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Research 811–840 of 1000+
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Update on hidradenitis suppurativa: connecting the tracts
- Inflammatory perspectives of polycystic ovary syndrome: role of specific mediators and markers
- Poster Presentations
- Treatment options for androgenetic alopecia: Efficacy, side effects, compliance, financial considerations, and ethics
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Eruptive vellus hair cyst: An uncommon and underdiagnosed entity
- Combined drug triads for synergic neuroprotection in retinal degeneration
- Off-Label Use of Botulinum Toxin in Dermatology—Current State of the Art
- Importance of Citrullination on Hair Protein Molecular Assembly During Trichocytic Differentiation
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Global hotspots and trends in Acanthosis nigricans research: A bibliometric and visualized analysis
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- The Use of Natural Ingredients in the Treatment of Alopecias with an Emphasis on Central Centrifugal Cicatricial Alopecia: A Systematic Review.
- The incidental pore: Ca<sub>V</sub>1.2 and stem cell activation in quiescent hair follicles
- Shock: A possible presenting manifestation of autoimmune polyendocrine syndrome type II
- A 40-Year-Old Woman of African Descent with the Central Scalp Hair Loss
- Central Centrifugal Cicatricial Alopecia
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review