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Research 661–690 of 784
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- The Mixed Lineage Kinase Leucine-Zipper Protein Kinase Exhibits a Differentiation-Associated Localization in Normal Human Skin and Induces Keratinocyte Differentiation upon Overexpression
- Immunopathology and Immunotherapy of Inflammatory Skin Diseases
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Targeted Delivery of Zinc Pyrithione to Skin Epithelia
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Cell death in skin function, inflammation, and disease
- 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
- 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
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Systematic characterization of the barrier function of diverse ex vivo models of damaged human skin
- Transglutaminase Activity Is Conserved in Stratified Epithelia and Skin Appendages of Mammals and Birds
- Microscopic polyangiitis secondary to Mycobacterium abscessus in a patient with bronchiectasis: a case report
- Metabolism and skin diseases
- Putting the Human Hair Follicle Cycle on the Map
- Frontal fibrosing alopecia: a review of eleven patients
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages