VERÓNICA RAMOS MEJIA-rekin lankidetzan egindako argitalpenak (27)

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

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. 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

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

  2. The role of RUNX1 isoforms in hematopoietic commitment of human pluripotent stem cells

    Blood