24107997,20529844,16407178,22242013,9326947,15254584,21152435,10097121,22374917[uid] - Search Results

Year	Number of Results
1997	1
1999	1
2004	1
2005	1
2006	1
2010	2
2012	2
2013	1
2024	0

1

Integrin-modulating therapy prevents fibrosis and autoimmunity in mouse models of scleroderma.

Gerber EE, Gallo EM, Fontana SC, Davis EC, Wigley FM, Huso DL, Dietz HC. Gerber EE, et al. Nature. 2013 Nov 7;503(7474):126-30. doi: 10.1038/nature12614. Epub 2013 Oct 9. Nature. 2013. PMID: 24107997 Free PMC article.

2

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. Charbonneau NL, et al. J Biol Chem. 2010 Aug 6;285(32):24943-55. doi: 10.1074/jbc.M110.130021. Epub 2010 Jun 7. J Biol Chem. 2010. PMID: 20529844 Free PMC article.

3

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. Carta L, et al. J Biol Chem. 2006 Mar 24;281(12):8016-23. doi: 10.1074/jbc.M511599200. Epub 2005 Dec 28. J Biol Chem. 2006. PMID: 16407178 Free PMC article.

4

Microenvironmental regulation by fibrillin-1.

Sengle G, Tsutsui K, Keene DR, Tufa SF, Carlson EJ, Charbonneau NL, Ono RN, Sasaki T, Wirtz MK, Samples JR, Fessler LI, Fessler JH, Sekiguchi K, Hayflick SJ, Sakai LY. Sengle G, et al. PLoS Genet. 2012 Jan;8(1):e1002425. doi: 10.1371/journal.pgen.1002425. Epub 2012 Jan 5. PLoS Genet. 2012. PMID: 22242013 Free PMC article.

5

Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.

Pereira L, Andrikopoulos K, Tian J, Lee SY, Keene DR, Ono R, Reinhardt DP, Sakai LY, Biery NJ, Bunton T, Dietz HC, Ramirez F. Pereira L, et al. Nat Genet. 1997 Oct;17(2):218-22. doi: 10.1038/ng1097-218. Nat Genet. 1997. PMID: 9326947

6

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. Judge DP, et al. J Clin Invest. 2004 Jul;114(2):172-81. doi: 10.1172/JCI20641. J Clin Invest. 2004. PMID: 15254584 Free PMC article.

7

A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression.

Lima BL, Santos EJ, Fernandes GR, Merkel C, Mello MR, Gomes JP, Soukoyan M, Kerkis A, Massironi SM, Visintin JA, Pereira LV. Lima BL, et al. PLoS One. 2010 Nov 30;5(11):e14136. doi: 10.1371/journal.pone.0014136. PLoS One. 2010. PMID: 21152435 Free PMC article.

8

Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1.

Pereira L, Lee SY, Gayraud B, Andrikopoulos K, Shapiro SD, Bunton T, Biery NJ, Dietz HC, Sakai LY, Ramirez F. Pereira L, et al. Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3819-23. doi: 10.1073/pnas.96.7.3819. Proc Natl Acad Sci U S A. 1999. PMID: 10097121 Free PMC article.

9

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. Cook JR, et al. Genesis. 2012 Aug;50(8):635-41. doi: 10.1002/dvg.22022. Epub 2012 Mar 31. Genesis. 2012. PMID: 22374917 Free PMC article.

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