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Research 241–270 of 1000+
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Primary cicatricial alopecia and inflammatory bowel disease – is there a link?
- Rapid Characterization of the Functional and Pharmacological Consequences of Cantú Syndrome K<sub>ATP</sub>Channel Mutations in Intact Cells
- Alopecia Areata
- Cell Types Promoting Goosebumps Form a Niche to Regulate Hair Follicle Stem Cells
- Physiological and pharmacological features of the non-saponin components in Korean Red Ginseng
- Epigenetic regulation in adult stem cells and cancers
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- RAGE and Its Ligands in Melanoma
- Perspectives on Dermatopathology
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors
- Anti-androgenic activities of Ganoderma lucidum
- American Academy of Dermatology
- Structure of human type II 5 alpha-reductase gene.
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Function of KLF4 in Stem Cell Biology
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Das weiße Hautfettgewebe initiiert die IL-33-abhängige Expression von Interleukin 4/13 in myeloischen Zellen während einer Entzündung
- Hair follicle differentiation and regulation.
- Alopecia Areata
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- <i>Pten</i> loss in Lgr5<sup>+</sup> hair follicle stem cells promotes SCC development
- Long COVID syndrome: An unfolding enigma
- Association Between Human Hair Loss and the Expression Levels of Nucleolin, Nucleophosmin, and<i>UBTF</i>Genes
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy