Works matching IS 1664-8021 AND DT 2025
Results: 277
Exploration of folate and its derivatives in grains of wheat with different colors.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1549122
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Life destiny of erythrocyte in high altitude erythrocytosis: mechanisms underlying the progression from physiological (moderate) to pathological (excessive) high-altitude erythrocytosis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1528935
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Improving accuracy and precision of heritability estimation in twin studies through hierarchical modeling: reassessing the measurement error assumption.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1522729
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Enhanced renal ischemia/reperfusion injury repair potential of exosomes derived from B7-H1<sup>high</sup> mesenchymal stem cells.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1516626
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Endoplasmic reticulum stress-related prognosis signature characterizes the immune landscape and predicts the prognosis of colon adenocarcinoma.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1516232
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Optical genome mapping with whole genome sequencing identifies complex chromosomal structural variations in acute leukemia.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1496847
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Thyroid function and hepatic fibrosis/cirrhosis: a two-sample Mendelian randomization study.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1399353
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Endoplasmic reticulum stress-related prognosis signature characterizes the immune landscape and predicts the prognosis of colon adenocarcinoma.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1516232
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De novo KCNK4 variant caused epilepsy with febrile seizures plus, neurodevelopmental abnormalities, and hypertrichosis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1499716
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Identification of a novel nonsense mutation and a recurrent missense mutation in UROS gene in a patient with congenital erythropoietic porphyria.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1486595
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A method for finding epistatic effects of maternal and fetal variants.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1420641
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Recent progress in exosomal non-coding RNAs research related to idiopathic pulmonary fibrosis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1556495
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Differentially expressed and alternately spliced genes as a novel tool for genotoxicity: a computerized study in ATT-myc transgenic mice for the recognition of genotoxic and non-genotoxic chemical.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1505379
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Etiology and clinical features of Han Chinese patients with Duane retraction syndrome.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1500090
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Integrated promoter-capture Hi-C and Hi-C analysis reveals fine-tuned regulation of the 3D chromatin architecture in colorectal cancer.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1553469
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Identification of candidate genes for drought tolerance in soybean through QTL mapping and gene expression analysis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1564160
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CirclizePlus: using ggplot2 feature to write readable R code for circular visualization.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1535368
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Natural vs. genetically engineered microbiomes: understanding public attitudes for indoor applications and pathways for future engagement.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1560601
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Adaptation of key bacterial vaginosis-associated bacteria to a medium simulating genital tract secretions: a transcriptomic analysis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1552307
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Genome-wide identification, phylogeny, and expression analysis of PEBP gene family in Castanea mollissima.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1530910
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Multi-omics pan-cancer analysis reveals the diagnostic and prognostic value of C8orf76, with experimental validation of its impact on lung adenocarcinoma cell proliferation.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1524422
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Identification of mitochondrial permeability transition-related lncRNAs as quantitative biomarkers for the prognosis and therapy of breast cancer.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1510154
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A comprehensive analysis of microRNA alteration in an ApoE(−/−) mice model of white adipose tissue injury induced by chronic intermittent hypoxia.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1474223
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Karyotype and genome size analyses for two spiders of the lycosidae family.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1544087
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Blood toxicogenomics reveals potential biomarkers for management of idiosyncratic drug-induced liver injury.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1524433
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Novel variations in the PLOD1, COL1A1, COL5A2 and COL4A1 genes related to keratoconus.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1497915
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Genetic analysis reveals the shared genetic architecture between breast cancer and atrial fibrillation.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1450259
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Genetic diversity, reproductive performance, and genetic enhancement strategies in Huang-Huai goats.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1549051
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Construction of a risk model associated with tryptophan metabolism and identification of related molecular subtypes in laryngeal squamous cell carcinoma.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1530334
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Genetic genealogy of Y-chromosome in the Zhetiru tribe of the Kazakh population from Kazakhstan.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1516130
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Multi-trait phenotypic modeling through factor analysis and bayesian network learning to develop latent reproductive, body conformational, and carcass-associated traits in admixed beef heifers.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1551967
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Cancer classification in high dimensional microarray gene expressions by feature selection using eagle prey optimization.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1528810
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Profiling X chromosome genes expression relevant to sex dimorphism in stroke: insights from transcriptomics landscape analysis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1479270
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Assessment of physician preparedness for implementation of pathology-supported genetic testing: solution-driven post-COVID-19 survey.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1543056
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A semi-supervised weighted SPCA- and convolution KAN-based model for drug response prediction.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1532651
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A panel of six immune-related mRNAs as biomarkers for tuberculosis diagnosis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1544007
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Identified five variants in CFTR gene that alter RNA splicing by minigene assay.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1543623
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Effects of drought pretreatment on the morphology traits, biomass, and stoichiometric characteristics of the desert ephemeral plant.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1534894
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MDNN-DTA: a multimodal deep neural network for drug-target affinity prediction.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1527300
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Discovery of therapeutic targets in cardiovascular diseases using high-throughput chromosome conformation capture (Hi-C).
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1515010
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Evolutionary history and divergence times of Tettigoniidae (Orthoptera) inferred from mitochondrial phylogenomics.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1495754
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Causal relationships between serum metabolites and coronary heart disease risk: a mendelian randomization study.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1440364
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Identification of key genes in periodontitis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1579848
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Editorial: Functional study of novel VUS (variant of uncertain significance) mutations in single-gene inherited disease.
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- 2025
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- Editorial
Functional analysis of a novel FBN1 deep intronic variant causing Marfan syndrome in a Chinese patient.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1564824
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Mechanism of action and experimental validation of key genes common to diabetic retinopathy and coronary heart disease based on multiple bioinformatics investigations.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1548147
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Multi-tissue transcriptomic characterization of endogenous retrovirus-derived transcripts in Capra hircus.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1544330
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Congenital heart disease presentations in the 15q11.2 microdeletion syndrome.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1535732
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Enhancing wheat β-glucan content through precision crossbreeding: development and evaluation of biofortified lines with improved nutritional and agronomic traits.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1532956
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Review of the role and potential clinical value of m6A methylation modifications in the biological process of osteosarcoma.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1522622
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