Publications en collaboration avec des chercheurs de Institut d'Investigació Biomédica de Bellvitge (19)

2023

  1. Apoptotic cell death in disease—Current understanding of the NCCD 2023

    Cell Death and Differentiation, Vol. 30, Núm. 5, pp. 1097-1154

2022

  1. Detection of early seeding of Richter transformation in chronic lymphocytic leukemia

    Nature Medicine, Vol. 28, Núm. 8, pp. 1662-1671

2020

  1. 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

  1. 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

  1. Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1

    Nature Communications, Vol. 9, Núm. 1

  2. Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance

    DMM Disease Models and Mechanisms, Vol. 11, Núm. 5

2017

  1. Stem cell-like transcriptional reprogramming mediates metastatic resistance to mTOR inhibition

    Oncogene, Vol. 36, Núm. 19, pp. 2737-2749

2016

  1. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

  3. Loss of the proteostasis factor AIRAPL causes myeloid transformation by deregulating IGF-1 signaling

    Nature Medicine, Vol. 22, Núm. 1, pp. 91-96

  4. Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis

    Scientific Reports, Vol. 6

2015

  1. 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

  2. Essential versus accessory aspects of cell death: Recommendations of the NCCD 2015

    Cell Death and Differentiation, Vol. 22, Núm. 1, pp. 58-73

  3. Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype

    Gut, Vol. 64, Núm. 2, pp. 355-356

  4. Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

    Gastroenterology, Vol. 149, Núm. 3, pp. 563-566

2010

  1. Epigenetic repression of ROR2 has a Wnt-mediated, pro-tumourigenic role in colon cancer

    Molecular Cancer, Vol. 9

2009

  1. Genetic inactivation of ADAMTS15 metalloprotease in human colorectal cancer

    Cancer Research, Vol. 69, Núm. 11, pp. 4926-4934

  2. The ADAMTS12 metalloprotease gene is epigenetically silenced in tumor cells and transcriptionally activated in the stroma during progression of colon cancer

    Journal of Cell Science, Vol. 122, Núm. 16, pp. 2906-2913

2007

  1. Molecular characterization of a t(9;12)(p21;q13) balanced chromosome translocation in combination with integrative genomics analysis identifies C9orf14 as a candidate tumor-suppressor

    Genes Chromosomes and Cancer, Vol. 46, Núm. 2, pp. 155-162