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Research 91–120 of 1000+
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- 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
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Genome-Wide Association Study of Fiber Diameter in Alpacas