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Research 151–180 of 1000+
- Alopecias in humans: biology, pathomechanisms and emerging therapies
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Technological Advances in Anti-hair Loss and Hair Regrowth Cosmeceuticals: Mechanistic Breakthroughs and Industrial Prospects Driven by Multidisciplinary Collaborative Innovation
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Design of Liposome Formulations for CRISPR/Cas9 Enzyme Immobilization: Evaluation of 5-Alpha-Reductase Enzyme Knockout for Androgenic Disorders
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Diverse cellular players orchestrate regeneration after wounding
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Regulatory T cells in dominant immunologic tolerance
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies