메뉴 건너뛰기




Volumn 30, Issue 5-6, 1998, Pages 443-448

The unexplored 5q13 locus: A role in hematopoietic malignancies

Author keywords

5q13; AML; MDS; Myeloblastic leukemia; Myelodysplastic syndromes; Physical mapping

Indexed keywords

DNA MARKER;

EID: 0031851185     PISSN: 10428194     EISSN: None     Source Type: Journal    
DOI: 10.3109/10428199809057556     Document Type: Review
Times cited : (17)

References (34)
  • 1
    • 0023478436 scopus 로고
    • Karyotype is prognostically more important than the FAB system's distinction between myelodysplastic syndrome and acute myelogenous leukemia
    • Estey, E. H., Keating, M. J., Dixon, D. O., Trujillo, J. M., McCredie, K. B. and Freiriech, E. J. (1987). Karyotype is prognostically more important than the FAB system's distinction between myelodysplastic syndrome and acute myelogenous leukemia. Hematologic Pathology, 1, 203-208.
    • (1987) Hematologic Pathology , vol.1 , pp. 203-208
    • Estey, E.H.1    Keating, M.J.2    Dixon, D.O.3    Trujillo, J.M.4    McCredie, K.B.5    Freiriech, E.J.6
  • 3
    • 0030592517 scopus 로고    scopus 로고
    • Lessons from hereditary colorectal cancer
    • Kinsler, K. W. and Vogelstein, B. (1996). Lessons from hereditary colorectal cancer. Cell, 87(2), 159-170.
    • (1996) Cell , vol.87 , Issue.2 , pp. 159-170
    • Kinsler, K.W.1    Vogelstein, B.2
  • 6
    • 0028214564 scopus 로고
    • Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: Delineation of the critical region on 5q and identification of a 5q- breakpoint
    • Boultwood, J., Fidler, C., Lewis, S., Kelly, S., Sheridan, H., Littlewood, T. J., Buckle, V. J. and Wainscoat, J. S. (1994). Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint. Genomics, 19, 425-432.
    • (1994) Genomics , vol.19 , pp. 425-432
    • Boultwood, J.1    Fidler, C.2    Lewis, S.3    Kelly, S.4    Sheridan, H.5    Littlewood, T.J.6    Buckle, V.J.7    Wainscoat, J.S.8
  • 9
    • 9544254827 scopus 로고    scopus 로고
    • Translocations and deletions of 5q13.1 in myelodysplasia and acute myelogenous leukemia: Evidence for a novel critical locus
    • Fairman, J., Wang, R. Y., Liang, H., Zhao, L., Saltman, D., Liang, J. C. and Nagarajan, L. (1996). Translocations and deletions of 5q13.1 in myelodysplasia and acute myelogenous leukemia: evidence for a novel critical locus. Blood, 88, 2259-2266.
    • (1996) Blood , vol.88 , pp. 2259-2266
    • Fairman, J.1    Wang, R.Y.2    Liang, H.3    Zhao, L.4    Saltman, D.5    Liang, J.C.6    Nagarajan, L.7
  • 10
    • 0029796608 scopus 로고    scopus 로고
    • Polymerase chain reaction-based diagnosis of del(5q) in acute myeloid leukemia and myelodysplastic syndrome identifies a minimal deletion interval
    • Horrigan, S. K., Westbrook, C. A., Kim, A. H., Banerjee, M., Stock, W. and Larson, R. A. (1996). Polymerase chain reaction-based diagnosis of del(5q) in acute myeloid leukemia and myelodysplastic syndrome identifies a minimal deletion interval. Blood, 88(7), 2665-2670.
    • (1996) Blood , vol.88 , Issue.7 , pp. 2665-2670
    • Horrigan, S.K.1    Westbrook, C.A.2    Kim, A.H.3    Banerjee, M.4    Stock, W.5    Larson, R.A.6
  • 11
    • 0030927835 scopus 로고    scopus 로고
    • Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map
    • Zhou, N., Stoffel, A., Wang, P. W., Eisenbart, J. D., Espinosa, R., Larson, R. A. and LeBeau, M. M. (1997). Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map. Proceedings of the National Academy of Science USA, 94, 6948-6953.
    • (1997) Proceedings of the National Academy of Science USA , vol.94 , pp. 6948-6953
    • Zhou, N.1    Stoffel, A.2    Wang, P.W.3    Eisenbart, J.D.4    Espinosa, R.5    Larson, R.A.6    LeBeau, M.M.7
  • 12
    • 0025777315 scopus 로고
    • Clinical and prognostic implications of chromosome 5q deletions: 96 high resolution studied patients
    • Pedersen, B. and Jensen, I. M. (1991). Clinical and prognostic implications of chromosome 5q deletions: 96 high resolution studied patients. Leukemia, 5, 566-573.
    • (1991) Leukemia , vol.5 , pp. 566-573
    • Pedersen, B.1    Jensen, I.M.2
  • 13
    • 0030466276 scopus 로고    scopus 로고
    • Anatomy of the 5q- deletion: Different sex ratios and deleted 5q bands in MDS and AML
    • Pedersen, B. (1996). Anatomy of the 5q- deletion: different sex ratios and deleted 5q bands in MDS and AML. Leukemia, 10, 1883-1890.
    • (1996) Leukemia , vol.10 , pp. 1883-1890
    • Pedersen, B.1
  • 14
    • 0029935947 scopus 로고    scopus 로고
    • A new translocation, t(5:21)(q13:q22) in acute myelogenous leukemia
    • Gogineni, S. K., da Costa, M. and Verma, R. S. (1996). A new translocation, t(5:21)(q13:q22) in acute myelogenous leukemia. Cancer Genetics Cytogenetics, 88, 167-169.
    • (1996) Cancer Genetics Cytogenetics , vol.88 , pp. 167-169
    • Gogineni, S.K.1    Da Costa, M.2    Verma, R.S.3
  • 16
    • 3543127249 scopus 로고
    • Detection of rare 21q22 translocation breakpoints within the AML1 gene in myeloid neoplasms by fluorescence in situ hybridization
    • Roulston, D., Nucifora, G., Dietz-Band, J., Lebeau, M. M. and Rowley, J. D. (1993). Detection of rare 21q22 translocation breakpoints within the AML1 gene in myeloid neoplasms by fluorescence in situ hybridization. Blood, 82, 532a.
    • (1993) Blood , vol.82
    • Roulston, D.1    Nucifora, G.2    Dietz-Band, J.3    Lebeau, M.M.4    Rowley, J.D.5
  • 17
    • 0028096970 scopus 로고
    • Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases
    • Kobayashi, H., Montgomery, K. T., Bohlander, S. K., Adra, C. N., Lim, B. L., Kucherlapati, R. S., Donis-Keller, H., Le Beau, M. M. and Rowley, J. D. (1994). Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases. Blood, 84(10), 3473-3482.
    • (1994) Blood , vol.84 , Issue.10 , pp. 3473-3482
    • Kobayashi, H.1    Montgomery, K.T.2    Bohlander, S.K.3    Adra, C.N.4    Lim, B.L.5    Kucherlapati, R.S.6    Donis-Keller, H.7    Le Beau, M.M.8    Rowley, J.D.9
  • 18
    • 0028269605 scopus 로고
    • Hairy cell leukemia is characterized by clonal chromosome abnormalities clustered to specific regions
    • Haglund, U., Juliusson, G., Stellan, B. and Gahrton, G. (1994). Hairy cell leukemia is characterized by clonal chromosome abnormalities clustered to specific regions. Blood, 83, 2637-2645.
    • (1994) Blood , vol.83 , pp. 2637-2645
    • Haglund, U.1    Juliusson, G.2    Stellan, B.3    Gahrton, G.4
  • 21
    • 0027415533 scopus 로고
    • Double t(1;7)(p36;p11) in a megakaryocytic crisis of chronic myelogenous leukemia with variant t(5;9;22)
    • Hirata, J., Umemura, T., Nishimura, J., Sadamura, S., Sato, H. and Nawata, H. (1992). Double t(1;7)(p36;p11) in a megakaryocytic crisis of chronic myelogenous leukemia with variant t(5;9;22). Cancer Genetics Cytogenetics, 65, 107-110.
    • (1992) Cancer Genetics Cytogenetics , vol.65 , pp. 107-110
    • Hirata, J.1    Umemura, T.2    Nishimura, J.3    Sadamura, S.4    Sato, H.5    Nawata, H.6
  • 22
    • 0028928283 scopus 로고
    • Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoiesis and a high incidence of p53 mutations
    • Lai, J-L., Preudhomme, C., Zandecki, M., Flactif, M., Vanrumbeke, M., Lepelley, P., Wattel, E. and Fenaux, P. (1995). Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoiesis and a high incidence of p53 mutations. Leukemia, 9, 370-381.
    • (1995) Leukemia , vol.9 , pp. 370-381
    • Lai, J.-L.1    Preudhomme, C.2    Zandecki, M.3    Flactif, M.4    Vanrumbeke, M.5    Lepelley, P.6    Wattel, E.7    Fenaux, P.8
  • 23
    • 0029878014 scopus 로고    scopus 로고
    • The enigma of common fragile sites
    • Simonic, I. and Gericke, G. S. (1996). The enigma of common fragile sites. Human Genetics, 97, 524-531.
    • (1996) Human Genetics , vol.97 , pp. 524-531
    • Simonic, I.1    Gericke, G.S.2
  • 24
    • 0021690129 scopus 로고
    • Constitutive fragile sites and cancer
    • Yunis, J. J. and Soreng, A. L. (1984). Constitutive fragile sites and cancer. Science, 226, 1199-1204.
    • (1984) Science , vol.226 , pp. 1199-1204
    • Yunis, J.J.1    Soreng, A.L.2
  • 27
    • 0030035692 scopus 로고    scopus 로고
    • Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21
    • Tavassoli, M., Steingrimsdottir, H., Pierce, E., Jiang, X., Alagox, M., Farzaneh, F. and Campbell, I. G. (1996). Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21. British Journal of Cancer, 74(1), 115-119.
    • (1996) British Journal of Cancer , vol.74 , Issue.1 , pp. 115-119
    • Tavassoli, M.1    Steingrimsdottir, H.2    Pierce, E.3    Jiang, X.4    Alagox, M.5    Farzaneh, F.6    Campbell, I.G.7
  • 31
    • 9544225039 scopus 로고    scopus 로고
    • Identification of a putative effector for Cdc42Hs with high sequence similarity to the RasGAP-related protein IQGAP1 and a Cdc42Hs binding partner with similarity to IQGAP2
    • McCallum, S. J., Wu, W. J. and Cerione, R. A. (1996). Identification of a putative effector for Cdc42Hs with high sequence similarity to the RasGAP-related protein IQGAP1 and a Cdc42Hs binding partner with similarity to IQGAP2. Journal of Biological Chemistry, 271(36), 21732-21737.
    • (1996) Journal of Biological Chemistry , vol.271 , Issue.36 , pp. 21732-21737
    • McCallum, S.J.1    Wu, W.J.2    Cerione, R.A.3
  • 32
    • 0029030415 scopus 로고
    • Regional localization of the XRCC4 human radiation repair gene
    • Otevrel, T. and Stamato, T. D. (1995). Regional localization of the XRCC4 human radiation repair gene. Genomics, 27(1), 211-214.
    • (1995) Genomics , vol.27 , Issue.1 , pp. 211-214
    • Otevrel, T.1    Stamato, T.D.2
  • 33
    • 0028892585 scopus 로고    scopus 로고
    • Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23
    • Hobson, G. M., Krahe, R., Garcia, E., Siciliano, M. J. and Funanage, V. L. Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23. Genomics, 29(3), 704-711.
    • Genomics , vol.29 , Issue.3 , pp. 704-711
    • Hobson, G.M.1    Krahe, R.2    Garcia, E.3    Siciliano, M.J.4    Funanage, V.L.5
  • 34
    • 0027976709 scopus 로고
    • Genetic analysis of the catalytic domain of the GAP gene in human lung cancer cell lines
    • Mitsudomi, T., Friedman, E., Gejman, P. V., McCormick, F. and Gazdar, A. F. (1994). Genetic analysis of the catalytic domain of the GAP gene in human lung cancer cell lines. Human Genetics, 93, 27-31.
    • (1994) Human Genetics , vol.93 , pp. 27-31
    • Mitsudomi, T.1    Friedman, E.2    Gejman, P.V.3    McCormick, F.4    Gazdar, A.F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.