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Research 241–270 of 552
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Immunolocalization of Scaffoldin, a Trichohyalin‐Like Protein, in the Epidermis of the Chicken Embryo
- A folliculocentric perspective of dandruff pathogenesis: Could a troublesome condition be caused by changes to a natural secretory mechanism?
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Integrated Meta-Analysis of Scalp Transcriptomics and Serum Proteomics Defines Alopecia Areata Subtypes and Core Disease Pathways
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Epidermal homeostasis: a balancing act of stem cells in the skin
- Cellular and molecular mechanisms of repair in acute and chronic wound healing
- Vaccines, adjuvants and autoimmunity
- Signaling Involved in Hair Follicle Morphogenesis and Development
- Evidence that Myc activation depletes the epidermal stem cell compartment by modulating adhesive interactions with the local microenvironment
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Proteome Analysis of Human Hair Shaft
- Human Eccrine Sweat Gland Cells Can Reconstitute a Stratified Epidermis
- Pemphigus Vulgaris IgG and Methylprednisolone Exhibit Reciprocal Effects on Keratinocytes
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- Stratum corneum dysfunction in dandruff
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- Keratins and disease at a glance
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation