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Research 241–270 of 1000+
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Functional enhancement strategies for immunomodulation of mesenchymal stem cells and their therapeutic application
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Metabolic Syndrome Prevalence in Psoriasis
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Evaluation of acute, subacute oral toxicity and wound healing activity of mother plant and callus of Teucrium polium L. subsp. geyrii Maire from Algeria
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Injectable platelet-rich fibrin promotes proliferation and trichogenic inductivityof dermal papilla cells through activating TGF-β/Smad signaling pathway
- The Cross-section Trichometer
- Efficacy and safety of diode laser for facial hair reduction in hirsutism—a clinico-trichoscopic evaluation
- Mesenchymal stem cell therapy for skin repair and rejuvenation
- Application and progress of induced pluripotent stem in chronic wound healing: a narrative review
- Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens)
- Polycystic ovary syndrome: Pathophysiology, Symptoms, Risk factors, and Pharmacological treatment
- Bioregenerative Applications of the Human Mesenchymal Stem Cell- Derived Secretome: Part-II
- Cancer risk in polycystic ovary syndrome patients: Common treatments and future perspectives
- Alopecia
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Modelling androgen synthesis and action during human sexual differentiation
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Dietary Vitamin D Supplementation Improves Hair Follicle Development and Affects Fatty Acid Metabolism in Rex Rabbits
- Cell-derived exosome therapy for diabetic peripheral neuropathy: a preclinical animal studies systematic review and meta-analysis
- The FRZB gene regulates hair follicle development in rabbits via the Wnt/β-catenin signaling pathway
- Caffeine Induces Autophagy and Apoptosis in Auditory Hair Cells via the SGK1/HIF-1α Pathway
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development