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Research 871–900 of 1000+
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerative Healing
- The brain–gut–skin axis in inflammatory and disfiguring skin diseases: mechanistic insights, clinical correlations, and therapeutic strategies
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerating Healing
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Genetic Insights into Acne, Androgenetic Alopecia, and Alopecia Areata: Implications for Mechanisms and Precision Dermatology
- Integrated Meta-Analysis of Scalp Transcriptomics and Serum Proteomics Defines Alopecia Areata Subtypes and Core Disease Pathways
- The Skin Microenvironment: A Dynamic Regulator of Hair Follicle Development, Cycling and Disease
- Bacteroides fragilis and Microbacterium as Microbial Signatures in Hashimoto’s Thyroiditis
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Low-Dose Dimethyl Sulfoxide (DMSO) Suppresses Androgen Receptor (AR) and Its Splice Variant AR-V7 in Castration-Resistant Prostate Cancer (CRPC) Cells
- Recent Advances in the Role of Fibroblast Growth Factors in Hair Follicle Growth
- Exploring lncRNA-Mediated Mechanisms in Muscle Regulation and Their Implications for Duchenne Muscular Dystrophy
- Modulating immune responses in alopecia: therapeutic insights and potential targets of antisense oligonucleotides
- The Impact of Sulforaphane on Sex-Specific Conditions and Hormone Balance: A Comprehensive Review
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Alk1 acts in non-endothelial VE-cadherin+ perineurial cells to maintain nerve branching during hair homeostasis
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- The JAK/STAT signaling pathway: from bench to clinic
- The microbiome in patients with atopic dermatitis
- Polycystic ovary syndrome
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Skin Cell Heterogeneity in Development, Wound Healing, and Cancer
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- FGF Family: From Drug Development to Clinical Application