About: Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III

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About: Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 2009

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2009 (uk) im Oktober 2009 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 2009 (ast) scientific article published on 01 October 2009 (en)
publication date	wds:Q84596356-52726609-428A-4F1E-9A8C-8917CACCB82D
publication date	2009-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q84596356-3200F2F3-0224-4E9D-8151-D25DD727FA9C wds:Q84596356-5FBF74FF-88E2-47A6-A9E8-74E8AC863A18 wds:Q84596356-7EE143E1-DFB8-4E22-9A7D-35BABB3F8220 wds:Q84596356-E49F5899-3865-4B9C-8FC6-986B2D93B59E wds:Q84596356-E87C671D-02B0-4AA5-BDC1-A1215B89F537
author name string	Magali Demoor Elise Duval Philippe Galéra Sylvain Leclercq Jean-Marc Elissalde
rdfs:label	Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III (en) Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III (nl)
skos:prefLabel	Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III (en) Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III (nl)
name	Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III (en) Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III (nl)
author	wds:Q84596356-099BDB52-6E8A-4066-A723-1CAFCE4129A6
author	Karim Boumediene
title	wds:Q84596356-945B38AC-4DD7-4ED6-BC89-C0DFCC2190BC
title	Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III collagen in the hypoxia-inducible factor 1alpha-dependent redifferentiation of chondrocytes (en)
page(s)	wds:Q84596356-9A8B576F-99DE-4748-975B-E911985257AC
page(s)	3038-3048
instance of	wds:Q84596356-9486AD61-2A02-4998-9CCE-24C67528F8F3
instance of	scholarly article
PubMed ID	wds:Q84596356-272A5DC7-A030-4C17-A031-7242875AD070
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19790048
PubMed ID	19790048
published in	wds:Q84596356-C9054879-87FE-4040-853B-E0C83C5855B8
published in	Arthritis and Rheumatism
issue	wds:Q84596356-23EB6507-C094-4776-A552-DBC499532154
volume	wds:Q84596356-9DC8EB3E-98BC-4C39-A6C5-DAE7898B7F66
issue	10
volume	60
DOI	wds:Q84596356-2B2AD47F-EA45-4290-938E-593355C909E3
DOI	http://dx.doi.org/10.1002/ART.24851
DOI	10.1002/ART.24851
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q84596356
is cites work of	Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases. Signaling pathways in cartilage repair Hypoxia-inducible factor-1 (HIF-1) but not HIF-2 is essential for hypoxic induction of collagen prolyl 4-hydroxylases in primary newborn mouse epiphyseal growth plate chondrocytes. Shifting HIFs in osteoarthritis Association of reduced type IX collagen gene expression in human osteoarthritic chondrocytes with epigenetic silencing by DNA hypermethylation Homeostatic mechanisms in articular cartilage and role of inflammation in osteoarthritis Hypoxia-inducible factor-2alpha is a catabolic regulator of osteoarthritic cartilage destruction The role of oxygen during fracture healing Hypoxia Inducible Factor Pathway and Physiological Adaptation: A Cell Survival Pathway? Culture expansion in low-glucose conditions preserves chondrocyte differentiation and enhances their subsequent capacity to form cartilage tissue in three-dimensional culture. Passing the baton: the HIF switch Regulation of H19 and its encoded microRNA-675 in osteoarthritis and under anabolic and catabolic in vitro conditions New findings in osteoarthritis pathogenesis: therapeutic implications. Anabolic and catabolic responses of human articular chondrocytes to varying oxygen percentages Developing functional musculoskeletal tissues through hypoxia and lysyl oxidase-induced collagen cross-linking Multifaceted signaling regulators of chondrogenesis: Implications in cartilage regeneration and tissue engineering Asporin expression is highly regulated in human chondrocytes. Responses to altered oxygen tension are distinct between human stem cells of high and low chondrogenic capacity BMP-2, hypoxia, and COL1A1/HtrA1 siRNAs favor neo-cartilage hyaline matrix formation in chondrocytes RNA Interference and BMP-2 Stimulation Allows Equine Chondrocytes Redifferentiation in 3D-Hypoxia Cell Culture Model: Application for Matrix-Induced Autologous Chondrocyte Implantation Characterization and use of Equine Bone Marrow Mesenchymal Stem Cells in Equine Cartilage Engineering. Study of their Hyaline Cartilage Forming Potential when Cultured under Hypoxia within a Biomaterial in the Presence of BMP-2 and TGF-ß1. Hypoxia promotes redifferentiation and suppresses markers of hypertrophy and degeneration in both healthy and osteoarthritic chondrocytes. Platelet-Rich Plasma Supports Proliferation and Redifferentiation of Chondrocytes during In Vitro Expansion. βig-h3 potentiates the profibrogenic effect of TGFβ signaling on connective tissue progenitor cells through the negative regulation of master chondrogenic genes Matrix forming characteristics of inner and outer human meniscus cells on 3D collagen scaffolds under normal and low oxygen tensions Calcium/Cobalt Alginate Beads as Functional Scaffolds for Cartilage Tissue Engineering Osteoarthritis pathogenesis: a review of molecular mechanisms Effects of the pro-inflammatory milieu on the dedifferentiation of cultured fibroblast-like synoviocytes Hypoxia-Inducible Factor 1 Is an Inductor of Transcription Factor Activating Protein 2 Epsilon Expression during Chondrogenic Differentiation Differential Regulation of Human Bone Marrow Mesenchymal Stromal Cell Chondrogenesis by Hypoxia Inducible Factor-1α Hydroxylase Inhibitors Engineering superficial zone features in tissue engineered cartilage. lncRNA MALAT1 Accelerates Wound Healing of Diabetic Mice Transfused with Modified Autologous Blood via the HIF-1α Signaling Pathway Suppressing mesenchymal stem cell hypertrophy and endochondral ossification in 3D cartilage regeneration with nanofibrous poly(l-lactic acid) scaffold and matrilin-3 Hypoxia promotes maintenance of the chondrogenic phenotype in rat growth plate chondrocytes through the HIF-1α/YAP signaling pathway Hypoxia regulates RhoA and Wnt/β-catenin signaling in a context-dependent way to control re-differentiation of chondrocytes. Chondrogenic Differentiation of Defined Equine Mesenchymal Stem Cells Derived from Umbilical Cord Blood for Use in Cartilage Repair Therapy. Cartilage tissue engineering using dermis isolated adult stem cells: the use of hypoxia during expansion versus chondrogenic differentiation Physiological oxygen tension modulates soluble growth factor profile after crosstalk between chondrocytes and osteoblasts. Hyperosmolar Potassium (K(+)) Treatment Suppresses Osteoarthritic Chondrocyte Catabolic and Inflammatory Protein Production in a 3-Dimensional In Vitro Model. Bioreactor-Controlled Physoxia Regulates TGF-β Signaling to Alter Extracellular Matrix Synthesis by Human Chondrocytes Human Articular Chondrocytes Retain Their Phenotype in Sustained Hypoxia While Normoxia Promotes Their Immunomodulatory Potential. Role of Norepinephrine in IL-1β-Induced Chondrocyte Dedifferentiation under Physioxia Copper-incorporated bioactive glass-ceramics inducing anti-inflammatory phenotype and regeneration of cartilage/bone interface Synoviocyte Derived-Extracellular Matrix Enhances Human Articular Chondrocyte Proliferation and Maintains Re-Differentiation Capacity at Both Low and Atmospheric Oxygen Tensions Disparate response of articular- and auricular-derived chondrocytes to oxygen tension. Cellular reprogramming for clinical cartilage repair. Role of growth factors and oxygen to limit hypertrophy and impact of high magnetic nanoparticles dose during stem cell chondrogenesis Identification of an easy to use 3D culture model to investigate invasion and anticancer drug response in chondrosarcomas Proteasomal function is impaired in human osteoarthritic chondrocytes and this can contribute to decreased SOX9 and aggrecan. Molecular Insights Into Lysyl Oxidases in Cartilage Regeneration and Rejuvenation Effects of different concentrations of type-I collagen hydrogel on the growth and differentiation of chondrocytes
is cites work of	wds:Q33755839-2C31AC07-AB68-4C48-81BF-0A58FBA8EE91 wds:Q36514312-6B32C9FE-9F5C-4386-848A-CD04E6FF283B wds:Q38610396-553FACBC-89FC-4223-BBA5-E4F946B853D5 wds:Q47169053-92710A19-4DAC-466F-81E8-4B6F377EA74D

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