Prolyl hydroxylase inhibitors increase neoangiogenesis and callus formation following femur fracture in mice.
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The hypoxia-inducible factor pathway, prolyl hydroxylase domain protein inhibitors, and their roles in bone repair and regenerationHypoxic regulation of osteoclast differentiation and bone resorption activityMolecular mechanisms of action and therapeutic uses of pharmacological inhibitors of HIF-prolyl 4-hydroxylases for treatment of ischemic diseasesFlavonoid Compound Icariin Activates Hypoxia Inducible Factor-1α in Chondrocytes and Promotes Articular Cartilage RepairAngiogenesis in bone regeneration.Localized deferoxamine injection augments vascularity and improves bony union in pathologic fracture healing after radiotherapy.HIF-1α activation results in actin cytoskeleton reorganization and modulation of Rac-1 signaling in endothelial cellsA central role for hypoxic signaling in cartilage, bone, and hematopoiesis.Cross-talk between hypoxia and insulin signaling through Phd3 regulates hepatic glucose and lipid metabolism and ameliorates diabetesAdvances in iron chelation: an update.Hypoxia-inducible factor regulates osteoclast-mediated bone resorption: role of angiopoietin-like 4The prolyl hydroxylase inhibitor dimethyloxalylglycine enhances dentin sialophoshoprotein expression through VEGF-induced Runx2 stabilizationDimethyloxalylglycine prevents bone loss in ovariectomized C57BL/6J mice through enhanced angiogenesis and osteogenesis.Restoring the secretory function of irradiation-damaged salivary gland by administrating deferoxamine in mice.Incorporation of a prolyl hydroxylase inhibitor into scaffolds: a strategy for stimulating vascularizationStimulating angiogenesis mitigates the unloading-induced reduction in osteogenesis in early-stage bone repair in rats.Oxygen-sensing PHDs regulate bone homeostasis through the modulation of osteoprotegerin.Contaminated open fracture and crush injury: a murine model.Deferoxamine enhances bone regeneration in mandibular distraction osteogenesis.MiRNA inhibition in tissue engineering and regenerative medicine.Deferoxamine reverses radiation induced hypovascularity during bone regeneration and repair in the murine mandible.Deferoxamine enhances the vascular response of bone regeneration in mandibular distraction osteogenesis.Quantitative analysis of vascular response after mandibular fracture repair using microcomputed tomography with vessel perfusion.Vascular development during distraction osteogenesis proceeds by sequential intramuscular arteriogenesis followed by intraosteal angiogenesis.Arterial calcification and bone physiology: role of the bone-vascular axis.Translational treatment paradigm for managing non-unions secondary to radiation injury utilizing adipose derived stem cells and angiogenic therapy.Bone regeneration in distraction osteogenesis demonstrates significantly increased vascularity in comparison to fracture repair in the mandibleDifferential fracture healing resulting from fixation stiffness variability: a mouse modelPrevention of radiation-induced bone pathology through combined pharmacologic cytoprotection and angiogenic stimulation.Targeting angiogenesis as a therapeutic means to reinforce osteocyte survival and prevent nonunions in the aftermath of radiotherapy.The role of oxygen during fracture healingDeferoxamine restores callus size, mineralization, and mechanical strength in fracture healing after radiotherapy.Prolyl hydroxylation regulates protein degradation, synthesis, and splicing in human induced pluripotent stem cell-derived cardiomyocytes.The effect of deferoxamine on angiogenesis and bone repair in steroid-induced osteonecrosis of rabbit femoral heads.Tunable delivery of siRNA from a biodegradable scaffold to promote angiogenesis in vivo.Evaluating effects of deferoxamine in a rat tibia critical bone defect modelHypoxia-driven pathways in bone development, regeneration and disease.Hypoxia signalling manipulation for bone regeneration.Prolyl hydroxylase inhibitors act as agents to enhance the efficiency of cell therapy.Glucocorticoids promote Von Hippel Lindau degradation and Hif-1α stabilization.
P2860
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P2860
Prolyl hydroxylase inhibitors increase neoangiogenesis and callus formation following femur fracture in mice.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Prolyl hydroxylase inhibitors ...... lowing femur fracture in mice.
@en
Prolyl hydroxylase inhibitors ...... lowing femur fracture in mice.
@nl
type
label
Prolyl hydroxylase inhibitors ...... lowing femur fracture in mice.
@en
Prolyl hydroxylase inhibitors ...... lowing femur fracture in mice.
@nl
prefLabel
Prolyl hydroxylase inhibitors ...... lowing femur fracture in mice.
@en
Prolyl hydroxylase inhibitors ...... lowing femur fracture in mice.
@nl
P2093
P2860
P356
P1476
Prolyl hydroxylase inhibitors ...... lowing femur fracture in mice.
@en
P2093
Alan Eberhart
Craig L Duvall
Girish Ramaswamy
Lian Fu Deng
Mahendra Mavalli
Robert E Guldberg
Shawn R Gilbert
Thomas L Clemens
P2860
P304
P356
10.1002/JOR.20886
P577
2009-10-01T00:00:00Z