Publicacións (13) Publicacións nas que participase algún/ha investigador/a

filter_list Molecular Biology

2020

  1. Modeling PrPSc Generation Through Deformed Templating

    Frontiers in Bioengineering and Biotechnology, Vol. 8

2018

  1. Cofactors influence the biological properties of infectious recombinant prions

    Acta Neuropathologica, Vol. 135, Núm. 2, pp. 179-199

2017

  1. The Structure of Mammalian Prions and Their Aggregates

    International Review of Cell and Molecular Biology (Elsevier Inc.), pp. 277-301

  2. The Structure of the Infectious Prion Protein and Its Propagation

    Progress in Molecular Biology and Translational Science (Elsevier B.V.), pp. 341-359

2016

  1. The Structural Architecture of an Infectious Mammalian Prion Using Electron Cryomicroscopy

    PLoS Pathogens, Vol. 12, Núm. 9

2015

  1. Proteinase K and the structure of PrPSc: The good, the bad and the ugly

    Virus Research, Vol. 207, pp. 120-126

2014

  1. Loss of Prion Protein Leads to Age-Dependent Behavioral Abnormalities and Changes in Cytoskeletal Protein Expression

    Molecular Neurobiology, Vol. 50, Núm. 3, pp. 923-936

2012

  1. Histological and molecular features of lipomatous and nonlipomatous adipose tissue in familial partial lipodystrophy caused by LMNA mutations

    Clinical Endocrinology, Vol. 76, Núm. 6, pp. 816-824

  2. Structural Organization of Mammalian Prions as Probed by Limited Proteolysis

    PLoS ONE, Vol. 7, Núm. 11

2009

  1. Oligomer assembly of the C-terminal DISC1 domain (640-854) is controlled by self-association motifs and disease-associated polymorphism S704C

    Biochemistry, Vol. 48, Núm. 32, pp. 7746-7755

2008

  1. Scrapie Prion Protein Structural Constraints Obtained by Limited Proteolysis and Mass Spectrometry

    Journal of Molecular Biology, Vol. 382, Núm. 1, pp. 88-98

2006

  1. Isolation and characterization of a proteinase K-sensitive PrP Sc fraction

    Biochemistry, Vol. 45, Núm. 51, pp. 15710-15717

  2. High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect

    Clinical Endocrinology, Vol. 64, Núm. 3, pp. 330-336