Publicacions en col·laboració amb investigadors/es de University of Chicago (10)

2017

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

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

2016

  1. Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease

    American Journal of Human Genetics, Vol. 98, Núm. 6, pp. 1193-1207

2014

  1. The role of complement in tumor growth

    Advances in Experimental Medicine and Biology

2003

  1. A t(11;15) fuses MLL to two different genes, AF15q14 and a novel gene MPFYVE on chromosome 15

    Oncogene, Vol. 22, Núm. 9, pp. 1400-1410

  2. Identification of candidate tumor-suppressor genes in 6q27 by combined deletion mapping and electronic expression profiling in lymphoid neoplasms

    Genes Chromosomes and Cancer, Vol. 37, Núm. 4, pp. 421-426

  3. Molecular cytogenetic characterization of breakpoints in 19 patients with hematologic malignancies and 12p unbalanced translocations

    Cancer Genetics and Cytogenetics, Vol. 142, Núm. 2, pp. 115-119

2002

  1. A novel gene, MDS2, is fused to ETV6/TEL in a t(1;12)(p36.1;p13) in a patient with myelodysplastic syndrome

    Genes Chromosomes and Cancer, Vol. 35, Núm. 1, pp. 11-19

2001

  1. Further characterization of complex chromosomal rearrangements in myeloid malignancies: Spectral karyotyping adds precision in defining abnormalities associated with poor prognosis [1]

    Leukemia

  2. Identification of new translocations involving ETV6 in hematologic malignancies by fluorescence in situ hybridization and spectral karyotyping

    Genes Chromosomes and Cancer, Vol. 31, Núm. 2, pp. 134-142

2000

  1. Cytogenetic and molecular analysis of the acute monocytic leukemia cell line THP-1 with an MLL-AF9 translocation

    Genes Chromosomes and Cancer, Vol. 29, Núm. 4, pp. 333-338