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Research 241–270 of 414
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Medical Dermatology
- Histological and molecular restoration of type VII collagen in Recessive dystrophic epidermolysis bullosa mouse skin by topical injection of keratinocyte-like cells differentiated from human adipose-derived mesenchymal stromal cells
- Rare Cutaneous Side Effects of Imiquimod: A Review on Its Mechanisms, Diagnosis, and Management
- Clinical manifestations of alopecia in autoimmune blistering diseases: A cross-sectional study
- Wnt signaling modulates mechanotransduction in the epidermis to drive hair follicle regeneration
- Telogen effluvium: a comprehensive review
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Genetic Hair Disorders: A Review
- New developments in the molecular treatment of ichthyosis: review of the literature
- Skin Barrier Dysfunction in Acne Vulgaris: Pathogenesis and Therapeutic Approaches
- Immunopathology and Immunotherapy of Inflammatory Skin Diseases
- Vitamin D and calcium signaling in epidermal stem cells and their regeneration
- Hair shaft disorders in children – An update
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Selection signatures for fiber production in commercial species: A review
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- SPRY1 Deficiency in Keratinocytes Induces Follicular Melanocyte Stem Cell Migration to the Epidermis through p53/Stem Cell Factor/C-KIT Signaling
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Bioinformatics analysis of genes associated with the patchy-type alopecia areata: CD2 may be a new therapeutic target
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Keratinocytes of the Upper Epidermis and Isthmus of Hair Follicles Express Hemoglobin mRNA and Protein
- Integrated Meta-Analysis of Scalp Transcriptomics and Serum Proteomics Defines Alopecia Areata Subtypes and Core Disease Pathways
- DataSheet1_Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature.zip
- Review of Promising Off-Label Use of Deucravacitinib