Publicaciones en colaboración con investigadoras/es de Universidad de Zaragoza (22)

2023

  1. Contribution of APOE Genetic Variants to Dyslipidemia

    Arteriosclerosis, Thrombosis, and Vascular Biology, Vol. 43, Núm. 6, pp. 1066-1077

2022

  1. Lipoprotein(a) in hereditary hypercholesterolemia: Influence of the genetic cause, defective gene and type of mutation

    Atherosclerosis, Vol. 349, pp. 211-218

2021

  1. All-or-none amyloid disassembly via chaperone-triggered fibril unzipping favors clearance of α-synuclein toxic species

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 118, Núm. 36

  2. Diagnostic yield of sequencing familial hypercholesterolemia genes in individuals with primary hypercholesterolemia

    Revista Espanola de Cardiologia, Vol. 74, Núm. 8, pp. 664-673

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

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

  4. Lipoprotein metabolism in familial hypercholesterolemia

    Journal of Lipid Research, Vol. 62

2020

  1. Dissecting the Structural and Chemical Determinants of the "open-To-Closed" Motion in the Mannosyltransferase PimA from Mycobacteria

    Biochemistry, Vol. 59, Núm. 32, pp. 2934-2945

  2. Predicted pathogenic mutations in STAP1 are not associated with clinically defined familial hypercholesterolemia

    Atherosclerosis, Vol. 292, pp. 143-151

  3. The extent of protein hydration dictates the preference for heterogeneous or homogeneous nucleation generating either parallel or antiparallel β-sheet α-synuclein aggregates

    Chemical Science, Vol. 11, Núm. 43, pp. 11902-11914

2019

  1. Fast and slow biomembrane solubilizing detergents: Insights into their mechanism of action

    Colloids and Surfaces B: Biointerfaces, Vol. 183

  2. Structural insights into the ability of nucleoplasmin to assemble and chaperone histone octamers for DNA deposition

    Scientific Reports, Vol. 9, Núm. 1

2018

  1. Site-specific O-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactions

    Journal of Biological Chemistry, Vol. 293, Núm. 19, pp. 7408-7422

2016

  1. A Quantitative Characterization of Nucleoplasmin/Histone Complexes Reveals Chaperone Versatility

    Scientific Reports, Vol. 6

  2. New clues to the evolutionary history of the main European paternal lineage M269: Dissection of the Y-SNP S116 in Atlantic Europe and Iberia

    European Journal of Human Genetics, Vol. 24, Núm. 3, pp. 437-441

  3. The p.Leu167del mutation in APOE gene causes autosomal dominant hypercholesterolemia by down-regulation of LDL receptor expression in hepatocytes

    Journal of Clinical Endocrinology and Metabolism, Vol. 101, Núm. 5, pp. 2113-2121

2015

  1. A Native Ternary Complex Trapped in a Crystal Reveals the Catalytic Mechanism of a Retaining Glycosyltransferase

    Angewandte Chemie - International Edition, Vol. 54, Núm. 34, pp. 9898-9902

  2. Histones cause aggregation and fusion of lipid vesicles containing phosphatidylinositol-4-phosphate

    Biophysical Journal, Vol. 108, Núm. 4, pp. 863-871

2010

  1. Energetics of nucleotide-induced DnaK conformational states

    Biochemistry, Vol. 49, Núm. 6, pp. 1338-1345

2009

  1. A Mechanism for Histone Chaperoning Activity of Nucleoplasmin: Thermodynamic and Structural Models

    Journal of Molecular Biology, Vol. 393, Núm. 2, pp. 448-463

2008

  1. Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients

    Clinical Endocrinology, Vol. 68, Núm. 6, pp. 873-878