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Journal Abstract Search

225 related items for PubMed ID: 25204799

  • 1. Divergence(s) in nodal signaling between aggressive melanoma and embryonic stem cells.
    Khalkhali-Ellis Z, Kirschmann DA, Seftor EA, Gilgur A, Bodenstine TM, Hinck AP, Hendrix MJ.
    Int J Cancer; 2015 Mar 01; 136(5):E242-51. PubMed ID: 25204799
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  • 2. Transforming growth factor-beta- and Activin-Smad signaling pathways are activated at distinct maturation stages of the thymopoeisis.
    Rosendahl A, Speletas M, Leandersson K, Ivars F, Sideras P.
    Int Immunol; 2003 Dec 01; 15(12):1401-14. PubMed ID: 14645149
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  • 3. An increased transforming growth factor beta receptor type I:type II ratio contributes to elevated collagen protein synthesis that is resistant to inhibition via a kinase-deficient transforming growth factor beta receptor type II in scleroderma.
    Pannu J, Gore-Hyer E, Yamanaka M, Smith EA, Rubinchik S, Dong JY, Jablonska S, Blaszczyk M, Trojanowska M.
    Arthritis Rheum; 2004 May 01; 50(5):1566-77. PubMed ID: 15146427
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  • 7. Requirement of TGFbeta signaling for SMO-mediated carcinogenesis.
    Fan Q, He M, Sheng T, Zhang X, Sinha M, Luxon B, Zhao X, Xie J.
    J Biol Chem; 2010 Nov 19; 285(47):36570-6. PubMed ID: 20858897
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  • 8. TGFbeta/activin/nodal signaling is necessary for the maintenance of pluripotency in human embryonic stem cells.
    James D, Levine AJ, Besser D, Hemmati-Brivanlou A.
    Development; 2005 Mar 19; 132(6):1273-82. PubMed ID: 15703277
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  • 9. Expression of nodal, lefty-a, and lefty-B in undifferentiated human embryonic stem cells requires activation of Smad2/3.
    Besser D.
    J Biol Chem; 2004 Oct 22; 279(43):45076-84. PubMed ID: 15308665
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  • 10. Activin-Nodal signaling is involved in propagation of mouse embryonic stem cells.
    Ogawa K, Saito A, Matsui H, Suzuki H, Ohtsuka S, Shimosato D, Morishita Y, Watabe T, Niwa H, Miyazono K.
    J Cell Sci; 2007 Jan 01; 120(Pt 1):55-65. PubMed ID: 17182901
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  • 13. Activin receptor-like kinase (ALK)1 is an antagonistic mediator of lateral TGFbeta/ALK5 signaling.
    Goumans MJ, Valdimarsdottir G, Itoh S, Lebrin F, Larsson J, Mummery C, Karlsson S, ten Dijke P.
    Mol Cell; 2003 Oct 01; 12(4):817-28. PubMed ID: 14580334
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  • 14. Transforming growth factor beta (TGFbeta ) signaling via differential activation of activin receptor-like kinases 2 and 5 during cardiac development. Role in regulating parasympathetic responsiveness.
    Ward SM, Desgrosellier JS, Zhuang X, Barnett JV, Galper JB.
    J Biol Chem; 2002 Dec 20; 277(51):50183-9. PubMed ID: 12393881
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  • 15. Quantification of transforming growth factor beta1 (TGFbeta1) mRNA expression in mouse preimplantation embryos and determination of TGFbeta receptor (type I and type II) expression in mouse embryos and reproductive tract.
    Chow JF, Lee KF, Chan ST, Yeung WS.
    Mol Hum Reprod; 2001 Nov 20; 7(11):1047-56. PubMed ID: 11675471
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  • 16. Nodal·Gdf1 heterodimers with bound prodomains enable serum-independent nodal signaling and endoderm differentiation.
    Fuerer C, Nostro MC, Constam DB.
    J Biol Chem; 2014 Jun 20; 289(25):17854-71. PubMed ID: 24798330
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  • 18. Growth differentiation factor-9 signaling is mediated by the type I receptor, activin receptor-like kinase 5.
    Mazerbourg S, Klein C, Roh J, Kaivo-Oja N, Mottershead DG, Korchynskyi O, Ritvos O, Hsueh AJ.
    Mol Endocrinol; 2004 Mar 20; 18(3):653-65. PubMed ID: 14684852
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  • 19. Graded Nodal/Activin signaling titrates conversion of quantitative phospho-Smad2 levels into qualitative embryonic stem cell fate decisions.
    Lee KL, Lim SK, Orlov YL, Yit le Y, Yang H, Ang LT, Poellinger L, Lim B.
    PLoS Genet; 2011 Jun 20; 7(6):e1002130. PubMed ID: 21731500
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  • 20. TGFbeta/Activin/Nodal pathway in inhibition of human embryonic stem cell differentiation by mechanical strain.
    Saha S, Ji L, de Pablo JJ, Palecek SP.
    Biophys J; 2008 May 15; 94(10):4123-33. PubMed ID: 18234825
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