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836 results
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Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.
Putnam EA, Zhang H, Ramirez F, Milewicz DM. Putnam EA, et al. Among authors: ramirez f. Nat Genet. 1995 Dec;11(4):456-8. doi: 10.1038/ng1295-456. Nat Genet. 1995. PMID: 7493032
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. Among authors: ramirez f. 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.
Biogenesis and function of fibrillin assemblies.
Ramirez F, Sakai LY. Ramirez F, et al. Cell Tissue Res. 2010 Jan;339(1):71-82. doi: 10.1007/s00441-009-0822-x. Epub 2009 Jun 10. Cell Tissue Res. 2010. PMID: 19513754 Free PMC article. Review.
Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events.
Ramirez F, Dietz HC. Ramirez F, et al. J Cell Physiol. 2007 Nov;213(2):326-30. doi: 10.1002/jcp.21189. J Cell Physiol. 2007. PMID: 17708531 Review.
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states.
Cohn RD, van Erp C, Habashi JP, Soleimani AA, Klein EC, Lisi MT, Gamradt M, ap Rhys CM, Holm TM, Loeys BL, Ramirez F, Judge DP, Ward CW, Dietz HC. Cohn RD, et al. Among authors: ramirez f. Nat Med. 2007 Feb;13(2):204-10. doi: 10.1038/nm1536. Epub 2007 Jan 21. Nat Med. 2007. PMID: 17237794 Free PMC article.
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. Sengle G, et al. Among authors: ramirez f. PLoS Genet. 2015 Jun 26;11(6):e1005340. doi: 10.1371/journal.pgen.1005340. eCollection 2015 Jun. PLoS Genet. 2015. PMID: 26114882 Free PMC article.
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. Nistala H, et al. Among authors: ramirez f. Hum Mol Genet. 2010 Dec 15;19(24):4790-8. doi: 10.1093/hmg/ddq409. Epub 2010 Sep 24. Hum Mol Genet. 2010. PMID: 20871099 Free PMC article.
Marfan syndrome: from molecular pathogenesis to clinical treatment.
Ramirez F, Dietz HC. Ramirez F, et al. Curr Opin Genet Dev. 2007 Jun;17(3):252-8. doi: 10.1016/j.gde.2007.04.006. Epub 2007 Apr 27. Curr Opin Genet Dev. 2007. PMID: 17467262 Review.
Recent progress towards a molecular understanding of Marfan syndrome.
Dietz HC, Loeys B, Carta L, Ramirez F. Dietz HC, et al. Among authors: ramirez f. Am J Med Genet C Semin Med Genet. 2005 Nov 15;139C(1):4-9. doi: 10.1002/ajmg.c.30068. Am J Med Genet C Semin Med Genet. 2005. PMID: 16273535 Review.
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. Neptune ER, et al. Among authors: ramirez f. Nat Genet. 2003 Mar;33(3):407-11. doi: 10.1038/ng1116. Epub 2003 Feb 24. Nat Genet. 2003. PMID: 12598898
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