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Research 211–240 of 1000+
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- Characterization of the Human Hair Shaft Cuticle–Specific Keratin-Associated Protein 10 Family
- Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Network Pharmacology Reveals Curcuma aeruginosa Roxb. Regulates MAPK and HIF-1 Pathways to Treat Androgenetic Alopecia
- Hox genes in development and beyond
- Extracellular matrix sensing by FERONIA and Leucine‐Rich Repeat Extensins controls vacuolar expansion during cellular elongation in <i>Arabidopsis thaliana</i>
- S100A6: molecular function and biomarker role
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Does an apple a day keep away diseases? Evidence and mechanism of action
- Enzymes
- Overexpression of the calcium sensing receptor accelerates epidermal differentiation and permeability barrier formation in vivo
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- RSPO1, a potent inducer of pancreatic β cell neogenesis
- Drug-associated insomnia: A pharmacovigilance study based on FDA adverse event reporting system
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Decision letter: A counter gradient of Activin A and follistatin instructs the timing of hair cell differentiation in the murine cochlea
- Decision letter: Hair follicle epidermal stem cells define a niche for tactile sensation
- Expression of NAD+dependent 15-hydroxyprostaglandin dehydrogenase and protection of prostaglandins in human hair follicle
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- Acne
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Study of<i>Demodex</i>mites: Challenges and Solutions
- How to diagnose a lipodystrophy syndrome
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia