메뉴 건너뛰기




Volumn 51, Issue 5, 2012, Pages 419-428

From cryptic chromosomal lesions to pathologically relevant genes: Integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN 2; CD34 ANTIGEN; PROTEIN; TRIB3 PROTEIN; UNCLASSIFIED DRUG;

EID: 84857997094     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.21927     Document Type: Article
Times cited : (16)

References (24)
  • 1
    • 78651539523 scopus 로고    scopus 로고
    • Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia
    • Bajaj R, Xu F, Xiang B, et al. 2001. Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia. Mol Cytogenet 4: 3.
    • (2001) Mol Cytogenet , vol.4 , pp. 3
    • Bajaj, R.1    Xu, F.2    Xiang, B.3
  • 2
    • 77956550865 scopus 로고    scopus 로고
    • The human SWI/SNF complex associates with RUNX1 to control transcription of hematopoietic target genes
    • Bakshi R, Hassan MQ, Pratap J, et al. 2010. The human SWI/SNF complex associates with RUNX1 to control transcription of hematopoietic target genes. J Cell Physiol 225: 569-576.
    • (2010) J Cell Physiol , vol.225 , pp. 569-576
    • Bakshi, R.1    Hassan, M.Q.2    Pratap, J.3
  • 3
    • 79959794787 scopus 로고    scopus 로고
    • Clinical effect of point mutations in myelodysplastic syndromes
    • Bejar R, Stevenson K, Abdel-Wahab O, et al. 2011. Clinical effect of point mutations in myelodysplastic syndromes. N Engl J Med 364: 2496-2506.
    • (2011) N Engl J Med , vol.364 , pp. 2496-2506
    • Bejar, R.1    Stevenson, K.2    Abdel-Wahab, O.3
  • 4
    • 13844255164 scopus 로고    scopus 로고
    • The presence of clonal cell subpopulations in peripheral blood and bone marrow of patients with refractory cytopenia with multilineage dysplasia but not in patients with refractory anemia may reflect a multistep pathogenesis of myelodysplasia
    • Cermák J, Belicková M, Krejcová H, et al. 2005. The presence of clonal cell subpopulations in peripheral blood and bone marrow of patients with refractory cytopenia with multilineage dysplasia but not in patients with refractory anemia may reflect a multistep pathogenesis of myelodysplasia. Leuk Res 29: 371-379.
    • (2005) Leuk Res , vol.29 , pp. 371-379
    • Cermák, J.1    Belicková, M.2    Krejcová, H.3
  • 5
    • 70449726860 scopus 로고    scopus 로고
    • Real-time quantitative polymerase chain reaction detection of minimal residual disease by standardized WT1 assay to enhance risk stratification in acute myeloid leukemia: A European leukemianet study
    • Cilloni D, Renneville A, Hermitte F, et al. 2009. Real-time quantitative polymerase chain reaction detection of minimal residual disease by standardized WT1 assay to enhance risk stratification in acute myeloid leukemia: A European leukemianet study. J Clin Oncol 27: 5195-5201.
    • (2009) J Clin Oncol , vol.27 , pp. 5195-5201
    • Cilloni, D.1    Renneville, A.2    Hermitte, F.3
  • 6
    • 27144478643 scopus 로고    scopus 로고
    • Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias
    • Fitzgibbon J, Smith LL, Raghavan M, et al. 2005. Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias. Cancer Res 65: 9152-9154.
    • (2005) Cancer Res , vol.65 , pp. 9152-9154
    • Fitzgibbon, J.1    Smith, L.L.2    Raghavan, M.3
  • 7
    • 38949123096 scopus 로고    scopus 로고
    • Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML
    • Gondek LP, Tiu R, O'Keefe CL, et al. 2008. Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML. Blood 111: 1534-1542.
    • (2008) Blood , vol.111 , pp. 1534-1542
    • Gondek, L.P.1    Tiu, R.2    O'Keefe, C.L.3
  • 8
    • 25844451158 scopus 로고    scopus 로고
    • Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype
    • Gorletta TA, Gasparini P, D'Elios MM, et al. 2005. Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype. Genes Chromosomes Cancer 44: 334-337.
    • (2005) Genes Chromosomes Cancer , vol.44 , pp. 334-337
    • Gorletta, T.A.1    Gasparini, P.2    D'Elios, M.M.3
  • 9
    • 44449158040 scopus 로고    scopus 로고
    • Cytogenetic features in myelodysplastic syndromes
    • Haase D. 2008. Cytogenetic features in myelodysplastic syndromes. Ann Hematol 87: 515-526.
    • (2008) Ann Hematol , vol.87 , pp. 515-526
    • Haase, D.1
  • 10
    • 70349306857 scopus 로고    scopus 로고
    • Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics
    • Heinrichs S, Kulkarni RV, Bueso-Ramos CE, et al. 2009. Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics. Leukemia 23: 1605-1613.
    • (2009) Leukemia , vol.23 , pp. 1605-1613
    • Heinrichs, S.1    Kulkarni, R.V.2    Bueso-Ramos, C.E.3
  • 11
    • 0036191941 scopus 로고    scopus 로고
    • Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera
    • Kralovics R, Guan Y, Prchal JT. 2002. Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera. Exp Hematol 30: 229-236.
    • (2002) Exp Hematol , vol.30 , pp. 229-236
    • Kralovics, R.1    Guan, Y.2    Prchal, J.T.3
  • 12
    • 79959214591 scopus 로고    scopus 로고
    • Pathogenesis and consequences of uniparental disomy in cancer
    • Makishima H, Maciejewski JP. 2011. Pathogenesis and consequences of uniparental disomy in cancer. Clin Cancer Res 17: 3913-3923.
    • (2011) Clin Cancer Res , vol.17 , pp. 3913-3923
    • Makishima, H.1    Maciejewski, J.P.2
  • 13
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF. 1988. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16: 1215.
    • (1988) Nucleic Acids Res , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 14
    • 36148993604 scopus 로고    scopus 로고
    • Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes
    • Mohamedali A, Gäken J, Twine NA, et al. 2007. Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes. Blood 110: 3365-3373.
    • (2007) Blood , vol.110 , pp. 3365-3373
    • Mohamedali, A.1    Gäken, J.2    Twine, N.A.3
  • 15
    • 69849110150 scopus 로고    scopus 로고
    • Novel TET2 mutations associated with UPD4q24 in myelodysplastic syndrome
    • Mohamedali AM, Smith AE, Gaken J, et al. 2009. Novel TET2 mutations associated with UPD4q24 in myelodysplastic syndrome. J Clin Oncol 27: 4002-4006.
    • (2009) J Clin Oncol , vol.27 , pp. 4002-4006
    • Mohamedali, A.M.1    Smith, A.E.2    Gaken, J.3
  • 16
    • 5744243856 scopus 로고    scopus 로고
    • Pathobiology, classification, and diagnosis of myelodysplastic syndrome
    • Mufti GJ. 2004. Pathobiology, classification, and diagnosis of myelodysplastic syndrome. Best Pract Res Clin Haematol 17: 543-557.
    • (2004) Best Pract Res Clin Haematol , vol.17 , pp. 543-557
    • Mufti, G.J.1
  • 17
    • 12544257171 scopus 로고    scopus 로고
    • Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias
    • Raghavan M, Lillington DM, Skoulakis S, et al. 2005. Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias. Cancer Res 65: 375-378.
    • (2005) Cancer Res , vol.65 , pp. 375-378
    • Raghavan, M.1    Lillington, D.M.2    Skoulakis, S.3
  • 18
    • 46749114860 scopus 로고    scopus 로고
    • Uniparental disomy may be associated with microsatellite instability in acute myeloid leukemia (AML) with a normal karyotype
    • Serrano E, Carnicer MJ, Orantes V, et al. 2008. Uniparental disomy may be associated with microsatellite instability in acute myeloid leukemia (AML) with a normal karyotype. Leuk Lymphoma 49: 1178-1183.
    • (2008) Leuk Lymphoma , vol.49 , pp. 1178-1183
    • Serrano, E.1    Carnicer, M.J.2    Orantes, V.3
  • 20
    • 79952362122 scopus 로고    scopus 로고
    • Copy number alterations at polymorphic loci may be acquired somatically in patients with myelodysplastic syndromes
    • Starczynowski DT, Vercauteren S, Sung S, et al. 2011. Copy number alterations at polymorphic loci may be acquired somatically in patients with myelodysplastic syndromes. Leuk Res 35: 444-447.
    • (2011) Leuk Res , vol.35 , pp. 444-447
    • Starczynowski, D.T.1    Vercauteren, S.2    Sung, S.3
  • 21
    • 0036951801 scopus 로고    scopus 로고
    • del11(p11-13) with overexpression of Wilms' tumor gene during leukemic transformation of myelodysplastic syndrome
    • Suzuki S, Hashino S, Yoshida S, et al. 2002. del11(p11-13) with overexpression of Wilms' tumor gene during leukemic transformation of myelodysplastic syndrome. Ann Hematol 81: 605-608.
    • (2002) Ann Hematol , vol.81 , pp. 605-608
    • Suzuki, S.1    Hashino, S.2    Yoshida, S.3
  • 22
    • 79955945973 scopus 로고    scopus 로고
    • Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies
    • Tiu RV, Gondek LP, O'Keefe CL, et al. 2011. Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies. Blood 117: 4552-4560.
    • (2011) Blood , vol.117 , pp. 4552-4560
    • Tiu, R.V.1    Gondek, L.P.2    O'Keefe, C.L.3
  • 23
    • 77957162079 scopus 로고    scopus 로고
    • A distinct expression of various gene subsets in CD34+ cells from patiens with early and advanced myelodysplastic syndrome
    • Vasikova A, Belickova M, Budinska E, et al. 2010. A distinct expression of various gene subsets in CD34+ cells from patiens with early and advanced myelodysplastic syndrome. Leuk Res 34: 1566-1572.
    • (2010) Leuk Res , vol.34 , pp. 1566-1572
    • Vasikova, A.1    Belickova, M.2    Budinska, E.3
  • 24
    • 79956220948 scopus 로고    scopus 로고
    • Tribbles in disease: Signaling pathways important for cellular function and neoplastic transformation
    • Yokoyama T, Nakamura T. 2011. Tribbles in disease: Signaling pathways important for cellular function and neoplastic transformation. Cancer Sci 102: 1115-1122.
    • (2011) Cancer Sci , vol.102 , pp. 1115-1122
    • Yokoyama, T.1    Nakamura, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.