Genetics & genomics
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- A high-resolution protein-RNA binding atlas for structure-aware interaction prediction and post-transcriptional regulatory modeling
- Convergent genome evolution reveals shared routes to salt tolerance in flowering plants
- Dog-human gene network colocalization links synaptic signalling and ubiquitination to compulsive disorders
- A Genome-Wide Association Study Links AEBP2 to Litter Size in Meishan Pigs.
- Adaptation and Retention of Digitally Fabricated Presurgical Orthopedic Plates for Infants with Cleft Lip and Palate.
- Multi-model genome-wide association analysis reveals natural allelic variation and candidate loci for kernel phytic acid content in quality protein maize.
- Global trends and hotspots of genetic research on non-syndromic cleft lip with or without cleft palate: a bibliometric and bioinformatics analysis.
- International practice patterns in the management of pouchitis: results from a global survey
- Genetic mapping of QTL controlling kernel protein content in maize using multiple DH populations
- Integrated GWAS, TWAS, and functional enrichment reveal candidate genes for claw and hoof traits in Jiangsu Jersey cattle
- Pitfalls and challenges in endoscopic assessment of ulcerative colitis.
- Architect or Destroyer: The Diversity of Glucocorticoid Receptor Signaling Pathways in the Brain
- The CYFIP2 Arg87Cys Mutation Reshapes the Interactome and Alters Stress Fiber-Associated Proteins
- High-altitude gastric disorders: insights into maladaptation pathophysiological mechanisms, disease spectrum and prevention strategies
- Cellular mechanism of gain-of-function mutation I173M in sheep MC4R gene identified in year-round and seasonal estrus breeds through whole-genome resequencing
- Mutational divergence over years in local populations of the selfing nematode Caenorhabditis elegans
- Repeated mutation of a GT92 glycosyltransferase gene confers antiviral resistance in two Caenorhabditis species
- Heterozygous Mutations in MAP3K7 , Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome
- Loss of function variants in ADAMTS6: a new connective tissue disorder with heart defect, aortic aneurysm and neurodevelopmental features
- Uncovering the historic genetic diversity of Ugandan Robusta coffee germplasm: a foundation for core collection design
- Hip region muscular dystrophy and emergence of motor deficits in dysferlin-deficient Bla/J mice
- Host‐Associated Bacterial Community Changes After Laboratory Introduction Vary With Wolbachia Presence
- KLK15 alters connective tissues in hypermobile Ehlers-Danlos syndrome
- Evaluating imputation methods for determining North American honey bee (Apis mellifera) ancestry from low-pass whole-genome sequencing data
- The multifaceted role of SsrB in S. Typhi H58 during THP-1 macrophage infection