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Research 781–810 of 1000+
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Activation of Cilia-Independent Hedgehog/GLI1 Signaling as a Novel Concept for Neuroblastoma Therapy
- Causal Effects of Lipids-Related Metabolites on Androgenic Alopecia: A Mendelian Randomization Study
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- The role of WNT10B in physiology and disease: A 10-year update
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Advances in single-cell transcriptomics in animal research
- A “hair‐raising” history of alopecia areata
- Metabolic Syndrome, Hepatic Steatosis and Testosterone: A Matter of Sex
- The correlation between corona virus disease 2019 and alopecia areata: a literature review
- The post-finasteride syndrome: possible etiological mechanisms and symptoms
- Long-lived proteins and DNA as candidate predictive biomarkers for tissue associated diseases
- Cutaneous Sequelae After Burn Injury: Pruritus, Dyspigmentation and Malignancy—Mechanisms and Management
- An (Ir)reversible Affection of the Sexual Sphere: A Case Report
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Insights into disparities observed with COVID‐19
- Central centrifugal cicatricial alopecia: challenges and solutions
- The Association of Hispanic Ethnicity with Nonalcoholic Fatty Liver Disease in Polycystic Ovary Syndrome
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Successful in situ 5-aminolevulinic acid photodynamic therapy in a 53-year-old female with cutaneous squamous cell carcinoma
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- A Complex Clinical Situation in Polycystic Ovary Syndrome: HAIR‐AN Syndrome ‘‘Case Report’’
- Frontal fibrosing alopecia: a review of eleven patients
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Cell Therapy for Androgenetic Alopecia: Elixir or Trick?
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders