scholarly article | Q13442814 |
P50 | author | Meenakshi A Chellaiah | Q89701683 |
P2093 | author name string | Tao Ma | |
Sunipa Majumdar | |||
P2860 | cites work | The architecture of the adhesive apparatus of cultured osteoclasts: from podosome formation to sealing zone assembly | Q21144466 |
Phosphorylation on Ser5 increases the F-actin-binding activity of L-plastin and promotes its targeting to sites of actin assembly in cells | Q24320052 | ||
Functional differences between L- and T-plastin isoforms | Q24673025 | ||
Fimbrin is a homologue of the cytoplasmic phosphoprotein plastin and has domains homologous with calmodulin and actin gelation proteins | Q24678811 | ||
The molecular dynamics of osteoclast adhesions | Q28287398 | ||
A Glanzmann's mutation in beta 3 integrin specifically impairs osteoclast function | Q28364534 | ||
Src kinase activity is essential for osteoclast function | Q28513236 | ||
A dynamic podosome-like structure of epithelial cells | Q28564794 | ||
Dramatic inhibition of osteoclast sealing ring formation and bone resorption in vitro by a WASP-peptide containing pTyr294 amino acid | Q28592212 | ||
Quantitative kinetic study of the actin-bundling protein L-plastin and of its impact on actin turn-over | Q33532623 | ||
Upregulation of L-plastin gene by testosterone in breast and prostate cancer cells: identification of three cooperative androgen receptor-binding sequences | Q33889475 | ||
Osteoclast motility: putting the brakes on bone resorption. | Q33925042 | ||
Mice lacking beta3 integrins are osteosclerotic because of dysfunctional osteoclasts | Q33939357 | ||
Regulation of sealing ring formation by L-plastin and cortactin in osteoclasts | Q34144752 | ||
Human T cell L-plastin bundles actin filaments in a calcium-dependent manner | Q34297620 | ||
Podosome organization drives osteoclast-mediated bone resorption. | Q34344623 | ||
FcgammaRII-mediated adhesion and phagocytosis induce L-plastin phosphorylation in human neutrophils. | Q34384522 | ||
Actin-bundling protein L-plastin regulates T cell activation. | Q34522338 | ||
Inhibition of osteoclast activation by phloretin through disturbing αvβ3 integrin-c-Src pathway | Q35193656 | ||
Actin-binding proteins | Q36035371 | ||
Rational identification of enoxacin as a novel V-ATPase-directed osteoclast inhibitor | Q36131284 | ||
Plastins: versatile modulators of actin organization in (patho)physiological cellular processes | Q36165372 | ||
A role for the actin-bundling protein L-plastin in the regulation of leukocyte integrin function | Q36257346 | ||
Gelsolin deficiency blocks podosome assembly and produces increased bone mass and strength | Q36316394 | ||
An atomic model of actin filaments cross-linked by fimbrin and its implications for bundle assembly and function | Q36326402 | ||
Podosomes as smart regulators of cellular adhesion. | Q36424991 | ||
Podosome and sealing zone: specificity of the osteoclast model | Q36424995 | ||
Pharmacologic shifting of a balance between protein refolding and degradation mediated by Hsp90 | Q37044062 | ||
Clear zone in osteoclast function: role of podosomes in regulation of bone-resorbing activity | Q37202816 | ||
Osteopontin stimulates gelsolin-associated phosphoinositide levels and phosphatidylinositol triphosphate-hydroxyl kinase | Q37380833 | ||
The osteoclast and its unique cytoskeleton | Q37968677 | ||
Invadopodia and matrix degradation, a new property of prostate cancer cells during migration and invasion | Q38291490 | ||
c-Src is required for stimulation of gelsolin-associated phosphatidylinositol 3-kinase | Q38336689 | ||
The actin-bundling protein L-plastin is essential for marginal zone B cell development | Q38361351 | ||
Osteoclast function and bone-resorbing activity: An overview | Q38828957 | ||
Characterization of L-plastin interaction with beta integrin and its regulation by micro-calpain | Q39735206 | ||
The actin-bundling protein L-plastin: a critical regulator of immune cell function | Q39802557 | ||
Characterization of the expression of variant and standard CD44 in prostate cancer cells: identification of the possible molecular mechanism of CD44/MMP9 complex formation on the cell surface | Q39828194 | ||
The leukocyte protein L-plastin induces proliferation, invasion and loss of E-cadherin expression in colon cancer cells. | Q40351667 | ||
Apatite-mediated actin dynamics in resorbing osteoclasts | Q40521404 | ||
L-Plastin promotes podosome longevity and supports macrophage motility | Q40544757 | ||
Cytoskeletal changes in osteoclasts during the resorption cycle | Q41142562 | ||
Dynamics of the sealing zone in cultured osteoclasts | Q42316781 | ||
Tyrosine phosphorylation of p130Cas and cortactin accompanies integrin-mediated cell adhesion to extracellular matrix | Q42824269 | ||
Protein transduction: delivery of Tat-GTPase fusion proteins into mammalian cells | Q43576972 | ||
Role for plastin in host defense distinguishes integrin signaling from cell adhesion and spreading | Q44519041 | ||
Biochemical characterization of the L-plastin-actin interaction shows a resemblance with that of alpha-actinin and allows a distinction to be made between the two actin-binding domains of the molecule | Q44781686 | ||
Rous sarcoma virus-transformed fibroblasts and cells of monocytic origin display a peculiar dot-like organization of cytoskeletal proteins involved in microfilament-membrane interactions | Q45835332 | ||
Activation of Src kinase by protein-tyrosine phosphatase-PEST in osteoclasts: comparative analysis of the effects of bisphosphonate and protein-tyrosine phosphatase inhibitor on Src activation in vitro | Q46058982 | ||
Characterization of a 64-kd protein phosphorylated during chemotactic activation with IL-8 and fMLP of human polymorphonuclear leukocytes. I. Phosphorylation of a 64-kd protein and other proteins. | Q50781411 | ||
A band of F-actin containing podosomes is involved in bone resorption by osteoclasts. | Q52484129 | ||
Role of alpha(v)beta(3) integrin in osteoclast migration and formation of the sealing zone. | Q52536880 | ||
Kinetics of the osteoclast cytoskeleton during the resorption cycle in vitro. | Q54258542 | ||
An atomic model of fimbrin binding to F-actin and its implications for filament crosslinking and regulation | Q58052717 | ||
Phosphorylation of a Wiscott-Aldrich syndrome protein-associated signal complex is critical in osteoclast bone resorption | Q64377259 | ||
Purification of the intestinal microvillus cytoskeletal proteins villin, fimbrin, and ezrin | Q69761052 | ||
Characterization of the M(r) 65,000 lymphokine-activated killer proteins phosphorylated after tumor target binding: evidence that pp65a and pp65b are phosphorylated forms of L-plastin | Q70866369 | ||
Fimbrin localized to an insoluble cytoskeletal fraction is constitutively phosphorylated on its headpiece domain in adherent macrophages | Q72560063 | ||
Fimbrin in podosomes of monocyte-derived osteoclasts | Q73590158 | ||
Rho-A is critical for osteoclast podosome organization, motility, and bone resorption | Q73680599 | ||
Transduction of full-length TAT fusion proteins into mammalian cells: TAT-p27Kip1 induces cell migration | Q77658726 | ||
TNFalpha potently activates osteoclasts, through a direct action independent of and strongly synergistic with RANKL | Q77679093 | ||
Murine osteoclast formation and function: differential regulation by humoral agents | Q82129423 | ||
L-plastin regulates polarization and migration in chemokine-stimulated human T lymphocytes | Q84121464 | ||
P433 | issue | 1 | |
P304 | page(s) | 73-82 | |
P577 | publication date | 2018-09-21 | |
P1433 | published in | Experimental Cell Research | Q1524289 |
P1476 | title | L-plastin phosphorylation regulates the early phase of sealing ring formation by actin bundling process in mouse osteoclasts | |
P478 | volume | 372 |
Q89701687 | C-phycocyanin attenuates RANKL-induced osteoclastogenesis and bone resorption in vitro through inhibiting ROS levels, NFATc1 and NF-κB activation |
Q64939376 | Engineering of L-Plastin Peptide-Loaded Biodegradable Nanoparticles for Sustained Delivery and Suppression of Osteoclast Function In Vitro. |
Q93015610 | L-Plastin deficiency produces increased trabecular bone due to attenuation of sealing ring formation and osteoclast dysfunction |
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