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Research 871–900 of 1000+
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- The role of vitamin D receptor signaling in hair follicle health and alopecia: Current understanding and therapeutic implications
- Long‐term culture of skin biopsies: maintenance of fibroblast production and competency of reprogramming
- 440 Charting the Spatially Resolved Hair Follicle Stem Cell Niche: A Multi-Omics Atlas of Healthy and Diseased Scalp
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Multiomics Analysis of the Response to Ritlecitinib in Alopecia Areata Subtypes and Correlation With Efficacy
- The GPR30 agonist G-1 promotes hair growth via Wnt/Hedgehog signaling in mice
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Restoration of Hair Luster via Novel Biomarker COL7A1 by Minoxidil, Caffeine, and Biotin
- Silk fibroin hydrogel with recombinant silk fibroin/NT3 protein enhances wound healing by promoting Type III collagen synthesis and hair follicle regeneration in skin injury
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Restoration of hair follicle inductive properties by depletion of senescent cells
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Disturbance of Immune Microenvironment in Androgenetic Alopecia through Spatial Transcriptomics
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Integrated edge information and pathway topology for drug-disease associations
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Regulation of Hair Follicle Growth and Development by Different Alternative Spliceosomes of FGF5 in Rabbits
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat
- Quantitative Analysis of Hair Luster in a Novel Ultraviolet-Irradiated Mouse Model
- Spatiotemporal Expression Characterization of KRTAP6 Family Genes and Its Effect on Wool Traits
- HDAC6-dependent deacetylation of NGF dictates its ubiquitination and maintains primordial follicle dormancy
- Ehlers-Danlos syndrome: From bedside to bench
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- A missense mutation in Lama3 causes androgen alopecia
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome