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Research 61–90 of 775
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- A computationally inferred regulatory heart aging model including post-transcriptional regulations
- Advances in Hair Diseases
- DNA Methylation‐Regulated ZDHHC17 Promotes the Risk of Facial Skin Aging
- Epigenetic control of adult stem cell function
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Congenital Adrenal Hyperplasia
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Current evaluation of amenorrhea
- Adverse effects of common medications on male fertility
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Nonclassic adrenal hyperplasia
- New insights into the functions of Cox-2 in skin and esophageal malignancies
- How to diagnose a lipodystrophy syndrome
- Regulation of masculinization: androgen signalling for external genitalia development
- Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
- Current evaluation of amenorrhea
- Morphological Approach to Hair Disorders
- Treatment options for alopecia: an update, looking to the future
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Genome-wide association study of skin complex diseases
- Comparative study on seasonal hair follicle cycling by analysis of the transcriptomes from cashmere and milk goats
- Management of the psychological comorbidities of dermatological conditions: practitioners' guidelines
- INTERFERONS IN DERMATOLOGY
- Is polycystic ovary syndrome a sexual conflict? A review
- Male fertility and skin diseases
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- The eye and the skin in endocrine metabolic diseases
- Human Fetal Scalp Dermal Papilla Enriched Genes and the Role of R-Spondin-1 in the Restoration of Hair Neogenesis in Adult Mouse Cells