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- 865 Single-cell protein activity inference analysis of full-thickness skin uncovers novel pathways and a rare Arg1+ macrophage population in AA
- 229 Single cell transcriptomics identifies a potential role for Arg1+ macrophages in alopecia areata pathogenesis
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p. Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother
- 757 Wound healing in aged skin exhibits systems-level alterations in cellular composition and cell-cell communication
- The Role of Methylacrylylated Hyaluronic Acid Hydrogels in Promoting Skin Wound Healing
- Impaired Arginine Metabolism in Hair Follicles: A Potential Mechanism in Androgenetic Alopecia
- Comprehensive single-cell transcriptomic profiling of the scalp from patients with moderate-to-severe alopecia areata
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
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