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Research 991–1000 of 1000+
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Drug repositioning: current approaches and their implications in the precision medicine era
- Identification of the Ovine Keratin-Associated Protein 22-1 (KAP22-1) Gene and Its Effect on Wool Traits
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Congenital hair loss disorders: Rare, but not too rare
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- Pubertal Development
- Male pattern baldness: current treatments, future prospects