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Research 121–150 of 1000+
- Insights into Male Androgenetic Alopecia: Differential Gene Expression Profiling of Plucked Hair Follicles and Integration with Genetic Data
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- Is the “Comb Over” Dying? A Mouse Model for Male Pattern Baldness (Androgenic Alopecia)
- 860 Understanding cellular & molecular responses in the treatment of pediatric lymphatic anomalies
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Poly(γ-Glutamic Acid)/Chitosan Hydrogel Nanoparticles For Effective Preservation And Delivery Of Fermented Herbal Extract For Enlarging Hair Bulb And Enhancing Hair Growth
- COVID‐19, androgens, and androgenic alopecia
- Hair cell toxicology: With the help of a little fish
- Drug Repositioning: New Opportunities for Older Drugs
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- Human pluripotent stem cell-derived skin organoids enabled pathophysiological model of Mycobacterium tuberculosis infection
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- The Rotterdam Study: 2016 objectives and design update
- Hair morphogenesis<i>in vitro</i>: formation of hair structures suitable for implantation
- Chronic overlapping pain conditions and nociplastic pain
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Developing Patient-Derived 3D-Bioprinting models of pancreatic cancer
- Androgens induce sebaceous differentiation in sebocyte cells expressing a stable functional androgen receptor
- STAT3 Partly Inhibits Cell Proliferation via Direct Negative Regulation of FST Gene Expression
- Biomedical applications of organoids in genetic diseases
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- CSI on steroids
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Pathogenicity and enzyme screening of some selected non-dermatophytic moulds
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant