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Research 30 of 57
- The Role of Histone Demethylases in Disease
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Inhibition of the CoREST Repressor Complex Promotes Wound Re-Epithelialization through the Regulation of Keratinocyte Migration
- Is There a Histone Code for Cellular Quiescence?
- Epigenetic control of skin and hair regeneration after wounding
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Disease causing homozygous variants in the human hairless gene
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- ATP-dependent chromatin remodeling during mammalian development
- Epigenetic control of adult stem cell function
- Exploring the Drug Repurposing Versatility of Valproic Acid as a Multifunctional Regulator of Innate and Adaptive Immune Cells
- Epigenetic regulation in adult stem cells and cancers
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- The role of protein lactylation in skin diseases: from molecular mechanisms to potential therapeutics
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- JMJD3 and NF-κB-dependent activation of Notch1 gene is required for keratinocyte migration during skin wound healing
- Non-histone Methylation of SET7/9 and its Biological Functions
- Novel anti-aging gene NM_026333 contributes to proton-induced aging via NCX1-pathway
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Identification of Drug-Disease Associations Using Information of Molecular Structures and Clinical Symptoms via Deep Convolutional Neural Network
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- Epigenetics of Colorectal Cancer
- Epidermal stem cells in wound healing and their clinical applications
- Progenitor Cell Dysfunctions Underlie Some Diabetic Complications
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells