Related references
Note: Only part of the references are listed.Genetics of crystallins: Cataract and beyond
Jochen Graw
EXPERIMENTAL EYE RESEARCH (2009)
Alpha crystallin: The quest for a homogeneous quaternary structure
Joseph Horwitz
EXPERIMENTAL EYE RESEARCH (2009)
Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA)
Leslie Richter et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Mechanism of insolubilization by a single-point mutation in αA-crystallin linked with hereditary human cataracts
Usha P. Andley et al.
BIOCHEMISTRY (2008)
Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging
Richard I. Morimoto
GENES & DEVELOPMENT (2008)
Mechanism of small heat shock protein function in vivo -: A knock-in mouse model demonstrates that the R49C mutation in αA-crystallin enhances protein insolubility and cell death
Jing-hua Xi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Mixed oligomer formation between human αA-Crystallin and its cataract-causing G98R mutant:: Structural, stability and functional differences
Devendra Singh et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
Genetic origins of cataract
Alan Shiels et al.
ARCHIVES OF OPHTHALMOLOGY (2007)
Crystallins in the eye: Function and pathology
Usha P. Andley
PROGRESS IN RETINAL AND EYE RESEARCH (2007)
N- and C-terminal motifs in human αB crystallin play an important role in the recognition, selection, and solubilization of substrates
Joy G. Ghosh et al.
BIOCHEMISTRY (2006)
Arginine 54 and tyrosine 118 residues of αA-crystallin are crucial for lens formation and transparency
Chun-hong Xia et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
A hypomorphic mutation in the mouse laminin α5 gene causes polycystic kidney disease
M. Brendan Shannon et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2006)
Mechanism of a hereditary cataract phenotype -: Mutations in αA-crystallin activate substrate binding
Hanane A. Koteiche et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Alpha-crystallin expression affects microtubule assembly and prevents their aggregation
Jing-Hua Xi et al.
FASEB JOURNAL (2006)
A transgenic mouse model for human autosomal dominant cataract
Cheng-Da Hsu et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
Effect of site-directed mutagenesis of methylglyoxal-modifiable arginine residues on the structure and chaperone function of human αA-crystallin
A Biswas et al.
BIOCHEMISTRY (2006)
Caspase-dependent secondary lens fiber cell disintegration in αA-/αB-crystallin double-knockout mice
V Morozov et al.
DEVELOPMENT (2006)
A novel αB-crystallin mutation associated with autosomal dominant congenital lamellar cataract
YZ Liu et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
α-Crystallin localizes to the leading edges of migrating lens epithelial cells
R Maddala et al.
EXPERIMENTAL CELL RESEARCH (2005)
R120G αB-crystallin promotes the unfolding of reduced α-lactalbumin and is inherently unstable
TM Treweek et al.
FEBS JOURNAL (2005)
Ageing and vision: structure, stability and function of lens crystallins
H Bloemendal et al.
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY (2004)
Congenital hereditary cataracts
J Graw
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY (2004)
Desmin aggregate formation by R120G αB-crystallin is caused by altered filament interactions and is dependent upon network status in cells
MD Perng et al.
MOLECULAR BIOLOGY OF THE CELL (2004)
Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q
DS Mackay et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2003)
Polydispersity of a mammalian chaperone:: Mass spectrometry reveals the population of oligomers in αB-crystallin
JA Aquilina et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Alteration of cadherin in dexamethasone-induced cataract organ-cultured rat lens
J Lyu et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2003)
Reduced survival of lens epithelial cells in the αA-crystallin-knockout mouse
JH Xi et al.
JOURNAL OF CELL SCIENCE (2003)
The genetic and molecular basis of congenital eye defects
J Graw
NATURE REVIEWS GENETICS (2003)
Mechanism of chaperone function in small heat shock proteins -: Two-mode binding of the excited states of T4 lysozyme mutants by αA-crystallin
HS Mchaourab et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
The R116C mutation in αA-crystallin diminishes its protective ability against stress-induced lens epithelial cell apoptosis
UP Andley et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
α-crystallin chaperone-like activity and membrane binding in age-related cataracts
BA Cobb et al.
BIOCHEMISTRY (2002)
Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice
PC Scacheri et al.
GENESIS (2001)
Structural and functional changes in the αA-crystallin R116C mutant in hereditary cataracts
BA Cobb et al.
BIOCHEMISTRY (2000)
Differential protective activity of αA- and αB-crystallin in lens epithelial cells
UP Andley et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Structure and function of small heat shock/α-crystallin proteins:: established concepts and emerging ideas
TH MacRae
CELLULAR AND MOLECULAR LIFE SCIENCES (2000)
Mutation of R116C results in highly oligomerized αA-crystallin with modified structure and defective chaperone-like function
NP Shroff et al.
BIOCHEMISTRY (2000)
Share Paper
