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Research 91–120 of 1000+
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function
- MicroRNA in skin diseases
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Combined Oral Contraception and Bicalutamide in Polycystic Ovary Syndrome and Severe Hirsutism: A Double-Blind Randomized Controlled Trial
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Group IID, IIE, IIF and III secreted phospholipase A2s
- The Pathogenesis of Alopecia Areata in Rodent Models
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Genetic basis of polycystic ovary syndrome
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Regeneration of Hair Follicles Is Modulated by Flightless I (Flii) in a Rodent Vibrissa Model
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Inhibition of 5α Reductase Impairs Cognitive Performance, Alters Dendritic Morphology and Increases Tau Phosphorylation in the Hippocampus of Male 3xTg-AD Mice
- Identifying molecular targets for reverse aging using integrated network analysis of transcriptomic and epigenomic changes during aging
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling
- Flightless I Expression Enhances Murine Claw Regeneration Following Digit Amputation
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Disease causing homozygous variants in the human hairless gene
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Involvement of the central hypothalamic-pituitary-adrenal axis in hair growth and melanogenesis among different mouse strains
- Differential impact of environmental factors on systemic and localized autoimmunity
- Association of a polymorphism in the ornithine decarboxylase gene with male androgenetic alopecia
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- Debatable Topics in PCOS Patients
- Atlas of Geriatric Dermatology
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta