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Research 601–630 of 1000+
- Skin melanocytes: biology and development
- Discovery of HAP Stem Cells
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Hair Follicles as a Critical Model for Monitoring the Circadian Clock
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- A Screen for Key Genes and Pathways Involved in High-Quality Brush Hair in the Yangtze River Delta White Goat
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems
- Scars or Regeneration?—Dermal Fibroblasts as Drivers of Diverse Skin Wound Responses
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Thymic Mesenchymal Cells Have a Distinct Transcriptomic Profile
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Epithelial-Mesenchymal Micro-niches Govern Stem Cell Lineage Choices
- Intelligent nanotherapeutic strategies for the delivery of CRISPR system
- Isolation and Characterization of Mouse High-glycine/Tyrosine Proteins
- Dendritic Cell–Associated MARCKSL1 Regulates Fibroblast Differentiation During Wound Healing
- Aligned membranes regulate wound healing via MMP12 secreted by macrophages
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- PR-independent neurosteroid regulation of α2-GABA-A receptors in the hippocampus subfields