Search
for
Sort by
Research 61–90 of 83
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Monovalent antibody-conjugated lipid-polymer nanohybrids for active targeting to desmoglein 3 of keratinocytes to attenuate psoriasiform inflammation
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Identification of Hypoxia and Mitochondrial-related Gene Signature and Prediction of Prognostic Model in Lung Adenocarcinoma
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Proteomics as a tool to improve novel insights into skin diseases: what we know and where we should be going
- 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
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Current Genetics in Hair Diseases
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- Integrated Meta-Analysis of Scalp Transcriptomics and Serum Proteomics Defines Alopecia Areata Subtypes and Core Disease Pathways
- Molecular Genetics of Human Hair Diseases
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- 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
- Animal models of human skin disease
- Intercellular junctions in normal epidermis
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness