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Research 571–600 of 677
- Microimaging of hairless rat skin by magnetic resonance at 900 MHz
- Anatomic Considerations in Rhytidectomy
- Rejuvenation of the Lower Eyelid Complex
- Transtemporal Midface Lifting to Blend the Lower Eyelid-Cheek Junction
- The Arrector Pili Muscle and the Follicular Unit of the Scalp
- Biomaterials for dermal substitutes
- Microneedles meet photomedicine: emerging strategies for diagnosis and therapy of skin diseases
- Complications in Esthetic Surgery
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Network pharmacology and molecular docking analysis on potential molecular targets and mechanism of action of BRAF inhibitors for application in wound healing
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Multi-omics analyses, cell experiments, and network pharmacology tools identified key proteins and candidate drugs for alopecia areata treatment
- Correction of Tear Trough Deformity Using Autologous Fibroblast Combined with Keratin: New Soft Tissue Filler
- Soft Tissue Augmentation of the Temporal Brow in Browlifting Surgery
- Pharmacogenetics of the Androgen Metabolic Pathway
- Collider bias undermines our understanding of COVID-19 disease risk and severity
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- 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
- Conditional epidermal expression of TGFβ1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia
- Phospholipase C 1 is required for skin stem cell lineage commitment
- 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