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Research 31–60 of 751
- 559 Visualization of sweat suppression following botulinum toxin A by soluble microneedle arrays
- 557 A peptide derivative with known anti-wrinkle properties was identified as potent dipeptiylpeptidase-4 inhibitor
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Two Dogs with Juvenile-Onset Skin Diseases with Involvement of Extremities
- Cutaneous manifestations of the COVID-19 pandemic in schoolchildren and adolescents
- Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Ichthyosis hystrix
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Pathology and pathogenesis of cutaneous lesions in beef cattle associated with buffalo fly infestation
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Building Models for Keratin Disorders
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Anhidrotic effect of intradermal injections of botulinum toxin—A comparison of different products and concentrations
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Painful thickened skin on the soles of the feet
- Skin Development and Disease: A Molecular Perspective
- Beyond Expectations