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Research 811–840 of 1000+
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerating Healing
- Unraveling Evolutionary Insights into AVT Peptide Conservation and Antimicrobial Motif Prediction Across Taxa
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Hair follicle stem cells promote epidermal regeneration under expanded condition
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- The biology and genetics of curly hair
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Effects of Curcumin and Its Different Formulations in Preclinical and Clinical Studies of Peripheral Neuropathic and Postoperative Pain: A Comprehensive Review
- Toll-like receptor-targeted anti-tumor therapies: Advances and challenges
- The Role of Nutrition on Thyroid Function
- Myotonic Dystrophy—A Progeroid Disease?
- Dynamic changes of genomic methylation profiles at different growth stages in Chinese Tan sheep
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Enriching Proteolysis Targeting Chimeras with a Second Modality: When Two Are Better Than One
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- RNA-Seq Reveals the Roles of Long Non-Coding RNAs (lncRNAs) in Cashmere Fiber Production Performance of Cashmere Goats in China
- Frontiers in Topical Photoprotection
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- The AR/miR-221/IGF-1 pathway mediates the pathogenesis of androgenetic alopecia
- Novel potential therapeutic targets of alopecia areata
- Plerixafor Engages β-Arrestin-Dependent CXCR4 Signaling to Promote Melanogenesis via β-Catenin-MITF Activation
- Advancements in Therapeutic Deep Eutectic Solvents as Multifunctional Transdermal Delivery Systems
- Enhancing Cancer Therapy with Hyperthermia: Synergistic Effects with Natural Compounds and Conventional Treatments
- Gene expression of FOXA1 and CCL2 in different phenotypes of infertile women with polycystic ovarian syndrome