222 related articles for article (PubMed ID: 20729550)
1. Extracellular microfibrils control osteoblast-supported osteoclastogenesis by restricting TGF{beta} stimulation of RANKL production.
Nistala H; Lee-Arteaga S; Smaldone S; Siciliano G; Ramirez F
J Biol Chem; 2010 Oct; 285(44):34126-33. PubMed ID: 20729550
[TBL] [Abstract][Full Text] [Related]
2. Fibrillin-1 and -2 differentially modulate endogenous TGF-β and BMP bioavailability during bone formation.
Nistala H; Lee-Arteaga S; Smaldone S; Siciliano G; Carta L; Ono RN; Sengle G; Arteaga-Solis E; Levasseur R; Ducy P; Sakai LY; Karsenty G; Ramirez F
J Cell Biol; 2010 Sep; 190(6):1107-21. PubMed ID: 20855508
[TBL] [Abstract][Full Text] [Related]
3. Abnormal Activation of BMP Signaling Causes Myopathy in Fbn2 Null Mice.
Sengle G; Carlberg V; Tufa SF; Charbonneau NL; Smaldone S; Carlson EJ; Ramirez F; Keene DR; Sakai LY
PLoS Genet; 2015 Jun; 11(6):e1005340. PubMed ID: 26114882
[TBL] [Abstract][Full Text] [Related]
4. Differential effects of alendronate and losartan therapy on osteopenia and aortic aneurysm in mice with severe Marfan syndrome.
Nistala H; Lee-Arteaga S; Carta L; Cook JR; Smaldone S; Siciliano G; Rifkin AN; Dietz HC; Rifkin DB; Ramirez F
Hum Mol Genet; 2010 Dec; 19(24):4790-8. PubMed ID: 20871099
[TBL] [Abstract][Full Text] [Related]
5. Establishment of fibrillin-deficient osteoprogenitor cell lines identifies molecular abnormalities associated with extracellular matrix perturbation of osteogenic differentiation.
Smaldone S; Carta L; Ramirez F
Cell Tissue Res; 2011 Jun; 344(3):511-7. PubMed ID: 21538048
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome.
Beene LC; Wang LW; Hubmacher D; Keene DR; Reinhardt DP; Annis DS; Mosher DF; Mecham RP; Traboulsi EI; Apte SS
Invest Ophthalmol Vis Sci; 2013 Dec; 54(13):8337-44. PubMed ID: 24265020
[TBL] [Abstract][Full Text] [Related]
8. Structure and function of the mammalian fibrillin gene family: implications for human connective tissue diseases.
Davis MR; Summers KM
Mol Genet Metab; 2012 Dec; 107(4):635-47. PubMed ID: 22921888
[TBL] [Abstract][Full Text] [Related]
9. Fibrillins 1 and 2 perform partially overlapping functions during aortic development.
Carta L; Pereira L; Arteaga-Solis E; Lee-Arteaga SY; Lenart B; Starcher B; Merkel CA; Sukoyan M; Kerkis A; Hazeki N; Keene DR; Sakai LY; Ramirez F
J Biol Chem; 2006 Mar; 281(12):8016-23. PubMed ID: 16407178
[TBL] [Abstract][Full Text] [Related]
10. Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.
Putnam EA; Zhang H; Ramirez F; Milewicz DM
Nat Genet; 1995 Dec; 11(4):456-8. PubMed ID: 7493032
[TBL] [Abstract][Full Text] [Related]
11. Mutation of the gene encoding fibrillin-2 results in syndactyly in mice.
Chaudhry SS; Gazzard J; Baldock C; Dixon J; Rock MJ; Skinner GC; Steel KP; Kielty CM; Dixon MJ
Hum Mol Genet; 2001 Apr; 10(8):835-43. PubMed ID: 11285249
[TBL] [Abstract][Full Text] [Related]
12. Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders.
Dietz HC; Pyeritz RE
Hum Mol Genet; 1995; 4 Spec No():1799-809. PubMed ID: 8541880
[TBL] [Abstract][Full Text] [Related]
13. Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events.
Ramirez F; Dietz HC
J Cell Physiol; 2007 Nov; 213(2):326-30. PubMed ID: 17708531
[TBL] [Abstract][Full Text] [Related]
14. ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2.
Miller G; Neilan M; Chia R; Gheryani N; Holt N; Charbit A; Wells S; Tucci V; Lalanne Z; Denny P; Fisher EM; Cheeseman M; Askew GN; Dear TN
PLoS One; 2010 Feb; 5(2):e9137. PubMed ID: 20161761
[TBL] [Abstract][Full Text] [Related]
15. In vivo studies of mutant fibrillin-1 microfibrils.
Charbonneau NL; Carlson EJ; Tufa S; Sengle G; Manalo EC; Carlberg VM; Ramirez F; Keene DR; Sakai LY
J Biol Chem; 2010 Aug; 285(32):24943-55. PubMed ID: 20529844
[TBL] [Abstract][Full Text] [Related]
16. The molecular genetics of Marfan syndrome and related microfibrillopathies.
Robinson PN; Godfrey M
J Med Genet; 2000 Jan; 37(1):9-25. PubMed ID: 10633129
[TBL] [Abstract][Full Text] [Related]
17. Biogenesis and function of fibrillin assemblies.
Ramirez F; Sakai LY
Cell Tissue Res; 2010 Jan; 339(1):71-82. PubMed ID: 19513754
[TBL] [Abstract][Full Text] [Related]
18. Role of the latent transforming growth factor beta binding protein 1 in fibrillin-containing microfibrils in bone cells in vitro and in vivo.
Dallas SL; Keene DR; Bruder SP; Saharinen J; Sakai LY; Mundy GR; Bonewald LF
J Bone Miner Res; 2000 Jan; 15(1):68-81. PubMed ID: 10646116
[TBL] [Abstract][Full Text] [Related]
19. Immunolocalisation of fibrillin microfibrils in the calf metacarpal and vertebral growth plate.
Yu J; Urban J
J Anat; 2013 Dec; 223(6):641-50. PubMed ID: 24117386
[TBL] [Abstract][Full Text] [Related]
20. Generation of Fbn1 conditional null mice implicates the extracellular microfibrils in osteoprogenitor recruitment.
Cook JR; Smaldone S; Cozzolino C; del Solar M; Lee-Arteaga S; Nistala H; Ramirez F
Genesis; 2012 Aug; 50(8):635-41. PubMed ID: 22374917
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]