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Research 841–870 of 1000+
- Physical attractiveness, same-sex stimuli, and male venture capitalists’ financial risk-taking
- Scalp Microbiome Composition in Young Women: Associations with Scalp Type, Sensitivity, and Lifestyle Factors
- Alopecia areata: a review of diagnosis, pathogenesis and the therapeutic landscape
- THE INFLUENCE OF SKIN MICROBIOME IMBALANCE ON SPECIFIC PATHOLOGICAL SKIN CONDITIONS
- Potential of Natural Products in Hangeshashinto Water Extract on the Direct Suppression of Stomatitis Induced by Intra-/Extracellular Advanced Glycation End-Products
- Main Plenary Sessions: Summaries of Papers
- Regulation of Involucrin Gene Expression
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- The Human Papillomavirus Type 11 Upstream Regulatory Region Triggers Hair-Follicle-Specific Gene Expression in Transgenic Mice
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Morphological Approach to Hair Disorders
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- In That Issue: Proceedings From the Third Intercontinental Meeting of Hair Research Societies
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- British Society for Dermatopathology: Summaries of Papers
- Ingestion of topical steroid triggering pustular psoriasis?
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Close Shave for a Keratin Disorder—K6hf Polymorphism Linked to Pseudofolliculitis Barbae
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Cutaneous manifestations associated with substance use disorders
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Viewpoint 6
- 368 The Unanticipated Costs, Deficits, and Other Unexpected Burdens in a Diagnosis of Alopecia Areata
- SEXUAL DIMORPHISM IN MAMMALS
- Androgenetic alopecia in men: the scale of the problem and prospects for treatment.
- Androgens in postmenopausal women