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Research 781–810 of 797
- Epidermal–dermal coupled spheroids are important for tissue pattern regeneration in reconstituted skin explant cultures
- Keratinocytes of the Upper Epidermis and Isthmus of Hair Follicles Express Hemoglobin mRNA and Protein
- Status of research on the development and regeneration of hair follicles
- Prospective Observational Study of a Non-Arthroscopic Autologous Cartilage Micrografting Technology for Knee Osteoarthritis
- Identification of immune microenvironment changes, immune-related pathways and genes in male androgenetic alopecia
- Alk1 acts in non-endothelial VE-cadherin+ perineurial cells to maintain nerve branching during hair homeostasis
- Novel Insights to Assess Climate Resilience in Goats Using a Holistic Approach of Skin-Based Advanced NGS Technologies
- Cell Therapy for Androgenetic Alopecia: Elixir or Trick?
- Repurposing DPP4-Inhibition to Improve Hair Follicle Activation and Regeneration
- Revolutionizing Radiotoxicity Management with Mesenchymal Stem Cells and Their Derivatives: A Focus on Radiation-Induced Cystitis
- Mechanical force drives the initial mesenchymal-epithelial interaction during skin organoid development
- The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism
- Adipogenic Differentiation of Canine Hair Follicle Stem Cells (cHFSCs)
- Current issues of skin aging and strategies for its correction
- Hair Follicle Stem Cells and Hair Regeneration
- Cells, growth factors and biomaterials used in tissue engineering for hair follicles regeneration
- Investigation of hub genes and immune infiltration in androgenetic alopecia using bioinformatics analysis
- Three Novel Homozygous Point Mutations and a New Polymorphism in the COL17A1 Gene: Relation to Biological and Clinical Phenotypes of Junctional Epidermolysis Bullosa
- 302 Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Mutational Analysis in Dystrophic Epidermolysis Bullosa
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- 304 Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
- The Genetics of Human Skin Disease
- 519 Phase I/IIa clinical trial for recessive dystrophic epidermolysis bullosa using genetically corrected autologous keratinocytes
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Comparative ubiquitinomics of human skin reveals insulin receptor ubiquitination as a regulator of collagen secretion
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- 572 Defining chronic wound types in recessive dystrophic epidermolysis bullosa patients for clinical outcome assessment