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Research 271–300 of 501
- A Study of Combined Genotype Effects of SHCBP1 on Wool Quality Traits in Chinese Merino
- Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Developmental genetics of color pattern establishment in cats
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- The autoimmune basis of alopecia areata: A comprehensive review
- Selective blockade of γc pathway ameliorates alopecia areata in a humanized murine model
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- The genetic link between thyroid dysfunction and alopecia areata: a bidirectional two-sample Mendelian randomization study
- Author response: Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- Whole-genome resequencing to investigate the genetic diversity and the molecular basis underlying key economic traits in indigenous sheep breeds adapted to hypoxic environments
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves