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Research 211–240 of 329
- Improving the treatment of bacterial infections caused by multidrug-resistant bacteria through drug repositioning
- Skin ultrasonography and magnetic resonance; new clinical applications and instrumentation
- Clinical characteristics in Taiwanese women with polycystic ovary syndrome
- Ranitidine and finasteride inhibit the synthesis and release of trimethylamine N-oxide and mitigates its cardiovascular and renal damage through modulating gut microbiota
- Optical Studies of Nanodiamond-Tissue Interaction: Skin Penetration and Localization
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- HGF/SF Increases Number of Skin Melanocytes but Does Not Alter Quality or Quantity of Follicular Melanogenesis
- Inorganic Nanomaterial for Biomedical Imaging of Brain Diseases
- Assessment of prescribing information for generic drugs manufactured in the Middle East and marketed in Saudi Arabia
- Are Nutraceuticals Effective in COVID-19 and Post-COVID Prevention and Treatment?
- Cell death in skin function, inflammation, and disease
- Phytochemicals and Nano-Phytopharmaceuticals Use in Skin, Urogenital and Locomotor Disorders: Are We There?
- The mechanical forces that shape our senses
- Influence of Extraction Techniques and Solvents on the Antioxidant and Biological Potential of Different Parts of Scorzonera undulata
- Isoxazole 9 (ISX9), a small molecule targeting Axin, activates Wnt/β‐catenin signalling and promotes hair regrowth
- On the Horizon From the ORS
- Differential Expression of Proteins Associated with the Hair Follicle Cycle - Proteomics and Bioinformatics Analyses
- Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA
- Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review
- The myeloid mineralocorticoid receptor regulates dermal angiogenesis and inflammation in glucocorticoid‐induced impaired wound healing
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Lateral oblique forehead lines: redefining sleeping lines and treatment with botulinum toxin A
- Phytochemicals With Anti 5-alpha-reductase Activity: A Prospective For Prostate Cancer Treatment
- Molecular Mechanisms of Vitexin: An Update on Its Anti-Cancer Functions
- Analysis of potentially toxic contaminants in milk powder
- Phosphatase Regulator NIPP1 Restrains Chemokine-Driven Skin Inflammation
- Benign prostatic hyperplasia, metabolic syndrome and androgenic alopecia: Is there a possible relationship?
- A 32‐year‐old woman with arthralgias and severe hypotension
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation