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Research 211–240 of 1000+
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Spironolactone and XPB: An Old Drug with a New Molecular Target
- More than one way to skin . . .
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Biomaterials for in situ tissue regeneration: development and perspectives
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- The genetic basis of dermatophytosis skin infection susceptibility
- Keratinocyte Growth Factor Modified Messenger RNA Accelerating Cell Proliferation and Migration of Keratinocytes
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Loss of Repressor Activator Protein 1 Precipitates Cardiac Aging in Mice via p53/PPARα Signaling
- Bald scalp in men with androgenetic alopecia retains hair follicle stem cells but lacks CD200-rich and CD34-positive hair follicle progenitor cells
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation
- Author response: Loss of Dnmt3a and Dnmt3b does not affect epidermal homeostasis but promotes squamous transformation through PPAR-γ
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- HOXC13 Is Involved in the Regulation of Human Hair Keratin Gene Expression
- A kindred with mutant IKAROS and autoimmunity
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Biomaterials for dermal substitutes
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Epigenetics of Colorectal Cancer
- Solution Blow Spinning of Programmable Biofunctionalized Polymer Fibers
- Melanocytes: The new Black
- Vitamin D receptor is essential for normal keratinocyte stem cell function
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation