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Research 211–240 of 1000+
- 870 Y27632 promotes proliferation via EGFR signaling in a newly isolated and characterized human primary sebocyte cell line
- Guidelines based management of androgenetic alopecia
- Oral Presentations
- Subject Index
- TONGUE, RED
- Overview of the Role of 308 Monochromatic Excimer Phototherapy for the Treatment of Alopecia Areata
- Madarosis: A marker of many Maladies
- Organ-Level Quorum Sensing Directs Regeneration in Hair Stem Cell Populations
- Frizzled Receptors in Development and Disease
- Alopecias in lupus erythematosus
- Chronic graft versus host disease and skin
- Tissue Resident Foxp3+ Regulatory T Cells: Sentinels and Saboteurs in Health and Disease
- The Basic Science of Radiofrequency-Based Devices
- Usefulness of Dermoscopy to Provide Accurate Assessment of Skin Cancers
- Maternal Faecalibacterium pathobionts and low-fiber diets synergize to impact offspring health: implications for atopic dermatitis
- The expanding impact of T-regs in the skin
- Off‐Label Use of Topical Ruxolitinib in Dermatology: A Systematic Literature Review and Current Perspectives
- Human Regulatory T Cells: Understanding the Role of Tregs in Select Autoimmune Skin Diseases and Post-Transplant Nonmelanoma Skin Cancers
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Overview of popular cosmeceuticals in dermatology
- Medical Dermatology
- Social Perception of Male Faces. Individuals, Clusters, Dimensions
- Pentacyclic Triterpenoid Maslinic Acid Promotes Hair Growth Comparable to Minoxidil: A New Insight on the Potential Involvement of Cilia Activity
- Localized in vivo genotypic and phenotypic correction of the albino mutation in skin by RNA-DNA oligonucleotide
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Treatment of localized scleroderma and lichen sclerosus with etretinate
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Localized syringolymphoid hyperplasia with alopecia and anhidrosis
- Reversible Alopecia with Localized Scalp Necrosis After Accidental Embolization of the Parietal Artery with Hyaluronic Acid