BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

282 related articles for article (PubMed ID: 33513792)

  • 21. Hereditary hemorrhagic telangiectasia in Japanese patients.
    Komiyama M; Ishiguro T; Yamada O; Morisaki H; Morisaki T
    J Hum Genet; 2014 Jan; 59(1):37-41. PubMed ID: 24196379
    [TBL] [Abstract][Full Text] [Related]  

  • 22. VEGF neutralization can prevent and normalize arteriovenous malformations in an animal model for hereditary hemorrhagic telangiectasia 2.
    Han C; Choe SW; Kim YH; Acharya AP; Keselowsky BG; Sorg BS; Lee YJ; Oh SP
    Angiogenesis; 2014 Oct; 17(4):823-830. PubMed ID: 24957885
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1.
    Albiñana V; Zafra MP; Colau J; Zarrabeitia R; Recio-Poveda L; Olavarrieta L; Pérez-Pérez J; Botella LM
    BMC Med Genet; 2017 Feb; 18(1):20. PubMed ID: 28231770
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Arterial endoglin does not protect against arteriovenous malformations.
    Singh E; Redgrave RE; Phillips HM; Arthur HM
    Angiogenesis; 2020 Nov; 23(4):559-566. PubMed ID: 32506200
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Bazedoxifene, a new orphan drug for the treatment of bleeding in hereditary haemorrhagic telangiectasia.
    Zarrabeitia R; Ojeda-Fernandez L; Recio L; Bernabéu C; Parra JA; Albiñana V; Botella LM
    Thromb Haemost; 2016 Jun; 115(6):1167-77. PubMed ID: 26818701
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Angiopoietin-2 Inhibition Rescues Arteriovenous Malformation in a Smad4 Hereditary Hemorrhagic Telangiectasia Mouse Model.
    Crist AM; Zhou X; Garai J; Lee AR; Thoele J; Ullmer C; Klein C; Zabaleta J; Meadows SM
    Circulation; 2019 Apr; 139(17):2049-2063. PubMed ID: 30744395
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia.
    Giraud S; Bardel C; Dupuis-Girod S; Carette MF; Gilbert-Dussardier B; Riviere S; Saurin JC; Eyries M; Patri S; Decullier E; Calender A; Lesca G
    Orphanet J Rare Dis; 2020 Sep; 15(1):254. PubMed ID: 32962750
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Pro-angiogenic changes of T-helper lymphocytes in hereditary hemorrhagic telangiectasia.
    Guilhem A; Ciudad M; Aubriot-Lorton MH; Greigert H; Cladière C; Leguy-Seguin V; Audia S; Samson M; Bonnotte B
    Front Immunol; 2023; 14():1321182. PubMed ID: 38143764
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel brain arteriovenous malformation mouse models for type 1 hereditary hemorrhagic telangiectasia.
    Choi EJ; Chen W; Jun K; Arthur HM; Young WL; Su H
    PLoS One; 2014; 9(2):e88511. PubMed ID: 24520391
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Common and distinctive pathogenetic features of arteriovenous malformations in hereditary hemorrhagic telangiectasia 1 and hereditary hemorrhagic telangiectasia 2 animal models--brief report.
    Garrido-Martin EM; Nguyen HL; Cunningham TA; Choe SW; Jiang Z; Arthur HM; Lee YJ; Oh SP
    Arterioscler Thromb Vasc Biol; 2014 Oct; 34(10):2232-6. PubMed ID: 25082229
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers.
    Sabbà C; Pasculli G; Lenato GM; Suppressa P; Lastella P; Memeo M; Dicuonzo F; Guant G
    J Thromb Haemost; 2007 Jun; 5(6):1149-57. PubMed ID: 17388964
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Enhanced responses to angiogenic cues underlie the pathogenesis of hereditary hemorrhagic telangiectasia 2.
    Choi EJ; Kim YH; Choe SW; Tak YG; Garrido-Martin EM; Chang M; Lee YJ; Oh SP
    PLoS One; 2013; 8(5):e63138. PubMed ID: 23675457
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease.
    Abdalla SA; Letarte M
    J Med Genet; 2006 Feb; 43(2):97-110. PubMed ID: 15879500
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Therapeutic targeting of vascular malformation in a zebrafish model of hereditary haemorrhagic telangiectasia.
    Snodgrass RO; Govindpani K; Plant K; Kugler EC; Doh C; Dawson T; McCormack LE; Arthur HM; Chico TJA
    Dis Model Mech; 2023 Apr; 16(4):. PubMed ID: 36861761
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia.
    Letteboer TG; Mager JJ; Snijder RJ; Koeleman BP; Lindhout D; Ploos van Amstel JK; Westermann CJ
    J Med Genet; 2006 Apr; 43(4):371-7. PubMed ID: 16155196
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Decreased Expression of Vascular Endothelial Growth Factor Receptor 1 Contributes to the Pathogenesis of Hereditary Hemorrhagic Telangiectasia Type 2.
    Thalgott JH; Dos-Santos-Luis D; Hosman AE; Martin S; Lamandé N; Bracquart D; Srun S; Galaris G; de Boer HC; Tual-Chalot S; Kroon S; Arthur HM; Cao Y; Snijder RJ; Disch F; Mager JJ; Rabelink TJ; Mummery CL; Raymond K; Lebrin F
    Circulation; 2018 Dec; 138(23):2698-2712. PubMed ID: 30571259
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: mutations and manifestations.
    Bayrak-Toydemir P; McDonald J; Markewitz B; Lewin S; Miller F; Chou LS; Gedge F; Tang W; Coon H; Mao R
    Am J Med Genet A; 2006 Mar; 140(5):463-70. PubMed ID: 16470787
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1.
    Snellings DA; Gallione CJ; Clark DS; Vozoris NT; Faughnan ME; Marchuk DA
    Am J Hum Genet; 2019 Nov; 105(5):894-906. PubMed ID: 31630786
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 99():118-26. PubMed ID: 25892364
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Non-invasive CT screening for pulmonary arteriovenous malformations in children with confirmed hereditary hemorrhagic telangiectasia: Results from two pediatric centers.
    Soysal N; Eyries M; Verlhac S; Escabasse V; Remus N; Tamalet A; Rioux JY; Franchi-Abella S; Vasile M; Robert S; Delestrain C; Hau I; Ducou-Le Pointe H; Soubrier F; Carette MF; Epaud R
    Pediatr Pulmonol; 2017 May; 52(5):642-649. PubMed ID: 28165669
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.