Search
for
Sort by
Research 331–360 of 737
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- Biotin and biotinidase deficiency
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- 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
- Cantú Syndrome Is Caused by Mutations in ABCC9
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- WNT Signaling in Disease
- Wounding induces dedifferentiation of epidermal Gata6+ cells and acquisition of stem cell properties
- FGF5 is a crucial regulator of hair length in humans
- 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
- Cell death in the skin
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- FGF Family: From Drug Development to Clinical Application
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- 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
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Pathology of Mouse Models of Accelerated Aging
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions