Works matching IS 1664-8021 AND DT 2025
Results: 224
Bioinformatics revealed biomarkers for diagnosis in kidney stones.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1542840
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Cotton under heat stress: a comprehensive review of molecular breeding, genomics, and multi-omics strategies.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1553406
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Retrospective analysis of inflammatory biomarkers and prognosis in non-small cell lung cancer without adenocarcinoma in situ.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1549602
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Genetic diversity and population structure of non-descript cattle in South African smallholder systems.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1535730
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Structural characteristics of mitochondrial genome of Spirobo-lus walkeri (Spirobolida: Spirobolidae), and phylogenetic analysis of Diplopoda.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1566634
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weIMPUTE: a user-friendly web-based genotype imputation platform.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1532464
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Exploring the oncogenic role and prognostic value of CKS1B in human lung adenocarcinoma and squamous cell carcinoma.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1449466
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Case report: Novel homozygous ACVRL1 missense variant in a family with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension: findings suggest a hypomorphic allele.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1554624
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Emotional dispositions and intracerebral hemorrhage: a Mendelian Randomization insight.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1330682
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Corrigendum: Case report and literature review: delayed diagnosis of ARCL1B due to a newly reported homozygous mutation c.464A>C p. (Tyr155Ser) in the EFEMP2 gene.
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- 2025
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- Correction Notice
Identification and validation of key biomarkers associated with immune and oxidative stress for preeclampsia by WGCNA and machine learning.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1500061
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Case Report and literature review: Delayed diagnosis of ARCL1B due to a newly reported homozygous mutation c.464A>C p. (Tyr155Ser) in the EFEMP2 gene.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1453195
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Editorial: The non-coding RNA world in animals and plants.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1558406
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Sequencing whole genomes of the West Javanese population in Indonesia reveals novel variants and improves imputation accuracy.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1492602
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ADAM-multi: software to simulate complex breeding programs for animals and plants with different ploidy levels and generalized genotypic effect models to account for multiple alleles.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1513615
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Negative frequency-dependent selection through variations in seedling fitness due to genetic differentiation of parents' pair in a tropical rainforest tree, Rubroshorea curtisii (Dipterocarpaceae).
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1552024
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Noncoding RNA profiling in omentum adipose tissue from obese patients and the identification of novel metabolic biomarkers.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1533637
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Editorial: Towards the embedding of artificial intelligence into synthetic organisms: engineering intelligence in microorganisms.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1562092
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Exploring the relationship between sepsis and Golgi apparatus dysfunction: bioinformatics insights and diagnostic marker discovery.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1483493
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A structural genomics approach to investigate Dystrophin mutations and their impact on the molecular pathways of Duchenne muscular dystrophy.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1517707
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Genomic selection for resistance to one pathogenic strain of Vibrio splendidus in blue mussel Mytilus edulis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1487807
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Genome-wide identification of oat TCP gene family and expression patterns under abiotic stress.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1533562
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Systematic review and meta-analysis of the impact of abnormal expression of long non coding RNA on the prognosis of acute myeloid leukemia.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1524449
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Enhancing the utility of polygenic scores in Alzheimer's disease through systematic curation and annotation.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1507395
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Circular RNA microarray expression profile and potential function of circDOCK1 in colorectal cancer.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1443876
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Fresh-cut watermelon: postharvest physiology, technology, and opportunities for quality improvement.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1523240
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Integrated analysis of M2 macrophage-related gene prognostic model and single-cell sequence to predict immunotherapy response in lung adenocarcinoma.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1519677
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Mendelian randomization and multiomics comprehensively reveal the causal relationship and potential mechanism between atrial fibrillation and gastric cancer.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1446661
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Molecular genetic analysis of Rubinstein–Taybi syndrome in Russian patients.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1516565
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Revealing study and breeding implications for production traits and tail characteristics in Simmental cattle by GWAS.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1491816
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Identification of a novel SPTB gene splicing mutation in hereditary spherocytosis: a case report and diagnostic insights.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1522204
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Clinical phenotype and genetic analysis of patients with severe oligoasthenospermia carrying heterozygous SOHLH1 c.346-1G>A mutation.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1531697
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GOLPH3 inhibits glioma cell apoptosis through the JNK signaling pathway.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1518573
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Antimicrobial resistance in diverse urban microbiomes: uncovering patterns and predictive markers.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1460508
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Genome-wide identification and expression analysis of GRAS transcription factors under cold stress in diploid and triploid Eucalyptus.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1436285
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Based on bioinformatics, SESN2 negatively regulates ferroptosis induced by ischemia reperfusion via the System Xc−/GPX4 pathway.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1504114
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Identifying health risk determinants and molecular targets in patients with idiopathic pulmonary fibrosis via combined differential and weighted gene co-expression analysis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1496462
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ZINQ-L: a zero-inflated quantile approach for differential abundance analysis of longitudinal microbiome data.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1494401
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Quadratic descriptors and reduction methods in a two-layered model for compound inference.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1483490
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Bibliometric analysis of ferroptosis: a comprehensive evaluation of its contribution to lung cancer.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1449491
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Corrigendum: Codon usage is influenced by compositional constraints in genes associated with dementia.
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- 2025
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- Correction Notice
Editorial: Systems biology approaches to psychiatric and psychological disorders: unraveling the complexities.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1547943
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Case report: Discovery of novel CTNNB1 mutations and comparison of clinical characteristics in two patients with NEDSDV.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1502756
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Impacts of stem cells from different sources on wound healing rate in diabetic foot ulcers: a systematic review and meta-analysis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1541992
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Machine learning potential predictor of idiopathic pulmonary fibrosis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1464471
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Mendelian randomization analysis reveals genetic evidence for a causal link between inflammatory bowel disease and uterine cervical neoplasms.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1436512
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Vitamin A family suppresses periodontitis by restoring mitochondrial metabolic reprogramming in macrophages through JAK-STAT pathway.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1505933
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Characterization of novel human endogenous retrovirus structures on chromosomes 6 and 7.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1498978
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The role of SPINK5 mutation distribution in phenotypes of Netherton syndrome.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1475054
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Identification of key genes underlying radiosensitivity and radioresistance in endometrial cancer through integrated bioinformatics analysis.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1469610
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