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Research 151–180 of 1000+
- The Roles of Smad2 and Smad3 in Mouse Skin Development
- Folliculin Deficient Renal Cancer Cells Show Higher Radiosensitivity through Autophagic Cell Death
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Medical Therapy for Female Pattern Hair Loss (FPHL)
- Polycystic Ovary Syndrome (PCOS): Causes, Symptoms, Diagnosis & Treatments
- Update on Polycystic Ovary Syndrome
- Epidemiology, diagnosis, and management of polycystic ovary syndrome
- Evaluation and Treatment of Hirsutism in Premenopausal Women: An Endocrine Society Clinical Practice Guideline
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Acne
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Ferrous Ferric Chloride Stimulates the Skin Cell Function and Hair Growth in Mice
- Polycystic ovary syndrome and iron overload: biochemical link and underlying mechanisms with potential novel therapeutic avenues
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Polycystic ovary syndrome [PCOS]: Comprehensive management in primary care
- No. 350-Hirsutism: Evaluation and Treatment
- FLCN regulates transferrin receptor 1 transport and iron homeostasis
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- The Case | Bilateral kidney tumors and lung cysts
- A 40-Year-Old Woman With Facial Papules and Flank Pain
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Hair Dyes in Pregnancy: A Systematic Review and Meta‐Analysis
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Association of Infant Physical Development and Rapid Growth With Pubertal Onset Among Girls in Rural China
- Sjogren-Larsson syndrome
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- <i>Hoxc13</i> mutant mice lack external hair
- Polyethylene-Glycol-Ornamented Small Intestinal Submucosa Biosponge for Skin Tissue Engineering
- Anaesthetics and platelets.