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Research 181–210 of 1000+
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- <i>Hoxc13</i> mutant mice lack external hair
- Association of a polymorphism in the ornithine decarboxylase gene with male androgenetic alopecia
- Clinical Management in Psychodermatology
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Antihelminthic Drugs
- A review on follicular targeting for the treatment of hirsutism
- Oral Presentations
- Light scattering from human hair fibers
- Androgen binding profiles of two distinct nuclear androgen receptors in Atlantic croaker (Micropogonias undulatus)
- Profiling the Response of Human Hair Follicles to Ultraviolet Radiation
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Genetic prediction of male pattern baldness
- Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possible pathophysiologic mechanisms
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Genetic basis of polycystic ovary syndrome
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- Causal Relationship Between Sleep Characteristics and Alopecia Areata and Other Non-Scarring Alopecia: A Two-Sample Bidirectional Mendelian Randomization Analysis