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Research 151–180 of 176
- The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus
- Characterization and functional analysis of Krtap11-1 during hair follicle development in Angora rabbits (Oryctolagus cuniculus)
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Eruptive vellus hair cysts: An underdiagnosed entity
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)
- Steatocystoma Multiplex
- Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Bioengineered skin organoids: from development to applications
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- Generalized multiple eruptive milia in an infant – An unusual presentation
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Acquired Localized Longitudinal Pachyonychia and Onychomatrical Tumors: A Comparative Study to Onychomatricomas (5 Cases) and Onychocytic Matricomas (4 Cases)
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Interventions for nail psoriasis
- Update on the Treatment of Alopecia Areata
- Optimal Management of Plaque Psoriasis in Adolescents: Current Perspectives
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita