research Identification of a novelPNPLA1mutation in a Spanish family with autosomal recessive congenital ichthyosis
This study identified a new PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis.
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research Study of gene expression alteration in male androgenetic alopecia: evidence of predominant molecular signalling pathways
This study identified overexpression of certain immune-related genes and underexpression of genes in specific signaling pathways in premature androgenetic alopecia, suggesting potential new therapeutic targets.
research The oestrogen receptor 2 (ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
This study reports an association between the ESR2 gene variant rs10137185 and female-pattern hair loss in German patients.
research Autosomal recessive congenital ichthyosis due to PNPLA1 mutation in a golden retriever–poodle cross‐bred dog and the effect of topical therapy
This case report describes how a long-term combination of oral fatty acids and topical therapy appeared beneficial for managing autosomal recessive congenital ichthyosis in a goldendoodle with a PNPLA1 mutation.
research Targeting the pre-receptor metabolism of cortisol as a novel therapy in obesity and diabetes
This study discusses the potential of targeting 11β-HSD1 for treating metabolic syndrome and highlights emerging promising data from human trials on selective 11β-HSD1 inhibitors.
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