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Netherton syndrome (NS) is a rare skin disease caused by loss-of-function mutations in the serine peptidase inhibitor Kazal type 5 (SPINK5) gene. Disease severity and the lack of efficacious treatments call for a better understanding of NS mechanisms. Here we describe a viable, Spink5 conditional kn...
ORGANISM(S): Mus Musculus (ncbitaxon:10090) 
2023-02-02 | MSV000091184 | MassIVE
Transcriptome profiling of lesional skin from Spink5 conditional knock-out mice
Transcriptome profiling of lymph nodes from Spink5 conditional knock-out mice.
Transcriptome profiling of lesional skin from neonate Spink5 constitutive knock-out mice
We generated a viable mouse model of Netherton syndrome by conditional ablation of Spink5 gene in the epidermis. To characterize this model at the molecular level, we induced Spink5 deletion in young adult mice and collected lesional skin samples for transcriptome analyses.
ORGANISM(S): Mus musculus 
2024-02-05 | GSE224280 | GEO
We generated a viable mouse model of Netherton syndrome by conditional ablation of Spink5 gene in the epidermis. To study the systemic inflammation phenotype of this mouse model at the molecular level, we induced Spink5 deletion in the skin of young adult mice and collected inguinal lymph nodes for ...
ORGANISM(S): Mus musculus 
2024-02-05 | GSE224409 | GEO
STAT3 maintains skin barrier integrity by modulating SPINK5 and KLK5 expression in keratinocytes
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