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Research 30 of 764
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- The Rotterdam Study: 2016 objectives and design update
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- The genetic basis of dermatophytosis skin infection susceptibility
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