BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 16830086)

  • 21. Respiratory failure, juvenile myelomonocytic leukemia, and neonatal Noonan syndrome.
    Cheong JL; Moorkamp MH
    J Pediatr Hematol Oncol; 2007 Apr; 29(4):262-4. PubMed ID: 17414570
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mild variable Noonan syndrome in a family with a novel PTPN11 mutation.
    Zenker M; Voss E; Reis A
    Eur J Med Genet; 2007; 50(1):43-7. PubMed ID: 17052965
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 39(1):70-4. PubMed ID: 17143285
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndrome.
    Sarkozy A; Obregon MG; Conti E; Esposito G; Mingarelli R; Pizzuti A; Dallapiccola B
    Eur J Hum Genet; 2004 Dec; 12(12):1069-72. PubMed ID: 15470362
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Systemic lupus erythematosus and other autoimmune disorders in children with Noonan syndrome.
    Lopez-Rangel E; Malleson PN; Lirenman DS; Roa B; Wiszniewska J; Lewis ME
    Am J Med Genet A; 2005 Dec; 139(3):239-42. PubMed ID: 16283670
    [No Abstract]   [Full Text] [Related]  

  • 26. Does the rare A172G mutation of PTPN11 gene convey a mild Noonan syndrome phenotype?
    Kitsiou-Tzeli S; Papadopoulou A; Kanaka-Gantenbein C; Fretzayas A; Daskalopoulos D; Kanavakis E; Nicolaidou P
    Horm Res; 2006; 66(3):124-31. PubMed ID: 16804314
    [TBL] [Abstract][Full Text] [Related]  

  • 27. No mutation in the gene for Noonan syndrome, PTPN11, in 18 patients with Costello syndrome.
    Tröger B; Kutsche K; Bolz H; Lüttgen S; Gal A; Almassy Z; Caliebe A; Freisinger P; Hobbiebrunken E; Morlot M; Stefanova M; Streubel B; Wieczorek D; Meinecke P
    Am J Med Genet A; 2003 Aug; 121A(1):82-4. PubMed ID: 12900909
    [No Abstract]   [Full Text] [Related]  

  • 28. [Clinical symptoms and molecular pathogenesis of Noonan syndrome--current concepts].
    Klapecki J; Obersztyn E; Laniewski-Wollk M; Szpecht-Potocka A; Mazurczak T
    Med Wieku Rozwoj; 2006; 10(1 Pt 2):289-308. PubMed ID: 17028394
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 64(24):8816-20. PubMed ID: 15604238
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism.
    Jafarov T; Ferimazova N; Reichenberger E
    Clin Genet; 2005 Aug; 68(2):190-1. PubMed ID: 15996221
    [No Abstract]   [Full Text] [Related]  

  • 31. Noonan syndrome mutation Q79R in Shp2 increases proliferation of valve primordia mesenchymal cells via extracellular signal-regulated kinase 1/2 signaling.
    Krenz M; Yutzey KE; Robbins J
    Circ Res; 2005 Oct; 97(8):813-20. PubMed ID: 16166557
    [TBL] [Abstract][Full Text] [Related]  

  • 32. PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13.
    Maheshwari M; Belmont J; Fernbach S; Ho T; Molinari L; Yakub I; Yu F; Combes A; Towbin J; Craigen WJ; Gibbs R
    Hum Mutat; 2002 Oct; 20(4):298-304. PubMed ID: 12325025
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetics and variation in phenotype in Noonan syndrome.
    Jongmans M; Otten B; Noordam K; van der Burgt I
    Horm Res; 2004; 62 Suppl 3():56-9. PubMed ID: 15539800
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Mutation analysis of PTPN11 gene in Noonan syndrome].
    Yang T; Meng Y; Shi HP; Zhao SM; Wang G; Huang SZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):554-8. PubMed ID: 20931536
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Noonan-like/multiple giant cell lesion syndrome: report of a case and review of the literature.
    Wolvius EB; de Lange J; Smeets EE; van der Wal KG; van den Akker HP
    J Oral Maxillofac Surg; 2006 Aug; 64(8):1289-92. PubMed ID: 16860226
    [No Abstract]   [Full Text] [Related]  

  • 36. Double-chambered right ventricle in an adult with Noonan syndrome.
    Patel AM; Kim JB; Roberts AE; Aragam J
    Cardiol Rev; 2006; 14(5):e16-20. PubMed ID: 16924159
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A 3-bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia.
    Yoshida R; Miyata M; Nagai T; Yamazaki T; Ogata T
    Am J Med Genet A; 2004 Jul; 128A(1):63-6. PubMed ID: 15211660
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutation analysis of PTPN11 in Noonan syndrome by WAVE.
    Elanko N; Jeffery S
    Methods Mol Med; 2006; 126():97-111. PubMed ID: 16930008
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Excellent growth response to growth hormone therapy in a child with PTPN11-negative Noonan syndrome and features of growth hormone resistance.
    Walton-Betancourth S; Martinelli CE; Thalange NK; Dyke MP; Acerini CL; White S; Camacho-Hübner C; Savage MO
    J Endocrinol Invest; 2007 May; 30(5):439-41. PubMed ID: 17598979
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel mitochondrial DNA mutations implicated in Noonan syndrome.
    Dhandapany PS; Sadayappan S; Vanniarajan A; Karthikeyan B; Nagaraj C; Gowrishankar K; Selvam GS; Singh L; Thangaraj K
    Int J Cardiol; 2007 Aug; 120(2):284-5. PubMed ID: 17092585
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.