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Research 61–90 of 1000+
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Highlights from the 68th Annual Meeting of the Society of Investigative Dermatology
- Stem-cell therapy in dermatology – Challenges and opportunities
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Stem Cell Use to Treat Dermatological Disorders
- Cutaneous gene therapy
- Skin Development and Disease: A Molecular Perspective
- Hair and Nail Relationship
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- Poster Presentations
- SATU KASUS DERMATOSIS PUSTULAR SUBKORNEAL YANG DITERAPI DENGAN KORTIKOSTEROID
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- 331 An open label clinical trial of the JAK inhibitor tofacitinib for alopecia areata
- Beyond Expectations
- Retinoids for Chemoprophylaxis of Nonmelanoma Skin Cancer
- Next generation human skin constructs as advanced tools for drug development
- Preparing regenerative therapies for clinical application: proposals for responsible translation
- Secondary cicatricial and other permanent alopecias
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- Extracellular vesicle-based drug overview: research landscape, quality control and nonclinical evaluation strategies
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- LITERATURE REVIEW
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Molecular Genetics of Alopecias
- Skin