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Research 121–150 of 1000+
- 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
- Skin penetration of active folate salts and their effects on wound healing in vitro: new approaches for dermal folate application
- Novel amino acid‐based surfactant for silicone emulsification and its application in hair care products: a promising alternative to quaternary ammonium cationic surfactants
- 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
- Immunomodulatory properties of mesenchymal stromal/stem cells: The link with metabolism
- 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
- Understanding human aging and the fundamental cell signaling link in age-related diseases: the middle-aging hypovascularity hypoxia hypothesis
- Characteristics and Differences in the Antler Velvet Microbiota During Regeneration
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Design of a RADA16-based self-assembling peptide nanofiber scaffold for biomedical applications
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- The role of vasoactive peptides in skin homeostasis—focus on adiponectin and the kallikrein-kinin system
- Wear characteristics of epoxy based hybrid composites reinforced with short hair fibers and glass micro spheres
- Central Centrifugal Cicatricial Alopecia
- Purified Vitexin Compound 1 Inhibits UVA-Induced Cellular Senescence in Human Dermal Fibroblasts by Binding Mitogen-Activated Protein Kinase 1
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Androgen Receptor Ligands: Agonists and Antagonists
- Central centrifugal cicatricial alopecia