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Research 121–150 of 1000+
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Developmental genetics of color pattern establishment in cats
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Identification of the Ovine Keratin-Associated Protein 26-1 Gene and Its Association with Variation in Wool Traits
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Hair & Cutaneous Development
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Novel lysophosphoplipid receptors: their structure and function
- The Genetic Architecture of Alopecia Areata
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Congenital Adrenal Hyperplasia
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness