Genetics & genomics
3,278 studies221 in 7 days1,369 in 30 days
Filters
Latest
3,278 studies
- Overcoming Detection Lag in a Cryptic Panzootic: Chytrid Invasion Linked to Historically Enigmatic Amphibian Declines in the Brazilian Atlantic Forest
- Rhizosphere Fungal Community Responses to Nitrogen Addition Reflect Genotypic Versus Trait Variation in the Marsh Sedge Schoenoplectus americanus Over Time
- CD180-Associated B-Cell Alterations in Type 1 Diabetes and the In Vitro Effects of Chlorogenic Acid: An Integrated Transcriptomic and Experimental Study
- Inter‐ and Intraspecific Variation in Web Architecture and Its Significance in Australian Funnel‐Web Spiders (Atracidae)
- AcNR1F orchestrates epidermal remodeling to enable host adaptation in Angiostrongylus cantonensis
- Genome-Wide DNA methylation profiling of tissue-plasma pairs identifies Novel cfDNA biomarkers for the diagnosis of gastric cancer
- Ten simple rules to build genomics capacity for routine laboratory practice in the Global South
- A systematic review and meta-analysis of immunosuppressive regimens and immune-related outcomes in adeno-associated virus-based gene therapy
- Public preferences for investigative genetic genealogy (IGG) programs: A discrete choice experiment.
- The ytrGABCDEF operon controls cell size, growth arrest, and lysis of distinct Bacillus subtilis subpopulations
- Population-scale immune multiome atlas reveals regulatory disease mechanisms
- From retina to brain: Viral tools for targeting retinal cells and mapping visual circuits
- Polygenic Risk Scores of Coronary Heart Disease in Chronic Kidney Disease Population: The CRIC Study
- Genomic and biochemical contexts determine the physiological role of a horizontally acquired gene
- Development and qualification of quantitative assays for detecting process-related nucleic acid impurities in recombinant AAV preparations
- Isolated add(12)(p13) in a BCR::ABL1-Negative Neutrophilic Myeloproliferative Neoplasm Lacking Canonical Driver Mutations: A Case Report
- Cockayne Syndrome Phenotype in a Sudanese Child With a Homozygous ERCC8 Splice-Site Variant of Uncertain Significance: A Case Report
- Blueberry Muffin Sign: A Diagnostic Histochemical Clue in Mitochondrial Myopathy
- Sex-dependent DNA methylation in amyotrophic lateral sclerosis
- PKA disrupts adult ovarian identity circuits through direct inhibition of TRIM28-chromatin binding
- Chromosome-scale genome assembly of the North American invasive Asteraceae, Tanacetum vulgare (common tansy)
- Synergistic effects of hypergravity and immune challenge on the zebrafish larval transcriptome
- Analysis of Naturally Arising Simple Deletions in Single Human Colon Crypts with Age
- Gene transcriptional profiling to assess Chinook salmon osmoregulatory resilience to salinity challenges
- Recent effective population size of the snowy owl (Bubo scandiacus) tracks historical climate variation