Search
for
Sort by
Research 571–600 of 787
- Hormonal interventions in skin wounds – a mini review
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- The Silent Syndrome of Long COVID and Gaps in Scientific Knowledge: A Narrative Review
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens)
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- PolyQ length co-evolution in neural proteins
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Coffea arabica: An Emerging Active Ingredient in Dermato-Cosmetic Applications
- The causal relationship between gut microbiota and alopecia areata: a Mendelian randomization analysis
- Genetically determined metabolites in allergic conjunctivitis: A Mendelian randomization study
- Update on the Potential of <i>Punica granatum</i> L. Traditional Uses and Pharmacological Uses: A Review
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Use of Antiandrogens as Therapeutic Agents in COVID-19 Patients
- Selection signatures for fiber production in commercial species: A review
- An update of polycystic ovary syndrome: causes and therapeutics options
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Case-Only Trees and Random Forests for Exploring Genotype-Specific Treatment Effects in Randomized Clinical Trials with Dichotomous End Points
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Genetic Control/Involvement in Hair Fiber Traits
- Forensic skeletal and molecular anthropology face to face: Combining expertise for identification of human remains
- MultiKano: an automatic cell type annotation tool for single-cell multi-omics data based on Kolmogorov–Arnold network and data augmentation