Search
for
Sort by
Research 661–690 of 1000+
- RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Polycystic ovary syndrome
- Androgenetic alopecia: a review
- Dermal Adipocyte Lipolysis and Myofibroblast Conversion Are Required for Efficient Skin Repair
- Obesity and polycystic ovary syndrome
- Real-time iTRAQ-based proteome profiling revealed the central metabolism involved in nitrogen starvation induced lipid accumulation in microalgae
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Recently Identified Forms of Epidermolysis Bullosa
- The role of WNT10B in physiology and disease: A 10-year update
- Alopecia Areata
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Advances in single-cell transcriptomics in animal research
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- The Changing Landscape of Alopecia Areata: The Translational Landscape
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Retinoids for Chemoprophylaxis of Nonmelanoma Skin Cancer
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- The role of multiomics in revealing the mechanism of skin repair and regeneration
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Role of Csdc2 in Regulating Secondary Hair Follicle Growth in Cashmere Goats
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development