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Research 421–450 of 1000+
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Tracing the developmental origin of tissue stem cells
- Role of regeneration in tissue repairing and therapies
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- A Threefold Association Between Vitiligo and Alopecia Areata: Results from a Nationwide Case-control Observational Study
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Adult female acne: Clinical and therapeutic particularities (Review)
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Abstracts
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Regulation and dysregulation of hair regeneration: aiming for clinical application
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Causes and therapeutic limitations of clinical alopecia and the advent of human pluripotent stem cell follicular transplantation
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Unusual symptoms of iron deficiency anemia (2 clinical observations)
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- First Symposium of Ichthyosis Experts
- Alopecia areata
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep