Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts
Author:
Funder
Ehlers-Danlos Society
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference85 articles.
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3. Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): clinical description and natural history;Tinkle;Am. J. Med. Genet. C Semin. Med. Genet.,2017
4. Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type;Chiarelli;PLoS One,2016
5. Dermal fibroblast-to-myofibroblast transition sustained by αvß3 integrin-ILK-Snail1/Slug signaling is a common feature for hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders;Zoppi;Biochim. Biophys. Acta Mol. basis Dis.,2018
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