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Research 30 of 119
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- 피부 발육과정에서 데스모콜린 1의 발현에 관한 면역조직화학적 연구
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- Intercellular junctions in normal epidermis
- A 4kb Fragment of the Desmocollin 3 Promoter Directs Reporter Gene Expression to Parakeratotic Epidermis and Primary Hair Follicles
- 010 Development of a Desmocollin-3 Active Mouse Model Recapitulating Human Atypical Pemphigus
- DEVELOPMENT OF A DESMOCOLLIN-3 ACTIVE MOUSE MODEL RECAPITULATING HUMAN ATYPICAL PEMPHIGUS
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- 195 Androgen action and 3D culture conditions influence dermal papilla cells inductive properties: the role of Wnt agonists/antagonists balance
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- 196 The endocannabinoid tone regulates human sebocyte biology
- 194 An underlying mechanism of hair loss in acrodermatitis enteropathica
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- MicroRNA in skin diseases
- A Novel In Vivo Active Pemphigus Model Targeting Desmoglein1 and Desmoglein3: A Tool Representing All Pemphigus Variants
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- Type 2 Cytokine–Dependent Skin Barrier Regulation in Personalized 2-Dimensional and 3-Dimensional Skin Models of Atopic Dermatitis: A Pilot Study
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Cell death by cornification
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Current Genetics in Hair Diseases
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Inherited Disorders of the Hair
- Bidirectional binding property of high glycine–tyrosine keratin-associated protein contributes to the mechanical strength and shape of hair
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate