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Research 91–120 of 136
- Inherited Disorders of the Hair
- Coexistence of bullous pemphigoid, intrahepatic cholangiocarcinoma, and alopecia areata: a case report of multifactorial autoimmunity in a surgical context
- 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
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris
- 464 Spatial transcriptomics links gene expression profiles to functional and structural traits of darkly pigmented skin
- In pemphigus, cell detachment, but not autoantibody binding, induces cell-wide, long-lasting transcriptomic and proteomic changes
- 219 Clinical and immunological impact of booster immunization with recombinant mRNA vaccines for SARS-CoV-2 in patients with pemphigus and bullous pemphigoid
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Comparative Characterization of Human Meibomian Glands, Free Sebaceous Glands, and Hair-Associated Sebaceous Glands Based on Biomarkers, Analysis of Secretion Composition, and Gland Morphology
- Editors’ Picks
- 1433 Role of BNC1 in keratinocytes proliferation and migration: A critical regulator of wound healing?
- Diverse Role of OX40 on T Cells as a Therapeutic Target for Skin Diseases
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Oxidative Stress and Skin Diseases: The Role of Lipid Peroxidation
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- New developments in the molecular treatment of ichthyosis: review of the literature
- Skin Development and Disease: A Molecular Perspective
- Immunopathology and Immunotherapy of Inflammatory Skin Diseases
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats