Publicacións nas que colabora con ROSA MARÍA MONTES LORENZO (19)

2023

  1. The pediatric leukemia oncoprotein NUP98-KDM5A induces genomic instability that may facilitate malignant transformation

    Cell Death and Disease, Vol. 14, Núm. 6

2022

  1. Generation of a H9 Clonal Cell Line With Inducible Expression of NUP98-KDM5A Fusion Gene in the AAVS1 Safe Harbor Locus

    Frontiers in Cell and Developmental Biology, Vol. 10

2020

  1. The molecular clock protein Bmal1 regulates cell differentiation in mouse embryonic stem cells

    Life Science Alliance, Vol. 3, Núm. 5

2019

  1. GENYOi004-A: An induced pluripotent stem cells (iPSCs)line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation

    Stem Cell Research, Vol. 37

  2. GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant

    Stem Cell Research, Vol. 41

2017

  1. Establishment of 2 control and 2 hPSC cell lines constitutively expressing the Notch ligand DLL4

    Stem Cell Research, Vol. 25, pp. 274-277

  2. Hoxa9 and EGFP reporter expression in human Embryonic Stem Cells (hESC) as useful tools for studying human development

    Stem Cell Research, Vol. 25, pp. 286-290

  3. Induced pluripotent stem cells derived from Bernard-Soulier Syndrome patient's peripheral blood cells with a p.Phe55Ser mutation in the GPIX gene

    Stem Cell Research, Vol. 20, pp. 10-13

  4. New hPSC-based human models to study pediatric Acute Megakaryoblastic Leukemia harboring the fusion oncogene RBM15-MKL1

    Stem Cell Research, Vol. 19, pp. 1-5

  5. RUNX1c Regulates Hematopoietic Differentiation of Human Pluripotent Stem Cells Possibly in Cooperation with Proinflammatory Signaling

    Stem Cells, Vol. 35, Núm. 11, pp. 2253-2266

2016

  1. Erratum: Corrigendum to “Generation of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX gene” (Stem Cell Research (2016) 16(3) (692–695) (S1873506116300253) (10.1016/j.scr.2016.04.013))

    Stem Cell Research

  2. Generation of a human induced pluripotent stem cell (iPSC) line from a Bernard-Soulier syndrome patient with the mutation p.Asn45Ser in the GPIX gene

    Stem Cell Research, Vol. 17, Núm. 3, pp. 603-606

  3. Generation of human pluripotent stem cell lines with suppressed expression of the Notch ligand DLL4 using short hairpin RNAs

    Stem Cell Research, Vol. 16, Núm. 3, pp. 735-739

  4. Generation of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX gene

    Stem Cell Research, Vol. 16, Núm. 3, pp. 692-695

2015

  1. Generation and characterization of the human iPSC line PBMC1-iPS4F1 from adult peripheral blood mononuclear cells

    Stem Cell Research, Vol. 15, Núm. 3, pp. 614-617

2013

  1. FLT3 activation cooperates with MLL-AF4 fusion protein to abrogate the hematopoietic specification of human ESCs

    Blood, Vol. 121, Núm. 19, pp. 3867-3878

2012

  1. A human ESC model for MLL-AF4 leukemic fusion gene reveals an impaired early hematopoietic-endothelial specification

    Cell Research, Vol. 22, Núm. 6, pp. 986-1002

  2. Intrahepatic transplantation of cord blood CD34+ cells into newborn NOD/SCID-IL2Rγnull mice allows efficient multi-organ and multi-lineage hematopoietic engraftment without accessory cells

    Clinical Immunology

2009

  1. Mesenchymal stem cells facilitate the derivation of human embryonic stem cells from cryopreserved poor-quality embryos

    Human Reproduction, Vol. 24, Núm. 8, pp. 1844-1851