Genetics & genomics
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- Dual maternal origin and dispersal history of peach (Prunus persica) from China
- Exploring the Pleiotropic Genetic Architecture of Substance Use Disorders: Findings From Phenome-Wide Association Studies.
- Pseudomonas aeruginosa mgtC gene is under the control of PhoP and CbrAB regulators, and its expression can be visualized in macrophages
- Prognostic impact of variants of uncertain significance (VUS) in BRCA genes and homologous recombination repair (HRR) genes in prostate cancer: a real-world multicenter study.
- GAMETE maps the genetic architecture of chromatin accessibility in rice pollen at single-nucleus resolution.
- Asphyxiating thoracic dystrophy associated with IFT74 pathogenic variant: a case report.
- Characterization of the frameshift c.515dupC knock-in mouse model of HSPB8-associated myopathy (MFM13) and evaluation of Trehalose as autophagy modulating therapy.
- Integration of multi-tissue transcriptomic data identifies key regulatory genes for porcine fat deposition.
- Genetic architecture of node-specific leaf length and candidate gene identification in maize revealed by a temperate-tropical multiparental population.
- Bee Microbiomes Across Phylogeny and Functional Traits: Examining Host-Cleptoparasite Associations.
- Germline genetic risk and prostate cancer–specific mortality in a population-based incident cohort
- Molecular methods for differentiating Phragmites australis subspecies and identification of hybrid stands in the Upper Midwestern United States
- A phage-derived promoter SD13 enables strong and cross-host gene expression in Streptomyces and Escherichia coli.
- Emanuel syndrome: a physiotherapy overview.
- Robotic surgery in inflammatory bowel disease: a systematic review.
- Multi-biobank genome-wide association study of dermatochalasis implicates genes involved in skin biology and morphology
- Protective Effect of the Apolipoprotein L1 p.N264K Variant Against CKD among People with HIV Carrying Apolipoprotein L1 High-Risk Genotypes
- Improved detection of low-level GNAQ mosaicism in Sturge-Weber syndrome through affected tissue testing, deep sequencing, and HRM-qPCR
- Birth order and disease risk across the human phenome
- Polarized macrophage-derived microvesicles differentially modulate intestinal barrier dysfunction and endoplasmic reticulum stress in ulcerative colitis.
- Contractile morning glory disc anomaly associated with total retinal detachment: a case report.
- Congenital fibrovascular pupillary membrane with secondary glaucoma and associated fundus anomalies: a case report and literature review.
- NDUFV1 activation mediates high glucose-induced apoptosis in peritoneal mesothelial cells.
- Epidemiological profile of accidents involving venomous animals: a descriptive and time series study, Maranhão, 2014-2024.
- Structure and Function of the Type IX Secretion System for Protein Secretion and Cellular Motility