Found: 13
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Genetics, diet, microbiota, and metabolome: partners in crime for colon carcinogenesis.
- Published in:
- Clinical & Experimental Medicine, 2024, v. 24, n. 1, p. 1, doi. 10.1007/s10238-024-01505-x
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- Article
BAP1 Loss, Nuclear Grading, and Nonepithelioid Features in the Diagnosis of Mesothelioma in Italy: Nevermore without the Pathology Report.
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- Journal of Personalized Medicine, 2024, v. 14, n. 4, p. 394, doi. 10.3390/jpm14040394
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- Article
Sensitivity to asbestos is increased in patients with mesothelioma and pathogenic germline variants in BAP1 or other DNA repair genes.
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- Genes, Chromosomes & Cancer, 2018, v. 57, n. 11, p. 573, doi. 10.1002/gcc.22670
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- Article
Distinct Signatures of Tumor-Associated Microbiota and Metabolome in Low-Grade vs. High-Grade Dysplastic Colon Polyps: Inference of Their Role in Tumor Initiation and Progression.
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- Cancers, 2023, v. 15, n. 12, p. 3065, doi. 10.3390/cancers15123065
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- Article
Serum Extracellular Vesicle-Derived microRNAs as Potential Biomarkers for Pleural Mesothelioma in a European Prospective Study.
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- Cancers, 2023, v. 15, n. 1, p. 125, doi. 10.3390/cancers15010125
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- Article
New DNA Methylation Signals for Malignant Pleural Mesothelioma Risk Assessment.
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- Cancers, 2021, v. 13, n. 11, p. 2636, doi. 10.3390/cancers13112636
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- Article
DNA Methylation of FKBP5 as Predictor of Overall Survival in Malignant Pleural Mesothelioma.
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- Cancers, 2020, v. 12, n. 11, p. 3470, doi. 10.3390/cancers12113470
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- Article
Heterogeneous RNA editing and influence of ADAR2 on mesothelioma chemoresistance and the tumor microenvironment.
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- Molecular Oncology, 2022, v. 16, n. 22, p. 3949, doi. 10.1002/1878-0261.13322
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- Article
Diagnostics of BAP1 -Tumor Predisposition Syndrome by a Multitesting Approach: A Ten-Year-Long Experience.
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- Diagnostics (2075-4418), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/diagnostics12071710
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- Article
Double-Stranded RNA Structural Elements Holding the Key to Translational Regulation in Cancer: The Case of Editing in RNA-Binding Motif Protein 8A.
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- Cells (2073-4409), 2021, v. 10, n. 12, p. 3543, doi. 10.3390/cells10123543
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- Article
Deficiency of ribosomal protein S26, which is mutated in a subset of patients with Diamond Blackfan anemia, impairs erythroid differentiation.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.1045236
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- Article
A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond–Blackfan anemia.
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- Human Mutation, 2018, v. 39, n. 8, p. 1102, doi. 10.1002/humu.23551
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- Article
Author Correction: Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35522-0
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- Article