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Research 241–270 of 1000+
- 865 Single-cell protein activity inference analysis of full-thickness skin uncovers novel pathways and a rare Arg1+ macrophage population in AA
- 229 Single cell transcriptomics identifies a potential role for Arg1+ macrophages in alopecia areata pathogenesis
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- HAIR LOSS AND REGENERATION PERFORMED ON ANIMAL MODELS
- The Fate of Trichohyalin
- Ion pairs of risedronate for transdermal delivery and enhanced permeation rate on hairless mouse skin
- Central Centrifugal Cicatricial Alopecia Associated With PDL1 Loss and Increased Expression of Caspase 3: A Case Series
- Effects of Wet Cupping on Blood Components Specially Skin-Related Parameters of Healthy Cases: A Case Control Metabonomic Study
- Nutritional Pharmacology and Mechanistic Insights of Saw Palmetto in Male Endocrine and Prostatic Disorders
- Nutritional Pharmacology and Mechanistic Insights of Saw Palmetto in Male Endocrine and Prostatic Disorders
- Nitric Oxide Donor and Minoxidil Co‐Loaded Microneedles Improving Hair Loss Treatment
- An ex vivo comparative study of the tensile strengthening efficacy of protein-derived actives on heavily bleached hair
- Citrullinome of Porphyromonas gingivalis Outer Membrane Vesicles: Confident Identification of Citrullinated Peptides
- Novel amino acid‐based surfactant for silicone emulsification and its application in hair care products: a promising alternative to quaternary ammonium cationic surfactants
- Unraveling Evolutionary Insights into AVT Peptide Conservation and Antimicrobial Motif Prediction Across Taxa
- A Hairy Cituation – PADIs in Regeneration and Alopecia
- Deimination in epidermal barrier and hair formation
- 5 alpha-reductase-2 gene mutations in the Dominican Republic.
- Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D
- Trichorrhexis Nodosa Secondary to Argininosuccinicaciduria
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- An in-depth study of DOPE:DOPC liposomes to maximize targeted drug delivery to cancer-associated cells
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- A functional study of a case of glucagonoma exhibiting typical glucagonoma syndrome
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- SAT-080 An Atypical Adenoma Presenting with Hyperandrogenism: A Rare Case Presentation on a Pituitary Germ Cell Tumor
- Characteristics and Differences in the Antler Velvet Microbiota During Regeneration
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor