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Research 361–390 of 1000+
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- SOX9 in organogenesis: shared and unique transcriptional functions
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- New Insights into Testosterone Biosynthesis: Novel Observations from HSD17B3 Deficient Mice
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- GDNF promotes hair formation and cutaneous wound healing by targeting bulge stem cells
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Non-classical congenital adrenal hyperplasia: current insights into clinical implications, diagnosis and treatment
- Nutritional Disorders of the Hair and Their Management
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Zinc and Zinc Transporters in Dermatology
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- FLCN regulates transferrin receptor 1 transport and iron homeostasis
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Ernährungsstörungen des Haares und deren Management
- The vitamin B5/coenzyme A axis: A target for immunomodulation?
- Endocrinology
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- The microbiome in patients with atopic dermatitis
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions
- Local heroes or villains: tissue-resident memory T cells in human health and disease