These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 12739139)

  • 1. 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]  

  • 2. [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]  

  • 3. [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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. [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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Genotypic and phenotypic characterization of Noonan syndrome: new data and review of the literature.
    Jongmans M; Sistermans EA; Rikken A; Nillesen WM; Tamminga R; Patton M; Maier EM; Tartaglia M; Noordam K; van der Burgt I
    Am J Med Genet A; 2005 Apr; 134A(2):165-70. PubMed ID: 15723289
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 11(1):85-8. PubMed ID: 12529711
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome.
    Tartaglia M; Mehler EL; Goldberg R; Zampino G; Brunner HG; Kremer H; van der Burgt I; Crosby AH; Ion A; Jeffery S; Kalidas K; Patton MA; Kucherlapati RS; Gelb BD
    Nat Genet; 2001 Dec; 29(4):465-8. PubMed ID: 11704759
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene.
    Sznajer Y; Keren B; Baumann C; Pereira S; Alberti C; Elion J; Cavé H; Verloes A
    Pediatrics; 2007 Jun; 119(6):e1325-31. PubMed ID: 17515436
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndrome.
    Binder G; Neuer K; Ranke MB; Wittekindt NE
    J Clin Endocrinol Metab; 2005 Sep; 90(9):5377-81. PubMed ID: 15985475
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation.
    Bertola DR; Pereira AC; de Oliveira PS; Kim CA; Krieger JE
    Am J Med Genet A; 2004 Nov; 130A(4):378-83. PubMed ID: 15384080
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia.
    Niihori T; Aoki Y; Ohashi H; Kurosawa K; Kondoh T; Ishikiriyama S; Kawame H; Kamasaki H; Yamanaka T; Takada F; Nishio K; Sakurai M; Tamai H; Nagashima T; Suzuki Y; Kure S; Fujii K; Imaizumi M; Matsubara Y
    J Hum Genet; 2005; 50(4):192-202. PubMed ID: 15834506
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.