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Research 361–390 of 651
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- 1619 Spatial transcriptomic analysis of imiquimod-treated mouse skin reveals deregulation of lipid raft-associated markers which could be reversed by re-introduction of caveolin scaffolding domain peptide
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Molecular Genetics of Human Hair Diseases
- Clinical Snippets
- Cell death by cornification
- Identification of Stem Cell Populations in Sweat Glands and Ducts Reveals Roles in Homeostasis and Wound Repair
- The epidermis: rising to the surface
- Basal cell carcinoma — molecular biology and potential new therapies
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Genetic hair and nail disorders
- Two Mechanisms Regulate Keratin K15 Expression In Keratinocytes: Role of PKC/AP-1 and FOXM1 Mediated Signalling
- Immunofluorescent findings and clinical overlap in two cases of follicular lichen planus
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- Regionalisation of the skin
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- New developments in occupational dermatology
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Topical L‐thyroxine: The Cinderella among hormones waiting to dance on the floor of dermatological therapy?
- Common Pediatric Skin Conditions with Protracted Courses
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Congenital atrichia associated with situs inversus and mesocardia
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion