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Research 601–630 of 1000+
- Lack of the Vitamin D Receptor is Associated with Reduced Epidermal Differentiation and Hair Follicle Growth
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- An Extended Epidermal Response Heals Cutaneous Wounds in the Absence of a Hair Follicle Stem Cell Contribution
- Fundamental hair follicle biology and fine fibre production in animals
- 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
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- WNT Signaling in Disease
- Vitamin D receptor is essential for normal keratinocyte stem cell function
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- The Vitamin D Receptor Is a Wnt Effector that Controls Hair Follicle Differentiation and Specifies Tumor Type in Adult Epidermis
- Frizzled Receptors in Development and Disease
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Conditional epidermal expression of TGFβ1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Identification of a link between Wnt/β-catenin signalling and the cell fusion pathway
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Does D matter? The role of vitamin D in hair disorders and hair follicle cycling
- The Many Faces of Calcineurin Inhibitor Toxicity—What the FK?
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Indian Medicinal Herbs and Formulations for Alzheimer’s Disease, from Traditional Knowledge to Scientific Assessment
- NEDD4 and NEDD4L regulate Wnt signalling and intestinal stem cell priming by degrading LGR5 receptor