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Research 271–300 of 1000+
- Biomedical applications of organoids in genetic diseases
- MiR‐200c‐3p as a novel genetic marker and therapeutic tool for alopecia areata
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients
- Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Biology of the hair follicle and mechanisms of nonscarring and scarring alopecia
- Recent omics advances in hair aging biology and hair biomarkers analysis
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss
- Claves diagnósticas en displasias pilosas II
- What does the research say about androgen use and cerebrovascular events?
- Overview of Alopecia Areata
- Poliosis circumscripta: Overview and underlying causes
- Keratinocyte biology and pathology
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- The exposome impact on hair health: etiology, pathogenesis and clinical features ‒ Part I
- Leveraging Single Nucleotide Polymorphism Profiling for Precision Skin Care: How SNPs Shape Individual Responses in Cosmetic Dermatology
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- Exploring the Relationship Between Immune Cells and Non-Scarring Hair Loss: A Mendelian Randomization Study
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Pathology in Practice
- Serum Paroxonase 1 Level and Androgenetic Alopecia: Correspondence