Publicaciones en colaboración con investigadores/as de Centro de Investigaciones Biológicas (7)

2021

  1. Generation of a soluble form of human endoglin fused to green fluorescent protein

    International Journal of Molecular Sciences, Vol. 22, Núm. 20

  2. Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT-like” syndrome in children

    Molecular Genetics and Genomic Medicine, Vol. 9, Núm. 12

2020

  1. Differential expression of circulating plasma mirna-370 and mirna-10a from patients with hereditary hemorrhagic telangiectasia

    Journal of Clinical Medicine, Vol. 9, Núm. 9, pp. 1-14

2019

  1. Characterization of a family mutation in the 5’ untranslated region of the endoglin gene causative of hereditary hemorrhagic telangiectasia

    Journal of Human Genetics, Vol. 64, Núm. 4, pp. 333-339

  2. Endoglin Protein Interactome Profiling Identifies TRIM21 and Galectin-3 as New Binding Partners

    Cells, Vol. 8, Núm. 9

2018

  1. Functional analysis of a novel ENG variant in a patient with hereditary hemorrhagic telangiectasia (HHT) identifies a new Sp1 binding-site

    Gene, Vol. 647, pp. 85-92

2017

  1. Endoglin and alk1 as therapeutic targets for hereditary hemorrhagic telangiectasia

    Expert Opinion on Therapeutic Targets, Vol. 21, Núm. 10, pp. 933-947