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EGR1 Regulates Transcription Downstream of Mechanical Signals during Tendon Formation and Healing
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5098749
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27820865%20AND%20SRC:MED&resulttype=core&format=json
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26 March 2020
title
EGR1 Regulates Transcription Downstream of Mechanical Signals during Tendon Formation and Healing
(English)
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5098749
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26 March 2020
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Anthony Delalande
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3
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5098749
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26 March 2020
Marie-Ange Bonnin
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5098749
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26 March 2020
Delphine Duprez
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6
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26 March 2020
Chantal Pichon
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Chantal Pichon
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5098749
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26 March 2020
author name string
Ludovic Gaut
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1
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5098749
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26 March 2020
Nicolas Robert
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2
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5098749
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26 March 2020
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English
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publication date
7 November 2016
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5098749
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26 March 2020
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PLOS One
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5098749
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26 March 2020
volume
11
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5098749
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26 March 2020
issue
11
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5098749
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26 March 2020
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e0166237
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5098749
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27820865%20AND%20SRC:MED&resulttype=core&format=json
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26 March 2020
copyright license
Creative Commons Attribution 4.0 International
start time
7 November 2016
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cites work
The transcription factor scleraxis is a critical regulator of cardiac fibroblast phenotype
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Tendon mechanobiology: Current knowledge and future research opportunities
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Loss of tenomodulin results in reduced self-renewal and augmented senescence of tendon stem/progenitor cells
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Mohawk promotes the tenogenesis of mesenchymal stem cells through activation of the TGFβ signaling pathway
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Fibrin gels exhibit improved biological, structural, and mechanical properties compared with collagen gels in cell-based tendon tissue-engineered constructs
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Embryonic mechanical and soluble cues regulate tendon progenitor cell gene expression as a function of developmental stage and anatomical origin
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One load to rule them all: mechanical control of the musculoskeletal system in development and aging
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Transcription factor EGR1 directs tendon differentiation and promotes tendon repair
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Smad3 binds Scleraxis and Mohawk and regulates tendon matrix organization.
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Dynamic compression of chondrocyte-agarose constructs reveals new candidate mechanosensitive genes
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Tendon biomechanics and mechanobiology--a minireview of basic concepts and recent advancements
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Physiological loading of tendons induces scleraxis expression in epitenon fibroblasts
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In vivo investigation of tendon responses to mechanical loading.
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EGR1 and EGR2 involvement in vertebrate tendon differentiation.
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Induction of Sirt1 by mechanical stretch of skeletal muscle through the early response factor EGR1 triggers an antioxidative response
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Synthesis of embryonic tendon-like tissue by human marrow stromal/mesenchymal stem cells requires a three-dimensional environment and transforming growth factor β3.
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Rat Achilles tendon healing: mechanical loading and gene expression
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Regulation of tendon differentiation by scleraxis distinguishes force-transmitting tendons from muscle-anchoring tendons
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Scleraxis and NFATc regulate the expression of the pro-alpha1(I) collagen gene in tendon fibroblasts
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Scleraxis positively regulates the expression of tenomodulin, a differentiation marker of tenocytes
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Release of tensile strain on engineered human tendon tissue disturbs cell adhesions, changes matrix architecture, and induces an inflammatory phenotype
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EGR1 induces tenogenic differentiation of tendon stem cells and promotes rabbit rotator cuff repair.
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Mechano-sensitive transcriptional factor Egr-1 regulates insulin-like growth factor-1 receptor expression and contributes to neointima formation in vein grafts.
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23 September 2018
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23 September 2018
Generation of transgenic tendon reporters, ScxGFP and ScxAP, using regulatory elements of the scleraxis gene.
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23 September 2018
Analysis of the tendon cell fate using Scleraxis, a specific marker for tendons and ligaments.
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23 September 2018
Microtrauma stimulates rat Achilles tendon healing via an early gene expression pattern similar to mechanical loading
1 reference
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PubMed
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https://pubmed.ncbi.nlm.nih.gov/27820865
retrieved
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based on heuristic
inferred from PubMed ID database lookup
Tension is required for fibripositor formation
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27820865
retrieved
12 December 2020
based on heuristic
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A comparison of the safety margins of botulinum neurotoxin serotypes A, B, and F in mice.
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27820865
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Rapid induction and translocation of Egr-1 in response to mechanical strain in vascular smooth muscle cells
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27820865
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1371/JOURNAL.PONE.0166237
1 reference
stated in
Europe PubMed Central
PMC publication ID
5098749
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27820865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 March 2020
ADS bibcode
2016PLoSO..1166237G
0 references
PMC publication ID
5098749
1 reference
stated in
Europe PubMed Central
PMC publication ID
5098749
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27820865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 March 2020
PubMed publication ID
27820865
1 reference
stated in
Europe PubMed Central
PMC publication ID
5098749
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27820865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 March 2020
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