Publicaciones en colaboración con investigadores/as de Universidad de Málaga (22)

2024

  1. NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

    Movement Disorders

  2. Toll-like receptors ligand immunomodulators for the treatment congenital diaphragmatic hernia

    Orphanet Journal of Rare Diseases , Vol. 19, Núm. 1

2021

  1. Aradyal: The spanish multidisciplinary research network for allergic diseases

    Journal of Investigational Allergology and Clinical Immunology, Vol. 31, Núm. 2, pp. 108-119

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

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

  3. Kidins220 deficiency causes ventriculomegaly via SNX27-retromer-dependent AQP4 degradation

    Molecular Psychiatry, Vol. 26, Núm. 11, pp. 6411-6426

  4. Nanoarchitectures for efficient IgE cross-linking on effector cells to study amoxicillin allergy

    Allergy: European Journal of Allergy and Clinical Immunology, Vol. 76, Núm. 10, pp. 3183-3193

2019

  1. Synergistic effect of Si-hydroxyapatite coating and VEGF adsorption on Ti6Al4V-ELI scaffolds for bone regeneration in an osteoporotic bone environment

    Acta Biomaterialia, Vol. 83, pp. 456-466

2018

  1. Phenotype-loci associations in networks of patients with rare disorders: application to assist in the diagnosis of novel clinical cases

    European Journal of Human Genetics, Vol. 26, Núm. 10, pp. 1451-1461

2017

  1. C3G promotes a selective release of angiogenic factors from activated mouse platelets to regulate angiogenesis and tumor metastasis

    Oncotarget, Vol. 8, Núm. 67, pp. 110994-111011

2016

  1. Single administration of recombinant IL-6 restores the gene expression of lipogenic enzymes in liver of fasting IL-6-deficient mice

    British Journal of Pharmacology, Vol. 173, Núm. 6, pp. 1070-1084

  2. Systematic identification of phenotypically enriched loci using a patient network of genomic disorders

    BMC Genomics, Vol. 17, Núm. 1

2015

  1. Kpath: Integration of metabolic pathway linked data

    Database, Vol. 2015

2014

  1. Biocomputational resources useful for drug discovery against compartmentalized targets

    Current Pharmaceutical Design, Vol. 20, Núm. 2, pp. 293-300

  2. PhenUMA: A tool for integrating the biomedical relationships among genes and diseases

    BMC Bioinformatics, Vol. 15, Núm. 1

2013

  1. Developmental and tumoral vascularization is regulated by G protein-coupled receptor kinase 2

    Journal of Clinical Investigation, Vol. 123, Núm. 11, pp. 4714-4730

  2. Global Analysis of the Human Pathophenotypic Similarity Gene Network Merges Disease Module Components

    PLoS ONE, Vol. 8, Núm. 2

  3. Met signaling in cardiomyocytes is required for normal cardiac function in adult mice

    Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1832, Núm. 12, pp. 2204-2215

2012

  1. A combined model of hepatic polyamine and sulfur amino acid metabolism to analyze S-adenosyl methionine availability

    Amino Acids, Vol. 42, Núm. 2-3, pp. 597-610

  2. Histamine: An undercover agent in multiple rare diseases?

    Journal of Cellular and Molecular Medicine, Vol. 16, Núm. 9, pp. 1947-1960

  3. Regulatory cross-talk of mouse liver polyamine and methionine metabolic pathways: A systemic approach to its physiopathological consequences

    Amino Acids, Vol. 42, Núm. 2-3, pp. 577-595