphoma. Cancer Genet Cytogenet 118 (2000) 35-41
    • (2000) Cancer Genet Cytogenet , vol.118 , pp. 35-41
    • Fan, Y.-S.1    Rizkalla, K.2    William, B.F.3    Engel, C.J.4
  • 15
    • 0021248730 scopus 로고
    • Does multisomy of chromosome 1q confer a proliferative advantage in B-cell acute lymphoblastic leukemia?
    • Morris C.M., Fitzgerald M., Neville M.A., Wyld R.J., and Beard M.E.J. Does multisomy of chromosome 1q confer a proliferative advantage in B-cell acute lymphoblastic leukemia?. Cancer 54 (1984) 48-53
    • (1984) Cancer , vol.54 , pp. 48-53
    • Morris, C.M.1    Fitzgerald, M.2    Neville, M.A.3    Wyld, R.J.4    Beard, M.E.J.5
  • 16
    • 0028286174 scopus 로고
    • Rapid method for obtaining high-quality chromosome banding in the study of hematopoietic neoplasia
    • Novak A., Kruškic M., Ludoski M., and Jurukovski V. Rapid method for obtaining high-quality chromosome banding in the study of hematopoietic neoplasia. Cancer Genet Cytogenet 74 (1994) 109-114
    • (1994) Cancer Genet Cytogenet , vol.74 , pp. 109-114
    • Novak, A.1    Kruškic, M.2    Ludoski, M.3    Jurukovski, V.4
  • 18
    • 0018392825 scopus 로고
    • Cloning of satellite III DNA: different components are on different chromosomes
    • Cooke H.J., and Hindley J. Cloning of satellite III DNA: different components are on different chromosomes. Nucleic Acids Res 6 (1979) 3177-3197
    • (1979) Nucleic Acids Res , vol.6 , pp. 3177-3197
    • Cooke, H.J.1    Hindley, J.2
  • 19
    • 51249105090 scopus 로고    scopus 로고
    • Generation of a whole chromosome painting probe from monochromosomal hybrid cells by the ALU-polymerase chain reaction
    • Drakulić D., Nikčević G., Djordjević V., and Stevanović M. Generation of a whole chromosome painting probe from monochromosomal hybrid cells by the ALU-polymerase chain reaction. Arch Biol Sci 59 (2007) 89-95
    • (2007) Arch Biol Sci , vol.59 , pp. 89-95
    • Drakulić, D.1    Nikčević, G.2    Djordjević, V.3    Stevanović, M.4
  • 21
    • 0025094268 scopus 로고
    • Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines
    • Lichter P., Ledbetter S.A., Ledbetter D.H., and Ward D.C. Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines. Proc Natl Acad Sci USA 87 (1990) 6634-6638
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 6634-6638
    • Lichter, P.1    Ledbetter, S.A.2    Ledbetter, D.H.3    Ward, D.C.4
  • 22
    • 0022573439 scopus 로고
    • Chromosome 1 aberrations in cancer
    • Atkin N.B. Chromosome 1 aberrations in cancer. Cancer Genet Cytogenet 21 (1986) 279-285
    • (1986) Cancer Genet Cytogenet , vol.21 , pp. 279-285
    • Atkin, N.B.1
  • 23
    • 0034005973 scopus 로고    scopus 로고
    • Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodisplasic syndrome following treatment for a primitive neuroectodermal tumor
    • Mathew S., Head D., Rodrigez-Galindo C., and Raimondi S.C. Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodisplasic syndrome following treatment for a primitive neuroectodermal tumor. Leuk Lymph 37 (2000) 213-218
    • (2000) Leuk Lymph , vol.37 , pp. 213-218
    • Mathew, S.1    Head, D.2    Rodrigez-Galindo, C.3    Raimondi, S.C.4
  • 24
    • 0035395724 scopus 로고    scopus 로고
    • Derivative (1;18)(q10;q10): a recurrent and novel unbalanced translocation involving 1q in myeloid disorderders
    • Wan T.S.K., Ma S.K., Au W.Y., and Chan L.C. Derivative (1;18)(q10;q10): a recurrent and novel unbalanced translocation involving 1q in myeloid disorderders. Cancer Genet Cytogenet 128 (2001) 35-38
    • (2001) Cancer Genet Cytogenet , vol.128 , pp. 35-38
    • Wan, T.S.K.1    Ma, S.K.2    Au, W.Y.3    Chan, L.C.4
  • 27
    • 0033081639 scopus 로고    scopus 로고
    • Frequent hypomethylation in Wilms' tumors of pericentric DNA in chromosomes 1 and 16
    • Qu G.-Z., Grundy P.E., Narayan A., and Ehrlich M. Frequent hypomethylation in Wilms' tumors of pericentric DNA in chromosomes 1 and 16. Cancer Genet Cytogenet 109 (1999) 34-39
    • (1999) Cancer Genet Cytogenet , vol.109 , pp. 34-39
    • Qu, G.-Z.1    Grundy, P.E.2    Narayan, A.3    Ehrlich, M.4
  • 28
    • 0032848853 scopus 로고    scopus 로고
    • Two children with acute lymphoblastic leukemia and "jumping" translocations: both involve 1q23 as the donor breakpoint
    • Jarvis A., Sharma P., Watson N., and Smith A. Two children with acute lymphoblastic leukemia and "jumping" translocations: both involve 1q23 as the donor breakpoint. Cancer Genet Cytogenet 114 (1999) 112-116
    • (1999) Cancer Genet Cytogenet , vol.114 , pp. 112-116
    • Jarvis, A.1    Sharma, P.2    Watson, N.3    Smith, A.4
  • 30
    • 0033992433 scopus 로고    scopus 로고
    • Do rosette, heterochromatin, and/or genomic imprinting influence preferential translocations in human neoplasia?
    • Verma R.S. Do rosette, heterochromatin, and/or genomic imprinting influence preferential translocations in human neoplasia?. Cancer Genet Cytogenet 116 (2000) 174-175
    • (2000) Cancer Genet Cytogenet , vol.116 , pp. 174-175
    • Verma, R.S.1
  • 31
    • 0033967643 scopus 로고    scopus 로고
    • Jumping translocation in acute leukemia of myelomonocytic lineage: a case report and review of the literature
    • Bernard M., Lemee F., Picard F., Ghandour C., Drenou B., Le Prise P.Y., and Lamy T. Jumping translocation in acute leukemia of myelomonocytic lineage: a case report and review of the literature. Leukemia 14 (2000) 119-122
    • (2000) Leukemia , vol.14 , pp. 119-122
    • Bernard, M.1    Lemee, F.2    Picard, F.3    Ghandour, C.4    Drenou, B.5    Le Prise, P.Y.6    Lamy, T.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.