Search
for
Sort by
Research 751–780 of 1000+
- Transcriptome sequencing and identification of cytochrome P450 monooxygenases involved in the biosynthesis of maslinic acid and corosolic acid in <i>Avicennia marina</i>
- Differential Expression of Proteins Associated with the Hair Follicle Cycle - Proteomics and Bioinformatics Analyses
- Proteolysis‐Targeting Chimera (PROTAC): Current Applications and Future Directions
- Extracellular Vesicles in Osteogenesis: A Comprehensive Review of Mechanisms and Therapeutic Potential for Bone Regeneration
- Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker
- Recent advances in preparation and biomedical applications of keratin based biomaterials
- <i>Pseudomonas aeruginosa</i> heme metabolites biliverdin IXβ and IXδ are integral to lifestyle adaptations associated with chronic infection
- Computer-Aided Designing Peptide Inhibitors of Human Hematopoietic Prostaglandin D2 Synthase Combined Molecular Docking and Molecular Dynamics Simulation
- The PI3K-Akt-mTOR and Associated Signaling Pathways as Molecular Drivers of Immune-Mediated Inflammatory Skin Diseases: Update on Therapeutic Strategy Using Natural and Synthetic Compounds
- Effects of Periplaneta americana extracts on the growth and proliferation of cutaneous interstitial cells in cutaneous-wound healing
- Virtual Screening for the Discovery of Microbiome β-Glucuronidase Inhibitors to Alleviate Cancer Drug Toxicity
- Mitochondria Dysfunction and Inflammation in Traumatic Brain Injury: Androgens to the Battlefront
- Monitoring spatially resolved trace elements in polar bear hair using single spot laser ablation ICP-MS
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Ovine placental steroid synthesis and metabolism in late gestation†
- Allopregnanolone Alters the Gene Expression Profile of Human Glioblastoma Cells
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- sPLA2-IIA Overexpression in Mice Epidermis Depletes Hair Follicle Stem Cells and Induces Differentiation Mediated Through Enhanced JNK/c-Jun Activation
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Targeted protein degradation of Wnt/β-catenin signaling pathway: an effective strategy for cancer therapy
- CD44 signaling in skin wound healing and regeneration
- Cellulose-Based Nanofibers in Wound Dressing
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- Identification of functional circRNAs regulating ovarian follicle development in goats
- Biomaterials Mimicking Mechanobiology: A Specific Design for a Specific Biological Application
- Drug repurposing of cyclin-dependent kinase inhibitors for neutrophilic acute respiratory distress syndrome and psoriasis
- The Role of PGC-1α in Aging Skin Barrier Function
- In Situ Self-Assembling Liver Spheroids with Synthetic Nanoscaffolds for Preclinical Drug Screening Applications
- Cuprorivaite/hardystonite/alginate composite hydrogel with thermionic effect for the treatment of peri-implant lesion
- Serum Zinc Levels in Women with Polycystic Ovarian Syndrome are Lower as Compared to Those without Polycystic Ovarian Syndrome: A Cohort Study