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Volumn 31, Issue 4, 2017, Pages 821-828

Germline activating TYK2 mutations in pediatric patients with two primary acute lymphoblastic leukemia occurrences

(19)  Waanders, E a   Scheijen, B a   Jongmans, M C J a,b   Venselaar, H c   Van Reijmersdal, S V a   Van Dijk, A H A a   Pastorczak, A d   Weren, R D A a   Van Der Schoot, C E e   Van De Vorst, M a   Sonneveld, E f   Hoogerbrugge, N a   Van Der Velden, V H J g   Gruhn, B h   Hoogerbrugge, P M i   Van Dongen, J J M g   Geurts Van Kessel, A a   Van Leeuwen, F N a   Kuiper, R P a  


Author keywords

[No Author keywords available]

Indexed keywords

BRCA2 PROTEIN; GENOMIC DNA; IMMUNOGLOBULIN; JANUS KINASE; PROTEIN KINASE TYK2; STAT PROTEIN; T LYMPHOCYTE RECEPTOR; PROTEIN BINDING;

EID: 84996802211     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/leu.2016.277     Document Type: Article
Times cited : (35)

References (60)
  • 1
    • 85016810145 scopus 로고    scopus 로고
    • Incidence of germline mutations in cancer-predisposition genes in children with hematologic malignancies: A report from the pediatric cancer genome project
    • Walsh M, Wu G, Edmonson M, Gruber TA, Easton J, Yergeau D et al. Incidence of germline mutations in cancer-predisposition genes in children with hematologic malignancies: a report from the pediatric cancer genome project. Blood 2014; 124: 127-127
    • (2014) Blood , vol.124 , pp. 127
    • Walsh, M.1    Wu, G.2    Edmonson, M.3    Gruber, T.A.4    Easton, J.5    Yergeau, D.6
  • 3
    • 84899934875 scopus 로고    scopus 로고
    • Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c 547G4A
    • Auer F, Ruschendorf F, Gombert M, Husemann P, Ginzel S, Izraeli S et al. Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G4A. Leukemia 2014; 28: 1136-1138
    • (2014) Leukemia , vol.28 , pp. 1136-1138
    • Auer, F.1    Ruschendorf, F.2    Gombert, M.3    Husemann, P.4    Ginzel, S.5    Izraeli, S.6
  • 4
    • 84884999671 scopus 로고    scopus 로고
    • A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
    • Shah S, Schrader KA, Waanders E, Timms AE, Vijai J, Miething C et al. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia. Nat Genet 2013; 45: 1226-1231
    • (2013) Nat Genet , vol.45 , pp. 1226-1231
    • Shah, S.1    Schrader, K.A.2    Waanders, E.3    Timms, A.E.4    Vijai, J.5    Miething, C.6
  • 5
    • 84926216729 scopus 로고    scopus 로고
    • Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy
    • Zhang MY, Churpek JE, Keel SB, Walsh T, Lee MK, Loeb KR et al. Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy. Nat Genet 2015; 47: 180-185
    • (2015) Nat Genet , vol.47 , pp. 180-185
    • Zhang, M.Y.1    Churpek, J.E.2    Keel, S.B.3    Walsh, T.4    Lee, M.K.5    Loeb, K.R.6
  • 6
    • 84937779216 scopus 로고    scopus 로고
    • Germline ETV6 mutations confer susceptibility to acute lymphoblastic leukemia and thrombocytopenia
    • Topka S, Vijai J, Walsh MF, Jacobs L, Maria A, Villano D et al. Germline ETV6 mutations confer susceptibility to acute lymphoblastic leukemia and thrombocytopenia. PLoS Genet 2015; 11: e1005262
    • (2015) PLoS Genet , vol.11 , pp. e1005262
    • Topka, S.1    Vijai, J.2    Walsh, M.F.3    Jacobs, L.4    Maria, A.5    Villano, D.6
  • 7
    • 84929130522 scopus 로고    scopus 로고
    • Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia
    • Noetzli L, Lo RW, Lee-Sherick AB, Callaghan M, Noris P, Savoia A et al. Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia. Nat Genet 2015; 47: 535-538
    • (2015) Nat Genet , vol.47 , pp. 535-538
    • Noetzli, L.1    Lo, R.W.2    Lee-Sherick, A.B.3    Callaghan, M.4    Noris, P.5    Savoia, A.6
  • 8
    • 84951304790 scopus 로고    scopus 로고
    • Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: A systematic genetic study
    • Moriyama T, Metzger ML, Wu G, Nishii R, Qian M, Devidas M et al. Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study. Lancet Oncol 2015; 16: 1659-1666
    • (2015) Lancet Oncol , vol.16 , pp. 1659-1666
    • Moriyama, T.1    Metzger, M.L.2    Wu, G.3    Nishii, R.4    Qian, M.5    Devidas, M.6
  • 9
    • 84958893989 scopus 로고    scopus 로고
    • New cellular markers at diagnosis are associated with isolated central nervous system relapse in paediatric B-cell precursor acute lymphoblastic leukaemia
    • van der Velden VH, de Launaij D, de Vries JF, de Haas V, Sonneveld E, Voerman JS et al. New cellular markers at diagnosis are associated with isolated central nervous system relapse in paediatric B-cell precursor acute lymphoblastic leukaemia. Br J Haematol 2016; 172: 769-781
    • (2016) Br J Haematol , vol.172 , pp. 769-781
    • Vander Velden, V.H.1    Launaij, D.2    Vries, J.F.3    Haas, V.4    Sonneveld, E.5    Voerman, J.S.6
  • 10
    • 79955043828 scopus 로고    scopus 로고
    • Late recurrence of childhood T-cell acute lymphoblastic leukemia frequently represents a second leukemia rather than a relapse: First evidence for genetic predisposition
    • Szczepanski T, van der Velden VH, Waanders E, Kuiper RP, Van Vlierberghe P, Gruhn B et al. Late recurrence of childhood T-cell acute lymphoblastic leukemia frequently represents a second leukemia rather than a relapse: first evidence for genetic predisposition. J Cin Oncol 2011; 29: 1643-1649
    • (2011) J Cin Oncol , vol.29 , pp. 1643-1649
    • Szczepanski, T.1    Vander Velden, V.H.2    Waanders, E.3    Kuiper, R.P.4    Van Vlierberghe, P.5    Gruhn, B.6
  • 11
    • 84891783452 scopus 로고    scopus 로고
    • The Database of Genomic Variants: A curated collection of structural variation in the human genome
    • (Database issue)
    • MacDonald JR, Ziman R, Yuen RK, Feuk L, Scherer SW. The Database of Genomic Variants: a curated collection of structural variation in the human genome. Nucleic Acids Res 2014; 42(Database issue): D986-D992
    • (2014) Nucleic Acids Res , vol.42 , pp. D986-D992
    • MacDonald, J.R.1    Ziman, R.2    Yuen, R.K.3    Feuk, L.4    Scherer, S.W.5
  • 12
    • 77956174929 scopus 로고    scopus 로고
    • Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individuals
    • Franke B, Vasquez AA, Veltman JA, Brunner HG, Rijpkema M, Fernandez G. Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individuals. Biol Psychiatry 2010; 68: 586-588
    • (2010) Biol Psychiatry , vol.68 , pp. 586-588
    • Franke, B.1    Vasquez, A.A.2    Veltman, J.A.3    Brunner, H.G.4    Rijpkema, M.5    Fernandez, G.6
  • 13
    • 79960913302 scopus 로고    scopus 로고
    • Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients
    • Venkatachalam R, Verwiel ET, Kamping EJ, Hoenselaar E, Gorgens H, Schackert HK et al. Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients. Int J Cancer 2011; 129: 1635-1642
    • (2011) J Cancer , vol.129 , pp. 1635-1642
    • Venkatachalam, R.1    Verwiel, E.T.2    Kamping, E.J.3    Hoenselaar, E.4    Gorgens, H.5    Schackert, H.K.6
  • 14
    • 65649143517 scopus 로고    scopus 로고
    • MRD detection in acute lymphoblastic leukemia patients using Ig/TCR gene rearrangements as targets for real-time quantitative PCR
    • van der Velden VH, van Dongen JJ. MRD detection in acute lymphoblastic leukemia patients using Ig/TCR gene rearrangements as targets for real-time quantitative PCR. Methods Mol Biol 2009; 538: 115-150
    • (2009) Methods Mol Biol , vol.538 , pp. 115-150
    • Vander Velden, V.H.1    Van Dongen, J.J.2
  • 18
    • 84905579746 scopus 로고    scopus 로고
    • Whole-genome sequence variation, population structure and demographic history of the Dutch population
    • Genome of The Netherlands Consortium
    • Genome of The Netherlands Consortium. Whole-genome sequence variation, population structure and demographic history of the Dutch population. Nat Genet 2014; 46: 818-825
    • (2014) Nat Genet , vol.46 , pp. 818-825
  • 20
    • 84901840527 scopus 로고    scopus 로고
    • Structure of the pseudokinase-kinase domains from protein kinase TYK2 reveals a mechanism for Janus kinase (JAK) autoinhibition
    • Lupardus PJ, Ultsch M, Wallweber H, Bir Kohli P, Johnson AR, Eigenbrot C. Structure of the pseudokinase-kinase domains from protein kinase TYK2 reveals a mechanism for Janus kinase (JAK) autoinhibition. Proc Natl Acad Sci USA 2014; 111: 8025-8030
    • (2014) Proc Natl Acad Sci USA , vol.111 , pp. 8025-8030
    • Lupardus, P.J.1    Ultsch, M.2    Wallweber, H.3    Bir Kohli, P.4    Johnson, A.R.5    Eigenbrot, C.6
  • 21
    • 17844383458 scopus 로고    scopus 로고
    • A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
    • James C, Ugo V, Le Couedic JP, Staerk J, Delhommeau F, Lacout C et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 2005; 434: 1144-1148
    • (2005) Nature , vol.434 , pp. 1144-1148
    • James, C.1    Ugo, V.2    Le Couedic, J.P.3    Staerk, J.4    Delhommeau, F.5    Lacout, C.6
  • 25
    • 70149087158 scopus 로고    scopus 로고
    • High frequency of PTEN, PI3K, and AKT abnormalities in T-cell acute lymphoblastic leukemia
    • Gutierrez A, Sanda T, Grebliunaite R, Carracedo A, Salmena L, Ahn Y et al. High frequency of PTEN, PI3K, and AKT abnormalities in T-cell acute lymphoblastic leukemia. Blood 2009; 114: 647-650
    • (2009) Blood , vol.114 , pp. 647-650
    • Gutierrez, A.1    Sanda, T.2    Grebliunaite, R.3    Carracedo, A.4    Salmena, L.5    Ahn, Y.6
  • 27
    • 84952916741 scopus 로고
    • ALK-related neuroblastic tumor susceptibility
    • Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH et al. (eds).: Seattle, WA, USA
    • Greengard EG, Park JR. ALK-related neuroblastic tumor susceptibility. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH et al. (eds). GeneReviews (R): Seattle, WA, USA, 1993
    • (1993) GeneReviews (R)
    • Greengard, E.G.1    Park, J.R.2
  • 28
    • 54049120220 scopus 로고    scopus 로고
    • Activating mutations in ALK provide a therapeutic target in neuroblastoma
    • George RE, Sanda T, Hanna M, Frohling S, Luther W 2nd, Zhang J et al. Activating mutations in ALK provide a therapeutic target in neuroblastoma. Nature 2008; 455: 975-978
    • (2008) Nature , vol.455 , pp. 975-978
    • George, R.E.1    Sanda, T.2    Hanna, M.3    Frohling, S.4    Luther, W.5    Zhang, J.6
  • 30
    • 84892565796 scopus 로고    scopus 로고
    • Molecular characterization and clinical impact of t(11;15)(q23;q14-15) MLL-CASC5 rearrangement
    • Yang JJ, Park TS, Lee ST, Seo JY, Oh SH, Cho EH et al. Molecular characterization and clinical impact of t(11;15)(q23;q14-15) MLL-CASC5 rearrangement. Haematologica 2014; 99: e11-e13
    • (2014) Haematologica , vol.99 , pp. e11-e13
    • Yang, J.J.1    Park, T.S.2    Lee, S.T.3    Seo, J.Y.4    Oh, S.H.5    Cho, E.H.6
  • 32
    • 84890921845 scopus 로고    scopus 로고
    • A robust methodology to subclassify pseudokinases based on their nucleotide-binding properties
    • Murphy JM, Zhang Q, Young SN, Reese ML, Bailey FP, Eyers PA et al. A robust methodology to subclassify pseudokinases based on their nucleotide-binding properties. Biochem J 2014; 457: 323-334
    • (2014) Biochem J , vol.457 , pp. 323-334
    • Murphy, J.M.1    Zhang, Q.2    Young, S.N.3    Reese, M.L.4    Bailey, F.P.5    Eyers, P.A.6
  • 33
    • 77956199736 scopus 로고    scopus 로고
    • Undifferentiated high-grade pleomorphic sarcomas in children: A clinicopathologic study of 10 cases and review of literature
    • Alaggio R, Collini P, Randall RL, Barnette P, Million L, Coffin CM. Undifferentiated high-grade pleomorphic sarcomas in children: a clinicopathologic study of 10 cases and review of literature. Pediatr Dev Pathol 2010; 13: 209-217
    • (2010) Pediatr Dev Pathol , vol.13 , pp. 209-217
    • Alaggio, R.1    Collini, P.2    Randall, R.L.3    Barnette, P.4    Million, L.5    Coffin, C.M.6
  • 34
    • 84928015700 scopus 로고    scopus 로고
    • Convergent mutations and kinase fusions lead to oncogenic STAT3 activation in anaplastic large cell lymphoma
    • Crescenzo R, Abate F, Lasorsa E, Tabbo F, Gaudiano M, Chiesa N et al. Convergent mutations and kinase fusions lead to oncogenic STAT3 activation in anaplastic large cell lymphoma. Cancer Cell 2015; 27: 516-532
    • (2015) Cancer Cell , vol.27 , pp. 516-532
    • Crescenzo, R.1    Abate, F.2    Lasorsa, E.3    Tabbo, F.4    Gaudiano, M.5    Chiesa, N.6
  • 36
    • 84878339471 scopus 로고    scopus 로고
    • Multiple myeloma is affected by multiple and heterogeneous somatic mutations in adhesion-and receptor tyrosine kinase signaling molecules
    • Leich E, Weissbach S, Klein HU, Grieb T, Pischimarov J, Stuhmer T et al. Multiple myeloma is affected by multiple and heterogeneous somatic mutations in adhesion-and receptor tyrosine kinase signaling molecules. Blood Cancer J 2013; 3: e102
    • (2013) Blood Cancer J , vol.3 , pp. e102
    • Leich, E.1    Weissbach, S.2    Klein, H.U.3    Grieb, T.4    Pischimarov, J.5    Stuhmer, T.6
  • 38
    • 84919663234 scopus 로고    scopus 로고
    • A novel recurrent NPM1-TYK2 gene fusion in cutaneous CD30-positive lymphoproliferative disorders
    • Velusamy T, Kiel MJ, Sahasrabuddhe AA, Rolland D, Dixon CA, Bailey NG et al. A novel recurrent NPM1-TYK2 gene fusion in cutaneous CD30-positive lymphoproliferative disorders. Blood 2014; 124: 3768-3771
    • (2014) Blood , vol.124 , pp. 3768-3771
    • Velusamy, T.1    Kiel, M.J.2    Sahasrabuddhe, A.A.3    Rolland, D.4    Dixon, C.A.5    Bailey, N.G.6
  • 39
    • 84865118132 scopus 로고    scopus 로고
    • Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia
    • Roberts KG, Morin RD, Zhang J, Hirst M, Zhao Y, Su X et al. Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia. Cancer Cell 2012; 22: 153-166
    • (2012) Cancer Cell , vol.22 , pp. 153-166
    • Roberts, K.G.1    Morin, R.D.2    Zhang, J.3    Hirst, M.4    Zhao, Y.5    Su, X.6
  • 40
    • 84907080295 scopus 로고    scopus 로고
    • Targetable kinase-activating lesions in Ph-like acute lymphoblastic leukemia
    • Roberts KG, Li Y, Payne-Turner D, Harvey RC, Yang YL, Pei D et al. Targetable kinase-activating lesions in Ph-like acute lymphoblastic leukemia. N Engl J Med 2014; 371: 1005-1015
    • (2014) N Engl J Med , vol.371 , pp. 1005-1015
    • Roberts, K.G.1    Li, Y.2    Payne-Turner, D.3    Harvey, R.C.4    Yang, Y.L.5    Pei, D.6
  • 41
    • 77954516863 scopus 로고    scopus 로고
    • Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia
    • Harvey RC, Mullighan CG, Chen IM, Wharton W, Mikhail FM, Carroll AJ et al. Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia. Blood 2010; 115: 5312-5321
    • (2010) Blood , vol.115 , pp. 5312-5321
    • Harvey, R.C.1    Mullighan, C.G.2    Chen, I.M.3    Wharton, W.4    Mikhail, F.M.5    Carroll, A.J.6
  • 43
    • 84862907593 scopus 로고    scopus 로고
    • The genetic basis of early T-cell precursor acute lymphoblastic leukaemia
    • Zhang J, Ding L, Holmfeldt L, Wu G, Heatley SL, Payne-Turner D et al. The genetic basis of early T-cell precursor acute lymphoblastic leukaemia. Nature 2012; 481: 157-163
    • (2012) Nature , vol.481 , pp. 157-163
    • Zhang, J.1    Ding, L.2    Holmfeldt, L.3    Wu, G.4    Heatley, S.L.5    Payne-Turner, D.6
  • 44
    • 80052922387 scopus 로고    scopus 로고
    • Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: A report from the Children's Oncology Group
    • Zhang J, Mullighan CG, Harvey RC, Wu G, Chen X, Edmonson M et al. Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group. Blood 2011; 118: 3080-3087
    • (2011) Blood , vol.118 , pp. 3080-3087
    • Zhang, J.1    Mullighan, C.G.2    Harvey, R.C.3    Wu, G.4    Chen, X.5    Edmonson, M.6
  • 46
    • 20144363192 scopus 로고    scopus 로고
    • Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
    • Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 2005; 365: 1054-1061
    • (2005) Lancet , vol.365 , pp. 1054-1061
    • Baxter, E.J.1    Scott, L.M.2    Campbell, P.J.3    East, C.4    Fourouclas, N.5    Swanton, S.6
  • 48
    • 20244369569 scopus 로고    scopus 로고
    • Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
    • Levine RL, Wadleigh M, Cools J, Ebert BL, Wernig G, Huntly BJ et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell 2005; 7: 387-397
    • (2005) Cancer Cell , vol.7 , pp. 387-397
    • Levine, R.L.1    Wadleigh, M.2    Cools, J.3    Ebert, B.L.4    Wernig, G.5    Huntly, B.J.6
  • 49
    • 13844292408 scopus 로고    scopus 로고
    • Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus
    • Sigurdsson S, Nordmark G, Goring HH, Lindroos K, Wiman AC, Sturfelt G et al. Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus. Am J Hum Genet 2005; 76: 528-537
    • (2005) Am J Hum Genet , vol.76 , pp. 528-537
    • Sigurdsson, S.1    Nordmark, G.2    Goring, H.H.3    Lindroos, K.4    Wiman, A.C.5    Sturfelt, G.6
  • 50
    • 35748981184 scopus 로고    scopus 로고
    • Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
    • Wellcome Trust Case Control Consortium and Australo-Anglo-American Spondylitis Consortium
    • Wellcome Trust Case Control Consortium and Australo-Anglo-American Spondylitis Consortium, Burton PR, Clayton DG, Cardon LR, Craddock N et al. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 2007; 39: 1329-1337
    • (2007) Nat Genet , vol.39 , pp. 1329-1337
    • Burton, P.R.1    Clayton, D.G.2    Cardon, L.R.3    Craddock, N.4
  • 51
    • 33845897463 scopus 로고    scopus 로고
    • Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity
    • Minegishi Y, Saito M, Morio T, Watanabe K, Agematsu K, Tsuchiya S et al. Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity. Immunity 2006; 25: 745-755
    • (2006) Immunity , vol.25 , pp. 745-755
    • Minegishi, Y.1    Saito, M.2    Morio, T.3    Watanabe, K.4    Agematsu, K.5    Tsuchiya, S.6
  • 53
    • 79960392815 scopus 로고    scopus 로고
    • Involvement of tyrosine kinase-2 in both the IL-12/Th1 and IL-23/Th17 axes in vivo
    • Ishizaki M, Akimoto T, Muromoto R, Yokoyama M, Ohshiro Y, Sekine Y et al. Involvement of tyrosine kinase-2 in both the IL-12/Th1 and IL-23/Th17 axes in vivo. J Immunol 2011; 187: 181-189
    • (2011) J Immunol , vol.187 , pp. 181-189
    • Ishizaki, M.1    Akimoto, T.2    Muromoto, R.3    Yokoyama, M.4    Ohshiro, Y.5    Sekine, Y.6
  • 54
    • 84899971013 scopus 로고    scopus 로고
    • Tyk2 is a therapeutic target for psoriasis-like skin inflammation
    • Ishizaki M, Muromoto R, Akimoto T, Sekine Y, Kon S, Diwan M et al. Tyk2 is a therapeutic target for psoriasis-like skin inflammation. Int Immunol 2014; 26: 257-267
    • (2014) Immunol , vol.26 , pp. 257-267
    • Ishizaki, M.1    Muromoto, R.2    Akimoto, T.3    Sekine, Y.4    Kon, S.5    Diwan, M.6
  • 56
    • 55949137903 scopus 로고    scopus 로고
    • Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes
    • Magnusson S, Borg A, Kristoffersson U, Nilbert M, Wiebe T, Olsson H. Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes. Fam Cancer 2008; 7: 331-337
    • (2008) Fam Cancer , vol.7 , pp. 331-337
    • Magnusson, S.1    Borg, A.2    Kristoffersson, U.3    Nilbert, M.4    Wiebe, T.5    Olsson, H.6
  • 57
    • 33751095620 scopus 로고    scopus 로고
    • Childhood cancer in families with and without BRCA1 or BRCA2 mutations ascertained at a high-risk breast cancer clinic
    • Brooks GA, Stopfer JE, Erlichman J, Davidson R, Nathanson KL, Domchek SM. Childhood cancer in families with and without BRCA1 or BRCA2 mutations ascertained at a high-risk breast cancer clinic. Cancer Biol Ther 2006; 5: 1098-1102
    • (2006) Cancer Biol Ther , vol.5 , pp. 1098-1102
    • Brooks, G.A.1    Stopfer, J.E.2    Erlichman, J.3    Davidson, R.4    Nathanson, K.L.5    Domchek, S.M.6
  • 58
    • 85010703579 scopus 로고    scopus 로고
    • Diagnostic yield of clinical tumor and germline whole-exome sequencing for children with solid tumors
    • Parsons DW, Roy A, Yang Y, Wang T, Scollon S, Bergstrom K et al. Diagnostic yield of clinical tumor and germline whole-exome sequencing for children with solid tumors. JAMA Oncol 2016
    • (2016) JAMA Oncol
    • Parsons, D.W.1    Roy, A.2    Yang, Y.3    Wang, T.4    Scollon, S.5    Bergstrom, K.6
  • 59
    • 0036837899 scopus 로고    scopus 로고
    • Identification of a family of mastermind-like transcriptional coactivators for mammalian notch receptors
    • Wu L, Sun T, Kobayashi K, Gao P, Griffin JD. Identification of a family of mastermind-like transcriptional coactivators for mammalian notch receptors. Mol Cell Biol 2002; 22: 7688-7700
    • (2002) Mol Cell Biol , vol.22 , pp. 7688-7700
    • Wu, L.1    Sun, T.2    Kobayashi, K.3    Gao, P.4    Griffin, J.D.5
  • 60
    • 84865187020 scopus 로고    scopus 로고
    • Notch and PI3K: How is the road traveled?
    • Bailis W, Pear WS. Notch and PI3K: how is the road traveled? Blood 2012; 120: 1349-1350
    • (2012) Blood , vol.120 , pp. 1349-1350
    • Bailis, W.1    Pear, W.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.