相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Loss of Thiol Repair Systems in Human Cataractous Lenses
Min Wei et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2015)
The βγ-crystallins: Native state stability and pathways to aggregation
Eugene Serebryany et al.
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY (2014)
Amyloid Fiber Formation in Human γD-Crystallin Induced by UV-B Photodamage
Sean D. Moran et al.
BIOCHEMISTRY (2013)
The Human W42R γD-Crystallin Mutant Structure Provides a Link between Congenital and Age-related Cataracts
Fangling Ji et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Deamidation of Asparagine to Aspartate Destabilizes Cu, Zn Superoxide Dismutase, Accelerates Fibrillization, and Mirrors ALS-Linked Mutations
Yunhua Shi et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2013)
Tryptophan Cluster Protects Human D-Crystallin from Ultraviolet Radiation-Induced Photoaggregation In Vitro
Nathaniel Schafheimer et al.
PHOTOCHEMISTRY AND PHOTOBIOLOGY (2013)
Crystal structure of the cataract-causing P23T D-crystallin mutant
Fangling Ji et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2013)
UV-radiation Induced Disruption of Dry-Cavities in Human γD-crystallin Results in Decreased Stability and Faster Unfolding
Zhen Xia et al.
SCIENTIFIC REPORTS (2013)
Structural and Biochemical Characterization of the Childhood Cataract-Associated R76S Mutant of Human γD-Crystallin
Fangling Ji et al.
BIOCHEMISTRY (2012)
The Evolution of Multimeric Protein Assemblages
Michael Lynch
MOLECULAR BIOLOGY AND EVOLUTION (2012)
Kinetic mechanism of p53 oncogenic mutant aggregation and its inhibition
Rainer Wilcken et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Protein misfolding and aggregation in cataract disease and prospects for prevention
Kate L. Moreau et al.
TRENDS IN MOLECULAR MEDICINE (2012)
Molecular basis of α1-antitrypsin deficiency revealed by the structure of a domain-swapped trimer
Masayuki Yamasaki et al.
EMBO REPORTS (2011)
A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family
Binbin Wang et al.
HUMAN MUTATION (2011)
Characterization of a Transient Unfolding Intermediate in a Core Mutant of γS-Crystallin
Bryon Mahler et al.
JOURNAL OF MOLECULAR BIOLOGY (2011)
α-Synuclein occurs physiologically as a helically folded tetramer that resists aggregation
Tim Bartels et al.
NATURE (2011)
Gain of function of mutant p53 by coaggregation with multiple tumor suppressors
Jie Xu et al.
NATURE CHEMICAL BIOLOGY (2011)
Dynamic local unfolding in the serpin α-1 antitrypsin provides a mechanism for loop insertion and polymerization
Beena Krishnan et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)
The ageing lens and cataract: a model of normal and pathological ageing
R. Michael et al.
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2011)
Lens fibre cell differentiation and organelle loss: many paths lead to clarity
Michael A. Wride
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2011)
Aggregation of γ-crystallins associated with human cataracts via domain swapping at the C-terminal β-strands
Payel Das et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Intermolecular transmission of superoxide dismutase 1 misfolding in living cells
Leslie I. Grad et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
The genes underlying the process of speciation
Patrik Nosil et al.
TRENDS IN ECOLOGY & EVOLUTION (2011)
A Single Destabilizing Mutation (F9S) Promotes Concerted Unfolding of an Entire Globular Domain in γS-Crystallin
Soojin Lee et al.
JOURNAL OF MOLECULAR BIOLOGY (2010)
Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS
Daryl A. Bosco et al.
NATURE NEUROSCIENCE (2010)
Wild-type human SOD1 overexpression does not accelerate motor neuron disease in mice expressing murine Sod1G86R
Jean-Nicolas Audet et al.
NEUROBIOLOGY OF DISEASE (2010)
Phase behavior of mixtures of human lens proteins Gamma D and Beta B1
Ying Wang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Heterozygosity for a coding SNP in COL1A2 confers a lower BMD and an increased stroke risk
Katarina Lindahl et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2009)
The Structure of the Cataract-Causing P23T Mutant of Human γD-Crystallin Exhibits Distinctive Local Conformational and Dynamic Changes
Jinwon Jung et al.
BIOCHEMISTRY (2009)
The Cataract-Associated R14C Mutant of Human γD-Crystallin Shows a Variety of Intermolecular Disulfide Cross-Links: A Raman Spectroscopic Study
Ajay Pande et al.
BIOCHEMISTRY (2009)
Mechanism of the Very Efficient Quenching of Tryptophan Fluorescence in Human γD- and γS-Crystallins: The γ-Crystallin Fold May Have Evolved To Protect Tryptophan Residues from Ultraviolet Photodamage
Jiejin Chen et al.
BIOCHEMISTRY (2009)
Hydrophobic Core Mutations Associated with Cataract Development in Mice Destabilize Human γD-Crystallin
Kate L. Moreau et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Transmission and spreading of tauopathy in transgenic mouse brain
Florence Clavaguera et al.
NATURE CELL BIOLOGY (2009)
Amyloid formation by globular proteins under native conditions
Fabrizio Chiti et al.
NATURE CHEMICAL BIOLOGY (2009)
Converging concepts of protein folding in vitro and in vivo
F. Ulrich Hartl et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2009)
Prions: Protein Aggregation and Infectious Diseases
Adriano Aguzzi et al.
PHYSIOLOGICAL REVIEWS (2009)
Proteomic analysis of the oxidation of cysteine residues in human age-related nuclear cataract lenses
Peter G. Hains et al.
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS (2008)
Heterodimer formation of wild-type and amyotrophic lateral sclerosis-causing mutant Cu/Zn-superoxide dismutase induces toxicity independent of protein aggregation
Heidrun Witan et al.
HUMAN MOLECULAR GENETICS (2008)
Intense neutral drifts yield robust and evolvable consensus proteins
Shimon Bershtein et al.
JOURNAL OF MOLECULAR BIOLOGY (2008)
Folding and stability of the isolated Greek key domains of the long-lived human lens proteins γD-crystallin and γS-crystallin
Ishara A. Mills et al.
PROTEIN SCIENCE (2007)
Post-translational modifications in the nuclear region of young, aged, and cataract human lenses
Peter G. Hains et al.
JOURNAL OF PROTEOME RESEARCH (2007)
Glutamine deamidation destabilizes human γD-crystallin and lowers the kinetic barrier to unfolding
Shannon L. Flaugh et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
The Hb A variant (β73 Asp→Leu) disrupts Hb S polymerization by a novel mechanism
Kazuhiko Adachi et al.
JOURNAL OF MOLECULAR BIOLOGY (2006)
Kinetics and thermodynamics of amyloid fibril assembly
Ronald Wetzel
ACCOUNTS OF CHEMICAL RESEARCH (2006)
Deposition diseases and 3D domain swapping
Melanie J. Bennett et al.
STRUCTURE (2006)
Interdomain side-chain interactions in human γD crystallin influencing folding and stability
SL Flaugh et al.
PROTEIN SCIENCE (2005)
Age-related nuclear cataract - oxidation is the key
RJW Truscott
EXPERIMENTAL EYE RESEARCH (2005)
Regulation of tissue oxygen levels in the mammalian lens
R McNulty et al.
JOURNAL OF PHYSIOLOGY-LONDON (2004)
Probing folding and fluorescence quenching in human γD crystallin Greek key domains using triple tryptophan mutant proteins
MS Kosinski-Collins et al.
PROTEIN SCIENCE (2004)
High-resolution X-ray crystal structures of human γD crystallin (1.25 Å) and the R58H mutant (1.15 Å) associated with aculeiform cataract
A Basak et al.
JOURNAL OF MOLECULAR BIOLOGY (2003)
In vitro unfolding, refolding, and polymerization of human γD crystallin, a protein involved in cataract formation
MS Kosinski-Collins et al.
PROTEIN SCIENCE (2003)
Protein aggregation and aggregate toxicity: new insights into protein folding, misfolding diseases and biological evolution
M Stefani et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2003)
Protein aggregation in disease: a role for folding intermediates forming specific multimeric interactions
A Horwich
JOURNAL OF CLINICAL INVESTIGATION (2002)
Three-dimensional domain swapping in p13suc1 occurs in the unfolded state and is controlled by conserved proline residues
F Rousseau et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)