Genetics & genomics
3,226 studies192 in 7 days1,333 in 30 days
Filters
Latest
3,226 studies
- IscR-mediated morphological regulation confers virulence and stress resistance by reducing stress molecule uptake in Acinetobacter baumannii
- Carboxypeptidase activity drives L,D-transpeptidase essentiality during vegetative growth and sporulation in Clostridioides difficile
- Comparative immunogenomics of Suidae reveals lineage-specific immune gene disruption and positive selection
- Integrative omics reveals candidate drug-repurposing targets in Tritrichomonas foetus
- Balancing Prolificacy and Lamb Meat Production: Links Among Litter Size, Prenatal Development, Carcass Traits, and Meat Quality in Sheep.
- Genome-Wide Association Study of Body Measurement Traits at Birth in Cattle.
- Biomechanical strain patterns in Meckel's cartilage underlie mandibular variation in FGFR2 mouse models.
- DNAAF19-RUVBL1/2 complex recruits multiple adaptors to promote dynein arm assembly.
- Two D-loop resolution systems enable natural genetic transformation in bacteria.
- Cell-type-specific repression reveals MC4R neurons as a site of action for ciliary obesity genes.
- Association of Topical Therapy and Surgical Management with Corneal Parameters in Congenital PAX6-Related Classical Aniridia: a Cross-Sectional Study.
- Introgression line libraries in melon (Cucumis melo L.): development, genetic insights, and applications in trait dissection and crop improvement.
- Design and model choices shape inference of age-varying genetic effects on complex traits.
- Evidence-Tiered Venomics of the BotG50 Toxic Fraction from Buthus tunetanus Reveals a Diversified Neurotoxin Repertoire
- Diagnostic pathways in developmental disorders: a decade-apart comparison of two multicenter cohorts (2012–2022)
- Genome-wide scans between two honeybee populations reveal putative signatures of human-mediated selection
- Loss of Snord115 mitigates Snord116-driven sleep abnormalities in mouse models of Prader-Willi syndrome
- Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears
- Mutations in the Endothelin Receptor Type A Cause Mandibulofacial Dysostosis with Alopecia
- Goat genome assemblies, nine breeds for pangenome contribution
- Chromosomal genomes assemblies of twelve sheep breeds
- CardamomOT: A mechanistic optimal transport-based framework for gene regulatory network inference, trajectory reconstruction and generative modeling
- GlRac regulates an ATG8-independent autophagy-like pathway in Giardia lamblia
- HiFIseek: Gene-specific enrichment of high-impact mutations in associated genomic regions
- Spatial Transcriptomics As Rasterized Image Tensors (STARIT) characterizes cell states with subcellular molecular heterogeneity