Genetics & genomics
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- Insights into the Evolution of Ohnologous Sequences and Their Epigenetic Marks Post-WGD in Malus Domestica
- Evolutionary transitions in social organization and the relationship between climate and queen number in ant societies
- Revisiting genome-guided RNA localization in bacteria
- A robust and accurate two-sample Mendelian randomization method with a large number of genetic variants
- Beyond the Vertebrate Model: Insights from Insect Stress Responses
- The Openness–Constraint Spectrum: Module Integrity and the Evolutionary Reversibility of Fungal Traits
- Double Mutations in the FLNA and MYH11 Genes Causing Familial Thoracic Aortic Aneurysm and Dissection: A Report of Two Cases
- From embryo flushing to in vitro production: global trends in livestock reproductive biotechnology
- The analysis of genetic variants in nine patients with nemaline myopathy: implications for diagnosis and genetic counseling
- From prompts to genomes: A constraint-first framework for AI-driven sequence design across life and viruses
- Sickle cell disease screening: Experiences of parents with positive newborns at Korle Bu TeachingHospital
- Recognition and function analysis of MKK6 in immune reaction against Vibrio Parahaemolyticus in Crassostrea hongkongensis
- Low-frequency parasitized cells in bone marrow alter myelopoiesis following immunization with the live attenuated Leishmania major Cen−/− vaccine
- An intrinsically disordered domain of transcription terminator Rho governs genome-wide Rho utilization ( Rut ) site selection in Mycobacterium tuberculosis
- Elevational Melanism in East African Honey Bees Involves a Major-Effect Locus
- Heterosis in crosses between remnant populations of the rare prairie forb Silene regia: Implications for restoration genetics
- A patient-derived missense mouse model of Kabuki syndrome 1
- Integrative taxonomy of Trichogramma vitessoides sp. nov. (Hymenoptera, Trichogrammatidae), an egg parasitoid of Heortia vitessoides from southern China.
- Case Report: Concurrent maternal uniparental disomy-type Prader-Willi syndrome and X-linked G6PD deficiency-an area of focus on multi-gene screening for imprinting disorders.
- Case Report: transient migratory pulmonary nodules with bronchial artery malformations in an autosomal dominant polycystic kidney disease patient: a case of recurrent hemoptysis.
- A novel LARP7 variant expands the phenotypic spectrum of Alazami syndrome and reveals transcriptomic dysregulation of developmental and extracellular matrix pathways.
- Dietary intake and nutritional profiles characterize patients with Inflammatory Bowel Disease from Argentina.
- Circulating cell-death-associated biomarkers and inflammatory severity in Hymenoptera sting envenomation: a single-center retrospective study.
- Synthetic genome shuffling of poxviruses in yeast generates novel poxvirus candidates with potential oncolytic properties.
- Transcriptomic identification of high-altitude illness candidate genes and physiological mechanisms: a multidimensional bioinformatics study with 106 drug-food homologous substance target prediction.