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Journal Abstract Search

175 related items for PubMed ID: 16078230

  • 1. Therapy-related acute myeloid leukemia in a child with Noonan syndrome and clonal duplication of the germline PTPN11 mutation.
    Chantrain CF, Jijon P, De Raedt T, Vermylen C, Poirel HA, Legius E, Brichard B.
    Pediatr Blood Cancer; 2007 Jan; 48(1):101-4. PubMed ID: 16078230
    [Abstract] [Full Text] [Related]

  • 2. Activating mutations of the noonan syndrome-associated SHP2/PTPN11 gene in human solid tumors and adult acute myelogenous leukemia.
    Bentires-Alj M, Paez JG, David FS, Keilhack H, Halmos B, Naoki K, Maris JM, Richardson A, Bardelli A, Sugarbaker DJ, Richards WG, Du J, Girard L, Minna JD, Loh ML, Fisher DE, Velculescu VE, Vogelstein B, Meyerson M, Sellers WR, Neel BG.
    Cancer Res; 2004 Dec 15; 64(24):8816-20. PubMed ID: 15604238
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  • 3. Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation.
    Matsubara K, Yabe H, Ogata T, Yoshida R, Fukaya T.
    Am J Hematol; 2005 Jun 15; 79(2):171-2. PubMed ID: 15929108
    [No Abstract] [Full Text] [Related]

  • 4. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia.
    Tartaglia M, Niemeyer CM, Fragale A, Song X, Buechner J, Jung A, Hählen K, Hasle H, Licht JD, Gelb BD.
    Nat Genet; 2003 Jun 15; 34(2):148-50. PubMed ID: 12717436
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  • 5. Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome.
    Karow A, Steinemann D, Göhring G, Hasle H, Greiner J, Harila-Saari A, Flotho C, Zenker M, Schlegelberger B, Niemeyer CM, Kratz CP.
    Leukemia; 2007 Jun 15; 21(6):1303-5. PubMed ID: 17361219
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  • 8. Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors.
    Mutesa L, Pierquin G, Janin N, Segers K, Thomée C, Provenzi M, Bours V.
    Cancer Genet Cytogenet; 2008 Apr 01; 182(1):40-2. PubMed ID: 18328949
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  • 10. PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning.
    Schollen E, Matthijs G, Gewillig M, Fryns JP, Legius E.
    Eur J Hum Genet; 2003 Jan 01; 11(1):85-8. PubMed ID: 12529711
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  • 11. Mutations of the PTPN11 gene in therapy-related MDS and AML with rare balanced chromosome translocations.
    Christiansen DH, Desta F, Andersen MK, Pedersen-Bjergaard J.
    Genes Chromosomes Cancer; 2007 Jun 01; 46(6):517-21. PubMed ID: 17330262
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  • 12. Germline gain-of-function mutations in SOS1 cause Noonan syndrome.
    Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Kucherlapati RS.
    Nat Genet; 2007 Jan 01; 39(1):70-4. PubMed ID: 17143285
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  • 13. Severe aortic valvar stenosis in familial Noonan syndrome with mutation of the PTPN11 gene.
    Abadir S, Edouard T, Julia S.
    Cardiol Young; 2007 Feb 01; 17(1):95-7. PubMed ID: 17184563
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  • 14. PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes.
    Ogata T, Yoshida R.
    Pediatr Endocrinol Rev; 2005 Jun 01; 2(4):669-74. PubMed ID: 16208280
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  • 15. Mutation analysis of the genes involved in the Ras-mitogen-activated protein kinase (MAPK) pathway in Korean patients with Noonan syndrome.
    Lee ST, Ki CS, Lee HJ.
    Clin Genet; 2007 Aug 01; 72(2):150-5. PubMed ID: 17661820
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  • 16. Respiratory failure, juvenile myelomonocytic leukemia, and neonatal Noonan syndrome.
    Cheong JL, Moorkamp MH.
    J Pediatr Hematol Oncol; 2007 Apr 01; 29(4):262-4. PubMed ID: 17414570
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  • 19. Genotype-phenotype correlations in Noonan syndrome.
    Zenker M, Buheitel G, Rauch R, Koenig R, Bosse K, Kress W, Tietze HU, Doerr HG, Hofbeck M, Singer H, Reis A, Rauch A.
    J Pediatr; 2004 Mar 01; 144(3):368-74. PubMed ID: 15001945
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  • 20. Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation.
    Araki T, Mohi MG, Ismat FA, Bronson RT, Williams IR, Kutok JL, Yang W, Pao LI, Gilliland DG, Epstein JA, Neel BG.
    Nat Med; 2004 Aug 01; 10(8):849-57. PubMed ID: 15273746
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