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Research 31–60 of 66
- Wasabi leaf extract changes the expression levels of cytokine related genes in dermal papilla cells, which identified by the whole transcriptome
- Comparative investigation of immune-related biomarkers related to alopecia areata subtypes
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- 1318 Both lesional and non-lesional skin from acne patients shows robust IL-17-skewing and upregulation of antimicrobial peptides
- 1320 Orchestrated cytotoxic and skin migratory ability lacking self-tolerance: circulating γδT-cells may promote alopecia areata
- 1317 Nicotinic acid suppresses sebaceous lipid synthesis of human sebocytes via activating hydroxycarboxylic acid receptor 2 (HCA2)
- Epidermis-specific ablation of claudin-1 in adult mice demonstrates the essential role of a tight junction barrier in skin homeostasis
- Analysis of the finasteride treatment and its withdrawal in the rat hypothalamus and hippocampus at whole-transcriptome level
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- p63 regulates <i>Satb1</i> to control tissue-specific chromatin remodeling during development of the epidermis
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Extracellular Vesicles from Activated Dermal Fibroblasts Stimulate Hair Follicle Growth Through Dermal Papilla-Secreted Norrin
- Rab5c-mediated endocytic trafficking regulates hematopoietic stem and progenitor cell development via Notch and AKT signaling
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Skin Barrier Dysfunction in Acne Vulgaris: Pathogenesis and Therapeutic Approaches
- Regulatory pathway analysis of coat color genes in Mongolian horses
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Keratin 6A promotes skin inflammation through JAK1-STAT3 activation in keratinocytes
- Hair Growth Promoting Effects of 650 nm Red Light Stimulation on Human Hair Follicles and Study of Its Mechanisms via RNA Sequencing Transcriptome Analysis
- Genetic targeting of lymphatic endothelial cells in mice: current strategies and future perspectives
- Seborrheic Dermatitis Revisited: Pathophysiology, Diagnosis, and Emerging Therapies—A Narrative Review
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Type 2 Cytokine–Dependent Skin Barrier Regulation in Personalized 2-Dimensional and 3-Dimensional Skin Models of Atopic Dermatitis: A Pilot Study
- Novel Quinazoline Derivative Induces Differentiation of Keratinocytes and Enhances Skin Barrier Functions against Th2 Cytokine-Mediated Signaling
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- DNA Methylation as an Epigenetic Memory Keeper during Skin Development and Regeneration
- Current Genetics in Hair Diseases
- Temporal Dynamics of Endothelium After Radiation Injury Reveal a Transient Pro-Angiogenic Capillary Subpopulation Associated with Skin Repair