Cargando…
Experimental Models for the Study of Hereditary Cornification Defects
Ichthyoses comprise a broad spectrum of keratinization disorders due to hereditary defects of cornification. Until now, mutations in more than 50 genes, mostly coding for structural proteins involved in epidermal barrier formation, have been identified as causes for different types of these keratini...
Autores principales: | Copic, Dragan, Laggner, Maria, Kalinina, Polina, Klas, Katharina, Tschachler, Erwin, Mildner, Michael |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996736/ https://www.ncbi.nlm.nih.gov/pubmed/33652877 http://dx.doi.org/10.3390/biomedicines9030238 |
Ejemplares similares
-
miR-155 Contributes to Normal Keratinocyte Differentiation and Is Upregulated in the Epidermis of Psoriatic Skin Lesions
por: Beer, Lucian, et al.
Publicado: (2020) -
Heme Oxygenase-1 Is Upregulated during Differentiation of Keratinocytes but Its Expression Is Dispensable for Cornification of Murine Epidermis
por: Surbek, Marta, et al.
Publicado: (2023) -
The transcriptional profile of keloidal Schwann cells
por: Direder, Martin, et al.
Publicado: (2022) -
Epidermal cornification is preceded by the expression of a keratinocyte-specific set of pyroptosis-related genes
por: Lachner, Julia, et al.
Publicado: (2017) -
Tissue-regenerative potential of the secretome of γ-irradiated peripheral blood mononuclear cells is mediated via TNFRSF1B-induced necroptosis
por: Simader, Elisabeth, et al.
Publicado: (2019)