184 related articles for article (PubMed ID: 35777360)
21. 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]
22. BMP Receptor Inhibition Enhances Tissue Repair in Endoglin Heterozygous Mice.
Bakker W; Dingenouts CKE; Lodder K; Wiesmeijer KC; de Jong A; Kurakula K; Mager HJ; Smits AM; de Vries MR; Quax PHA; Goumans MJTH
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33670533
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations.
Pawlikowska L; Nelson J; Guo DE; McCulloch CE; Lawton MT; Young WL; Kim H; Faughnan ME;
Am J Med Genet A; 2015 Jun; 167(6):1262-7. PubMed ID: 25847705
[TBL] [Abstract][Full Text] [Related]
25. Hereditary hemorrhagic telangiectasia, a vascular dysplasia affecting the TGF-beta signaling pathway.
Fernández-L A; Sanz-Rodriguez F; Blanco FJ; Bernabéu C; Botella LM
Clin Med Res; 2006 Mar; 4(1):66-78. PubMed ID: 16595794
[TBL] [Abstract][Full Text] [Related]
26. Curaçao diagnostic criteria for hereditary hemorrhagic telangiectasia is highly predictive of a pathogenic variant in ENG or ACVRL1 (HHT1 and HHT2).
McDonald J; Bayrak-Toydemir P; DeMille D; Wooderchak-Donahue W; Whitehead K
Genet Med; 2020 Jul; 22(7):1201-1205. PubMed ID: 32300199
[TBL] [Abstract][Full Text] [Related]
27. Estrogen therapy for hereditary haemorrhagic telangiectasia (HHT): Effects of raloxifene, on Endoglin and ALK1 expression in endothelial cells.
Albiñana V; Bernabeu-Herrero ME; Zarrabeitia R; Bernabéu C; Botella LM
Thromb Haemost; 2010 Mar; 103(3):525-34. PubMed ID: 20135064
[TBL] [Abstract][Full Text] [Related]
28. Functional analysis of endoglin mutations from hereditary hemorrhagic telangiectasia type 1 patients reveals different mechanisms for endoglin loss of function.
Mallet C; Lamribet K; Giraud S; Dupuis-Girod S; Feige JJ; Bailly S; Tillet E
Hum Mol Genet; 2015 Feb; 24(4):1142-54. PubMed ID: 25312062
[TBL] [Abstract][Full Text] [Related]
29. Mutation analysis in Spanish patients with hereditary hemorrhagic telangiectasia: deficient endoglin up-regulation in activated monocytes.
Sanz-Rodriguez F; Fernandez-L A; Zarrabeitia R; Perez-Molino A; Ramírez JR; Coto E; Bernabeu C; Botella LM
Clin Chem; 2004 Nov; 50(11):2003-11. PubMed ID: 15375013
[TBL] [Abstract][Full Text] [Related]
30. Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1.
Heimdal K; Dalhus B; Rødningen OK; Kroken M; Eiklid K; Dheyauldeen S; Røysland T; Andersen R; Kulseth MA
Clin Genet; 2016 Feb; 89(2):182-6. PubMed ID: 25970827
[TBL] [Abstract][Full Text] [Related]
31. Deficiency in hereditary hemorrhagic telangiectasia-associated Endoglin elicits hypoxia-driven heart failure in zebrafish.
Lelièvre E; Bureau C; Bordat Y; Frétaud M; Langevin C; Jopling C; Kissa K
Dis Model Mech; 2023 May; 16(5):. PubMed ID: 37264878
[TBL] [Abstract][Full Text] [Related]
32. [Genetic diagnostics of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease)].
Major T; Gindele R; Szabó Z; Jóni N; Kis Z; Bora L; Bárdossy P; Rácz T; Karosi T; Bereczky Z
Orv Hetil; 2019 May; 160(18):710-719. PubMed ID: 31030535
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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]
35. Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia.
Kitayama K; Ishiguro T; Komiyama M; Morisaki T; Morisaki H; Minase G; Hamanaka K; Miyatake S; Matsumoto N; Kato M; Takahashi T; Yorifuji T
BMC Med Genomics; 2021 Dec; 14(1):288. PubMed ID: 34872578
[TBL] [Abstract][Full Text] [Related]
36. ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasia.
Tørring PM; Kjeldsen AD; Ousager LB; Brusgaard K
Mol Genet Genomic Med; 2018 Jan; 6(1):121-125. PubMed ID: 29243366
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network.
Lesca G; Olivieri C; Burnichon N; Pagella F; Carette MF; Gilbert-Dussardier B; Goizet C; Roume J; Rabilloud M; Saurin JC; Cottin V; Honnorat J; Coulet F; Giraud S; Calender A; Danesino C; Buscarini E; Plauchu H;
Genet Med; 2007 Jan; 9(1):14-22. PubMed ID: 17224686
[TBL] [Abstract][Full Text] [Related]
39. [Hereditary hemorrhagic telangiectasia. Report of a pediatric case].
Maaloul I; Aloulou H; Fourati H; Sfaihi L; Chabchoub I; Kamoun T; Mnif Z; Hachicha M
Arch Pediatr; 2014 Jul; 21(7):768-71. PubMed ID: 24935454
[TBL] [Abstract][Full Text] [Related]
40. Increase of circulating endothelial cells in patients with Hereditary Hemorrhagic Telangiectasia.
Massa M; Canzonieri C; Campanelli R; Ornati F; Fois G; Pagella F; Matti E; Buscarini E; Danesino C; Rosti V; Olivieri C
Int J Hematol; 2015 Jan; 101(1):23-31. PubMed ID: 25465912
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
