Publications in collaboration with researchers from Institut d'Investigació Biomédica de Bellvitge (22)

2024

  1. TDP-43 regulates LC3ylation in neural tissue through ATG4B cryptic splicing inhibition

    Acta Neuropathologica, Vol. 148, Núm. 1

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

  2. Neurofibromatosis type 1 families with first-degree relatives harbouring distinct NF1 pathogenic variants. Genetic counselling and familial diagnosis: what should be offered?

    Journal of Medical Genetics, Vol. 59, Núm. 10, pp. 1017-1023

2019

  1. Chromatin regulation by Histone H4 acetylation at Lysine 16 during cell death and differentiation in the myeloid compartment

    Nucleic Acids Research, Vol. 47, Núm. 10, pp. 5016-5037

  2. 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

2012

  1. A DNA methylation signature associated with aberrant promoter DNA hypermethylation of DNMT3B in human colorectal cancer

    European Journal of Cancer, Vol. 48, Núm. 14, pp. 2270-2281

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