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Research 151–180 of 711
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- Convergent Evolution of Cysteine-Rich Keratins in Hard Skin Appendages of Terrestrial Vertebrates
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- A curated catalog of canine and equine keratin genes
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- Identification of the key proteins associated with different hair types in sheep and goats
- Unlocking the genetic secrets of Dorper sheep: insights into wool shedding and hair follicle development
- Hair follicle stem cells promote epidermal regeneration under expanded condition
- The human keratins: biology and pathology
- Epidermal homeostasis: a balancing act of stem cells in the skin
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons
- SFRP2/DPP4 and FMO1/LSP1 Define Major Fibroblast Populations in Human Skin
- Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men
- Mesenchymal Stem Cells from Adipose Tissue in Clinical Applications for Dermatological Indications and Skin Aging
- Comparative Transcriptome Analysis of Fetal Skin Reveals Key Genes Related to Hair Follicle Morphogenesis in Cashmere Goats
- Epithelial Skin Biology
- Keratin disorders: from gene to therapy
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Differentiation of Mouse Induced Pluripotent Stem Cells into a Multipotent Keratinocyte Lineage
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Biology and Genetics of Hair
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Physiologic functions of PP2A: Lessons from genetically modified mice
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- The Changing Landscape of Alopecia Areata: The Therapeutic Paradigm
- Beyond Expectations