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Research 631–660 of 1000+
- Approach to androgen excess in women: Clinical and biochemical insights
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Allopregnanolone is required for prepulse inhibition deficits induced by D1 dopamine receptor activation
- Lrig1-expression confers suppressive function to CD4+ cells and is essential for averting autoimmunity via the Smad2/3/Foxp3 axis
- Proopiomelanocortin (POMC) and Psychodermatology
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Past, Present and Future Perspectives of Forensic Genetics
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Frontiers in Topical Photoprotection
- Canadian Expert Recommendations on Safety Overview and Toxicity Management Strategies for Sacituzumab Govitecan Based on Use in Metastatic Triple-Negative Breast Cancer
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Immune therapies for alopecia areata: evidence and new perspectives
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Matricellular Proteins in the Homeostasis, Regeneration, and Aging of Skin
- Tradescantia-Based Test Systems Can Be Used for the Evaluation of the Toxic Potential of Harmful Algal Blooms
- TRPV3 Ion Channel: From Gene to Pharmacology