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Research 721–750 of 1000+
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Polycystic Ovarian Syndrome in Adolescents
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Integrative insights into polycystic ovarian syndrome (PCOS): A comparative review of unani and modern medical perspective
- Recent advances in the genetics of alopecia areata
- Clinical Snippets
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- TREATMENT OF KERATOSIS PILARIS: A NARRATIVE LITERATURE REVIEW OF TOPICAL, PROCEDURAL, AND VARIANT-SPECIFIC THERAPIES
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Polycystic Ovary Syndrome: A Comprehensive Review of Its Clinical Presentation, Comorbidities, Long-Term Complications and Management
- The Link Between Obesity and the Skin
- Cutaneous Side Effects of Modern Targeted Therapy and Immunotherapy in Patients with Dermatological Malignancies
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Trichoscopy in genetic hair shaft abnormalities
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Update on Melasma—Part I: Pathogenesis
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Uveodermatological syndrome in dogs: A review of diagnosis, management, and ophthalmic patient needs
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- Advances in Microengineered Platforms for Skin Research
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- Erosive Pustular Dermatosis of the Scalp: A Clinicopathologic Study of Fifty Cases
- Prevalence of Cutaneous Disorders in Patients with Polycystic Ovary Syndrome
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development