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Research 121–150 of 777
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- “Degeneration” in Dermatopathology
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Vitamin D and the Skin: A Review for Dermatologists
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Off-label uses of retinoids in dermatology
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Medical aesthetics – Current trends and a review of its applications
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Regulation of Epidermal Ferritin Expression Influences Systemic Iron Homeostasis
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Acne Syndromes and Mosaicism
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Immunostaining study of cytokeratins in human hair follicle development