PEDRO JOSÉ REAL LUNA-rekin lankidetzan egindako argitalpenak (30)

2023

  1. Lentiviral gene therapy reverts GPIX expression and phenotype in Bernard-Soulier syndrome type C

    Molecular Therapy - Nucleic Acids, Vol. 33, pp. 75-92

  2. 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

2019

  1. Enhanced hemato-endothelial specification during human embryonic differentiation through developmental cooperation between AF4-MLL and MLL-AF4 fusions

    Haematologica, Vol. 104, Núm. 6, pp. 1189-1201

  2. 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

  3. 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

2018

  1. The IS2 Element Improves Transcription Efficiency of Integration-Deficient Lentiviral Vector Episomes

    Molecular Therapy - Nucleic Acids, Vol. 13, pp. 16-28

2017

  1. 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

  2. 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. Absence of WASp enhances hematopoietic and megakaryocytic differentiation in a human embryonic stem cell model

    Molecular Therapy, Vol. 24, Núm. 2, pp. 342-353

  2. 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

  3. 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

  4. 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

  5. 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

  2. Generation of human iPSC line GRX-MCiPS4F-A2 from adult peripheral blood mononuclear cells (PBMCs) with Spanish genetic background

    Stem Cell Research, Vol. 15, Núm. 2, pp. 337-340

  3. SCL/TAL1-mediated transcriptional network enhances megakaryocytic specification of human embryonic stem cells

    Molecular Therapy, Vol. 23, Núm. 1, pp. 158-170

  4. The Notch ligand DLL4 specifically marks human hematoendothelial progenitors and regulates their hematopoietic fate

    Leukemia, Vol. 29, Núm. 8, pp. 1741-1753

2014

  1. HOXA9 promotes hematopoietic commitment of human embryonic stem cells

    Blood, Vol. 124, Núm. 20, pp. 3065-3075

  2. Ligand-independent FLT3 activation does not cooperate with MLL-AF4 to immortalize/transform cord blood CD34+ cells

    Leukemia, Vol. 28, Núm. 3, pp. 666-674