Search
for
Sort by
Research 241–270 of 1000+
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Trichilemmal cyst of the neck: case report and review of the literature
- Fundamental research on the action mechanism of the 800 nm semiconductor laser on skin blackheads and coarse pores
- Dissecting Cellulitis of the Scalp: Linking Pathogenesis to Therapy
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- A systematic review of neutrophilic alopecias of the scalp in the pediatric population
- Hypotrichosis in a child with olmsted syndrome
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Hyperpigmentation Associated with the Use of Topical Cidofovir for Treatment of Trichodysplasia Spinulosa in an Immunosuppressed Adult: Case Report and Review of the Literature
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- Ulerythema ophryogenes with multiple congenital anomalies
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Cell death in the skin
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Histologic Changes in the Skin of Hairless Mice Following Peeling With Salicylic Acid
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- A rare case of woolly hair with unusual associations
- Regulation of Epidermal Ferritin Expression Influences Systemic Iron Homeostasis
- Off-label uses of retinoids in dermatology
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Immunostaining study of cytokeratins in human hair follicle development