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Volumn 139, Issue 11, 2013, Pages 1879-1886

Intron 3 of the ARID5B gene: A hot spot for acute lymphoblastic leukemia susceptibility

Author keywords

Acute lymphoblastic leukemia; ARID5B; Childhood; Function; Polymorphisms; Susceptibility

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ARID5B GENE; ARTICLE; CANCER CELL CULTURE; CANCER INCIDENCE; CANCER RISK; CANCER SUSCEPTIBILITY; CHILD; CONTROLLED STUDY; COPY NUMBER VARIATION; CYTOGENETICS; FEMALE; GENE; GENE EXPRESSION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN CELL; INTRON; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SPAIN; BIOSYNTHESIS; DIPLOIDY; GENE DOSAGE; GENETIC PREDISPOSITION; GENETICS; METABOLISM;

EID: 84892675481     PISSN: 01715216     EISSN: 14321335     Source Type: Journal    
DOI: 10.1007/s00432-013-1512-3     Document Type: Article
Times cited : (22)

References (26)
  • 1
    • 33644759290 scopus 로고    scopus 로고
    • Identification of distinct molecular phenotypes in acute megakaryoblastic leukemia by gene expression profiling
    • Bourquin JP, Subramanian A et al (2006) Identification of distinct molecular phenotypes in acute megakaryoblastic leukemia by gene expression profiling. Proc Natl Acad Sci USA 103(9):3339-3344
    • (2006) Proc Natl Acad Sci USA , vol.103 , Issue.9 , pp. 3339-3344
    • Bourquin, J.P.1    Subramanian, A.2
  • 2
    • 46749127803 scopus 로고    scopus 로고
    • Computational identification of the normal and perturbed genetic networks involved in myeloid differentiation and acute promyelocytic leukemia
    • Chang LW, Payton JE et al (2008) Computational identification of the normal and perturbed genetic networks involved in myeloid differentiation and acute promyelocytic leukemia. Genome Biol 9(2):R38
    • (2008) Genome Biol , vol.9 , Issue.2
    • Chang, L.W.1    Payton, J.E.2
  • 3
    • 84860709956 scopus 로고    scopus 로고
    • Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia
    • Ellinghaus E, Stanulla M et al (2012) Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. Leukemia 26(5):902-909
    • (2012) Leukemia , vol.26 , Issue.5 , pp. 902-909
    • Ellinghaus, E.1    Stanulla, M.2
  • 4
    • 59949088494 scopus 로고    scopus 로고
    • Whole population, genome-wide mapping of hidden relatedness
    • Gusev A, Lowe JK et al (2009) Whole population, genome-wide mapping of hidden relatedness. Genome Res 19(2):318-326
    • (2009) Genome Res , vol.19 , Issue.2 , pp. 318-326
    • Gusev, A.1    Lowe, J.K.2
  • 5
    • 77955983842 scopus 로고    scopus 로고
    • Genome-wide association study of childhood acute lymphoblastic leukemia in Korea
    • Han S, Lee KM et al (2010) Genome-wide association study of childhood acute lymphoblastic leukemia in Korea. Leuk Res 34(10):1271-1274
    • (2010) Leuk Res , vol.34 , Issue.10 , pp. 1271-1274
    • Han, S.1    Lee, K.M.2
  • 6
    • 77956865056 scopus 로고    scopus 로고
    • Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia
    • Healy J, Richer C et al (2010) Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia. Haematologica 95(9):1608-1611
    • (2010) Haematologica , vol.95 , Issue.9 , pp. 1608-1611
    • Healy, J.1    Richer, C.2
  • 7
    • 84855379048 scopus 로고    scopus 로고
    • Copy number variation at 6q13 functions as a long-range regulator and is associated with pancreatic cancer risk
    • Huang L, Yu D et al (2012) Copy number variation at 6q13 functions as a long-range regulator and is associated with pancreatic cancer risk. Carcinogenesis 33(1):94-100
    • (2012) Carcinogenesis , vol.33 , Issue.1 , pp. 94-100
    • Huang, L.1    Yu, D.2
  • 8
    • 78650178429 scopus 로고    scopus 로고
    • Childhood cancer survival: A report from the United Kingdom Childhood Cancer Study
    • Johnston WT, Lightfoot TJ et al (2010) Childhood cancer survival: a report from the United Kingdom Childhood Cancer Study. Cancer Epidemiol 34(6):659-666
    • (2010) Cancer Epidemiol , vol.34 , Issue.6 , pp. 659-666
    • Johnston, W.T.1    Lightfoot, T.J.2
  • 9
    • 0028857136 scopus 로고
    • Mathematical formulae for the prediction of the residual beta cell function during the first two years of disease in children and adolescents with insulin-dependent diabetes mellitus
    • Klipper-Aurbach Y, Wasserman M et al (1995) Mathematical formulae for the prediction of the residual beta cell function during the first two years of disease in children and adolescents with insulin-dependent diabetes mellitus. Med Hypotheses 45(5):486-490
    • (1995) Med Hypotheses , vol.45 , Issue.5 , pp. 486-490
    • Klipper-Aurbach, Y.1    Wasserman, M.2
  • 10
    • 0034893767 scopus 로고    scopus 로고
    • Gene targeting of Desrt, a novel ARID class DNA-binding protein, causes growth retardation and abnormal development of reproductive organs
    • Lahoud MH, Ristevski S et al (2001) Gene targeting of Desrt, a novel ARID class DNA-binding protein, causes growth retardation and abnormal development of reproductive organs. Genome Res 11(8):1327-1334
    • (2001) Genome Res , vol.11 , Issue.8 , pp. 1327-1334
    • Lahoud, M.H.1    Ristevski, S.2
  • 11
    • 84866679598 scopus 로고    scopus 로고
    • Candidate gene association study in pediatric acute lymphoblastic leukemia evaluated by Bayesian network based Bayesian multilevel analysis of relevance
    • Lautner-Csorba O, Gézsi A et al (2012) Candidate gene association study in pediatric acute lymphoblastic leukemia evaluated by Bayesian network based Bayesian multilevel analysis of relevance. BMC Med Genomics 5:42
    • (2012) BMC Med Genomics , vol.5 , pp. 42
    • Lautner-Csorba, O.1    Gézsi, A.2
  • 12
    • 38549158538 scopus 로고    scopus 로고
    • F-SNP: Computationally predicted functional SNPs for disease association studies
    • Lee PH, Shatkay H (2008) F-SNP: computationally predicted functional SNPs for disease association studies. Nucleic Acids Res 36(Database issue): D820-D824
    • (2008) Nucleic Acids Res , vol.36 , Issue.DATABASE ISSUE
    • Lee, P.H.1    Shatkay, H.2
  • 13
    • 0035710746 scopus 로고    scopus 로고
    • Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method
    • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25(4):402-408
    • (2001) Methods , vol.25 , Issue.4 , pp. 402-408
    • Livak, K.J.1    Schmittgen, T.D.2
  • 14
    • 79961178050 scopus 로고    scopus 로고
    • Polymorphisms of the SLCO1B1 gene predict methotrexate-related toxicity in childhood acute lymphoblastic leukemia
    • Lopez-Lopez E, Martin-Guerrero I et al (2011) Polymorphisms of the SLCO1B1 gene predict methotrexate-related toxicity in childhood acute lymphoblastic leukemia. Pediatr Blood Cancer 57(4):612-619
    • (2011) Pediatr Blood Cancer , vol.57 , Issue.4 , pp. 612-619
    • Lopez-Lopez, E.1    Martin-Guerrero, I.2
  • 15
    • 84871208154 scopus 로고    scopus 로고
    • Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE)
    • Orsi L, Rudant J et al (2012) Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE). Leukemia 26(12):2561-2564
    • (2012) Leukemia , vol.26 , Issue.12 , pp. 2561-2564
    • Orsi, L.1    Rudant, J.2
  • 16
    • 84867852880 scopus 로고    scopus 로고
    • Alternative transcription and alternative splicing in cancer
    • Pal S, Gupta R et al (2012) Alternative transcription and alternative splicing in cancer. Pharmacol Ther 136(3):283-294
    • (2012) Pharmacol Ther , vol.136 , Issue.3 , pp. 283-294
    • Pal, S.1    Gupta, R.2
  • 17
    • 69349101565 scopus 로고    scopus 로고
    • Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
    • Papaemmanuil E, Hosking FJ et al (2009) Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Nat Genet 41(9):1006-1010
    • (2009) Nat Genet , vol.41 , Issue.9 , pp. 1006-1010
    • Papaemmanuil, E.1    Hosking, F.J.2
  • 18
    • 80053953634 scopus 로고    scopus 로고
    • Role of 657del5 NBN mutation and 7p12.2IKZF1 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population
    • Pastorczak A, Górniak P et al (2011) Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population. Leuk Res 35(11):1534-1536
    • (2011) Leuk Res , vol.35 , Issue.11 , pp. 1534-1536
    • Pastorczak, A.1    Górniak, P.2
  • 19
    • 78650745577 scopus 로고    scopus 로고
    • Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia
    • Paulsson K, Forestier E et al (2010) Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA 107(50):21719-21724
    • (2010) Proc Natl Acad Sci USA , vol.107 , Issue.50 , pp. 21719-21724
    • Paulsson, K.1    Forestier, E.2
  • 20
    • 41149140876 scopus 로고    scopus 로고
    • The fine-scale and complex architecture of human copy-number variation
    • Perry GH, Ben-Dor A et al (2008) The fine-scale and complex architecture of human copy-number variation. Am J Hum Genet 82(3):685-695
    • (2008) Am J Hum Genet , vol.82 , Issue.3 , pp. 685-695
    • Perry, G.H.1    Ben-Dor, A.2
  • 21
    • 77950349468 scopus 로고    scopus 로고
    • Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood
    • Prasad RB, Hosking FJ et al (2010) Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood. Blood 115(9):1765-1767
    • (2010) Blood , vol.115 , Issue.9 , pp. 1765-1767
    • Prasad, R.B.1    Hosking, F.J.2
  • 22
    • 79955864597 scopus 로고    scopus 로고
    • Frequent somatic demethylation of RAPGEF1/C3G intronic sequences in gastrointestinal and gynecological cancer
    • Samuelsson J, Alonso S et al (2011) Frequent somatic demethylation of RAPGEF1/C3G intronic sequences in gastrointestinal and gynecological cancer. Int J Oncol 38(6):1575-1577
    • (2011) Int J Oncol , vol.38 , Issue.6 , pp. 1575-1577
    • Samuelsson, J.1    Alonso, S.2
  • 23
    • 69349091330 scopus 로고    scopus 로고
    • Germline genomic variants associated with childhood acute lymphoblastic leukemia
    • Treviño LR, Yang W et al (2009) Germline genomic variants associated with childhood acute lymphoblastic leukemia. Nat Genet 41(9):1001-1005
    • (2009) Nat Genet , vol.41 , Issue.9 , pp. 1001-1005
    • Treviño, L.R.1    Yang, W.2
  • 24
    • 77957735025 scopus 로고    scopus 로고
    • Variation at 7p12.2 and 10q21.2 influences childhood acute lymphoblastic leukemia risk in the Thai population and may contribute to racial differences in leukemia incidence
    • Vijayakrishnan J, Sherborne AL et al (2010) Variation at 7p12.2 and 10q21.2 influences childhood acute lymphoblastic leukemia risk in the Thai population and may contribute to racial differences in leukemia incidence. Leuk Lymphoma 51(10):1870-1874
    • (2010) Leuk Lymphoma , vol.51 , Issue.10 , pp. 1870-1874
    • Vijayakrishnan, J.1    Sherborne, A.L.2
  • 25
    • 84863162896 scopus 로고    scopus 로고
    • ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment outcome of childhood acute lymphoblastic leukemia
    • Xu H, Cheng C et al (2012) ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment outcome of childhood acute lymphoblastic leukemia. J Clin Oncol 30(7):751-757
    • (2012) J Clin Oncol , vol.30 , Issue.7 , pp. 751-757
    • Xu, H.1    Cheng, C.2
  • 26
    • 77950955951 scopus 로고    scopus 로고
    • ARID5B SNP rs10821936 is associated with risk of childhood acute lymphoblastic leukemia in blacks and contributes to racial differences in leukemia incidence
    • Yang W, Treviño LR et al (2010) ARID5B SNP rs10821936 is associated with risk of childhood acute lymphoblastic leukemia in blacks and contributes to racial differences in leukemia incidence. Leukemia 24(4):894-896
    • (2010) Leukemia , vol.24 , Issue.4 , pp. 894-896
    • Yang, W.1    Treviño, L.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.