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Research 151–180 of 1000+
- Regrowth of Alopecia Areata Simulating the Pattern of Androgenetic Alopecia
- Pyodermatitis vegetans associated with multiple myeloma
- Clinical and trichoscopic features of scalp discoid lupus erythematosus in skin of colour: A retrospective analysis
- Non-scarring Alopecia in Pemphigus Foliaceus
- Non-Neoplastic Disorders of Hair
- Elastic tissue in scars and alopecia
- Profiling the Response of Human Hair Follicles to Ultraviolet Radiation
- Responses of hair follicle–associated structures to loss of planar cell polarity signaling
- Acne and Hidden Iodides
- The Editor's Choice
- Clinical manifestations of cutaneous lupus erythematosus
- Alopecia areata update
- Dermatoses of pregnancy
- Cicatricial alopecia
- A study on dermatoses of pregnancy
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Clinical features of 109 patients with primary cicatricial alopecia: a 15-year retrospective study
- SUMMARIES OF PAPERS
- Dedifferentiation of committed epithelial cells into stem cells in vivo
- Control of hair growth and follicle size by VEGF-mediated angiogenesis
- Leucine-Rich Repeat-Containing G-Protein-Coupled Receptors as Markers of Adult Stem Cells
- Mechanical stretch induces hair regeneration through the alternative activation of macrophages
- Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes
- Probing the Effects of Stress Mediators on the Human Hair Follicle
- Wnt and Notch signaling pathway involved in wound healing by targeting c-Myc and Hes1 separately
- Differentiation of Mouse Induced Pluripotent Stem Cells into a Multipotent Keratinocyte Lineage
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice