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Research 691–720 of 1000+
- Spironolactone May Reduce the Risk of Incident Rosacea
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- Protein kinase C is a key target for attenuation of Leigh syndrome by rapamycin
- Acne in Dark Skin
- Association of a polymorphism in the ornithine decarboxylase gene with male androgenetic alopecia
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Nanofibers: An Effective Biomedical Tool for Burn Management
- Progeroide Syndrome
- The urine as a diagnostic key for a homozygous EGFR mutation
- Skin
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Causality of Aging Hallmarks
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Metabolomic analysis of SMP30/GNL knockout mice treated with fermented vegetable and fruit extract (OM-X®)
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Rac-dependent signaling from keratinocytes promotes differentiation of intradermal white adipocytes
- Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities
- Mister XX
- SOX2 in the Skin
- Melanocytes and Vitiligo (and Hair Graying)
- The Skin and Subcutaneous Tissues
- Stem Cells and their Niches
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Somatic mutations distinguish melanocyte subpopulations in human skin