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Research 211–240 of 1000+
- Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
- Contaminants of emerging concern in the fetal environment
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Ethnicity, obesity and the prevalence of impaired glucose tolerance and type 2 diabetes in PCOS: a systematic review and meta-regression
- Defining the identity of mouse embryonic dermal fibroblasts
- Data-driven strategies for drug repurposing: insights, recommendations, and case studies
- Does a male polycystic ovarian syndrome equivalent exist?
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- Factors associated with early-onset androgenetic alopecia: A scoping review
- 9. Immunology and Genetics
- Ottawa, Ontario, Canada, February 13–16, 2013
- 5. HIV, Fungal and Infectious Diseases
- The Rotterdam Study: 2016 objectives and design update
- TGF-β family signaling in stem cells
- Evaluation of the Relationship between Alopecia Areata and Viral Antigen Exposure
- Male pattern baldness and incidence of prostate cancer
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Mechanisms Involved in the Relationship between Vitamin D and Insulin Resistance: Impact on Clinical Practice
- Drug Repositioning with GraphSAGE and Clustering Constraints Based on Drug and Disease Networks
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- E-Poster
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Evaluating the Causal Relationship Between Human Blood Metabolites and the Susceptibility to Alopecia Areata
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases