BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 15886577)

  • 1. [Noonan syndrome and Leopard syndrome linked to mutation of the gene PTPN11].
    Dereure O
    Ann Dermatol Venereol; 2005 Apr; 132(4):400. PubMed ID: 15886577
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel PTPN11 gene mutation in a patient with LEOPARD Syndrome.
    Du-Thanh A; Cave H; Bessis D; Puso C; Guilhou JJ; Dereure O
    Arch Dermatol; 2007 Sep; 143(9):1210-1. PubMed ID: 17875892
    [No Abstract]   [Full Text] [Related]  

  • 3. PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype".
    Digilio MC; Sarkozy A; Pacileo G; Limongelli G; Marino B; Dallapiccola B
    Eur J Pediatr; 2006 Nov; 165(11):803-5. PubMed ID: 16733669
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes.
    Ogata T; Yoshida R
    Pediatr Endocrinol Rev; 2005 Jun; 2(4):669-74. PubMed ID: 16208280
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel and one recurrent PTPN11 mutations in LEOPARD syndrome.
    Yoshida R; Nagai T; Hasegawa T; Kinoshita E; Tanaka T; Ogata T
    Am J Med Genet A; 2004 Nov; 130A(4):432-4. PubMed ID: 15389709
    [No Abstract]   [Full Text] [Related]  

  • 6. [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]  

  • 7. Noonan syndrome with leukaemoid reaction and overproduction of catecholamines: a case report.
    Kondoh T; Ishii E; Aoki Y; Shimizu T; Zaitsu M; Matsubara Y; Moriuchi H
    Eur J Pediatr; 2003 Jul; 162(7-8):548-549. PubMed ID: 12739139
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. PTPN11 gene analysis in 74 Brazilian patients with Noonan syndrome or Noonan-like phenotype.
    Bertola DR; Pereira AC; Albano LM; De Oliveira PS; Kim CA; Krieger JE
    Genet Test; 2006; 10(3):186-91. PubMed ID: 17020470
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activation.
    Fragale A; Tartaglia M; Wu J; Gelb BD
    Hum Mutat; 2004 Mar; 23(3):267-77. PubMed ID: 14974085
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.
    Kalidas K; Shaw AC; Crosby AH; Newbury-Ecob R; Greenhalgh L; Temple IK; Law C; Patel A; Patton MA; Jeffery S
    J Hum Genet; 2005; 50(1):21-25. PubMed ID: 15690106
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 144(3):368-74. PubMed ID: 15001945
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Regulation of the immune system by protein tyrosine phosphatases].
    Mizuno K; Yakura H
    Seikagaku; 2005 Oct; 77(10):1281-90. PubMed ID: 16296320
    [No Abstract]   [Full Text] [Related]  

  • 19. Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
    Pandit B; Sarkozy A; Pennacchio LA; Carta C; Oishi K; Martinelli S; Pogna EA; Schackwitz W; Ustaszewska A; Landstrom A; Bos JM; Ommen SR; Esposito G; Lepri F; Faul C; Mundel P; López Siguero JP; Tenconi R; Selicorni A; Rossi C; Mazzanti L; Torrente I; Marino B; Digilio MC; Zampino G; Ackerman MJ; Dallapiccola B; Tartaglia M; Gelb BD
    Nat Genet; 2007 Aug; 39(8):1007-12. PubMed ID: 17603483
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Noonan's syndrome caused by a mutation in the PTPN11 gene].
    Lloreda-García JM; Martínez-Aedo MJ; Tarttaglia M; López-Siguero JP
    An Pediatr (Barc); 2006 Dec; 65(6):635-6. PubMed ID: 17194341
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.