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Research 661–690 of 845
- The Dermatology Life Quality Index (DLQI) used as the benchmark in validation of 101 quality‐of‐life instruments: A systematic review
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Keratosis follicularis spinulosa decalvans in a female
- The Mixed Lineage Kinase Leucine-Zipper Protein Kinase Exhibits a Differentiation-Associated Localization in Normal Human Skin and Induces Keratinocyte Differentiation upon Overexpression
- Clinical photography for trichology practice: Tips and tricks
- Immunopathology and Immunotherapy of Inflammatory Skin Diseases
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Targeted Delivery of Zinc Pyrithione to Skin Epithelia
- A Systemic Review on Topical Marketed Formulations, Natural Products, and Oral Supplements to Prevent Androgenic Alopecia: A Review
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Hair shaft disorders in children – An update
- Cell death in skin function, inflammation, and disease
- Male fertility and skin diseases
- Self-consistent field theory for the interactions between keratin intermediate filaments
- A rare case of woolly hair with unusual associations
- Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte
- Skin manifestations associated with systemic diseases – Part I
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Skin, a mirror reflecting diabetes mellitus: A longitudinal study in a tertiary care hospital in Gujarat
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Ultrastructure of the contrasting types of keratinization seen in the tail epidermis of the laboratory mouseMus musculus
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Micronutrients in hair loss
- Advancements in Dermatological Imaging Modalities
- The PI3K-Akt-mTOR and Associated Signaling Pathways as Molecular Drivers of Immune-Mediated Inflammatory Skin Diseases: Update on Therapeutic Strategy Using Natural and Synthetic Compounds
- Solubility of Foreign Molecules in Stratum Corneum Brick and Mortar Structure