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Research 301–330 of 1000+
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Advances in the Molecular Pathogenesis and Targeted Therapy of Psoriasis
- The Role of the Vitamin D Receptor in the Epidermal Stem Cell Response to Wounding
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome
- SFRP2/DPP4 and FMO1/LSP1 Define Major Fibroblast Populations in Human Skin
- Bone morphogenetic protein signaling drives rete ridge morphogenesis: a distinct epidermal appendage program
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- The urine as a diagnostic key for a homozygous EGFR mutation
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Hair follicle-derived epithelial sheet has potential in vitiligo treatment
- JAK-centric explainable few-shot gene-expression diagnosis framework for alopecia via MultiPLIER priors and relation-style set-to-set comparison
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- LncRNAs regulate the cyclic growth and development of hair follicles in Dorper sheep
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Cell Types Promoting Goosebumps Form a Niche to Regulate Hair Follicle Stem Cells
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- Single cell analysis of transcriptome and open chromatin reveals the dynamics of hair follicle stem cell aging
- LB1053 Dysregulation of antioxidant enzyme PRDX5 in alopecia areata
- Transcriptomic landscape of early hair follicle and epidermal development
- Prediction of cell states and key transcription factors of the human cornea through integrated single-cell omics analyses
- Single-Cell RNA Profiling of Human Skin Reveals Age-Related Loss of Dermal Sheath Cells and Their Contribution to a Juvenile Phenotype
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- Drug Repurposing for Rare Diseases