All Stories

  1. Microencapsulated rabbit adipose stem cells initiate tissue regeneration in a rabbit ear defect model
  2. Surface modification of bulk titanium substrates for biomedical applications via low-temperature microwave hydrothermal oxidation
  3. Imaging analysis of the interface between osteoblasts and microrough surfaces of laser-sintered titanium alloy constructs
  4. Inhibition of angiogenesis impairs bone healing in an in vivo murine rapid resynostosis model
  5. Galectin-1 promotes an M2 macrophage response to polydioxanone scaffolds
  6. Osteogenic response of human MSCs and osteoblasts to hydrophilic and hydrophobic nanostructured titanium implant surfaces
  7. Distribution of BMPs in craniosynostotic sutures
  8. Comparable responses of osteoblast lineage cells to microstructured hydrophilic titanium-zirconium and microstructured hydrophilic titanium
  9. Novel hydrophilic nanostructured microtexture on direct metal laser sintered Ti-6Al-4V surfaces enhances osteoblast responsein vitroand osseointegration in a rabbit model
  10. Implant Surface Design Regulates Mesenchymal Stem Cell Differentiation and Maturation
  11. Membrane-mediated actions of 1,25-dihydroxy vitamin D3: A review of the roles of phospholipase A2 activating protein and Ca2+/calmodulin-dependent protein kinase II
  12. Osteoblasts Secrete Pro-Inflammatory Cytokines on PEEK but Anti-inflammatory Cytokines on Microstructured Titanium
  13. Additively manufactured 3D porous Ti-6Al-4V constructs mimic trabecular bone structure and regulate osteoblast proliferation, differentiation and local factor production in a porosity and surface roughness dependent manner
  14. Role of integrin α2β1in mediating osteoblastic differentiation on three-dimensional titanium scaffolds with submicron-scale texture
  15. Osteoblast maturation on microtextured titanium involves paracrine regulation of bone morphogenetic protein signaling
  16. Rapid 1α,25(OH)2D3membrane-mediated activation of Ca2+/calmodulin-dependent protein kinase II in growth plate chondrocytes requires Pdia3, PLAA and caveolae
  17. Superposition of nanostructures on microrough titanium–aluminum–vanadium alloy surfaces results in an altered integrin expression profile in osteoblasts
  18. Role of α2β1 integrins in mediating cell shape on microtextured titanium surfaces
  19. Micro/nanorough titanium-aluminum-vanadium alloy surfaces trigger alternate osteoblast integrin expression profile
  20. Role of ERα36 in membrane-associated signaling by estrogen
  21. New insights on membrane mediated effects of 1α,25-dihydroxy vitamin D3 signaling in the musculoskeletal system
  22. Osteoblast response to nanocrystalline calcium hydroxyapatite depends on carbonate content
  23. Osteoblast Response to Nanocrystalline Calcium Hydroxyapatite Depends on Carbonate Content
  24. 17Beta-Estradiol Promotes Aggressive Laryngeal Cancer Through Membrane-Associated Estrogen Receptor-Alpha 36
  25. Mineralization of three-dimensional osteoblast cultures is enhanced by the interaction of 1α,25-dihydroxyvitamin D3 and BMP2 via two specific vitamin D receptors
  26. Sex-specific response of rat costochondral cartilage growth plate chondrocytes to 17β-estradiol involves differential regulation of plasma membrane associated estrogen receptors
  27. Microstructured titanium regulates interleukin production by osteoblasts, an effect modulated by exogenous BMP-2
  28. Amelogenin Peptide Extract Increases Differentiation and Angiogenic and Local Factor Production and Inhibits Apoptosis in Human Osteoblasts
  29. Addressing the gaps: sex differences in osteoarthritis of the knee
  30. Hormonal modulation of connective tissue homeostasis and sex differences in risk for osteoarthritis of the knee
  31. Rapid membrane responses to dihydrotestosterone are sex dependent in growth plate chondrocytes
  32. Sex Differences in Osteoarthritis of the Knee
  33. BMP2 induces osteoblast apoptosis in a maturation state and noggin‐dependent manner
  34. Mechanism of Pdia3-dependent 1α,25-dihydroxy vitamin D3 signaling in musculoskeletal cells
  35. Abstract 33P
  36. Osteogenic Differentiation of Stem Cells Alters Vitamin D Receptor Expression
  37. Effects of resveratrol on enrichment of adipose-derived stem cells and their differentiation to osteoblasts in two-and three-dimensional cultures
  38. Osteoblasts exhibit a more differentiated phenotype and increased bone morphogenetic protein production on titanium alloy substrates than on poly-ether-ether-ketone
  39. Membrane Estrogen Signaling Enhances Tumorigenesis and Metastatic Potential of Breast Cancer Cells via Estrogen Receptor- 36 (ER 36)
  40. Mechanical contributors to sex differences in idiopathic knee osteoarthritis
  41. Neural and psychosocial contributions to sex differences in knee osteoarthritic pain
  42. Coordinated tether formation in anatomically distinct mice growth centers is dependent on a functional vitamin D receptor and is tightly linked to three-dimensional tissue morphology
  43. Enhancement of Surface Wettability via the Modification of Microtextured Titanium Implant Surfaces with Polyelectrolytes
  44. Electrical Implications of Corrosion for Osseointegration of Titanium Implants
  45. 16: GENE EXPRESSION PROFILE IN NON-SYNDROMIC METOPIC CRANIOSYNOSTOSIS
  46. 21: TEMPORAL CHANGES IN GENE EXPRESSION REGULATING MOUSE POSTERIOR FRONTAL SUTURE FUSION
  47. 124: A NOVEL ALGORITHM TO ANALYZE CORONAL SUTURE DEVELOPMENT IN MICE
  48. 109: INCREASED OSTEOBLASTOGENESIS AND WNT/BMP GENE REGULATION IN NON-SYNDROMIC LAMBDOID CRANIOSYNOSTOSIS
  49. The effects of combined micron-/submicron-scale surface roughness and nanoscale features on cell proliferation and differentiation
  50. Dendritic cell responses to surface properties of clinical titanium surfaces
  51. Osteoblast response to titanium surfaces functionalized with extracellular matrix peptide biomimetics
  52. Cartilage
  53. The Effect of Substrate Microtopography on Osseointegration of Titanium Implants
  54. 17β-Estradiol Regulates Rat Growth Plate Chondrocyte Apoptosis Through a Mitochondrial Pathway Not Involving Nitric Oxide or MAPKs
  55. Protein-disulfide Isomerase-associated 3 (Pdia3) Mediates the Membrane Response to 1,25-Dihydroxyvitamin D3 in Osteoblasts
  56. Disruption of Pdia3 gene results in bone abnormality and affects 1α,25-dihydroxy-vitamin D3-induced rapid activation of PKC
  57. 161A: PHARMACOLOGICAL ENRICHMENT: A NEW APPROACH TO ADIPOSE-DERIVED STEM CELL ENRICHMENT
  58. 197A: THE DEVELOPMENT OF NOVEL MICRO-COMPUTED TOMOGRAPHY SNAKE ALGORITHM TO DETERMINE TIME COURSE OF POSTERIOR FRONTAL SUTURE CLOSURE IN MICE
  59. Proceedings from the Scientific Symposium: Sex Differences in Cardiovascular Disease and Implications for Therapies
  60. Bacterial Adhesion on Polyelectrolyte Modified Microstructured Titanium Surfaces
  61. Sex dependent regulation of osteoblast response to implant surface properties by systemic hormones
  62. Inhibition of 1,25-(OH)2D3- and 24,25-(OH)2D3-dependent stimulation of alkaline phosphatase activity by A23187 suggests a role for calcium in the mechanism of vitamin D regulation of chondrocyte cultures
  63. Effects of vitamin D metabolites on collagen production and cell proliferation of growth zone and resting zone cartilage cells in vitro
  64. Mechanisms regulating increased production of osteoprotegerin by osteoblasts cultured on microstructured titanium surfaces
  65. Formation of Tethers Linking the Epiphysis and Metaphysis Is Regulated by Vitamin D Receptor-Mediated Signaling
  66. Lysophosphatidic acid signaling promotes proliferation, differentiation, and cell survival in rat growth plate chondrocytes
  67. Inhibition of Phosphate-Induced Apoptosis in Resting Zone Chondrocytes by Thrombin Peptide 508
  68. 1,25-Dihydroxy Vitamin D3 Is an Autocrine Regulator of Extracellular Matrix Turnover and Growth Factor Release via ERp60-Activated Matrix Vesicle Matrix Metalloproteinases
  69. Thrombin peptide TP508 prevents nitric oxide mediated apoptosis in chondrocytes in the endochondral developmental pathway
  70. Beta-1 integrins mediate substrate dependent effects of 1α,25(OH)2D3 on osteoblasts
  71. Integrin α5 controls osteoblastic proliferation and differentiation responses to titanium substrates presenting different roughness characteristics in a roughness independent manner
  72. Requirement for both micron- and submicron scale structure for synergistic responses of osteoblasts to substrate surface energy and topography
  73. Osteoinductivity of demineralized bone matrix in immunocompromised mice and rats is decreased by ovariectomy and restored by estrogen replacement
  74. Regulation of Growth Plate Chondrocytes by 1,25-Dihydroxyvitamin D3 Requires Caveolae and Caveolin-1
  75. Integrin β1 silencing in osteoblasts alters substrate-dependent responses to 1,25-dihydroxy vitamin D3
  76. Plasma membrane requirements for 1α,25(OH)2D3 dependent PKC signaling in chondrocytes and osteoblasts
  77. Sex-specific regulation of growth plate chondrocytes by estrogen is via multiple MAP kinase signaling pathways
  78. Response of MG63 osteoblast-like cells to titanium and titanium alloy is dependent on surface roughness and composition
  79. Growth-plate chondrocytes respond to 17β-estradiol with sex-specific increases in IP3 and intracellular calcium ion signalling via a capacitative entry mechanism
  80. Differential regulation of osteoblasts by substrate microstructural features
  81. Human articular chondrocytes exhibit sexual dimorphism in their responses to 17β-estradiol
  82. Pulsed Electromagnetic Fields Have Direct Effects on Growth Plate Chondrocytes
  83. Sexual dimorphism of growth plate prehypertrophic and hypertrophic chondrocytes in response to testosterone requires metabolism to dihydrotestosterone (DHT) by steroid 5-alpha reductase type 1
  84. Cartilage and Vitamin D: Genomic and Nongenomic Regulation by 1,25(OH)2D3 and 24,25(OH)2D3
  85. Phospholipase A2activating protein (PLAA) is required for 1α,25(OH)2D3signaling in growth plate chondrocytes
  86. Rapid vitamin D-dependent PKC signaling shares features with estrogen-dependent PKC signaling in cartilage and bone
  87. Membrane actions of vitamin D metabolites 1?,25(OH)2D3 and 24R,25(OH)2D3 are retained in growth plate cartilage cells from vitamin D receptor knockout mice
  88. Estrogen-Dependent Rapid Activation of Protein Kinase C in Estrogen Receptor-Positive MCF-7 Breast Cancer Cells and Estrogen Receptor-Negative HCC38 Cells Is Membrane-Mediated and Inhibited by Tamoxifen
  89. Vitamin D and Cartilage
  90. Response of normal female human osteoblasts (NHOst) to 17?-estradiol is modulated by implant surface morphology
  91. Transforming growth factor-β1 regulation of growth zone chondrocytes is mediated by multiple interacting pathways
