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Research 871–900 of 1000+
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- Poster Presentations
- The impact of VDR expression and regulation in vivo
- Mettl3-catalyzed m <sup>6</sup> A regulates histone modifier and modification expression in self-renewing somatic tissue
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Innate type 2 immunity controls hair follicle commensalism by Demodex mites
- Transcriptomic landscape of early hair follicle and epidermal development
- Testosterone in COVID-19: An Adversary Bane or Comrade Boon
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Hair Growth Cycle Is Arrested in SCD1 Deficiency by Impaired Wnt3a-Palmitoleoylation and Retrieved by the Artificial Lipid Barrier
- Activating β-catenin signaling in CD133-positive dermal papilla cells increases hair inductivity
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Cell cycle controls long-range calcium signaling in the regenerating epidermis
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- PTEN Mediates Activation of Core Clock Protein BMAL1 and Accumulation of Epidermal Stem Cells
- The Molecular Revolution in Cutaneous Biology: Noncoding RNAs: New Molecular Players in Dermatology and Cutaneous Biology
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- New developments in the molecular treatment of ichthyosis: review of the literature
- Thiopurines: Recent Topics and Their Role in the Treatment of Inflammatory Bowel Diseases
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Cutaneous Lesions in the Rat Following Administration of an Irreversible Inhibitor of erbB Receptors, Including the Epidermal Growth Factor Receptor
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- The TOR–Auxin Connection Upstream of Root Hair Growth