961 related articles for article (PubMed ID: 12598898)
1. Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome.
Neptune ER; Frischmeyer PA; Arking DE; Myers L; Bunton TE; Gayraud B; Ramirez F; Sakai LY; Dietz HC
Nat Genet; 2003 Mar; 33(3):407-11. PubMed ID: 12598898
[TBL] [Abstract][Full Text] [Related]
2. TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome.
Ng CM; Cheng A; Myers LA; Martinez-Murillo F; Jie C; Bedja D; Gabrielson KL; Hausladen JM; Mecham RP; Judge DP; Dietz HC
J Clin Invest; 2004 Dec; 114(11):1586-92. PubMed ID: 15546004
[TBL] [Abstract][Full Text] [Related]
3. miR-29b participates in early aneurysm development in Marfan syndrome.
Merk DR; Chin JT; Dake BA; Maegdefessel L; Miller MO; Kimura N; Tsao PS; Iosef C; Berry GJ; Mohr FW; Spin JM; Alvira CM; Robbins RC; Fischbein MP
Circ Res; 2012 Jan; 110(2):312-24. PubMed ID: 22116819
[TBL] [Abstract][Full Text] [Related]
4. Fibrillin in Marfan syndrome and tight skin mice provides new insights into transforming growth factor-beta regulation and systemic sclerosis.
Lemaire R; Bayle J; Lafyatis R
Curr Opin Rheumatol; 2006 Nov; 18(6):582-7. PubMed ID: 17053502
[TBL] [Abstract][Full Text] [Related]
5. Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome.
Judge DP; Biery NJ; Keene DR; Geubtner J; Myers L; Huso DL; Sakai LY; Dietz HC
J Clin Invest; 2004 Jul; 114(2):172-81. PubMed ID: 15254584
[TBL] [Abstract][Full Text] [Related]
6. Recent progress towards a molecular understanding of Marfan syndrome.
Dietz HC; Loeys B; Carta L; Ramirez F
Am J Med Genet C Semin Med Genet; 2005 Nov; 139C(1):4-9. PubMed ID: 16273535
[TBL] [Abstract][Full Text] [Related]
7. Molecular pathogenesis of Marfan syndrome.
Ramachandra CJ; Mehta A; Guo KW; Wong P; Tan JL; Shim W
Int J Cardiol; 2015; 187():585-91. PubMed ID: 25863307
[TBL] [Abstract][Full Text] [Related]
8. Exogenous activation of BMP-2 signaling overcomes TGFβ-mediated inhibition of osteogenesis in Marfan embryonic stem cells and Marfan patient-specific induced pluripotent stem cells.
Quarto N; Li S; Renda A; Longaker MT
Stem Cells; 2012 Dec; 30(12):2709-19. PubMed ID: 23037987
[TBL] [Abstract][Full Text] [Related]
9. A Pkd1-Fbn1 genetic interaction implicates TGF-β signaling in the pathogenesis of vascular complications in autosomal dominant polycystic kidney disease.
Liu D; Wang CJ; Judge DP; Halushka MK; Ni J; Habashi JP; Moslehi J; Bedja D; Gabrielson KL; Xu H; Qian F; Huso D; Dietz HC; Germino GG; Watnick T
J Am Soc Nephrol; 2014 Jan; 25(1):81-91. PubMed ID: 24071006
[TBL] [Abstract][Full Text] [Related]
10. Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice.
Guo G; Muñoz-García B; Ott CE; Grünhagen J; Mousa SA; Pletschacher A; von Kodolitsch Y; Knaus P; Robinson PN
Hum Mol Genet; 2013 Feb; 22(3):433-43. PubMed ID: 23100322
[TBL] [Abstract][Full Text] [Related]
11. Determination of the molecular basis of Marfan syndrome: a growth industry.
Byers PH
J Clin Invest; 2004 Jul; 114(2):161-3. PubMed ID: 15254580
[TBL] [Abstract][Full Text] [Related]
12. Microfibrils: a cornerstone of extracellular matrix and a key to understand Marfan syndrome.
Bonetti MI
Ital J Anat Embryol; 2009; 114(4):201-24. PubMed ID: 20578676
[TBL] [Abstract][Full Text] [Related]
13. [Molecular biological aspects of Marfan syndromes].
Belsing TZ; Lund AM; Abildstrøm SZ; Søndergaard L; Friis-Hansen L
Ugeskr Laeger; 2011 Jan; 173(5):333-7. PubMed ID: 21276395
[TBL] [Abstract][Full Text] [Related]
14. Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia--a novel mouse model providing insights into geleophysic dysplasia.
Hubmacher D; Wang LW; Mecham RP; Reinhardt DP; Apte SS
Dis Model Mech; 2015 May; 8(5):487-99. PubMed ID: 25762570
[TBL] [Abstract][Full Text] [Related]
15. Dimorphic effects of transforming growth factor-β signaling during aortic aneurysm progression in mice suggest a combinatorial therapy for Marfan syndrome.
Cook JR; Clayton NP; Carta L; Galatioto J; Chiu E; Smaldone S; Nelson CA; Cheng SH; Wentworth BM; Ramirez F
Arterioscler Thromb Vasc Biol; 2015 Apr; 35(4):911-7. PubMed ID: 25614286
[TBL] [Abstract][Full Text] [Related]
16. Marfan syndrome and mitral valve prolapse.
Weyman AE; Scherrer-Crosbie M
J Clin Invest; 2004 Dec; 114(11):1543-6. PubMed ID: 15578086
[TBL] [Abstract][Full Text] [Related]
17. ADAMTSL6β protein rescues fibrillin-1 microfibril disorder in a Marfan syndrome mouse model through the promotion of fibrillin-1 assembly.
Saito M; Kurokawa M; Oda M; Oshima M; Tsutsui K; Kosaka K; Nakao K; Ogawa M; Manabe RI; Suda N; Ganjargal G; Hada Y; Noguchi T; Teranaka T; Sekiguchi K; Yoneda T; Tsuji T
J Biol Chem; 2011 Nov; 286(44):38602-38613. PubMed ID: 21880733
[TBL] [Abstract][Full Text] [Related]
18. Molecular genetics of Marfan syndrome.
Boileau C; Jondeau G; Mizuguchi T; Matsumoto N
Curr Opin Cardiol; 2005 May; 20(3):194-200. PubMed ID: 15861007
[TBL] [Abstract][Full Text] [Related]
19. [Interactions between fibrillin-1 and tgf-beta: consequences and human pathology].
Wipff J; Allanore Y; Boileau C
Med Sci (Paris); 2009 Feb; 25(2):161-7. PubMed ID: 19239848
[TBL] [Abstract][Full Text] [Related]
20. New insights into the assembly of extracellular microfibrils from the analysis of the fibrillin 1 mutation in the tight skin mouse.
Gayraud B; Keene DR; Sakai LY; Ramirez F
J Cell Biol; 2000 Aug; 150(3):667-80. PubMed ID: 10931876
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
