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- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- 487 Exploring ribosomal RNA modifications and corresponding snoRNAs in human skin cell senescence
- Lateral plate mesoderm directs human amnion and ventral skin organoid formation
- 1338 Dermal Wnt/β-catenin activation tunably controls hair follicle initiation
- 1458 EMT-inhibiting transcription factor Ovol2 regulates directional cell migration and proliferation in adult skin epithelia
- Deep facial mycosis due to <i>Trichophyton verrucosum</i>—molecular genetic identification of the dermatophyte in paraffin‐embedded tissue—case report and review of the literature
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Absence of vitamin D receptor (VDR)‐mediated PPARγ suppression causes alopecia in VDR‐null mice
- Bone morphogenetic protein signaling drives rete ridge morphogenesis: a distinct epidermal appendage program
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