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Research 631–660 of 1000+
- Connexin mutations in human disease
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- An overview of risk factors for androgenetic alopecia among women at Pasar Ambacang, Kuranji, Padang
- Factors affecting the development of alopecia areata in children
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Marie-unna hereditary hypotrichosis
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Molecular mechanisms of androgenetic alopecia
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- Both low circulating insulin-like growth factor-1 and high-density lipoprotein cholesterol are associated with hair loss in middle-aged women
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Associations of Sleep Quality and Perceived Stress with Skin, Scalp, and Hair Health Among 1,017 Chinese Women: A Cross-Sectional Observational Study
- Alterations in scalp blood flow after the epicutaneous application of 3% minoxidil and 0.1% hexyl nicotinate in alopecia
- Reversal of Baldness in Patient Receiving Minoxidil for Hypertension
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Role of vitamin D and calcium signaling in epidermal wound healing
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere goats
- Androgenetic alopecia – is contact dermatitis an accelerating factor?
- The human keratins: biology and pathology
- The role of vasoactive peptides in skin homeostasis—focus on adiponectin and the kallikrein-kinin system
- Modulating testosterone pathway: a new strategy to tackle male skin aging?
- Alopecia areata: recognition, diagnosis and management
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Role of caffeine in the management of androgenetic alopecia