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S100A4 regulates macrophage chemotaxis.

Li ZH, Dulyaninova NG, House RP, Almo SC, Bresnick AR.

Mol Biol Cell. 2010 Aug 1;21(15):2598-610. doi: 10.1091/mbc.E09-07-0609.


Metastatic potential of B16-F10 melanoma cells is enhanced by extracellular S100A4 derived from RAW264.7 macrophages.

Haase-Kohn C, Wolf S, Herwig N, Mosch B, Pietzsch J.

Biochem Biophys Res Commun. 2014 Mar 28;446(1):143-8. doi: 10.1016/j.bbrc.2014.02.126.


CD148/DEP-1 association with areas of cytoskeletal organisation in macrophages.

Dave RK, Hume DA, Elsegood C, Kellie S.

Exp Cell Res. 2009 Jun 10;315(10):1734-44. doi: 10.1016/j.yexcr.2009.02.023.


The chemotactic defect in wiskott-Aldrich syndrome macrophages is due to the reduced persistence of directional protrusions.

Ishihara D, Dovas A, Park H, Isaac BM, Cox D.

PLoS One. 2012;7(1):e30033. doi: 10.1371/journal.pone.0030033.


A biosensor of S100A4 metastasis factor activation: inhibitor screening and cellular activation dynamics.

Garrett SC, Hodgson L, Rybin A, Toutchkine A, Hahn KM, Lawrence DS, Bresnick AR.

Biochemistry. 2008 Jan 22;47(3):986-96.


Expression of metastasin S100A4 is essential for bone resorption and regulates osteoclast function.

Erlandsson MC, Svensson MD, Jonsson IM, Bian L, Ambartsumian N, Andersson S, Peng Z, Vääräniemi J, Ohlsson C, Andersson KM, Bokarewa MI.

Biochim Biophys Acta. 2013 Dec;1833(12):2653-63. doi: 10.1016/j.bbamcr.2013.06.020.


Two functional S100A4 monomers are necessary for regulating nonmuscle myosin-IIA and HCT116 cell invasion.

House RP, Pozzuto M, Patel P, Dulyaninova NG, Li ZH, Zencheck WD, Vitolo MI, Weber DJ, Bresnick AR.

Biochemistry. 2011 Aug 16;50(32):6920-32. doi: 10.1021/bi200498q.


VEGF-A and Tenascin-C produced by S100A4+ stromal cells are important for metastatic colonization.

O'Connell JT, Sugimoto H, Cooke VG, MacDonald BA, Mehta AI, LeBleu VS, Dewar R, Rocha RM, Brentani RR, Resnick MB, Neilson EG, Zeisberg M, Kalluri R.

Proc Natl Acad Sci U S A. 2011 Sep 20;108(38):16002-7. doi: 10.1073/pnas.1109493108.


S100A4-neutralizing antibody suppresses spontaneous tumor progression, pre-metastatic niche formation and alters T-cell polarization balance.

Grum-Schwensen B, Klingelhöfer J, Beck M, Bonefeld CM, Hamerlik P, Guldberg P, Grigorian M, Lukanidin E, Ambartsumian N.

BMC Cancer. 2015 Feb 12;15:44. doi: 10.1186/s12885-015-1034-2.


Structure of the S100A4/myosin-IIA complex.

Ramagopal UA, Dulyaninova NG, Varney KM, Wilder PT, Nallamsetty S, Brenowitz M, Weber DJ, Almo SC, Bresnick AR.

BMC Struct Biol. 2013 Nov 20;13:31. doi: 10.1186/1472-6807-13-31.


Macrophages require Skap2 and Sirpα for integrin-stimulated cytoskeletal rearrangement.

Alenghat FJ, Baca QJ, Rubin NT, Pao LI, Matozaki T, Lowell CA, Golan DE, Neel BG, Swanson KD.

J Cell Sci. 2012 Nov 15;125(Pt 22):5535-45. doi: 10.1242/jcs.111260.


Lung metastasis fails in MMTV-PyMT oncomice lacking S100A4 due to a T-cell deficiency in primary tumors.

Grum-Schwensen B, Klingelhöfer J, Grigorian M, Almholt K, Nielsen BS, Lukanidin E, Ambartsumian N.

Cancer Res. 2010 Feb 1;70(3):936-47. doi: 10.1158/0008-5472.CAN-09-3220.


Metastasis-inducing S100A4 and RANTES cooperate in promoting tumor progression in mice.

Forst B, Hansen MT, Klingelhöfer J, Møller HD, Nielsen GH, Grum-Schwensen B, Ambartsumian N, Lukanidin E, Grigorian M.

PLoS One. 2010 Apr 28;5(4):e10374. doi: 10.1371/journal.pone.0010374.


Imbalanced gp130-dependent signaling in macrophages alters macrophage colony-stimulating factor responsiveness via regulation of c-fms expression.

Jenkins BJ, Grail D, Inglese M, Quilici C, Bozinovski S, Wong P, Ernst M.

Mol Cell Biol. 2004 Feb;24(4):1453-63.


Cysteine 81 is critical for the interaction of S100A4 and myosin-IIA.

Dulyaninova NG, Hite KM, Zencheck WD, Scudiero DA, Almo SC, Shoemaker RH, Bresnick AR.

Biochemistry. 2011 Aug 23;50(33):7218-27. doi: 10.1021/bi200853y.

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