GENOMAS, CÁNCER Y ENVEJECIMIENTO (PROVISIONAL)
GenCanAge
Institut d'Investigació Biomédica de Bellvitge
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Institut d'Investigació Biomédica de Bellvitge (11)
2022
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Detection of early seeding of Richter transformation in chronic lymphocytic leukemia
Nature Medicine, Vol. 28, Núm. 8, pp. 1662-1671
2020
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The MNT transcription factor autoregulates its expression and supports proliferation in MYC-associated factor X (MAX)-deficient cells
Journal of Biological Chemistry, Vol. 295, Núm. 7, pp. 2001-2017
2019
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Chromosome 12p amplification in triple-negative/BRCA1-mutated breast cancer associates with emergence of docetaxel resistance and carboplatin sensitivity
Cancer Research, Vol. 79, Núm. 16, pp. 4258-4270
2018
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Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1
Nature Communications, Vol. 9, Núm. 1
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Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance
DMM Disease Models and Mechanisms, Vol. 11, Núm. 5
2017
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Stem cell-like transcriptional reprogramming mediates metastatic resistance to mTOR inhibition
Oncogene, Vol. 36, Núm. 19, pp. 2737-2749
2016
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Loss of the proteostasis factor AIRAPL causes myeloid transformation by deregulating IGF-1 signaling
Nature Medicine, Vol. 22, Núm. 1, pp. 91-96
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Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis
Scientific Reports, Vol. 6
2015
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Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine
EMBO Molecular Medicine, Vol. 7, Núm. 5, pp. 608-627
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Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype
Gut, Vol. 64, Núm. 2, pp. 355-356
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Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair
Gastroenterology, Vol. 149, Núm. 3, pp. 563-566