  92. Membrane mediated signaling mechanisms are used differentially by metabolites of vitamin D3 in musculoskeletal cells
  93. Tamoxifen elicits its anti-estrogen effects in growth plate chondrocytes by inhibiting protein kinase C
  94. DifferentialRegulation ofGrowthPlateChondrocytes by1α,25-(OH)2D3and24R,25-(OH)2D3InvolvesCell-maturation-specificMembrane-receptor-activatedPhospholipidMetabolism
  95. Evidence for distinct membrane receptors for 1α,25-(OH)2D3 and 24R,25-(OH)2D3 in osteoblasts
  96. Shear force modulates osteoblast response to surface roughness
  97. Rat costochondral chondrocytes produce 17β-estradiol and regulate its production by 1α,25(OH)2D3
  98. The First Stage of Transforming Growth Factor β1 Activation is Release of the Large Latent Complex from the Extracellular Matrix of Growth Plate Chondrocytes by Matrix Vesicle Stromelysin-1 (MMP-3)
  99. 1a,25-(OH)2D3 Regulates 25-Hydroxyvitamin D3 24R-Hydroxylase Activity in Growth Zone Costochondral Growth Plate Chondrocytes via Protein Kinase C
  100. Characterization of PGE2 receptors (EP) and their role as mediators of 1α,25-(OH)2D3 effects on growth zone chondrocytes
  101. The effect of 24R,25-(OH)2D3 on protein kinase C activity in chondrocytes is mediated by phospholipase D whereas the effect of 1α,25-(OH)2D3 is mediated by phospholipase C
  102. Inhibition of cyclooxygenase by indomethacin modulates osteoblast response to titanium surface roughness in a time-dependent manner
  103. 17?-estradiol-BSA conjugates and 17?-estradiol regulate growth plate chondrocytes by common membrane associated mechanisms involving PKC dependent and independent signal transduction
  104. Stathmin Levels in Growth Plate Chondrocytes Are Modulated by Vitamin D3 Metabolites and Transforming Growth Factor-β1 and Are Associated with Proliferation
  105. Effects of 1?,25-(OH)2D3 on rat growth zone chondrocytes are mediated via cyclooxygenase-1 and phospholipase A2
  106. Regulation of phospholipase D (PLD) in growth plate chondrocytes by 24R,25-(OH)2D3 is dependent on cell maturation state (resting zone cells) and is specific to the PLD2 isoform
  107. Osteoblast response to titanium surface roughness and 1?,25-(OH)2D3 is mediated through the mitogen-activated protein kinase (MAPK) pathway
  108. Both cyclooxygenase-1 and cyclooxygenase-2 mediate osteoblast response to titanium surface roughness
  109. The Titanium-Bone Cell Interface In Vitro: The Role of the Surface in Promoting Osteointegration
  110. Expression and production of stathmin in growth plate chondrocytes is cell‐maturation dependent
  111. Maturation State Determines the Response of Osteogenic Cells to Surface Roughness and 1,25-Dihydroxyvitamin D3
  112. Transforming growth factor-β1 regulation of resting zone chondrocytes is mediated by two separate but interacting pathways
  113. 24R,25-(OH)2D3 mediates its membrane receptor-dependent effects on protein kinase C and alkaline phosphatase via phospholipase A2 and cyclooxygenase-1 but not cyclooxygenase-2 in growth plate chondrocytes
  114. 24R,25-(OH)2D3 mediates its membrane receptor-dependent effects on protein kinase C and alkaline phosphatase via phospholipase A2 and cyclooxygenase-1 but not cyclooxygenase-2 in growth plate chondrocytes
  115. Phagocytosis of wear debris by osteoblasts affects differentiation and local factor production in a manner dependent on particle composition
  116. The phenotype and pretreatment of chondrocytes with PDGF regulate cartilage formation in biodegradable scaffolds in vivo
  117. Characterization of prostaglandin E2 receptors and their role in 24,25-(OH)2D3-mediated effects on resting zone chondrocytes
  118. Pretreatment with platelet derived growth factor-BB modulates the ability of costochondral resting zone chondrocytes incorporated into PLA/PGA scaffolds to form new cartilage in vivo
  119. Expression and production of stathmin in growth plate chondrocytes is cell-maturation dependent
  120. Potential Mechanisms for the Plasmin-Mediated Release and Activation of Latent Transforming Growth Factor-β1 from the Extracellular Matrix of Growth Plate Chondrocytes1
  121. Surface roughness mediates its effects on osteoblasts via protein kinase A and phospholipase A2
  122. Surface roughness modulates the response of MG63 osteoblast-like cells to 1,25-(OH)2D3 through regulation of phospholipase A2 activity and activation of protein kinase A
  123. Arachidonic Acid Directly Mediates the Rapid Effects of 24,25-Dihydroxyvitamin D3Via Protein Kinase C and Indirectly through Prostaglandin Production in Resting Zone Chondrocytes1
  124. Effect of surface roughness and composition on costochondral chondrocytes is dependent on cell maturation state
  125. Prostaglandins mediate the effects of 1,25-(OH)2D3 and 24,25-(OH)2D3 on growth plate chondrocytes in a metabolite-specific and cell maturation-dependent manner
  126. Altered Expression of Bone Sialoproteins in Vitamin D-Deficient rBSP2.7Luc Transgenic Mice
  127. Vitamin D3 metabolites regulate LTBP1 and latent TGF‐β1 expression and latent TGF‐β1 incorporation in the extracellular matrix of chondrocytes
  128. TGFβ1 Regulates 25-Hydroxyvitamin D3 1α- and 24-Hydroxylase Activity in Cultured Growth Plate Chondrocytes in a Maturation-Dependent Manner
  129. Vitamin D3 metabolites regulate LTBP1 and latent TGF-?1 expression and latent TGF-?1 incorporation in the extracellular matrix of chondrocytes
  130. Treatment of resting zone chondrocytes with transforming growth factor-β1 induces differentiation into a phenotype characteristic of growth zone chondrocytes by downregulating responsiveness to 24,25-(OH)2D3 and upregulating responsiveness to 1,25-(OH)2D3
  131. Growth plate chondrocytes store latent transforming growth factor (TGF)-β1 in their matrix through latent TGF-β1 binding protein-1
  132. Prostaglandins mediate the effects of titanium surface roughness on MG63 osteoblast‐like cells and alter cell responsiveness to 1α,25‐(OH)2D3
  133. Prostaglandins mediate the effects of titanium surface roughness on MG63 osteoblast-like cells and alter cell responsiveness to 1?,25-(OH)2D3
  134. Arachidonic acid is an autocoid mediator of the differential action of 1,25‐(OH)2D3 and 24,25‐(OH)2D3 on growth plate chondrocytes
  135. Arachidonic acid is an autocoid mediator of the differential action of 1,25-(OH)2D3 and 24,25-(OH)2D3 on growth plate chondrocytes
  136. 17β-Estradiol regulation of protein kinase C activity in chondrocytes is sex-dependent and involves nongenomic mechanisms
  137. 1,25(OH)2D3 Regulates Protein Kinase C Activity Through Two Phospholipid-Dependent Pathways Involving Phospholipase A2 and Phospholipase C in Growth Zone Chondrocytes
  138. The Synergistic Effects of Vitamin D Metabolites and Transforming Growth Factor-β on Costochondral Chondrocytes Are Mediated by Increases in Protein Kinase C Activity Involving Two Separate Pathways1
  139. Treatment of Resting Zone Chondrocytes with Bone Morphogenetic Protein-2 Induces Maturation into a Phenotype Characteristic of Growth Zone Chondrocytes by Downregulating Responsiveness to 24,25(OH)2D3 and Upregulating Responsivene...
  140. Titanium surface roughness alters responsiveness of MG63 osteoblast-like cells to 1?,25-(OH)2D3
  141. Response of MG63 osteoblast-like cells to titanium and titanium alloy is dependent on surface roughness and composition
  142. The effects of 17\-estradiol on chondrocyte differentiation are modulated by vitamin D3 metabolites
  143. Interleukin-1α and β in Growth Plate Cartilage Are Regulated by Vitamin D Metabolites In Vivo
  144. Rapid and long-term effects of PTH(1-34) on growth plate chondrocytes are mediated through two different pathways in a cell-maturation-dependent manner
  145. A‐ring analogues of 1,25‐(OH)2D3 with low affinity for the vitamin D receptor modulate chondrocytes via membrane effects that are dependent on cell maturation
  146. A-ring analogues of 1,25-(OH)2D3 with low affinity for the vitamin D receptor modulate chondrocytes via membrane effects that are dependent on cell maturation
  147. Recombinant bone morphogenetic protein (BMP)-2 regulates costochondral growth plate chondrocytes and induces expression of BMP-2 and BMP-4 in a cell maturation-dependent manner
  148. Vitamin D3 regulation of stromelysin-1 (MMP-3) in chondrocyte cultures is mediated by protein kinase C
  149. Vitamin D3 regulation of stromelysin‐1 (MMP‐3) in chondrocyte cultures is mediated by protein kinase C
  150. Surface roughness modulates the local production of growth factors and cytokines by osteoblast-like MG-63 cells
  151. Vitamin D Metabolites Regulate Matrix Vesicle Metalloproteinase Content in a Cell Maturation-Dependent Manner
  152. Nongenomic regulation of protein kinase C isoforms by the vitamin D metabolites 1α,25-(OH)2D3 and 24R,25-(OH)2D3
  153. Effect of titanium surface roughness on chondrocyte proliferation, matrix production, and differentiation depends on the state of cell maturation
  154. Effect of titanium surface roughness on chondrocyte proliferation, matrix production, and differentiation depends on the state of cell maturation
  155. The Synergistic Effect of TGFβ and 24, 25-(OH)2D3on Resting Zone Chondrocytes is Metabolite-Specific and Mediated by PKC
  156. Vitamin D Regulation of Metal loproteinase Activity in Matrix Vesicles
  157. Effect of titanium surface roughness on proliferation, differentiation, and protein synthesis of human osteoblast-like cells (MG63)
  158. Treatment of resting zone chondrocytes with 24,25-dihydroxyvitamin D3 [24,25-(OH)2D3] induces differentiation into a 1,25-(OH)2D3-responsive phenotype characteristic of growth zone chondrocytes.
  159. Nongenomic regulation of extracellular matrix events by vitamin D metabolites
  160. Gender-specific, maturation-dependent effects of testosterone on chondrocytes in culture.
  161. Gender-related effects of vitamin D metabolites on cartilage and bone
  162. Maturation-dependent regulation of protein kinase C activity by vitamin D3 metabolites in chondrocyte cultures
  163. Direct effects of transforming growth factor-beta on chondrocytes are modulated by vitamin D metabolites in a cell maturation-specific manner.
  164. Regulation of prostaglandin E2 production by vitamin D metabolites in growth zone and resting zone chondrocyte cultures is dependent on cell maturation
  165. Production of 1,25-dihydroxyvitamin D3 and 24,25-dihydroxyvitamin D3 by growth zone and resting zone chondrocytes is dependent on cell maturation and is regulated by hormones and growth factors.
  166. α2-HS-glycoprotein: Expression in chondrocytes and augmentation of alkaline phosphatase and phospholipase A2 activity
  167. Regulation of Matrix Vesicle Metabolism by Vitamin D Metabolites
  168. DIRECT EFFECT OF VITAMIN D METABOLITES ON MATRIX VESICLE ALKALINE PHOSPHATASE
  169. The Effects of Vitamin D Metabolites on the Plasma and Matrix Vesicle Membranes of Growth and Resting Cartilage Cellsin Vitro*
  170. The Effects of Vitamin D Metabolites on Phospholipase A2Activity of Growth Zone and Resting Zone Cartilage Cellsin Vitro*
  171. Differential expression of phenotype by resting zone and growth region costochondral chondrocytes in vitro
  172. Proteolipid-lipid relationships in normal and vitamin D-deficient chick cartilage
  173. Chapter 13—Bone Graft Substitutes: Basic Information for Successful Clinical Use with Special Focus on Synthetic Graft Substitutes