메뉴 건너뛰기




Volumn 19, Issue 8, 2011, Pages 870-874

Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN TYROSINE PHOSPHATASE SHP 2;

EID: 79960636001     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2011.37     Document Type: Article
Times cited : (142)

References (46)
  • 1
    • 77955574059 scopus 로고    scopus 로고
    • Noonan syndrome: Clinical aspects and molecular pathogenesis
    • Tartaglia M, Zampino G, Gelb BD: Noonan syndrome: clinical aspects and molecular pathogenesis. Mol Syndromol 2010; 1: 2-26.
    • (2010) Mol Syndromol , vol.1 , pp. 2-26
    • Tartaglia, M.1    Zampino, G.2    Gelb, B.D.3
  • 3
    • 33645280589 scopus 로고    scopus 로고
    • Inherited predispositions and hyperactive Ras in myeloid leukemogenesis
    • Lauchle JO, Braun BS, Loh ML, Shannon K: Inherited predispositions and hyperactive Ras in myeloid leukemogenesis. Pediatr Blood Cancer 2006; 46: 579-585.
    • (2006) Pediatr Blood Cancer , vol.46 , pp. 579-585
    • Lauchle, J.O.1    Braun, B.S.2    Loh, M.L.3    Shannon, K.4
  • 5
  • 6
    • 56649102280 scopus 로고    scopus 로고
    • Clinical and molecular characterization of 40 patients with Noonan syndrome
    • Ferrero GB, Baldassarre G, Delmonaco AG et al: Clinical and molecular characterization of 40 patients with Noonan syndrome. Eur J Med Genet 2008; 51: 566-572.
    • (2008) Eur J Med Genet , vol.51 , pp. 566-572
    • Ferrero, G.B.1    Baldassarre, G.2    Delmonaco, A.G.3
  • 9
    • 60049097249 scopus 로고    scopus 로고
    • Hodgkin's lymphoma in a patient with Noonan syndrome with germ-line PTPN11 mutations
    • Lo FS, Kuo TT, Wang CJ, Kuo MT, Kuo MC: Hodgkin's lymphoma in a patient with Noonan syndrome with germ-line PTPN11 mutations. Int J Hematol 2008; 88: 287-290.
    • (2008) Int J Hematol , vol.88 , pp. 287-290
    • Lo, F.S.1    Kuo, T.T.2    Wang, C.J.3    Kuo, M.T.4    Kuo, M.C.5
  • 10
    • 20044362426 scopus 로고    scopus 로고
    • Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation [2]
    • DOI 10.1002/ajh.20326
    • Matsubara K, Yabe H, Ogata T, Yoshida R, Fukaya T: Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation. Am J Hematol 2005; 79: 171-172. (Pubitemid 40770681)
    • (2005) American Journal of Hematology , vol.79 , Issue.2 , pp. 171-172
    • Matsubara, K.1    Yabe, H.2    Ogata, T.3    Yoshida, R.4    Fukaya, T.5
  • 11
    • 33645823187 scopus 로고    scopus 로고
    • Acute lymphoblastic leukaemia in Noonan syndrome
    • Roti G, La SR, Ballanti S et al: Acute lymphoblastic leukaemia in Noonan syndrome. Br J Haematol 2006; 133: 448-450.
    • (2006) Br J Haematol , vol.133 , pp. 448-450
    • Roti, G.1    La, S.R.2    Ballanti, S.3
  • 13
    • 0034091082 scopus 로고    scopus 로고
    • A case of Noonan's syndrome with possible associated neuroblastoma (multiple letters)
    • Ijiri R, Tanaka Y, Keisuke K, Masuno M, Imaizumi K: A case of Noonan's syndrome with possible associated neuroblastoma. Pediatr Radiol 2000; 30: 432-433. (Pubitemid 30330454)
    • (2000) Pediatric Radiology , vol.30 , Issue.6 , pp. 432-433
    • Ijiri, R.1    Tanaka, Y.2    Kato, K.3    Masuno, M.4    Imaizumi, K.5
  • 15
    • 0029027050 scopus 로고
    • Vaginal rhabdomyosarcoma in a patient with Noonan syndrome
    • Khan S, McDowell H, Upadhyaya M, Fryer A: Vaginal rhabdomyosarcoma in a patient with Noonan syndrome. J Med Genet 1995; 32: 743-745.
    • (1995) J Med Genet , vol.32 , pp. 743-745
    • Khan, S.1    McDowell, H.2    Upadhyaya, M.3    Fryer, A.4
  • 18
    • 40049093061 scopus 로고    scopus 로고
    • Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors
    • DOI 10.1016/j.cancergencyto.2007.12.005, PII S0165460807008114
    • Mutesa L, Pierquin G, Janin N et al: Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors. Cancer Genet Cytogenet 2008; 182: 40-42. (Pubitemid 351323957)
    • (2008) Cancer Genetics and Cytogenetics , vol.182 , Issue.1 , pp. 40-42
    • Mutesa, L.1    Pierquin, G.2    Janin, N.3    Segers, K.4    Thomee, C.5    Provenzi, M.6    Bours, V.7
  • 21
    • 18844428291 scopus 로고    scopus 로고
    • Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome
    • Lee JS, Tartaglia M, Gelb BD et al: Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome. J Med Genet 2005; 42: e11.
    • (2005) J Med Genet , vol.42
    • Lee, J.S.1    Tartaglia, M.2    Gelb, B.D.3
  • 26
    • 44849138413 scopus 로고    scopus 로고
    • Isolation of a distinct class of gain-of-function SHP-2 mutants with oncogenic RAS-like transforming activity from solid tumors
    • DOI 10.1038/sj.onc.1211019, PII 1211019
    • Miyamoto D, Miyamoto M, Takahashi A et al: Isolation of a distinct class of gain-offunction SHP-2 mutants with oncogenic RAS-like transforming activity from solid tumors. Oncogene 2008; 27: 3508-3515. (Pubitemid 351793798)
    • (2008) Oncogene , vol.27 , Issue.25 , pp. 3508-3515
    • Miyamoto, D.1    Miyamoto, M.2    Takahashi, A.3    Yomogita, Y.4    Higashi, H.5    Kondo, S.6    Hatakeyama, M.7
  • 32
    • 45549108065 scopus 로고    scopus 로고
    • Use of human androgen receptor gene analysis to aid the diagnosis of JMML in female noonan syndrome patients
    • DOI 10.1002/pbc.21591
    • Lavin VA, Hamid R, Patterson J, Alford C, Ho R, Yang E: Use of human androgen receptor gene analysis to aid the diagnosis of JMML in female noonan syndrome patients. Pediatr Blood Cancer 2008; 51: 298-302. (Pubitemid 351874432)
    • (2008) Pediatric Blood and Cancer , vol.51 , Issue.2 , pp. 298-302
    • Lavin, V.A.1    Hamid, R.2    Patterson, J.3    Alford, C.4    Ho, R.5    Yang, E.6
  • 33
    • 59449106107 scopus 로고    scopus 로고
    • Primary mixed glioneuronal tumor of the central nervous system in a patient with noonan syndrome: A case report and review of the literature
    • Sherman CB, li-Nazir A, Gonzales-Gomez I, Finlay JL, Dhall G: Primary mixed glioneuronal tumor of the central nervous system in a patient with noonan syndrome: a case report and review of the literature. J Pediatr Hematol Oncol 2009; 31: 61-64.
    • (2009) J Pediatr Hematol Oncol , vol.31 , pp. 61-64
    • Sherman, C.B.1    Li-Nazir, A.2    Gonzales-Gomez, I.3    Finlay, J.L.4    Dhall, G.5
  • 34
    • 33646022879 scopus 로고    scopus 로고
    • Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors
    • Martinelli S, Carta C, Flex E et al: Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors. Cancer Genet Cytogenet 2006; 166: 124-129.
    • (2006) Cancer Genet Cytogenet , vol.166 , pp. 124-129
    • Martinelli, S.1    Carta, C.2    Flex, E.3
  • 37
    • 42349111238 scopus 로고    scopus 로고
    • Hepatoblastoma in a Noonan syndrome patient with a PTPN11 mutation
    • DOI 10.1002/pbc.21509
    • Yoshida R, Ogata T, Masawa N, Nagai T: Hepatoblastoma in a Noonan syndrome patient with a PTPN11 mutation. Pediatr Blood Cancer 2008; 50: 1274-1276. (Pubitemid 351555559)
    • (2008) Pediatric Blood and Cancer , vol.50 , Issue.6 , pp. 1274-1276
    • Yoshida, R.1    Ogata, T.2    Masawa, N.3    Nagai, T.4
  • 38
    • 49149115868 scopus 로고    scopus 로고
    • The RAS/MAPK syndromes: Novel roles of the RAS pathway in human genetic disorders
    • Aoki Y, Niihori T, Narumi Y, Kure S, Matsubara Y: The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders. Hum Mutat 2008; 29: 992-1006.
    • (2008) Hum Mutat , vol.29 , pp. 992-1006
    • Aoki, Y.1    Niihori, T.2    Narumi, Y.3    Kure, S.4    Matsubara, Y.5
  • 41
    • 0023748414 scopus 로고
    • Genetic alterations during colorectal-tumor development
    • Vogelstein B, Fearon ER, Hamilton SR et al: Genetic alterations during colorectal-tumor development. N Engl J Med 1988; 319: 525-532.
    • (1988) N Engl J Med , vol.319 , pp. 525-532
    • Vogelstein, B.1    Fearon, E.R.2    Hamilton, S.R.3
  • 43
    • 34447562827 scopus 로고    scopus 로고
    • Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screening
    • DOI 10.1136/jmg.2007.049346
    • Sharif S, Moran A, Huson SM et al: Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screening. J Med Genet 2007; 44: 481-484. (Pubitemid 47325733)
    • (2007) Journal of Medical Genetics , vol.44 , Issue.8 , pp. 481-484
    • Sharif, S.1    Moran, A.2    Huson, S.M.3    Iddenden, R.4    Shenton, A.5    Howard, E.6    Evans, D.G.R.7
  • 44
    • 24744465207 scopus 로고    scopus 로고
    • Diverse biochemical properties of Shp2 mutants: Implications for disease phenotypes
    • DOI 10.1074/jbc.M504699200
    • Keilhack H, David FS, McGregor M, Cantley LC, Neel BG: Diverse biochemical properties of Shp2 mutants. Implications for disease phenotypes. J Biol Chem 2005; 280: 30984-30993. (Pubitemid 41291831)
    • (2005) Journal of Biological Chemistry , vol.280 , Issue.35 , pp. 30984-30993
    • Keilhack, H.1    David, F.S.2    McGregor, M.3    Cantley, L.C.4    Neel, B.G.5
  • 46
    • 2342525088 scopus 로고    scopus 로고
    • Cancer risk following growth hormone use in childhood: Implications for current practice
    • DOI 10.2165/00002018-200427060-00002
    • Ogilvy-Stuart AL, Gleeson H: Cancer risk following growth hormone use in childhood: implications for current practice. Drug Saf 2004; 27: 369-382. (Pubitemid 38608456)
    • (2004) Drug Safety , vol.27 , Issue.6 , pp. 369-382
    • Ogilvy-Stuart, A.L.1    Gleeson, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.