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Research 121–150 of 1000+
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Alopecia Areata
- Ottawa, Ontario, Canada, February 13–16, 2013
- The Rotterdam Study: 2016 objectives and design update
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Single-Cell Omics Advances in Understanding Tissue Development and Complex Trait Formation in Sheep and Goats
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Biology and Genetics of Hair
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Neuropsychiatric Adverse Events of Montelukast: An Analysis of Real-World Datasets and drug−gene Interaction Network
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Ophthalmologic Comorbidities in Alopecia Areata
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Risk factors for prostate cancer: An umbrella review of prospective observational studies and mendelian randomization analyses
- Data-driven strategies for drug repurposing: insights, recommendations, and case studies
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Chronic overlapping pain conditions and nociplastic pain