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Research 931–960 of 1000+
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Vitamin D resistance
- Hair Restoration in the Gender-Affirming Patient
- Rare Conditions of Hyperandrogenism Through Lifespan: A Case Series
- Inflammatory Skin Disease in Latin America: Treatment Challenges and Opportunities
- Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children
- Cepharanthine Inhibits Doxorubicin-Induced Cellular Senescence by Activating Autophagy via the mTOR Signaling Pathway
- Polycystic Ovarian Syndrome
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Gender-affirming hair procedures
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Novel acquisitions on the immunoprotective roles of the EGF receptor in the skin
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Viruses, Variants, and Vaccines: How COVID-19 Has Changed the Way We Look at Skin
- The effects of infrared radiation on the human skin
- Cell-free fat extract improves embryo development and clinical outcomes in older women with previous in-vitro fertilization failure
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Concurrent autoimmune and endocrine dysregulation in polycystic ovary syndrome
- Activity‐based therapeutic algorithm for folliculitis decalvans: A practical tool for effective management
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Transcriptome-guided development of a fibrosis-reversal compound reduces skin scarring and allows regeneration via mitochondrial uncoupling
- POLYCYSTIC OVARY SYNDROME: DIAGNOSTIC CRITERIA AND TREATMENT METHODS
- A narrative review on cutaneous manifestations in polycystic ovary syndrome: pathophysiology, diagnosis, management, and psychosocial impact
- Biology, diagnosis and treatment of <i>Malassezia</i> dermatitis in dogs and cats