(Q33411157)

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Opposite effects of PDGF-BB and prostaglandin E1 on cell-motility related processes are paralleled by modifications of distinct actin-binding proteins

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Europe PubMed Central

PubMed publication ID

26 July 2017

Opposite effects of PDGF-BB and prostaglandin E1 on cell-motility related processes are paralleled by modifications of distinct actin-binding proteins (English)

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Europe PubMed Central

PubMed publication ID

26 July 2017

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Stanley G Kimani

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Stanley G Kimani

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Tijs van Wieringen

1

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Europe PubMed Central

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26 July 2017

Anna-Karin Hultgård-Ekwall

3

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Europe PubMed Central

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26 July 2017

Jens Forsberg

4

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Europe PubMed Central

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26 July 2017

Vahid Reyhani

5

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Europe PubMed Central

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26 July 2017

Ake Engström

6

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26 July 2017

Kristofer Rubin

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26 July 2017

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20 February 2009

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26 July 2017

Experimental Cell Research

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26 July 2017

315

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Europe PubMed Central

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26 July 2017

10

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Europe PubMed Central

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26 July 2017

1745-1758

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Europe PubMed Central

PubMed publication ID

26 July 2017

Interstitial-lymphatic mechanisms in the control of extracellular fluid volume.

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A novel physiological function for platelet-derived growth factor-BB in rat dermis

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Platelet-derived growth factor BB-mediated normalization of dermal interstitial fluid pressure after mast cell degranulation depends on beta3 but not beta1 integrins

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Cell interactions with collagen matrices in vivo and in vitro depend on phosphatidylinositol 3-kinase and free cytoplasmic calcium

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P21-activated kinase 1: convergence point in PDGF- and LPA-stimulated collagen matrix contraction by human fibroblasts

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Induction of circular membrane ruffling on human fibroblasts by platelet-derived growth factor

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Platelet-derived growth factor-BB modulates membrane mobility of beta1 integrins

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Epidermal growth factor (EGF) promotes human keratinocyte locomotion on collagen by increasing the alpha 2 integrin subunit

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The anti-inflammatory agent alpha-trinositol exerts its edema-preventing effects through modulation of beta 1 integrin function

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Rapid methods for isolation of human plasma fibronectin

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Beta 1 integrin-mediated collagen gel contraction is stimulated by PDGF.

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Linking genome and proteome by mass spectrometry: large-scale identification of yeast proteins from two dimensional gels

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Probability-based protein identification by searching sequence databases using mass spectrometry data

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Measurement of cell numbers by means of the endogenous enzyme hexosaminidase. Applications to detection of lymphokines and cell surface antigens

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Increased myosin light chain phosphorylation is not required for growth factor stimulation of collagen matrix contraction

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Immobilized gallium(III) affinity chromatography of phosphopeptides

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Cortical actin organization: lessons from ERM (ezrin/radixin/moesin) proteins

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Mapping of phosphorylated proteins on two-dimensional polyacrylamide gels using protein phosphatase

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Phosphorylation of caldesmon during smooth muscle contraction and cell migration or proliferation

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Hepatic stellate cell protrusions couple platelet-derived growth factor-BB to chemotaxis

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Platelet isoforms of platelet-derived growth factor stimulate fibroblasts to contract collagen matrices

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Cytochalasin D induces edema formation and lowering of interstitial fluid pressure in rat dermis

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A secreted collagen- and fibronectin-binding streptococcal protein modulates cell-mediated collagen gel contraction and interstitial fluid pressure

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Prostacyclin analogs inhibit fibroblast contraction of collagen gels through the cAMP-PKA pathway

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Differential regulation of free-floating collagen gel contraction by human fetal and adult dermal fibroblasts in response to prostaglandin E2 mediated by an EP2/cAMP-dependent mechanism.

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Ca2+ sensitivity of smooth muscle and nonmuscle myosin II: modulated by G proteins, kinases, and myosin phosphatase

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Nonmuscle caldesmon: its distribution and involvement in various cellular processes. Review article.

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10.1016/J.YEXCR.2009.02.005

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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