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Research 391–420 of 1000+
- Endocrine Influences on Hair Growth
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- The role of vitamin D receptor signaling in hair follicle health and alopecia: Current understanding and therapeutic implications
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Natural Molecules in the Management of Polycystic Ovary Syndrome (PCOS): An Analytical Review
- The quantification of reproductive hormones in the hair of captive adult brown bears and their application as indicators of sex and reproductive state
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Is polycystic ovary syndrome a sexual conflict? A review
- Regulation of pathophysiological and tissue regenerative functions of MSCs mediated via the WNT signaling pathway (Review)
- Congenital atrichia and hypotrichosis
- Ketoconazole Shampoo for Seborrheic Dermatitis of the Scalp: A Narrative Review
- Melatonin Receptors and Their Role in Human Diseases
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- From basic biology to engineered therapies: the keratinocyte stem cell playbook
- Langerin+ Dendritic Cells in Cutaneous Fibrosis: The TGF-β1 Signaling Axis
- TRICOSCOPIA – ESTRUTURAS TRICOSCÓPICAS E SUA APLICABILIDADE NAS PATOLOGIAS DO CABELO E DO COURO CABELUDO
- CME examination for volume 43
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Endocrine Regulation of Hair Growth and Loss: Current Evidence and Clinical Implications
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Diagnostic approach to low‐renin hypertension
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Animal Models and the Developmental Origins of Polycystic Ovary Syndrome: Increasing Evidence for the Role of Androgens in Programming Reproductive and Metabolic Dysfunction
- Hair and nail involvement in lupus erythematosus
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome