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Research 271–300 of 1000+
- Flightless I Expression Enhances Murine Claw Regeneration Following Digit Amputation
- Single-cell analysis reveals fibroblast heterogeneity and myeloid-derived adipocyte progenitors in murine skin wounds
- The role of PPAR<i>γ</i>-mediated signalling in skin biology and pathology: new targets and opportunities for clinical dermatology
- LB881 Unraveling mechanisms of scarring alopecia in discoid lupus: Insights from spatial transcriptomics
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Loss of TET2 Tips the Scales Toward Tumorigenesis
- In vivo monitoring of hair cycle stages via bioluminescence imaging of hair follicle NG2 cells
- The remarkable legacy of the K6/ODC mouse: mechanisms of polyamine-promoted tumorigenesis revealed
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Transcriptional and epigenetic mechanisms governing epidermal stem cell regulation
- Scratching the surface of skin development
- Integrin signalling regulates YAP/TAZ to control skin homeostasis
- Diverse cellular players orchestrate regeneration after wounding
- Single-Cell Proteomics Uncovers Dual Traits of Dermal Sheath Cells in Wound Repair
- Progenitor-derived endothelin controls dermal sheath contraction for hair follicle regression
- The cell-surface marker MTS24 identifies a novel population of follicular keratinocytes with characteristics of progenitor cells
- Relation of Skin Polyamines to the Hairless Phenotype in Transgenic Mice Overexpressing Spermidine/Spermine N1-Acetyltransferase
- The nude gene and the skin
- Melanocortin receptor type 2 (MC2R, ACTH receptor) expression in patients with alopecia areata
- S100A6 Protein—Expression and Function in Norm and Pathology
- Double mutation of <i>claudin‐1</i> and <i>claudin‐3</i> causes alopecia in infant mice
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Regeneration of a bioengineered 3D integumentary organ system from iPS cells
- IMMUNE-DRIVEN ACTIVATION OF HAIR FOLLICLE STEM CELLS AS A TRANSLATIONAL MODEL FOR FUTURE CELL-BASED THERAPY DEVELOPMENT
- There and Back Again: Hair Follicle Stem Cell Dynamics
- Four murine monoclonal antibodies specific for the inner root sheath in the human hair follicle