Caricamento...
Genetic activation of Nrf2 reduces cutaneous symptoms in a murine model of Netherton syndrome
Netherton syndrome is a monogenic autosomal recessive disorder primarily characterized by the detachment of the uppermost layer of the epidermis, the stratum corneum. It results from mutations in the SPINK5 gene, which codes for a kallikrein inhibitor. Uncontrolled kallikrein activity leads to prema...
Salvato in:
| Pubblicato in: | Dis Model Mech |
|---|---|
| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The Company of Biologists Ltd
2020
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7286291/ https://ncbi.nlm.nih.gov/pubmed/32457102 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.042648 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|