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Research 511–540 of 1000+
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- Smart Biomaterials and Dressings for the Treatment of Chronic Inflammatory Skin Diseases
- Familial frontal fibrosing alopecia: A cross‐sectional study of 20 cases from nine families
- Impacts of Anabolic-androgenic steroid supplementation on female health and offspring: Mechanisms, side effects, and medical perspectives
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- The quantification of reproductive hormones in the hair of captive adult brown bears and their application as indicators of sex and reproductive state
- Applications of Engineered Skin Tissue for Cosmetic Component and Toxicology Detection
- Melatonin supplement induced the hair follicle development in offspring rex rabbits
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Australasian Society for Dermatology Research Meeting, May 2006
- Androgenetic alopecia: pathogenesis and potential for therapy
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Biotinidase deficiency characterized by skin and hair findings
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Dermatomyositis Disease in Dogs
- Congenital adrenal hyperplasia
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels