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Research 721–750 of 1000+
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- 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
- Managing Cutaneous Manifestations of Hyperandrogenic Disorders
- Update on Melasma—Part I: Pathogenesis
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Zebrafish Model of Hereditary Pigmentary Disorders
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Scoping Review on the Use of Drugs Targeting JAK/STAT Pathway in Atopic Dermatitis, Vitiligo, and Alopecia Areata
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- Hair cross-sectioning in uncombable hair syndrome: An easy tool for complex diagnosis
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Long-term Prophylaxis with Androgens in the management of Hereditary Angioedema (HAE) in emerging countries
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- The color of skin: white diseases of the skin, nails, and mucosa