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Research 901–930 of 1000+
- Fibroblast state switching orchestrates dermal maturation and wound healing
- Scars or Regeneration?—Dermal Fibroblasts as Drivers of Diverse Skin Wound Responses
- MicroRNA-302 Increases Reprogramming Efficiency via Repression of NR2F2
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- The Pathobiology of Skin Aging
- Proteome Analysis of Human Hair Shaft
- Resting no more: re‐defining telogen, the maintenance stage of the hair growth cycle
- Nitrate‐inducible NIGT1 proteins modulate phosphate uptake and starvation signalling via transcriptional regulation of <i>SPX</i> genes
- Dermal fibroblast in cutaneous development and healing
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- The Skin Microbiome: Current Landscape and Future Opportunities
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- The Auxin-Regulated CrRLK1L Kinase ERULUS Controls Cell Wall Composition during Root Hair Tip Growth
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- A slow-cycling LGR5 tumour population mediates basal cell carcinoma relapse after therapy
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- Recent advances in understanding and managing male infertility
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Cell fate decisions: emerging roles for metabolic signals and cell morphology
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Activated Polyamine Catabolism Depletes Acetyl-CoA Pools and Suppresses Prostate Tumor Growth in TRAMP Mice
- Switching roles: the functional plasticity of adult tissue stem cells
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease