Works matching IS 1756994X AND DT 2025 AND VI 17 AND IP 1
Results: 12
Digital twins as global learning health and disease models for preventive and personalized medicine.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01435-7
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- Article
Imaging flow cytometry-based cellular screening elucidates pathophysiology in individuals with Variants of Uncertain Significance.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01433-9
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Multi-omics uncovers immune-modulatory molecules in plasma contributing to resistance exercise-ameliorated locomotor disability after incomplete spinal cord injury.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01434-8
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- Article
Intricate interplay of CRISPR-Cas systems, anti-CRISPR proteins, and antimicrobial resistance genes in a globally successful multi-drug resistant Klebsiella pneumoniae clone.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01428-6
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A new method for detecting mixed Mycobacterium tuberculosis infection and reconstructing constituent strains provides insights into transmission.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01430-y
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- Article
Integrating pharmacogenomics and cheminformatics with diverse disease phenotypes for cell type-guided drug discovery.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01431-x
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- Article
Nanopore-based random genomic sampling for intraoperative molecular diagnosis.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01427-7
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- Article
Meta-analyses of mouse and human prostate single-cell transcriptomes reveal widespread epithelial plasticity in tissue regression, regeneration, and cancer.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01432-w
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- Article
A rare haplotype of the GJD3 gene segregating in familial Meniere's disease interferes with connexin assembly.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-024-01425-1
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- Article
TP53 germline testing and hereditary cancer: how somatic events and clinical criteria affect variant detection rate.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-025-01429-5
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- Article
SenPred: a single-cell RNA sequencing-based machine learning pipeline to classify deeply senescent dermal fibroblast cells for the detection of an in vivo senescent cell burden.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-024-01418-0
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- Article
Clinical evaluation of long-read sequencing-based episignature detection in developmental disorders.
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- Genome Medicine, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13073-024-01419-z
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- Article