메뉴 건너뛰기




Volumn 95, Issue 46, 2016, Pages

A childhood acute lymphoblastic leukemia genome-wide association study identifies novel sex-specific risk variants

Author keywords

Acute lymphoblastic leukemia; Case only study; Effect modification; Expression quantitative trait loci; Gene expression regulation; Genome wide association study; Sex specific association

Indexed keywords

COX6B1 PROTEIN; ESTROGEN RECEPTOR; HLA DQA1 ANTIGEN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; K LYSINE ACETYLTRANSFERASE 7; MICRORNA; MIR 17 92; PROTEIN; RASSF2 PROTEIN; SEX HORMONE; UNCLASSIFIED DRUG; HLA DQ ANTIGEN; HLA-DQA1 ANTIGEN; RASSF2 PROTEIN, HUMAN; TUMOR SUPPRESSOR PROTEIN;

EID: 85012005500     PISSN: 00257974     EISSN: 15365964     Source Type: Journal    
DOI: 10.1097/MD.0000000000005300     Document Type: Article
Times cited : (16)

References (68)
  • 1
    • 79958043675 scopus 로고    scopus 로고
    • 1975-2012,National Cancer Institute. Bethesda, MD, based on November 2014 SEER data submission, posted to the SEER web site, April 2015 (accessed May 31, 2016)
    • Howlader N, Noone AM, Krapcho M, et al (eds). SEER Cancer Statistics Review, 1975-2012,National Cancer Institute. Bethesda, MD, Available at: http://seer.cancer.gov/csr/1975-2012/, based on November 2014 SEER data submission, posted to the SEER web site, April 2015 (accessed May 31, 2016).
    • SEER Cancer Statistics Review
    • Howlader, N.1    Noone, A.M.2    Krapcho, M.3
  • 4
    • 84882264567 scopus 로고    scopus 로고
    • Gender differences in cancer susceptibility: An inadequately addressed issue
    • Dorak MT, Karpuzoglu E. Gender differences in cancer susceptibility: an inadequately addressed issue. Front Appl Genet Epidemiol 2012;3:268.
    • (2012) Front Appl Genet Epidemiol , vol.3 , pp. 268
    • Dorak, M.T.1    Karpuzoglu, E.2
  • 6
    • 84887309148 scopus 로고    scopus 로고
    • Health problems in survivors of childhood cancer: The need for international collaboration in longterm follow-up care
    • Mulder RL, Hudson MM, Skinner R, et al. Health problems in survivors of childhood cancer: the need for international collaboration in longterm follow-up care. Future Oncol 2013;9:1667-70.
    • (2013) Future Oncol , vol.9 , pp. 1667-1670
    • Mulder, R.L.1    Hudson, M.M.2    Skinner, R.3
  • 7
    • 84879677633 scopus 로고    scopus 로고
    • Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits
    • Randall JC, Winkler TW, Kutalik Z, et al. Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits. PLoS Genet 2013;9:e1003500.
    • (2013) PLoS Genet , vol.9
    • Randall, J.C.1    Winkler, T.W.2    Kutalik, Z.3
  • 8
    • 84921914031 scopus 로고    scopus 로고
    • Sex differences in disease genetics: Evidence, evolution, and detection
    • Gilks WP, Abbott JK, Morrow EH. Sex differences in disease genetics: evidence, evolution, and detection. Trends Genet 2014;30:453-63.
    • (2014) Trends Genet , vol.30 , pp. 453-463
    • Gilks, W.P.1    Abbott, J.K.2    Morrow, E.H.3
  • 9
    • 74149093117 scopus 로고    scopus 로고
    • An intronic polymorphism of IRF4 gene influences gene transcription in vitro and shows a risk association with childhood acute lymphoblastic leukemia in males
    • Do TN, Ucisik-Akkaya E, Davis CF, et al. An intronic polymorphism of IRF4 gene influences gene transcription in vitro and shows a risk association with childhood acute lymphoblastic leukemia in males. Biochim Biophys Acta 2010;1802:292-300.
    • (2010) Biochim Biophys Acta , vol.1802 , pp. 292-300
    • Do, T.N.1    Ucisik-Akkaya, E.2    Davis, C.F.3
  • 10
    • 78149435367 scopus 로고    scopus 로고
    • Multiple sclerosis risk markers in HLA-DRA, HLA-C, and IFNG genes are associated with sexspecific childhood leukemia risk
    • Morrison BA, Ucisik-Akkaya E, Flores H, et al. Multiple sclerosis risk markers in HLA-DRA, HLA-C, and IFNG genes are associated with sexspecific childhood leukemia risk. Autoimmunity 2010;43:690-7.
    • (2010) Autoimmunity , vol.43 , pp. 690-697
    • Morrison, B.A.1    Ucisik-Akkaya, E.2    Flores, H.3
  • 11
    • 84922371201 scopus 로고    scopus 로고
    • Genetic markers in a multiethnic sample for childhood acute lymphoblastic leukemia risk
    • Kennedy AE, Kamdar KY, Lupo PJ, et al. Genetic markers in a multiethnic sample for childhood acute lymphoblastic leukemia risk. Leuk Lymphoma 2015;56:169-74.
    • (2015) Leuk Lymphoma , vol.56 , pp. 169-174
    • Kennedy, A.E.1    Kamdar, K.Y.2    Lupo, P.J.3
  • 12
    • 77956865056 scopus 로고    scopus 로고
    • Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia
    • Healy J, Richer C, Bourgey M, et al. Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia. Haematologica 2010;95:1608-11.
    • (2010) Haematologica , vol.95 , pp. 1608-1611
    • Healy, J.1    Richer, C.2    Bourgey, M.3
  • 13
    • 33748302858 scopus 로고    scopus 로고
    • Polymorphisms in ERCC1 and susceptibility to childhood acute lymphoblastic leukemia in a Chinese population
    • Wang SL, Zhao H, Zhou B, et al. Polymorphisms in ERCC1 and susceptibility to childhood acute lymphoblastic leukemia in a Chinese population. Leuk Res 2006;30:1341-5.
    • (2006) Leuk Res , vol.30 , pp. 1341-1345
    • Wang, S.L.1    Zhao, H.2    Zhou, B.3
  • 14
    • 84877969387 scopus 로고    scopus 로고
    • Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations
    • Xu H, Yang W, Perez-Andreu V, et al. Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. J Natl Cancer Inst 2013;105:733-42.
    • (2013) J Natl Cancer Inst , vol.105 , pp. 733-742
    • Xu, H.1    Yang, W.2    Perez-Andreu, V.3
  • 15
    • 69349091330 scopus 로고    scopus 로고
    • Germline genomic variants associated with childhood acute lymphoblastic leukemia
    • Trevino LR, Yang W, French D, et al. Germline genomic variants associated with childhood acute lymphoblastic leukemia. Nat Genet 2009;41:1001-5.
    • (2009) Nat Genet , vol.41 , pp. 1001-1005
    • Trevino, L.R.1    Yang, W.2    French, D.3
  • 16
    • 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, Vijayakrishnan J, et al. Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Nat Genet 2009;41:1006-10.
    • (2009) Nat Genet , vol.41 , pp. 1006-1010
    • Papaemmanuil, E.1    Hosking, F.J.2    Vijayakrishnan, J.3
  • 17
    • 80052263017 scopus 로고    scopus 로고
    • IFNG genotype and sex interact to influence the risk of childhood asthma
    • Loisel DA, Tan Z, Tisler CJ, et al. IFNG genotype and sex interact to influence the risk of childhood asthma. J Allergy Clin Immunol 2011;128:524-31.
    • (2011) J Allergy Clin Immunol , vol.128 , pp. 524-531
    • Loisel, D.A.1    Tan, Z.2    Tisler, C.J.3
  • 18
    • 84962948889 scopus 로고    scopus 로고
    • Genome-wide interaction studies reveal sex-specific asthma risk alleles
    • Myers RA, Scott NM, Gauderman WJ, et al. Genome-wide interaction studies reveal sex-specific asthma risk alleles. Hum Mol Genet 2014;23: 5251-9.
    • (2014) Hum Mol Genet , vol.23 , pp. 5251-5259
    • Myers, R.A.1    Scott, N.M.2    Gauderman, W.J.3
  • 19
    • 84904051753 scopus 로고    scopus 로고
    • Sex- And age-interacting eQTLs in human complex diseases
    • Yao C, Joehanes R, Johnson AD, et al. Sex- and age-interacting eQTLs in human complex diseases. Hum Mol Genet 2014;23:1947-56.
    • (2014) Hum Mol Genet , vol.23 , pp. 1947-1956
    • Yao, C.1    Joehanes, R.2    Johnson, A.D.3
  • 20
    • 84870516488 scopus 로고    scopus 로고
    • Sex-biased genetic effects on gene regulation in humans
    • Dimas AS, Nica AC, Montgomery SB, et al. Sex-biased genetic effects on gene regulation in humans. Genome Res 2012;22:2368-75.
    • (2012) Genome Res , vol.22 , pp. 2368-2375
    • Dimas, A.S.1    Nica, A.C.2    Montgomery, S.B.3
  • 21
    • 84892471805 scopus 로고    scopus 로고
    • Sex differences in the human peripheral blood transcriptome
    • Jansen R, Batista S, Brooks AI, et al. Sex differences in the human peripheral blood transcriptome. BMC Genom 2014;15:33.
    • (2014) BMC Genom , vol.15 , pp. 33
    • Jansen, R.1    Batista, S.2    Brooks, A.I.3
  • 22
    • 84859504942 scopus 로고    scopus 로고
    • Sex differences in disease risk from reported genome-wide association study findings
    • Liu LY, Schaub MA, Sirota M, et al. Sex differences in disease risk from reported genome-wide association study findings. Hum Genet 2012;131: 353-64.
    • (2012) Hum Genet , vol.131 , pp. 353-364
    • Liu, L.Y.1    Schaub, M.A.2    Sirota, M.3
  • 23
    • 84867625599 scopus 로고    scopus 로고
    • Sex-specific differences in effect size estimatesatestablishedcomplextraitloci
    • Orozco G, Ioannidis JP,Morris A, et al. Sex-specific differences in effect size estimatesatestablishedcomplextraitloci.Int JEpidemiol2012;41:1376-82.
    • (2012) Int JEpidemiol , vol.41 , pp. 1376-1382
    • Orozco, G.1    Ioannidis, J.P.2    Morris, A.3
  • 24
    • 0035922669 scopus 로고    scopus 로고
    • Epidemiological methods for studying genes and environmental factors in complex diseases
    • Clayton D, McKeigue PM. Epidemiological methods for studying genes and environmental factors in complex diseases. Lancet 2001;358:1356-60.
    • (2001) Lancet , vol.358 , pp. 1356-1360
    • Clayton, D.1    McKeigue, P.M.2
  • 25
    • 78651100696 scopus 로고    scopus 로고
    • Data quality control in genetic case-control association studies
    • Anderson CA, Pettersson FH, Clarke GM, et al. Data quality control in genetic case-control association studies. Nat Protoc 2010;5:1564-73.
    • (2010) Nat Protoc , vol.5 , pp. 1564-1573
    • Anderson, C.A.1    Pettersson, F.H.2    Clarke, G.M.3
  • 26
    • 16544380910 scopus 로고    scopus 로고
    • Genomic control to the extreme
    • Devlin B, Bacanu SA, Roeder K. Genomic control to the extreme. Nat Genet 2004;36:1129-30.
    • (2004) Nat Genet , vol.36 , pp. 1129-1130
    • Devlin, B.1    Bacanu, S.A.2    Roeder, K.3
  • 27
    • 77956534324 scopus 로고    scopus 로고
    • ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
    • Wang K, Li M, Hakonarson H. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 2010;38:e164.
    • (2010) Nucleic Acids Res , vol.38 , pp. e164
    • Wang, K.1    Li, M.2    Hakonarson, H.3
  • 28
    • 61449107734 scopus 로고    scopus 로고
    • SNPnexus: A web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms
    • Chelala C, Khan A, Lemoine NR. SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms. Bioinformatics 2009;25:655-61.
    • (2009) Bioinformatics , vol.25 , pp. 655-661
    • Chelala, C.1    Khan, A.2    Lemoine, N.R.3
  • 29
    • 84895858942 scopus 로고    scopus 로고
    • A general framework for estimating the relative pathogenicity of human genetic variants
    • Kircher M, Witten DM, Jain P, et al. A general framework for estimating the relative pathogenicity of human genetic variants. Nat Genet 2014;46:310-5.
