Publikationen, an denen er mitarbeitet Borja Sáez Ochoa (14)

2023

  1. In vivo screening characterizes chromatin factor functions during normal and malignant hematopoiesis

    Nature Genetics, Vol. 55, Núm. 9, pp. 1542-1554

2022

  1. Deconvolution of the hematopoietic stem cell microenvironment reveals a high degree of specialization and conservation

    iScience, Vol. 25, Núm. 5

  2. The bone marrow niche regulates redox and energy balance in MLL::AF9 leukemia stem cells

    Leukemia, Vol. 36, Núm. 8, pp. 1969-1979

2021

  1. Molecular and Cellular Mechanisms of Delayed Fracture Healing in Mmp10 (Stromelysin 2) Knockout Mice

    Journal of Bone and Mineral Research, Vol. 36, Núm. 11, pp. 2203-2213

  2. Notch3 deficiency attenuates pulmonary fibrosis and impedes lung-function decline

    American Journal of Respiratory Cell and Molecular Biology, Vol. 64, Núm. 4, pp. 465-476

2020

  1. Characterization of freshly isolated mesenchymal stromal cells from healthy and multiple myeloma bone marrow: Transcriptional modulation of the microenvironment.

    Haematologica, Vol. 105, Núm. 5

  2. Engineering a humanised niche to support human haematopoiesis in mice: novel opportunities in modelling cancer

    Cancers, Vol. 12, Núm. 8, pp. 1-23

2019

  1. Role of the Extracellular Matrix in Stem Cell Maintenance

    Current Stem Cell Reports, Vol. 5, Núm. 1

2008

  1. Down-regulation of hsa-miR-10a in chronic myeloid leukemia CD34+ cells increases USF2-mediated cell growth

    Molecular Cancer Research, Vol. 6, Núm. 12, pp. 1830-1840

2007

  1. Multicolor interphase cytogenetics for the study of plasma cell dyscrasias

    Oncology Reports, Vol. 18, Núm. 5, pp. 1099-1106

  2. Multiple myeloma primary cells show a highly rearranged unbalanced genome with amplifications and homozygous deletions irrespective of the presence of immunoglobulin-related chromosome translocations

    Haematologica, Vol. 92, Núm. 6, pp. 795-802

  3. Simultaneous translocations of FGFR3/MMSET and CCND1 into two different IGH alleles in multiple myeloma: lack of concurrent activation of both proto-oncogenes

    Cancer Genetics and Cytogenetics, Vol. 175, Núm. 1, pp. 65.e1-65.e5

2006

  1. Identification of recurrent chromosomal breakpoints in multiple myeloma with complex karyotypes by combined G-banding, spectral karyotyping, and fluorescence in situ hybridization analyses

    Cancer Genetics and Cytogenetics, Vol. 169, Núm. 2, pp. 143-149

  2. Interphase FISH for the detection of breakpoints in IG loci and chromosomal changes with adverse prognostic impact in multiple myeloma with normal karyotypes

    Cancer Genetics and Cytogenetics