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Research 271–300 of 665
- Regulatory T Cells: the Many Faces of Foxp3
- MicroRNA-302 Increases Reprogramming Efficiency via Repression of NR2F2
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- The Tissue-dependent Keratin 19 Gene Transcription Is Regulated by GKLF/KLF4 and Sp1
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- A Receptor-Like Kinase Mediates Ammonium Homeostasis and Is Important for the Polar Growth of Root Hairs in<i>Arabidopsis</i>
- Immunological challenges associated with artificial skin grafts: available solutions and stem cells in future design of synthetic skin
- Targeting of Smoothened for therapeutic gain
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Dissecting the Impact of Chemotherapy on the Human Hair Follicle
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- NEDD4 and NEDD4L regulate Wnt signalling and intestinal stem cell priming by degrading LGR5 receptor
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- TCF/Lef1 activity controls establishment of diverse stem and progenitor cell compartments in mouse epidermis
- Switching roles: the functional plasticity of adult tissue stem cells
- Keratins and disease at a glance
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Epidermal Development in Mammals: Key Regulators, Signals from Beneath, and Stem Cells
- The role of pregnane neurosteroids in ethanol withdrawal: behavioral genetic approaches
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis