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Research 31–60 of 860
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Next generation human skin constructs as advanced tools for drug development
- The Genetics of Human Skin Disease
- 773 Generation of human hair follicle organoids in vitro and ex vivo by co-culture of primary human hair matrix keratinocytes and dermal papilla fibroblasts
- 9. Immunology and Genetics
- Keratin disorders: from gene to therapy
- An Intrinsic Oscillation of Gene Networks Inside Hair Follicle Stem Cells: An Additional Layer That Can Modulate Hair Stem Cell Activities
- Human Fetal Scalp Dermal Papilla Enriched Genes and the Role of R-Spondin-1 in the Restoration of Hair Neogenesis in Adult Mouse Cells
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Beyond Expectations
- Morpho-Regulation of Ectodermal Organs
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Conditional Gene Expression in the Epidermis of Transgenic Mice Using the Tetracycline-Regulated Transactivators tTA and rTA Linked to the Keratin 5 Promoter
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- TSA restores hair follicle-inductive capacity of skin-derived precursors
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- Estrogen modulates mesenchymal-epidermal interactions in the adult nipple
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Distinct stem cells contribute to mammary gland development and maintenance
- Identification of the cell lineage at the origin of basal cell carcinoma
- Identifying the Target Cells and Mechanisms of Merkel Cell Polyomavirus Infection
- Development and homeostasis of the sebaceous gland
- Maternal PPARγ protects nursing neonates by suppressing the production of inflammatory milk
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases