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Research 301–330 of 1000+
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- Fibroblast growth factors: key players in regeneration and tissue repair
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- Zeb2 recruits HDAC–NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
- The Pathobiology of Skin Aging
- Resting no more: re‐defining telogen, the maintenance stage of the hair growth cycle
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Overexpression of Smad7 results in severe pathological alterations in multiple epithelial tissues
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Prolactin and Its Receptor Are Expressed in Murine Hair Follicle Epithelium, Show Hair Cycle-Dependent Expression, and Induce Catagen
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Structure and expression of genes for a class of cysteine-rich proteins of the cuticle layers of differentiating wool and hair follicles.
- The Paradox of p53: What, How, and Why?
- Role of FGFR2-signaling in the pathogenesis of acne
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Stem cell plasticity enables hair regeneration following Lgr5+ cell loss
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex