Lista de obras - Jesús Zurdo - Dominio Público Uruguay

Amyloid fibril formation and seeding by wild-type human lysozyme and its disease-related mutational variants.

artículo científico publicado en 2000

Assembly ofSaccharomyces cerevisiaeRibosomal Stalk: Binding of P1 Proteins Is Required for the Interaction of P2 Proteins†

artículo científico publicado en 2000

Competing intrachain interactions regulate the formation of beta-sheet fibrils in bovine PrP peptides.

artículo científico publicado en 2003

Cryo-electron microscopy structure of an SH3 amyloid fibril and model of the molecular packing

artículo científico publicado en 1999

De novo designed peptide-based amyloid fibrils

artículo científico publicado en 2002

Exploring amyloid formation by a de novo design

scholarly article

Formation and seeding of amyloid fibrils from wild-type hen lysozyme and a peptide fragment from the β-domain

artículo científico publicado en 2000

Formation of insulin amyloid fibrils followed by FTIR simultaneously with CD and electron microscopy.

artículo científico publicado en 2000

Identification of a novel human islet amyloid polypeptide beta-sheet domain and factors influencing fibrillogenesis

artículo científico publicado en 2001

Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases

artículo científico publicado en 2002

Molecular recycling within amyloid fibrils

artículo científico publicado en 2005

Polypeptide models to understand misfolding and amyloidogenesis and their relevance in protein design and therapeutics.

artículo científico publicado en 2005

Prediction of "aggregation-prone" and "aggregation-susceptible" regions in proteins associated with neurodegenerative diseases

artículo científico publicado en 2005

Prediction of the Absolute Aggregation Rates of Amyloidogenic Polypeptide Chains

Preparation and Characterization of Purified Amyloid Fibrils

artículo científico publicado en 2001

Probing the mechanism of amyloidogenesis through a tandem repeat of the PI3-SH3 domain suggests a generic model for protein aggregation and fibril formation

artículo científico publicado en 2006

Protein aggregation and amyloid fibril formation by an SH3 domain probed by limited proteolysis

artículo científico publicado en 2003

Protein folding and misfolding: a paradigm of self-assembly and regulation in complex biological systems

artículo científico publicado en 2003

Short amino acid stretches can mediate amyloid formation in globular proteins: the Src homology 3 (SH3) case

artículo científico publicado en 2004

Structural Differences betweenSaccharomyces cerevisiaeRibosomal Stalk Proteins P1 and P2 Support Their Functional Diversity†

artículo científico publicado en 2000

The structural role of the carotenoid in the bacterial light-harvesting protein 2 (LH2) of Rhodonbacter capsulatus. A Fourier transform Raman spectroscopy and circular dichroism study.

artículo científico publicado en 1995

Transition from natively unfolded to folded state induced by desiccation in an anhydrobiotic nematode protein

artículo científico publicado en 2003

Lista de obras de Jesús Zurdo

Amyloid fibril formation and seeding by wild-type human lysozyme and its disease-related mutational variants.

Assembly ofSaccharomyces cerevisiaeRibosomal Stalk: Binding of P1 Proteins Is Required for the Interaction of P2 Proteins†

Competing intrachain interactions regulate the formation of beta-sheet fibrils in bovine PrP peptides.

Cryo-electron microscopy structure of an SH3 amyloid fibril and model of the molecular packing

De novo designed peptide-based amyloid fibrils

Exploring amyloid formation by a de novo design

Formation and seeding of amyloid fibrils from wild-type hen lysozyme and a peptide fragment from the β-domain

Formation of insulin amyloid fibrils followed by FTIR simultaneously with CD and electron microscopy.

Identification of a novel human islet amyloid polypeptide beta-sheet domain and factors influencing fibrillogenesis

Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases

Molecular recycling within amyloid fibrils

Polypeptide models to understand misfolding and amyloidogenesis and their relevance in protein design and therapeutics.

Prediction of "aggregation-prone" and "aggregation-susceptible" regions in proteins associated with neurodegenerative diseases

Prediction of the Absolute Aggregation Rates of Amyloidogenic Polypeptide Chains

Preparation and Characterization of Purified Amyloid Fibrils

Probing the mechanism of amyloidogenesis through a tandem repeat of the PI3-SH3 domain suggests a generic model for protein aggregation and fibril formation

Protein aggregation and amyloid fibril formation by an SH3 domain probed by limited proteolysis

Protein folding and misfolding: a paradigm of self-assembly and regulation in complex biological systems

Short amino acid stretches can mediate amyloid formation in globular proteins: the Src homology 3 (SH3) case

Structural Differences betweenSaccharomyces cerevisiaeRibosomal Stalk Proteins P1 and P2 Support Their Functional Diversity†

The structural role of the carotenoid in the bacterial light-harvesting protein 2 (LH2) of Rhodonbacter capsulatus. A Fourier transform Raman spectroscopy and circular dichroism study.

Transition from natively unfolded to folded state induced by desiccation in an anhydrobiotic nematode protein