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Research 301–330 of 1000+
- 3D bioprinting of calcium molybdate nanoparticles-containing immunomodulatory bioinks for hair regrowth
- The Diameter Factor of Aligned Membranes Facilitates Cutaneous Wound Healing by Promoting Epithelialization in an Immune Way
- DEVELOPMENT OF A DESMOCOLLIN-3 ACTIVE MOUSE MODEL RECAPITULATING HUMAN ATYPICAL PEMPHIGUS
- From the Microscopic Sweat Gland to Large Datasets: The Power of Quantitative Traits in Dermatology
- 1322 A non-cell autonomous dermal hedgehog signaling mechanism for follicular neoplasia and induction
- Dysregulation of Grainyhead-like 3 expression causes widespread developmental defects
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- Hypotrichosis in a child with olmsted syndrome
- Stem Cells and Peripheral Nerve
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Editors' Picks
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Multifunctional DNA Hydrogels with Hydrocolloid‐Cotton Structure for Regeneration of Diabetic Infectious Wounds
- Clonal Growth of Dermal Papilla Cells in Hydrogels Reveals Intrinsic Differences between Sox2-Positive and -Negative Cells In Vitro and In Vivo
- A Keratinocyte-specific Epoxygenase, CYP2B12, Metabolizes Arachidonic Acid with Unusual Selectivity, Producing a Single Major Epoxyeicosatrienoic Acid
- Effect of Hyaluronic Acid and Poly-L-Lactic Acid Dermal Fillers on Collagen Synthesis: An in vitro and in vivo Study
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Insertional mutation of the hairless locus on mouse Chromosome 14
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- Runx Family Genes in Tissue Stem Cell Dynamics
- Regulation and Role of GLI1 in Cutaneous Squamous Cell Carcinoma Pathogenesis
- Scarless wound healing – a literature review
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- 090 Reactive lipids from the secretome of senescent fibroblasts modify the extracellular matrix with functional consequences for resident cells
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- 361 p120-catenin regulates epidermal inflammation in a cadherin-dependent manner