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Research 181–210 of 341
- Epidermal Stem Cells Are Defined by Global Histone Modifications that Are Altered by Myc-Induced Differentiation
- JunB defines functional and structural integrity of the epidermo-pilosebaceous unit in the skin
- Different Requirements for GFRα2-Signaling in Three Populations of Cutaneous Sensory Neurons
- Enhanced restoration of<i>in situ</i>-damaged hairs by intradermal transplantation of trichogenous dermal cells
- Three-dimensional ultrastructural analysis of human skin with the arrector pili muscle interacting with the hair follicle epithelium
- Effects of a phasic oral contraceptive containing desogestrel on facial seborrhea and acne
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Alopezien und Hypotrichosen im Kindesalter
- 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
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- 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
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Diverse Role of OX40 on T Cells as a Therapeutic Target for Skin Diseases
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- The Transient Role for Calcium and Vitamin D during the Developmental Hair Follicle Cycle
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Value of dermoscopy for the diagnosis of monilethrix
- Intercellular junctions in normal epidermis
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- Co-occurrence of monilethrix and Type 1 diabetes mellitus