Search
for
Sort by
Research 541–570 of 548
- 655 In vitro cultivation of dermal-epidermal composites in a single medium supports human hair follicle neogenesis in xenografts
- Transcriptomic Analysis Reveals Candidate Ligand-Receptor Pairs and Signaling Networks Mediating Intercellular Communication between Hair Matrix Cells and Dermal Papilla Cells from Cashmere Goats
- Regulation of epidermal proliferation and hair follicle cycling by synthetic photostable retinoid EC23
- DataSheet1_Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature.zip
- A Niche Above: A Novel Modality of Stem Cell Regulation in Mammalian Skin Epidermis
- Deflúvio Telogénico Crónico
- SnapshotDx Quiz: May 2020
- Anti-Aging Medicine for Hair
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- 1422 Uncoupling desmosomal cadherin adhesion activates quiescent hair follicle stem cells and orchestrates self-organized regeneration through outside-in signaling
- 876 Imaging nanoscale changes in desmosome protein organization
- Congenital hair loss disorders: Rare, but not too rare
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Intercellular junctions in normal epidermis
- Biology and Genetics of Hair
- A function for Rac1 in the terminal differentiation and pigmentation of hair
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- 320 Desmoglein 3-mediated mechanical transadhesion controls epithelial stem cell quiescence
- Pseudo Pemphigus Phenotypes in Mice with Inactivated Desmoglein 3
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- Inherited Disorders of the Hair
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Immunolocalization of junctional proteins in human hairs indicates that the membrane complex stabilizes the inner root sheath while desmosomes contact the companion layer through specific keratins
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Molecular Genetics of Alopecias