    • (2014) Nat Genet , vol.46 , pp. 310-315
    • Kircher, M.1    Witten, D.M.2    Jain, P.3
  • 30
    • 84865777825 scopus 로고    scopus 로고
    • Linking disease associations with regulatory information in the human genome
    • Schaub MA, Boyle AP, Kundaje A, et al. Linking disease associations with regulatory information in the human genome. Genome Res 2012;22:1748-59.
    • (2012) Genome Res , vol.22 , pp. 1748-1759
    • Schaub, M.A.1    Boyle, A.P.2    Kundaje, A.3
  • 31
    • 84976873328 scopus 로고    scopus 로고
    • HaploReg v4: Systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease
    • Ward LD, Kellis M. HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease. Nucleic Acids Res 2016;44:D877-81.
    • (2016) Nucleic Acids Res , vol.44 , pp. D877-D881
    • Ward, L.D.1    Kellis, M.2
  • 32
    • 84927747554 scopus 로고    scopus 로고
    • SNiPA: An interactive, genetic variant-centered annotation browser
    • Arnold M, Raffler J, Pfeufer A, et al. SNiPA: an interactive, genetic variant-centered annotation browser. Bioinformatics 2015;31:1334-6.
    • (2015) Bioinformatics , vol.31 , pp. 1334-1336
    • Arnold, M.1    Raffler, J.2    Pfeufer, A.3
  • 33
    • 84976878613 scopus 로고    scopus 로고
    • RVarBase: An updated database for regulatory features of human variants
    • Guo L, Du Y, Qu S, et al. rVarBase: an updated database for regulatory features of human variants. Nucleic Acids Res 2016;44:D888-93.
    • (2016) Nucleic Acids Res , vol.44 , pp. D888-D893
    • Guo, L.1    Du, Y.2    Qu, S.3
  • 34
    • 84883583576 scopus 로고    scopus 로고
    • GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications
    • Li MJ, Wang LY, Xia Z, et al. GWAS3D: detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications. Nucleic Acids Res 2013;41: W150-8.
    • (2013) Nucleic Acids Res , vol.41 , pp. W150-W158
    • Li, M.J.1    Wang, L.Y.2    Xia, Z.3
  • 36
    • 84885018609 scopus 로고    scopus 로고
    • Systematic identification of trans eQTLs as putative drivers of known disease associations
    • Westra HJ, Peters MJ, Esko T, et al. Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat Genet 2013;45:1238-43.
    • (2013) Nat Genet , vol.45 , pp. 1238-1243
    • Westra, H.J.1    Peters, M.J.2    Esko, T.3
  • 37
    • 85015350236 scopus 로고    scopus 로고
    • Systematic identification of genetic influences on methylation across the human life course
    • Gaunt TR, Shihab HA, Hemani G, et al. Systematic identification of genetic influences on methylation across the human life course. Genome Biol 2016;17:61.
    • (2016) Genome Biol , vol.17 , pp. 61
    • Gaunt, T.R.1    Shihab, H.A.2    Hemani, G.3
  • 38
    • 84876580265 scopus 로고    scopus 로고
    • SwissRegulon, a database of genome-wide annotations of regulatory sites: Recent updates
    • Pachkov M, Balwierz PJ, Arnold P, et al. SwissRegulon, a database of genome-wide annotations of regulatory sites: recent updates. Nucleic Acids Res 2013;41:D214-20.
    • (2013) Nucleic Acids Res , vol.41 , pp. D214-D220
    • Pachkov, M.1    Balwierz, P.J.2    Arnold, P.3
  • 39
    • 58549112996 scopus 로고    scopus 로고
    • Bioinformatics enrichment tools: Paths toward the comprehensive functional analysis of large gene lists
    • Huang da W, Sherman BT, Lempicki RA. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic Acids Res 2009;37:1-3.
    • (2009) Nucleic Acids Res , vol.37 , pp. 1-3
    • Huang Da, W.1    Sherman, B.T.2    Lempicki, R.A.3
  • 40
    • 84964777775 scopus 로고    scopus 로고
    • NPInter v3.0: An upgraded database of noncoding RNA-associated interactions
    • Hao Y, Wu W, Li H, et al. NPInter v3.0: an upgraded database of noncoding RNA-associated interactions. Database (Oxford) 2016;pii: baw2057.
    • (2016) Database (Oxford)
    • Hao, Y.1    Wu, W.2    Li, H.3
  • 41
    • 84940502214 scopus 로고    scopus 로고
    • Predicting effective microRNA target sites in mammalian mRNAs
    • Agarwal V, Bell GW, Nam JW, et al. Predicting effective microRNA target sites in mammalian mRNAs. Elife 2015;4:e05005.
    • (2015) Elife , vol.4
    • Agarwal, V.1    Bell, G.W.2    Nam, J.W.3
  • 42
    • 77955134007 scopus 로고    scopus 로고
    • Clinical utility of microarray-based gene expression profiling in the diagnosis and subclassification of leukemia: Report from the International Microarray Innovations in Leukemia Study Group
    • Haferlach T, Kohlmann A, Wieczorek L, et al. Clinical utility of microarray-based gene expression profiling in the diagnosis and subclassification of leukemia: report from the International Microarray Innovations in Leukemia Study Group. J Clin Oncol 2010;28:2529-37.
    • (2010) J Clin Oncol , vol.28 , pp. 2529-2537
    • Haferlach, T.1    Kohlmann, A.2    Wieczorek, L.3
  • 43
    • 70349174971 scopus 로고    scopus 로고
    • The RASSF proteins in cancer; from epigenetic silencing to functional characterization
    • Richter AM, Pfeifer GP, Dammann RH. The RASSF proteins in cancer; from epigenetic silencing to functional characterization. Biochim Biophys Acta 2009;1796:114-28.
    • (2009) Biochim Biophys Acta , vol.1796 , pp. 114-128
    • Richter, A.M.1    Pfeifer, G.P.2    Dammann, R.H.3
  • 44
    • 53049109135 scopus 로고    scopus 로고
    • Mutation of genes affecting the RAS pathway is common in childhood acute lymphoblastic leukemia
    • Case M, Matheson E, Minto L, et al. Mutation of genes affecting the RAS pathway is common in childhood acute lymphoblastic leukemia. Cancer Res 2008;68:6803-9.
    • (2008) Cancer Res , vol.68 , pp. 6803-6809
    • Case, M.1    Matheson, E.2    Minto, L.3
  • 45
    • 77951841445 scopus 로고    scopus 로고
    • Reprogramming of miRNA networks in cancer and leukemia
    • Volinia S, Galasso M, Costinean S, et al. Reprogramming of miRNA networks in cancer and leukemia. Genome Res 2010;20:589-99.
    • (2010) Genome Res , vol.20 , pp. 589-599
    • Volinia, S.1    Galasso, M.2    Costinean, S.3
  • 46
    • 84863241188 scopus 로고    scopus 로고
    • Ablation of Rassf2 induces bone defects and subsequent haematopoietic anomalies in mice
    • Song H, KimH, Lee K, et al. Ablation of Rassf2 induces bone defects and subsequent haematopoietic anomalies in mice. EMBO J 2012;31: 1147-59.
    • (2012) EMBO J , vol.31 , pp. 1147-1159
    • Song, H.1    Kim, H.2    Lee, K.3
  • 47
    • 84905120617 scopus 로고    scopus 로고
    • RASSF tumor suppressor gene family: Biological functions and regulation
    • Volodko N, Gordon M, Salla M, et al. RASSF tumor suppressor gene family: biological functions and regulation. FEBS Lett 2014;588: 2671-84.
    • (2014) FEBS Lett , vol.588 , pp. 2671-2684
    • Volodko, N.1    Gordon, M.2    Salla, M.3
  • 48
    • 84899633950 scopus 로고    scopus 로고
    • Linkage of DNA methylation quantitative trait loci to human cancer risk
    • Heyn H, Sayols S, Moutinho C, et al. Linkage of DNA methylation quantitative trait loci to human cancer risk. Cell Rep 2014;7:331-8.
    • (2014) Cell Rep , vol.7 , pp. 331-338
    • Heyn, H.1    Sayols, S.2    Moutinho, C.3
  • 49
    • 84914106704 scopus 로고    scopus 로고
    • Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition
    • Irving J, Matheson E, Minto L, et al. Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition. Blood 2014;124:3420-30.
    • (2014) Blood , vol.124 , pp. 3420-3430
    • Irving, J.1    Matheson, E.2    Minto, L.3
  • 50
    • 84933278041 scopus 로고    scopus 로고
    • Whole-genome fingerprint of the DNA methylome during human B cell differentiation
    • Kulis M, Merkel A, Heath S, et al. Whole-genome fingerprint of the DNA methylome during human B cell differentiation. Nat Genet 2015;47: 746-56.
    • (2015) Nat Genet , vol.47 , pp. 746-756
    • Kulis, M.1    Merkel, A.2    Heath, S.3
  • 51
    • 20444467290 scopus 로고    scopus 로고
    • A microRNA polycistron as a potential human oncogene
    • He L, Thomson JM, Hemann MT, et al. A microRNA polycistron as a potential human oncogene. Nature 2005;435:828-33.
    • (2005) Nature , vol.435 , pp. 828-833
    • He, L.1    Thomson, J.M.2    Hemann, M.T.3
  • 52
    • 39749143354 scopus 로고    scopus 로고
    • Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters
    • Ventura A, Young AG, Winslow MM, et al. Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters. Cell 2008;132:875-86.
    • (2008) Cell , vol.132 , pp. 875-886
    • Ventura, A.1    Young, A.G.2    Winslow, M.M.3
  • 53
    • 84982671396 scopus 로고    scopus 로고
    • Regulation of B-cell development and tolerance by different members of the miR-17∼92 family microRNAs
    • Lai M, Gonzalez-Martin A, Cooper AB, et al. Regulation of B-cell development and tolerance by different members of the miR-17∼92 family microRNAs. Nat Commun 2016;7:12207.
    • (2016) Nat Commun , vol.7 , pp. 12207
    • Lai, M.1    Gonzalez-Martin, A.2    Cooper, A.B.3
  • 54
    • 59149104026 scopus 로고    scopus 로고
    • Consistent deregulation of gene expression between human and murine MLL rearrangement leukemias
    • Li Z, Luo RT, Mi S, et al. Consistent deregulation of gene expression between human and murine MLL rearrangement leukemias. Cancer Res 2009;69:1109-16.
    • (2009) Cancer Res , vol.69 , pp. 1109-1116
    • Li, Z.1    Luo, R.T.2    Mi, S.3
  • 55
    • 70349463161 scopus 로고    scopus 로고
    • The estrogen receptor-alphainduced microRNA signature regulates itself and its transcriptional response
    • Castellano L, Giamas G, Jacob J, et al. The estrogen receptor-alphainduced microRNA signature regulates itself and its transcriptional response. Proc Natl Acad Sci U S A 2009;106:15732-7.
    • (2009) Proc Natl Acad Sci U S A , vol.106 , pp. 15732-15737
    • Castellano, L.1    Giamas, G.2    Jacob, J.3
  • 56
    • 80052290466 scopus 로고    scopus 로고
    • Estrogen induces c-myc gene expression via an upstream enhancer activated by the estrogen receptor and the AP-1 transcription factor
    • Wang C, Mayer JA, Mazumdar A, et al. Estrogen induces c-myc gene expression via an upstream enhancer activated by the estrogen receptor and the AP-1 transcription factor. Mol Endocrinol 2011;25:1527-38.
    • (2011) Mol Endocrinol , vol.25 , pp. 1527-1538
    • Wang, C.1    Mayer, J.A.2    Mazumdar, A.3
  • 57
    • 84925863686 scopus 로고    scopus 로고
    • Microarray analysis on gene regulation by estrogen, progesterone and tamoxifen in human endometrial stromal cells
    • Ren CE, Zhu X, Li J, et al. Microarray analysis on gene regulation by estrogen, progesterone and tamoxifen in human endometrial stromal cells. Int J Mol Sci 2015;16:5864-85.
    • (2015) Int J Mol Sci , vol.16 , pp. 5864-5885
    • Ren, C.E.1    Zhu, X.2    Li, J.3
  • 59
    • 72849120988 scopus 로고    scopus 로고
    • MiR-19 is a key oncogenic component of mir-17-92
    • Olive V, Bennett MJ, Walker JC, et al. miR-19 is a key oncogenic component of mir-17-92. Genes Dev 2009;23:2839-49.
    • (2009) Genes Dev , vol.23 , pp. 2839-2849
    • Olive, V.1    Bennett, M.J.2    Walker, J.C.3
  • 60
    • 70449521473 scopus 로고    scopus 로고
    • Hormone-behavior associations in early infancy
    • Alexander GM, Wilcox T, Farmer ME. Hormone-behavior associations in early infancy. Horm Behav 2009;56:498-502.
    • (2009) Horm Behav , vol.56 , pp. 498-502
    • Alexander, G.M.1    Wilcox, T.2    Farmer, M.E.3
  • 62
    • 84960098132 scopus 로고    scopus 로고
    • The early postnatal period, minipuberty, provides a window on the role of testosterone in human neurobehavioural development
    • Hines M, Spencer D, Kung KT, et al. The early postnatal period, minipuberty, provides a window on the role of testosterone in human neurobehavioural development. Curr Opin Neurobiol 2016;38:69-73.
    • (2016) Curr Opin Neurobiol , vol.38 , pp. 69-73
    • Hines, M.1    Spencer, D.2    Kung, K.T.3
  • 63
    • 0031927226 scopus 로고    scopus 로고
    • Evidence that an HLA-DQA1- DQB1 haplotype influences susceptibility to childhood common acute lymphoblastic leukaemia in boys provides further support for an infection-related aetiology
    • Taylor GM, Dearden S, Payne N, et al. Evidence that an HLA-DQA1- DQB1 haplotype influences susceptibility to childhood common acute lymphoblastic leukaemia in boys provides further support for an infection-related aetiology. Br J Cancer 1998;78:561-5.
    • (1998) Br J Cancer , vol.78 , pp. 561-565
    • Taylor, G.M.1    Dearden, S.2    Payne, N.3
  • 64
    • 78449296221 scopus 로고    scopus 로고
    • Characterization of a candidate tumor suppressor gene uroplakin 1A in esophageal squamous cell carcinoma
    • Kong KL, Kwong DL, Fu L, et al. Characterization of a candidate tumor suppressor gene uroplakin 1A in esophageal squamous cell carcinoma. Cancer Res 2010;70:8832-41.
    • (2010) Cancer Res , vol.70 , pp. 8832-8841
    • Kong, K.L.1    Kwong, D.L.2    Fu, L.3
  • 65
    • 84867814813 scopus 로고    scopus 로고
    • Genome-wide meta-analysis of common variant differences between men and women
    • Boraska V, Jeroncic A, Colonna V, et al. Genome-wide meta-analysis of common variant differences between men and women. Hum Mol Genet 2012;21:4805-15.
    • (2012) Hum Mol Genet , vol.21 , pp. 4805-4815
    • Boraska, V.1    Jeroncic, A.2    Colonna, V.3
  • 66
    • 84960104882 scopus 로고    scopus 로고
    • K-Ras protein as a drug target
    • McCormick F. K-Ras protein as a drug target. J Mol Med (Berl) 2016;94:253-8.
    • (2016) J Mol Med (Berl) , vol.94 , pp. 253-258
    • McCormick, F.1
  • 67
    • 84896815728 scopus 로고    scopus 로고
    • MicroRNA-17∼92 is a powerful cancer driver and a therapeutic target
    • Jin HY, Lai M, Xiao C. microRNA-17∼92 is a powerful cancer driver and a therapeutic target. Cell Cycle 2014;13:495-6.
    • (2014) Cell Cycle , vol.13 , pp. 495-496
    • Jin, H.Y.1    Lai, M.2    Xiao, C.3
  • 68
    • 84883310620 scopus 로고    scopus 로고
    • MicroRNA-17∼92 plays a causative role in lymphomagenesis by coordinating multiple oncogenic pathways
    • Jin HY, Oda H, LaiM, et al. MicroRNA-17∼92 plays a causative role in lymphomagenesis by coordinating multiple oncogenic pathways. EMBO J 2013;32:2377-91.
    • (2013) EMBO J , vol.32 , pp. 2377-2391
    • Jin, H.Y.1    Oda, H.2    Lai, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.