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Research 121–150 of 1000+
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- Toward understanding scarless skin wound healing and pathological scarring
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Recent advances in understanding and managing male infertility
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Alopecias in humans: biology, pathomechanisms and emerging therapies
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Lineage Analysis of Epidermal Stem Cells
- Challenges and Strategies for Improving the Regenerative Effects of Mesenchymal Stromal Cell-Based Therapies
- The structure of people’s hair
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Predicting hair cortisol levels with hair pigmentation genes: a possible hair pigmentation bias
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- New developments in the molecular treatment of ichthyosis: review of the literature
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- 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
- 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
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature