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Journal Abstract Search

668 related items for PubMed ID: 16595794

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  • 3. ALK5- and TGFBR2-independent role of ALK1 in the pathogenesis of hereditary hemorrhagic telangiectasia type 2.
    Park SO, Lee YJ, Seki T, Hong KH, Fliess N, Jiang Z, Park A, Wu X, Kaartinen V, Roman BL, Oh SP.
    Blood; 2008 Jan 15; 111(2):633-42. PubMed ID: 17911384
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  • 6. Endoglin and alk1 as therapeutic targets for hereditary hemorrhagic telangiectasia.
    Ruiz-Llorente L, Gallardo-Vara E, Rossi E, Smadja DM, Botella LM, Bernabeu C.
    Expert Opin Ther Targets; 2017 Oct 15; 21(10):933-947. PubMed ID: 28796572
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  • 7. Global gene expression profiling of telangiectasial tissue from patients with hereditary hemorrhagic telangiectasia.
    Tørring PM, Larsen MJ, Kjeldsen AD, Ousager LB, Tan Q, Brusgaard K.
    Microvasc Res; 2015 May 15; 99():118-26. PubMed ID: 25892364
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  • 9. Propranolol as antiangiogenic candidate for the therapy of hereditary haemorrhagic telangiectasia.
    Albiñana V, Recio-Poveda L, Zarrabeitia R, Bernabéu C, Botella LM.
    Thromb Haemost; 2012 Jul 15; 108(1):41-53. PubMed ID: 22552254
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  • 11. 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 15; 40(8):585-90. PubMed ID: 12920067
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  • 12. Gene expression fingerprinting for human hereditary hemorrhagic telangiectasia.
    Fernandez-L A, Garrido-Martin EM, Sanz-Rodriguez F, Pericacho M, Rodriguez-Barbero A, Eleno N, Lopez-Novoa JM, Düwell A, Vega MA, Bernabeu C, Botella LM.
    Hum Mol Genet; 2007 Jul 01; 16(13):1515-33. PubMed ID: 17420163
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  • 13. Hereditary haemorrhagic telangiectasia: a clinical and scientific review.
    Govani FS, Shovlin CL.
    Eur J Hum Genet; 2009 Jul 01; 17(7):860-71. PubMed ID: 19337313
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  • 14. Endoglin-mediated vascular remodeling: mechanisms underlying hereditary hemorrhagic telangiectasia.
    Lebrin F, Mummery CL.
    Trends Cardiovasc Med; 2008 Jan 01; 18(1):25-32. PubMed ID: 18206806
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  • 15. Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1.
    Fernandez-L A, Sanz-Rodriguez F, Zarrabeitia R, Perez-Molino A, Morales C, Restrepo CM, Ramirez JR, Coto E, Lenato GM, Bernabeu C, Botella LM.
    Hum Mutat; 2006 Mar 01; 27(3):295. PubMed ID: 16470589
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  • 16. Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasia.
    Kim MJ, Kim ST, Lee HD, Lee KY, Seo J, Lee JB, Lee YJ, Oh SP.
    BMC Med Genet; 2011 Oct 03; 12():130. PubMed ID: 21967607
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  • 17. Overexpression of Activin Receptor-Like Kinase 1 in Endothelial Cells Suppresses Development of Arteriovenous Malformations in Mouse Models of Hereditary Hemorrhagic Telangiectasia.
    Hwan Kim Y, Vu PN, Choe SW, Jeon CJ, Arthur HM, Vary CPH, Lee YJ, Oh SP.
    Circ Res; 2020 Oct 09; 127(9):1122-1137. PubMed ID: 32762495
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  • 20. Activin receptor-like kinase 1 modulates transforming growth factor-beta 1 signaling in the regulation of angiogenesis.
    Oh SP, Seki T, Goss KA, Imamura T, Yi Y, Donahoe PK, Li L, Miyazono K, ten Dijke P, Kim S, Li E.
    Proc Natl Acad Sci U S A; 2000 Mar 14; 97(6):2626-31. PubMed ID: 10716993
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