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Research 121–150 of 1000+
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Answer
- Poster Presentations
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Disease causing homozygous variants in the human hairless gene
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Endocrine disorders and hormonal therapy for adolescent acne
- Diffuse loss of hair with papules
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome
- Trichodystrophies: A hair-raising differential diagnosis
- Understanding Polycystic Ovary Syndrome
- Syndromes of Severe Insulin Resistance (SSIRs)
- Acne and acneiform eruptions
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- Endocrine-skin interactions
- Molecular Genetics of Human Hair Diseases
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene