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Research 661–690 of 808
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- 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
- 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
- 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
- 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
- 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
- Medical aesthetics – Current trends and a review of its applications
- 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
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions