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3. Identification of hereditary hemorrhagic telangiectasia type 1 in newborns by protein expression and mutation analysis of endoglin. Cymerman U; Vera S; Pece-Barbara N; Bourdeau A; White RI; Dunn J; Letarte M Pediatr Res; 2000 Jan; 47(1):24-35. PubMed ID: 10625079 [TBL] [Abstract][Full Text] [Related]
4. Cerebral vascular abnormalities in a murine model of hereditary hemorrhagic telangiectasia. Satomi J; Mount RJ; Toporsian M; Paterson AD; Wallace MC; Harrison RV; Letarte M Stroke; 2003 Mar; 34(3):783-9. PubMed ID: 12624308 [TBL] [Abstract][Full Text] [Related]
5. Soluble endoglin regulates expression of angiogenesis-related proteins and induction of arteriovenous malformations in a mouse model of hereditary hemorrhagic telangiectasia. Gallardo-Vara E; Tual-Chalot S; Botella LM; Arthur HM; Bernabeu C Dis Model Mech; 2018 Sep; 11(9):. PubMed ID: 30108051 [TBL] [Abstract][Full Text] [Related]
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7. A role for endoglin in coupling eNOS activity and regulating vascular tone revealed in hereditary hemorrhagic telangiectasia. Toporsian M; Gros R; Kabir MG; Vera S; Govindaraju K; Eidelman DH; Husain M; Letarte M Circ Res; 2005 Apr; 96(6):684-92. PubMed ID: 15718503 [TBL] [Abstract][Full Text] [Related]
8. Potential role of modifier genes influencing transforming growth factor-beta1 levels in the development of vascular defects in endoglin heterozygous mice with hereditary hemorrhagic telangiectasia. Bourdeau A; Faughnan ME; McDonald ML; Paterson AD; Wanless IR; Letarte M Am J Pathol; 2001 Jun; 158(6):2011-20. PubMed ID: 11395379 [TBL] [Abstract][Full Text] [Related]
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10. Cloning of the promoter region of human endoglin, the target gene for hereditary hemorrhagic telangiectasia type 1. Ríus C; Smith JD; Almendro N; Langa C; Botella LM; Marchuk DA; Vary CP; Bernabéu C Blood; 1998 Dec; 92(12):4677-90. PubMed ID: 9845534 [TBL] [Abstract][Full Text] [Related]
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13. Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1. Pece-Barbara N; Cymerman U; Vera S; Marchuk DA; Letarte M Hum Mol Genet; 1999 Nov; 8(12):2171-81. PubMed ID: 10545596 [TBL] [Abstract][Full Text] [Related]
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16. Reduced endothelial secretion and plasma levels of transforming growth factor-beta1 in patients with hereditary hemorrhagic telangiectasia type 1. Letarte M; McDonald ML; Li C; Kathirkamathamby K; Vera S; Pece-Barbara N; Kumar S Cardiovasc Res; 2005 Oct; 68(1):155-64. PubMed ID: 15907823 [TBL] [Abstract][Full Text] [Related]
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20. Mutant endoglin in hereditary hemorrhagic telangiectasia type 1 is transiently expressed intracellularly and is not a dominant negative. Pece N; Vera S; Cymerman U; White RI; Wrana JL; Letarte M J Clin Invest; 1997 Nov; 100(10):2568-79. PubMed ID: 9366572 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]