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Research 151–180 of 157
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- Viewpoint 4
- Malignant Melanoma and Its Stromal Nonimmune Microecosystem
- Desmoplastic tricholemmoma in a dog
- The protective role of FTY720 in promoting survival of allograft fat in mice
- Hydrogels: current biomedical applications and future directions
- In vitro strategies for mimicking dynamic cell–ECM reciprocity in 3D culture models
- Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Novel compound heterozygous mutations in the<i>desmoplakin</i>gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Novel insights into cardiocutaneous syndromes
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Alopecia in Epidermolysis Bullosa
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Molecular Genetics of Alopecias
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- The Genetics of Human Skin Disease
- Effects of a complex mixture prepared from agrimonia, houttuynia, licorice, peony, and phellodendron on human skin cells
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Congenital hair loss disorders: Rare, but not too rare
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease