BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 9184539)

  • 21. Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.
    Johnson DW; Berg JN; Baldwin MA; Gallione CJ; Marondel I; Yoon SJ; Stenzel TT; Speer M; Pericak-Vance MA; Diamond A; Guttmacher AE; Jackson CE; Attisano L; Kucherlapati R; Porteous ME; Marchuk DA
    Nat Genet; 1996 Jun; 13(2):189-95. PubMed ID: 8640225
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: evidence for a founder effect.
    Gallione CJ; Scheessele EA; Reinhardt D; Duits AJ; Berg JN; Westermann CJ; Marchuk DA
    Hum Genet; 2000 Jul; 107(1):40-4. PubMed ID: 10982033
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.
    Vincent P; Plauchu H; Hazan J; Fauré S; Weissenbach J; Godet J
    Hum Mol Genet; 1995 May; 4(5):945-9. PubMed ID: 7633456
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms.
    Shovlin CL; Letarte M
    Thorax; 1999 Aug; 54(8):714-29. PubMed ID: 10413726
    [No Abstract]   [Full Text] [Related]  

  • 25. Association of hereditary hemorrhagic telangiectasia and hereditary nonpolyposis colorectal cancer in the same kindred.
    Goldschmidt N; Metzger S; Wexler ID; Goldshmidt O; Hershcovici T; Chajek-Shaul T
    Int J Cancer; 2005 Sep; 116(5):808-12. PubMed ID: 15849752
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel missense mutation in the endoglin gene in hereditary hemorrhagic telangiectasia.
    Yamaguchi H; Azuma H; Shigekiyo T; Inoue H; Saito S
    Thromb Haemost; 1997 Feb; 77(2):243-7. PubMed ID: 9157574
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hereditary hemorrhagic telangiectasia: an update on clinical manifestations and diagnostic measures.
    Sadick H; Sadick M; Götte K; Naim R; Riedel F; Bran G; Hörmann K
    Wien Klin Wochenschr; 2006 Mar; 118(3-4):72-80. PubMed ID: 16703249
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles.
    Gallione CJ; Klaus DJ; Yeh EY; Stenzel TT; Xue Y; Anthony KB; McAllister KA; Baldwin MA; Berg JN; Lux A; Smith JD; Vary CP; Craigen WJ; Westermann CJ; Warner ML; Miller YE; Jackson CE; Guttmacher AE; Marchuk DA
    Hum Mutat; 1998; 11(4):286-94. PubMed ID: 9554745
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2.
    Berg JN; Gallione CJ; Stenzel TT; Johnson DW; Allen WP; Schwartz CE; Jackson CE; Porteous ME; Marchuk DA
    Am J Hum Genet; 1997 Jul; 61(1):60-7. PubMed ID: 9245985
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Glaxo/MRS Young Investigator Medal. Molecular studies on adenosine deaminase deficiency and hereditary haemorrhagic telangiectasia.
    Shovlin CL
    Clin Sci (Lond); 1998 Mar; 94(3):207-18. PubMed ID: 9616253
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia.
    Harrison RE; Flanagan JA; Sankelo M; Abdalla SA; Rowell J; Machado RD; Elliott CG; Robbins IM; Olschewski H; McLaughlin V; Gruenig E; Kermeen F; Halme M; Räisänen-Sokolowski A; Laitinen T; Morrell NW; Trembath RC
    J Med Genet; 2003 Dec; 40(12):865-71. PubMed ID: 14684682
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Vascular endothelial growth factor induces abnormal microvasculature in the endoglin heterozygous mouse brain.
    Xu B; Wu YQ; Huey M; Arthur HM; Marchuk DA; Hashimoto T; Young WL; Yang GY
    J Cereb Blood Flow Metab; 2004 Feb; 24(2):237-44. PubMed ID: 14747750
    [TBL] [Abstract][Full Text] [Related]  

  • 33. What Benjamin Babington, William Osler, Frederick Weber, and Henri Rendu did not know.
    Hirschberg R
    Cardiovasc Res; 2005 Nov; 68(2):180-2. PubMed ID: 16198324
    [No Abstract]   [Full Text] [Related]  

  • 34. Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension.
    Chaouat A; Coulet F; Favre C; Simonneau G; Weitzenblum E; Soubrier F; Humbert M
    Thorax; 2004 May; 59(5):446-8. PubMed ID: 15115879
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients.
    Letteboer TG; Zewald RA; Kamping EJ; de Haas G; Mager JJ; Snijder RJ; Lindhout D; Hennekam FA; Westermann CJ; Ploos van Amstel JK
    Hum Genet; 2005 Jan; 116(1-2):8-16. PubMed ID: 15517393
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. Online.
    Klaus DJ; Gallione CJ; Anthony K; Yeh EY; Yu J; Lux A; Johnson DW; Marchuk DA
    Hum Mutat; 1998; 12(2):137. PubMed ID: 10694922
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Vascular abnormalities in the fingers of patients affected with hereditary hemorrhagic telangiectasia (HHT) as assessed by color doppler sonography.
    Draghi F; Precerutti M; Danesino GM; Olivieri C; Valacca C; Danesino C; Pagella F; Semino L; Lanzarini L; Buscarini E; Danesino C
    Am J Med Genet A; 2005 May; 135(1):106-9. PubMed ID: 15779017
    [No Abstract]   [Full Text] [Related]  

  • 38. No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia.
    Karabegovic A; Shinawi M; Cymerman U; Letarte M
    J Med Genet; 2004 Nov; 41(11):e119. PubMed ID: 15520401
    [No Abstract]   [Full Text] [Related]  

  • 39. Hereditary haemorrhagic telangiectasia: From symptomatic management to pathogenesis based treatment.
    Fernández-Fernández FJ
    Eur J Hum Genet; 2010 Apr; 18(4):404; author reply. PubMed ID: 19888298
    [No Abstract]   [Full Text] [Related]  

  • 40. Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.
    Berg J; Porteous M; Reinhardt D; Gallione C; Holloway S; Umasunthar T; Lux A; McKinnon W; Marchuk D; Guttmacher A
    J Med Genet; 2003 Aug; 40(8):585-90. PubMed ID: 12920067
    [TBL] [Abstract][Full Text] [Related]  

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