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Research 481–510 of 868
- Predominance of CD27-PD-1- Effector Memory T Cells Re-Expressing CD45RA Characterizes Treatment-Resistant Severe Alopecia Areata
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Preventable effect of L-threonate, an ascorbate metabolite, on androgen-driven balding via repression of dihydrotestosteroneinduced dickkopf-1 expression in human hair dermal papilla cells
- Lichen Planopilaris: The first biopsy layer microbiota inspection
- Alignment control and softness creation in hair with glycylglycine.
- Identification of Epigenetic Regulator‐Associated Genes in Keloid Disease Through Integrated Bulk and Single‐Cell Transcriptomics With RT ‐ qPCR Validation
- Efficacy of Rituximab in Successful Management of Refractory Juvenile Systemic Lupus Erythematosus Complicated with Macrophage Activation Syndrome: A Case Report with Literature Overview
- 87: Examining Representations of Alopecia and Trichotillomania in Children’s Literature
- The efficacy of light-guiding microneedle patch for stimulating hair growth in androgenetic alopecia
- Development and Evaluation of a Novel Fish-Derived Protein Peptide Conditioner Formulated with Pneumatophorus japonicus Heads Peptides
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Granzyme B in skin aging, injury and repair
- Factors associated with female pattern hair loss and its prevalence in Taiwanese women: A community-based survey
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Multi-Stage Transcriptome Analysis Revealed the Growth Mechanism of Feathers and Hair Follicles during Induction Molting by Fasting in the Late Stage of Egg Laying
- Efficacy and safety of dutasteride in the treatment of alopecia: a comprehensive review
- Hair cosmetics: An overview
- Keratin gene mutations in disorders of human skin and its appendages
- The neurosteroidogenic enzyme 5α-reductase modulates the role of D1 dopamine receptors in rat sensorimotor gating
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Ceramic flat irons: Improper use leading to acquired trichorrhexis nodosa
- Degradation of Hair Surface: Importance of 18-MEA and Epicuticle
- Hair and nail diseases in the mature patient
- Potential use of human hair shaft keratin peptide signatures to distinguish gender and ethnicity
- Ultramicroscopic study on the hair of newly found 15th century mummy in Daejeon, Korea
- Toll-like receptor 4 (TLR4): new insight immune and aging
- Disorders of hair in infants and children other than alopecia
- Monilethrix: A rare hereditary condition
- Unique Hair Properties that Emerge from Combinations of Multiple Races
- Nail abnormalities in patients with vitiligo