Publications (20) Publications in which a researcher has participated

filter_list Molecular Biology

2024

  1. Insights into the pathogenesis of primary hyperoxaluria type I from the structural dynamics of alanine:glyoxylate aminotransferase variants

    FEBS Letters, Vol. 598, Núm. 4, pp. 485-499

2023

  1. Counterintuitive structural and functional effects due to naturally occurring mutations targeting the active site of the disease-associated NQO1 enzyme*

    FEBS Journal, Vol. 290, Núm. 7, pp. 1855-1873

2022

  1. Allosteric Communication in the Multifunctional and Redox NQO1 Protein Studied by Cavity‐Making Mutations

    Antioxidants, Vol. 11, Núm. 6

  2. Different phenotypic outcome due to site-specific phosphorylation in the cancer-associated NQO1 enzyme studied by phosphomimetic mutations

    Archives of Biochemistry and Biophysics, Vol. 729

2019

  1. Correction: DUB3 and USP7 de-ubiquitinating enzymes control replication inhibitor Geminin: molecular characterization and associations with breast cancer (Oncogene, (2017), 36, 33, (4802-4809), 10.1038/onc.2017.21)

    Oncogene

  2. Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses

    Human Molecular Genetics, Vol. 28, Núm. 1, pp. 1-15

2018

  1. Evolutionary divergent suppressor mutations in conformational diseases

    Genes, Vol. 9, Núm. 7

  2. Natural (and Unnatural) Small Molecules as Pharmacological Chaperones and Inhibitors in Cancer

    Handbook of Experimental Pharmacology (Springer New York LLC), pp. 155-190

2017

  1. Erratum: DUB3 and USP7 de-ubiquitinating enzymes control replication inhibitor Geminin: molecular characterization and associations with breast cancer (Oncogene (2017) 36 33 (4802-4809))

    Oncogene

2014

  1. The consensus-Based approach for gene/enzyme replacement therapies and crystallization strategies: The case of human alanine-Glyoxylate aminotransferase

    Biochemical Journal, Vol. 462, Núm. 3, pp. 453-463

  2. The lower limits for protein stability and foldability in primary hyperoxaluria type i

    Biochimica et Biophysica Acta - Proteins and Proteomics, Vol. 1844, Núm. 12, pp. 2355-2365

2013

  1. The Role of Protein Denaturation Energetics and Molecular Chaperones in the Aggregation and Mistargeting of Mutants Causing Primary Hyperoxaluria Type I

    PLoS ONE, Vol. 8, Núm. 8

2012

  1. The hMSH2(M688R) lynch syndrome mutation may function as a dominant negative

    Carcinogenesis, Vol. 33, Núm. 9, pp. 1647-1654

2011

  1. Phenotypic correction of a mouse model for primary hyperoxaluria with adeno-associated virus gene transfer

    Molecular Therapy, Vol. 19, Núm. 5, pp. 870-875

  2. Role of low native state kinetic stability and interaction of partially unfolded states with molecular chaperones in the mitochondrial protein mistargeting associated with primary hyperoxaluria

    Amino Acids, Vol. 41, Núm. 5, pp. 1233-1245

2010

  1. Differential expression of liver and kidney proteins in a mouse model for primary hyperoxaluria type I

    FEBS Journal, Vol. 277, Núm. 22, pp. 4766-4774

  2. Structure of GroEL in complex with an early folding intermediate of alanine glyoxylate aminotransferase

    Journal of Biological Chemistry, Vol. 285, Núm. 9, pp. 6371-6376

2008

  1. Much to know about proteolysis: Intricate proteolytic machineries compromise essential cellular functions

    Biochemical Society Transactions

1996

  1. Genetic mapping of the adenine nucleotide translocase-2 gene (Ant2) to the mouse proximal X chromosome

    Genomics, Vol. 36, Núm. 2, pp. 369-371

1994

  1. Isolation and characterization of XE169, a novel human gene that escapes x-inactivation

    Human Molecular Genetics, Vol. 3, Núm. 1, pp. 153-160