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Research 151–180 of 181
- Molecular Genetics of Inherited Disorders of Epidermal Keratins
- Clinical Snippets
- The keratins and their disorders
- Androgenetic Alopecia
- New Activators and Inhibitors in the Hair Cycle Clock: Targeting Stem Cells’ State of Competence
- 554 Repurposing a clinical antimalarial for the therapeutic induction of lethal ER stress targeting BRAF-kinase inhibitor-resistant malignant melanoma
- 556 α 1 -AR agonist induced piloerection protects against the development of traction alopecia
- 557 A peptide derivative with known anti-wrinkle properties was identified as potent dipeptiylpeptidase-4 inhibitor
- Feather on the Cap of Medicine
- SkIndia Quiz 24: Itchy papules over face
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Keratin gene mutations in disorders of human skin and its appendages
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Eruptive vellus hair cysts: An underdiagnosed entity
- Botulinum Toxins in Medical and Cosmetic Dermatology
- Dermatology Patient Support Groups
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- 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
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- 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