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Research 931–960 of 1000+
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Efficacy and Safety of Platelet-Rich Plasma Therapy in Alopecia Areata Patients: A Systematic Review
- Clinical manifestations of alopecia in autoimmune blistering diseases: A cross-sectional study
- Estrogens
- Ectopic olfactory receptors in human: New therapeutic possibilities
- Subject Index
- Cells, growth factors and biomaterials used in tissue engineering for hair follicles regeneration
- Mesenchymal Stem Cell Secretome: Toward Cell-Free Therapeutic Strategies in Regenerative Medicine
- Mechanisms and applications of the anti-inflammatory effects of photobiomodulation
- Cepharanthine: An update of its mode of action, pharmacological properties and medical applications
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Oral Lichen Planus
- Exosomes based advancements for application in medical aesthetics
- Zinc and Zinc Transporters in Dermatology
- Insights from Tandem Mass Tag (TMT) Proteomic Analysis on Protein Network Modification in Control of Yak Hair Follicle Cycle
- Medical Dermatology
- The Multifaceted Functions of TRPV4 and Calcium Oscillations in Tissue Repair
- Organoids in skin wound healing
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Alopecia areata incognita: clinical characteristics and use of the Sinclair shedding scale
- The JAK/STAT signaling pathway: from bench to clinic
- Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
- Histopathology of alopecia: a clinicopathological approach to diagnosis
- Evidence-based (S3) guideline for the treatment of androgenetic alopecia in women and in men – short version
- Dermal adipose tissue has high plasticity and undergoes reversible dedifferentiation in mice
- K channel therapeutics at the bedside
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions