Publikationen in Zusammenarbeit mit Forschern von Centro de Investigaciones Biológicas (61)

2023

  1. Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration

    Autophagy, Vol. 19, Núm. 3, pp. 784-804

  2. Ag2S Biocompatible Ensembles as Dual OCT Contrast Agents and NIR Ocular Imaging Probes

    Small, Vol. 19, Núm. 49

  3. The Absence of FAIM Leads to a Delay in Dark Adaptation and Hampers Arrestin-1 Translocation upon Light Reception in the Retina

    Cells, Vol. 12, Núm. 3

2022

  1. Insulin receptor activation by proinsulin preserves synapses and vision in retinitis pigmentosa

    Cell Death and Disease, Vol. 13, Núm. 4

  2. Targeting retinoic acid receptor alpha-corepressor interaction activates chaperone-mediated autophagy and protects against retinal degeneration

    Nature Communications, Vol. 13, Núm. 1

  3. The inhibition of NCS-1 binding to Ric8a rescues fragile X syndrome mice model phenotypes

    Frontiers in Neuroscience, Vol. 16

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. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

  3. HDAC inhibition ameliorates cone survival in retinitis pigmentosa mice

    Cell Death and Differentiation, Vol. 28, Núm. 4, pp. 1317-1332

  4. 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

  5. Tlr2 gene deletion delays retinal degeneration in two genetically distinct mouse models of retinitis pigmentosa

    International Journal of Molecular Sciences, Vol. 22, Núm. 15

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

  2. Oxidative Stress and Lymphocyte Alterations in Chronic Relapsing Experimental Allergic Encephalomyelitis in the Rat Hippocampus and Protective Effects of an Ethanolamine Phosphate Salt

    Molecular Neurobiology, Vol. 57, Núm. 2, pp. 860-878

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

  3. Insights into real-time chemical processes in a calcium sensor protein-directed dynamic library

    Nature Communications, Vol. 10, Núm. 1

2018

  1. Deciphering the Inhibition of the Neuronal Calcium Sensor 1 and the Guanine Exchange Factor Ric8a with a Small Phenothiazine Molecule for the Rational Generation of Therapeutic Synapse Function Regulators

    Journal of Medicinal Chemistry, Vol. 61, Núm. 14, pp. 5910-5921

  2. 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

  3. Modulation of GSK-3 provides cellular and functional neuroprotection in the rd10 mouse model of retinitis pigmentosa

    Molecular Neurodegeneration, Vol. 13, Núm. 1

2017

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

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