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Research 31–60 of 78
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Inherited Epidermolysis Bullosa: A Clinical Case
- Pemphigus Vulgaris IgG and Methylprednisolone Exhibit Reciprocal Effects on Keratinocytes
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- Monovalent antibody-conjugated lipid-polymer nanohybrids for active targeting to desmoglein 3 of keratinocytes to attenuate psoriasiform inflammation
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- DNA Methylation‐Regulated ZDHHC17 Promotes the Risk of Facial Skin Aging
- An Investigation of Hair and its Keratin Associated Proteins using Advanced Light Microscopy
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Epithelial–mesenchymal transition in cutaneous fibrosis disease: from mechanisms to therapy
- Dysfunction of keratinocyte adhesion
- Skin fragility, diffuse ecchymosis and blisters on a yellowish waxy base
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- The Genetics of Human Skin Disease
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Integrated Meta-Analysis of Scalp Transcriptomics and Serum Proteomics Defines Alopecia Areata Subtypes and Core Disease Pathways
- Molecular Genetics of Human Hair Diseases
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- The Roles of WNT Signaling Pathways in Skin Development and Mechanical-Stretch-Induced Skin Regeneration
- Multifaceted role of keratins in epithelial cell differentiation and transformation
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Alopecia in Epidermolysis Bullosa
- Dermatopathology and molecular genetics