BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

354 related articles for article (PubMed ID: 19438935)

  • 21. High resolution melting analysis for mutation detection for PTPN11 gene: applications of this method for diagnosis of Noonan syndrome.
    Lo FS; Luo JD; Lee YJ; Shu SG; Kuo MT; Chiou CC
    Clin Chim Acta; 2009 Nov; 409(1-2):75-7. PubMed ID: 19737548
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?
    Brasil AS; Malaquias AC; Wanderley LT; Kim CA; Krieger JE; Jorge AA; Pereira AC; Bertola DR
    Arq Bras Endocrinol Metabol; 2010 Nov; 54(8):717-22. PubMed ID: 21340158
    [TBL] [Abstract][Full Text] [Related]  

  • 23. PTPN11 and KRAS gene analysis in patients with Noonan and Noonan-like syndromes.
    Brasil AS; Pereira AC; Wanderley LT; Kim CA; Malaquias AC; Jorge AA; Krieger JE; Bertola DR
    Genet Test Mol Biomarkers; 2010 Jun; 14(3):425-32. PubMed ID: 20578946
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Noonan syndrome, the Ras-MAPK signalling pathway and short stature.
    Binder G
    Horm Res; 2009 Apr; 71 Suppl 2():64-70. PubMed ID: 19407499
    [TBL] [Abstract][Full Text] [Related]  

  • 25. PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome.
    Ko JM; Kim JM; Kim GH; Yoo HW
    J Hum Genet; 2008; 53(11-12):999-1006. PubMed ID: 19020799
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Noonan syndrome, the SOS1 gene and embryonal rhabdomyosarcoma.
    Jongmans MC; Hoogerbrugge PM; Hilkens L; Flucke U; van der Burgt I; Noordam K; Ruiterkamp-Versteeg M; Yntema HG; Nillesen WM; Ligtenberg MJ; van Kessel AG; Kuiper RP; Hoogerbrugge N
    Genes Chromosomes Cancer; 2010 Jul; 49(7):635-41. PubMed ID: 20461756
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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]  

  • 28. 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; 182(1):40-2. PubMed ID: 18328949
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Noonan-like/multiple giant cell lesion syndrome in two adult patients with SOS1 gene mutations.
    Slezak R; Luczak K; Kalscheuer V; Neumann TE; Sasiadek MM
    Clin Dysmorphol; 2010 Jul; 19(3):157-160. PubMed ID: 20305546
    [No Abstract]   [Full Text] [Related]  

  • 30. Coronary artery ectasia in Noonan syndrome: Report of an individual with SOS1 mutation and literature review.
    Calcagni G; Baban A; De Luca E; Leonardi B; Pongiglione G; Digilio MC
    Am J Med Genet A; 2016 Mar; 170(3):665-9. PubMed ID: 26686981
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome.
    Shoji Y; Ida S; Niihori T; Aoki Y; Okamoto N; Etani Y; Kawai M
    Endocr J; 2019 Nov; 66(11):983-994. PubMed ID: 31292302
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Differential allelic expression of SOS1 and hyperexpression of the activating SOS1 c.755C variant in a Noonan syndrome family.
    Moncini S; Bonati MT; Morella I; Ferrari L; Brambilla R; Riva P
    Eur J Hum Genet; 2015 Nov; 23(11):1531-7. PubMed ID: 25712082
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A severe form of Noonan syndrome and autosomal dominant café-au-lait spots - evidence for different genetic origins.
    Nyström AM; Ekvall S; Strömberg B; Holmström G; Thuresson AC; Annerén G; Bondeson ML
    Acta Paediatr; 2009 Apr; 98(4):693-8. PubMed ID: 19120036
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Noonan-like/multiple giant cell lesion syndrome.
    Cohen MM; Gorlin RJ
    Am J Med Genet; 1991 Aug; 40(2):159-66. PubMed ID: 1897569
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Alterations in RAS-MAPK genes in 200 Spanish patients with Noonan and other neuro-cardio-facio-cutaneous syndromes. Genotype and cardiopathy.
    Ezquieta B; Santomé JL; Carcavilla A; Guillén-Navarro E; Pérez-Aytés A; Sánchez del Pozo J; García-Miñaur S; Castillo E; Alonso M; Vendrell T; Santana A; Maroto E; Galbis L
    Rev Esp Cardiol (Engl Ed); 2012 May; 65(5):447-55. PubMed ID: 22465605
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pilocytic astrocytoma in a child with Noonan syndrome.
    Schuettpelz LG; McDonald S; Whitesell K; Desruisseau DM; Grange DK; Gurnett CA; Wilson DB
    Pediatr Blood Cancer; 2009 Dec; 53(6):1147-9. PubMed ID: 19621452
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hepatoblastoma in a Noonan syndrome patient with a PTPN11 mutation.
    Yoshida R; Ogata T; Masawa N; Nagai T
    Pediatr Blood Cancer; 2008 Jun; 50(6):1274-6. PubMed ID: 18253957
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A mother and son with Noonan syndrome resulting from a PTPN11 mutation: first report of molecularly proven cases from Turkey.
    Demir K; Yntema HG; Altincik A; Böber E
    Turk J Pediatr; 2010; 52(3):321-4. PubMed ID: 20718194
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.