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Research 121–150 of 644
- Autophagy: Guardian of Skin Barrier
- Clinically relevant aberrant Filip1l DNA methylation detected in a murine model of cutaneous squamous cell carcinoma
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Ex Vivo Treatment with Allogenic Mesenchymal Stem Cells of a Healthy Donor on Peripheral Blood Mononuclear Cells of Patients with Severe Alopecia Areata: Targeting Dysregulated T Cells and the Acquisition of Immunotolerance
- Rejuvenation by Design: Building Cosmetic Products with Extracellular Vesicle Technology, the Example of Exo.Reset®
- Scar Inhibition in Wound Healing: Mechanisms, Design, and Recent Advances
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- Disturbance of Immune Microenvironment in Androgenetic Alopecia through Spatial Transcriptomics
- Pathogenesis of Alopecia Areata and Vitiligo: Commonalities and Differences
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single‐cell RNA‐sequencing
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Induced Pluripotent Stem Cells from Human Hair Follicle Mesenchymal Stem Cells
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Differential Expression of miR-93 and miR-21 in Granulosa Cells and Follicular Fluid of Polycystic Ovary Syndrome Associating with Different Phenotypes
- Prospect of Stem Cell Conditioned Medium in Regenerative Medicine
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Amelioration of psoriasis-like skin lesions by human amniotic mesenchymal stem cells: insights from multiomics profiling in mice
- Transcriptomic analyses of regenerating adult feathers in chicken
- Prediction of the Development of Depression in Patients with Autoimmune Thyroiditis and Hypothyroidism
- FOXN1 deficient nude severe combined immunodeficiency
- Nrf2-Mediated Expansion of Pilosebaceous Cells Accelerates Cutaneous Wound Healing
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Major Differences in Expression of Inflammatory Pathways in Skin from Different Body Sites of Healthy Individuals