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Research 31–60 of 83
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Identification of Hypoxia and Mitochondrial-related Gene Signature and Prediction of Prognostic Model in Lung Adenocarcinoma
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Birt–Hogg–Dubé syndrome
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Biology and Genetics of Hair
- The Genetics of Human Skin Disease
- 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
- Congenital hair loss disorders: Rare, but not too rare
- 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
- 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
- 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