Signatures of Dermal Fibroblasts from RDEB Pediatric Patients

The recessive form of dystrophic epidermolysis bullosa (RDEB) is a debilitating disease caused by impairments in the junctions of the dermis and the basement membrane of the epidermis. Mutations in the COL7A1 gene induce multiple abnormalities, including chronic inflammation and profibrotic changes...

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Pubblicato in:Int J Mol Sci
Autori principali: Beilin, Arkadii K., Evtushenko, Nadezhda A., Lukyanov, Daniil K., Murashkin, Nikolay N., Ambarchian, Eduard T., Pushkov, Alexander A., Savostyanov, Kirill V., Fisenko, Andrey P., Rogovaya, Olga S., Vasiliev, Andrey V., Vorotelyak, Ekaterina A., Gurskaya, Nadya G.
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2021
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7918539/
https://ncbi.nlm.nih.gov/pubmed/33670258
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22041792
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