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Research 211–240 of 1000+
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerative Healing
- Innovations in skin microphysiological systems for nonclinical testing and FDA modernization
- RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Dynamics and Epigenetics of the Epidermal Differentiation Complex
- Comparison of three different lactic acid bacteria-fermented proteins on RAW 264.7 osteoclast and MC3T3-E1 osteoblast differentiation
- Hair & Cutaneous Development
- Subject Index
- 513 Demonstration of hair health benefits using an oral supplement
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Vitamin D and skin diseases: A review
- Variation in the ovine trichohyalin gene and its association with wool curvature
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Dextran hydrogel scaffolds enhance angiogenic responses and promote complete skin regeneration during burn wound healing
- Autoantigen Discovery in the Hair Loss Disorder, Alopecia Areata: Implication of Post-Translational Modifications
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Retinoic Acid-Induced Epidermal Transdifferentiation in Skin
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- Ichthyosis
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- TRP Channels in Skin Biology and Pathophysiology
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- The biology and genetics of curly hair
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex