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Research 211–240 of 1000+
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Emerging Topical and Systemic JAK Inhibitors in Dermatology
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- Novel lysophosphoplipid receptors: their structure and function
- WNT Signaling in Disease
- Autoimmunity: Alopecia Areata
- TRP Channels in Skin Biology and Pathophysiology
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- The molecular basis of human keratin disorders
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Regulation of stem cell function by protein ubiquitylation
- Role of janus kinase inhibitors in the treatment of alopecia areata
- Human Hair and the Impact of Cosmetic Procedures: A Review on Cleansing and Shape-Modulating Cosmetics
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Coronavirus 2019 Infectious Disease Epidemic: Where We Are, What Can Be Done and Hope For
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- The influence of interferon on healthy and diseased skin
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Follicular and Scarring Disorders in Skin of Color: Presentation and Management
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System