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Research 481–510 of 683
- Pharmacogenetics of the Androgen Metabolic Pathway
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Mitochondrial Reactive Oxygen Species Promote Epidermal Differentiation and Hair Follicle Development
- Drug Repurposing for Rare Diseases
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Lipoatrophy and severe metabolic disturbance in mice with fat-specific deletion of PPARγ
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Competitive balance of intrabulge BMP/Wnt signaling reveals a robust gene network ruling stem cell homeostasis and cyclic activation
- Biotin and biotinidase deficiency
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Conditional epidermal expression of TGFβ1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Phospholipase C 1 is required for skin stem cell lineage commitment
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- mTOR signaling promotes stem cell activation via counterbalancing BMP-mediated suppression during hair regeneration
- Exploring the new horizons of drug repurposing: A vital tool for turning hard work into smart work
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Mitochondrial Function in Murine Skin Epithelium Is Crucial for Hair Follicle Morphogenesis and Epithelial–Mesenchymal Interactions
- Functional Interpretation of Genome-Wide Association Study Evidence in Alopecia Areata
- Ceramide Synthase 4 Regulates Stem Cell Homeostasis and Hair Follicle Cycling
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis