(Q37678803)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20090208%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

review article

1 reference

title

Mouse models of cataract (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20090208%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20090208%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

author name string

Jochen Graw

series ordinal

1

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21 August 2017

1 December 2009

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20090208%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20090208%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

volume

88

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20090208%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20090208%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

page(s)

469-486

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20090208%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s12041-009-0066-2

17 January 2020

exact match

0 references

cites work

Induction of gene mutations in mice: the multiple endpoint approach.

1 reference

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The genetic and molecular basis of congenital eye defects

21 January 2018

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Looking forward to 20/20: a focus on the epidemiology of eye diseases

21 January 2018

1 reference

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Ephrin-A5 regulates the formation of the ascending midbrain dopaminergic pathways

21 January 2018

1 reference

12 December 2020

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin

1 reference

12 December 2020

Cataracts and abnormal proliferation of the lens epithelium in mice carrying the CatFr gene

1 reference

12 December 2020

Genetical and biochemical studies of a dominant cataract mutant in mice

1 reference

12 December 2020

The gene mutated in bare patches and striated mice encodes a novel 3beta-hydroxysteroid dehydrogenase

1 reference

12 December 2020

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

1 reference

12 December 2020

AlphaB-crystallin in lens development and muscle integrity: a gene knockout approach

1 reference

12 December 2020

Altered Na,K-ATPase pattern in gamma-crystallin mutant mice.

1 reference

12 December 2020

A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice

1 reference

12 December 2020

v-maf, a viral oncogene that encodes a "leucine zipper" motif

1 reference

12 December 2020

Deletion mutation in an eye lens beta-crystallin. An animal model for inherited cataracts

1 reference

12 December 2020

Selective loss of dopaminergic neurons in the substantia nigra of Pitx3-deficient aphakia mice

1 reference

12 December 2020

Glucose intolerance in a xenotransplantation model: studies in alpha-gal knockout mice.

1 reference

12 December 2020

Dominant cataract mutations induced by gamma-irradiation of male mice

1 reference

12 December 2020

Novel HSF4 mutation causes congenital total white cataract in a Chinese family

1 reference

12 December 2020

Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma

1 reference

12 December 2020

Novel ENU-induced eye mutations in the mouse: models for human eye disease

1 reference

12 December 2020

A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation

1 reference

12 December 2020

Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse.

1 reference

12 December 2020

Cardiac malformation in neonatal mice lacking connexin43.

1 reference

12 December 2020

Mutation screening of HSF4 in 150 age-related cataract patients

1 reference

12 December 2020

Congenital hereditary cataracts

1 reference

12 December 2020

The gamma S-crystallin gene is mutated in autosomal recessive cataract in mouse

1 reference

12 December 2020

Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataract

1 reference

12 December 2020

Changes in connexin expression and distribution during chick lens development.

1 reference

12 December 2020

Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene

1 reference

12 December 2020

A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in Asians

1 reference

12 December 2020

Late onset hereditary cataract of the emory mouse. A model for human senile cataract

1 reference

12 December 2020

A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract

1 reference

12 December 2020

EPHA2 is associated with age-related cortical cataract in mice and humans

1 reference

12 December 2020

Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract

1 reference

12 December 2020

Genetics of crystallins: cataract and beyond.

1 reference

12 December 2020

Targeted disruption of the mouse alpha A-crystallin gene induces cataract and cytoplasmic inclusion bodies containing the small heat shock protein alpha B-crystallin

1 reference

12 December 2020

A gene location for the inheritance of the cataract Fraser (CatFr) mouse congenital cataract

1 reference

12 December 2020

A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish family

1 reference

12 December 2020

Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations

1 reference

12 December 2020

Pax6 3' deletion results in aniridia, autism and mental retardation

1 reference

12 December 2020

Novel allele of crybb2 in the mouse and its expression in the brain.

1 reference

12 December 2020

A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q

1 reference

12 December 2020

Defining a link between gap junction communication, proteolysis, and cataract formation

1 reference

12 December 2020

Genetic and environmental factors in age-related nuclear cataracts in monozygotic and dizygotic twins

1 reference

12 December 2020

Nuclear breakdown during terminal differentiation of primary lens fibres in mice: a transmission electron microscopic study

1 reference

12 December 2020

Pitx3 is required for development of substantia nigra dopaminergic neurons.

1 reference

12 December 2020

Differential expression of alpha A- and alpha B-crystallin during murine ocular development.

1 reference

12 December 2020

Human gamma-crystallin genes. A gene family on its way to extinction

1 reference

12 December 2020

Identification of a mutation in the MP19 gene, Lim2, in the cataractous mouse mutant To3

1 reference

12 December 2020

Targeted ablation of connexin50 in mice results in microphthalmia and zonular pulverulent cataracts.

1 reference

12 December 2020

A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice

1 reference

12 December 2020

Implementing large-scale ENU mutagenesis screens in North America

1 reference

12 December 2020

Bilateral congenital cataracts result from a gain-of-function mutation in the gene for aquaporin-0 in mice

1 reference

12 December 2020

Structural changes in lenses of mice lacking the gap junction protein connexin43

1 reference

12 December 2020

Recessive congenital total cataract with microcornea and heterozygote carrier signs caused by a novel missense CRYAA mutation (R54C)

1 reference

12 December 2020

A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2

1 reference

12 December 2020

DNase activity in murine lenses: implications for cataractogenesis.

1 reference

12 December 2020

Subfertility in mice harboring a mutation in betaB2-crystallin

1 reference

12 December 2020

Sox1 directly regulates the gamma-crystallin genes and is essential for lens development in mice

1 reference

12 December 2020

Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract

1 reference

12 December 2020

Mouse small eye results from mutations in a paired-like homeobox-containing gene

1 reference

12 December 2020

Recessive transmission of a multiple endocrine neoplasia syndrome in the rat

1 reference

12 December 2020

Disruption of alpha3 connexin gene leads to proteolysis and cataractogenesis in mice

1 reference

12 December 2020

Spectrum of ENU-induced mutations in phenotype-driven and gene-driven screens in the mouse.

1 reference

12 December 2020

A novel function of DNA repair molecule Nbs1 in terminal differentiation of the lens fibre cells and cataractogenesis.

1 reference

12 December 2020

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

1 reference

12 December 2020

The EPHA2 gene is associated with cataracts linked to chromosome 1p

1 reference

12 December 2020

A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan

1 reference

12 December 2020

Lens opacity: a new gene for congenital cataract on chromosome 10 of the mouse

1 reference

12 December 2020

Expression of betaB(2)-crystallin mRNA and protein in retina, brain, and testis

1 reference

12 December 2020

Mutations in the founder of the MIP gene family underlie cataract development in the mouse.

1 reference

12 December 2020

Cooperative action between L-Maf and Sox2 on delta-crystallin gene expression during chick lens development.

1 reference

12 December 2020

Gap junctions containing alpha8-connexin (MP70) in the adult mammalian lens epithelium suggests a re-evaluation of its role in the lens

1 reference

12 December 2020

Two new cataract loci, Ccw and To3, and further mapping of the Npp and Opj cataracts in the mouse

1 reference

12 December 2020

Early developmental failure of substantia nigra dopamine neurons in mice lacking the homeodomain gene Pitx3

1 reference

12 December 2020

gammaN-crystallin and the evolution of the betagamma-crystallin superfamily in vertebrates

1 reference

12 December 2020

Elongation of axons during regeneration involves retinal crystallin beta b2 (crybb2).

1 reference

12 December 2020

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

1 reference

12 December 2020

Pairing SOX off: with partners in the regulation of embryonic development

1 reference

12 December 2020

A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family

1 reference

12 December 2020

Histological and biochemical characterization of the murine cataract mutant Nop

1 reference

12 December 2020

The mouse Cat4 locus maps to chromosome 8 and mutants express lens-corneal adhesion

1 reference

12 December 2020

Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genes.

1 reference

12 December 2020

Morphological study of the cataractous lens of the senescence accelerated mouse

1 reference

12 December 2020

A mouse model of galactose-induced cataracts

1 reference

12 December 2020

Targeted deletion of the lens fiber cell-specific intermediate filament protein filensin

1 reference

12 December 2020

Focus on molecules: Pax-6, the eye master

1 reference

12 December 2020

Induction of lens differentiation by activation of a bZIP transcription factor, L-Maf.

1 reference

12 December 2020

Cataract- and lens-specific upregulation of ARK receptor tyrosine kinase in Emory mouse cataract.

1 reference

12 December 2020

Relationship of Pax6 activity levels to the extent of eye development in the mouse, Mus musculus

1 reference

12 December 2020

Denucleation process of the lens.

1 reference

12 December 2020

Radiation cataracts: mechanisms involved in their long delayed occurrence but then rapid progression.

1 reference

12 December 2020

Atm heterozygous mice are more sensitive to radiation-induced cataracts than are their wild-type counterparts.

1 reference

12 December 2020

Xcat, a novel mouse model for Nance-Horan syndrome inhibits expression of the cytoplasmic-targeted Nhs1 isoform

1 reference

12 December 2020

Impaired learning and memory in Pitx3 deficient aphakia mice: a genetic model for striatum-dependent cognitive symptoms in Parkinson's disease

1 reference

12 December 2020

Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse

1 reference

12 December 2020

A frameshift mutation in the gamma E-crystallin gene of the Elo mouse

1 reference

12 December 2020

Synergistic effect of osmotic and oxidative stress in slow-developing cataract formation

1 reference

12 December 2020

Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy

1 reference

12 December 2020

Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2

1 reference

12 December 2020

Temporal expression of three mouse lens fiber cell membrane protein genes during early development.

1 reference

12 December 2020

A mutation in the Pax-6 gene in rat small eye is associated with impaired migration of midbrain crest cells

1 reference

12 December 2020

Regulation of mouse lens fiber cell development and differentiation by the Maf gene

1 reference

12 December 2020

Knockout of the intermediate filament protein CP49 destabilises the lens fibre cell cytoskeleton and decreases lens optical quality, but does not induce cataract

1 reference

12 December 2020

Connexins: functions without junctions

1 reference

12 December 2020

Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice.

1 reference

12 December 2020

Autosomal recessive juvenile onset cataract associated with mutation in BFSP1.

1 reference

12 December 2020

The cataract-inducing S50P mutation in Cx50 dominantly alters the channel gating of wild-type lens connexins.

1 reference

12 December 2020

Structural function of MIP/aquaporin 0 in the eye lens; genetic defects lead to congenital inherited cataracts

1 reference

12 December 2020

Sry and Sox9: mammalian testis-determining genes.

1 reference

12 December 2020

A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract

1 reference

12 December 2020

Crystallin gene mutations in Indian families with inherited pediatric cataract

1 reference

12 December 2020

Targeted ablation of NrCAM or ankyrin-B results in disorganized lens fibers leading to cataract formation

1 reference

12 December 2020

Identification of vimentin as a novel target of HSF4 in lens development and cataract by proteomic analysis.

1 reference

12 December 2020

Prenatal lens development in connexin43 and connexin50 double knockout mice

1 reference

12 December 2020

Osmotic state of lenses in three dominant murine cataract mutants.

1 reference

12 December 2020

A missense mutation in LIM2 causes autosomal recessive congenital cataract

1 reference

12 December 2020

A temperature-sensitive mutation of Crygs in the murine Opj cataract

1 reference

12 December 2020

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye

1 reference

12 December 2020

Hyperphenylalaninemia and impaired glucose tolerance in mice lacking the bifunctional DCoH gene

1 reference

12 December 2020

Radiation cataractogenesis: a review of recent studies.

1 reference

12 December 2020

Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene

1 reference

12 December 2020

SPARC deficiency leads to early-onset cataractogenesis.

1 reference

12 December 2020

Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse

1 reference

12 December 2020

Arginine 54 and Tyrosine 118 residues of {alpha}A-crystallin are crucial for lens formation and transparency

1 reference

12 December 2020

Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17.

1 reference

12 December 2020

Aphakia, a new mutation in the mouse

1 reference

12 December 2020

The Emory mouse cataract: an animal model for human senile cataract

1 reference

12 December 2020

Aberrant expression of the gene for lens major intrinsic protein in the CAT mouse

1 reference

12 December 2020

Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype

1 reference

12 December 2020

A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle

1 reference

12 December 2020

Loss of ephrin-A5 function disrupts lens fiber cell packing and leads to cataract

1 reference

12 December 2020

Gene expression changes during cataract progression in Sparc null mice: differential regulation of mouse globins in the lens.

1 reference

12 December 2020

Bfsp2 mutation found in mouse 129 strains causes the loss of CP49' and induces vimentin-dependent changes in the lens fibre cell cytoskeleton

1 reference

12 December 2020

Role of INK4a locus in normal eye development and cataract genesis.

1 reference

12 December 2020

Altered aggregation properties of mutant gamma-crystallins cause inherited cataract

1 reference

12 December 2020

A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD

1 reference

12 December 2020

A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding

1 reference

12 December 2020

Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts

1 reference

12 December 2020

The heritability of age-related cortical cataract: the twin eye study.

1 reference

12 December 2020

Targeted genomic deletion of the lens-specific intermediate filament protein CP49.

1 reference

12 December 2020

Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract

1 reference

12 December 2020

Mapping of six dominant cataract genes in the mouse

1 reference

12 December 2020

Involvement of Sox1, 2 and 3 in the early and subsequent molecular events of lens induction.

1 reference

12 December 2020

Characterization of dominant cataract mutations in mice: penetrance, fertility and homozygous viability of mutations recovered after 250 mg/kg ethylnitrosourea paternal treatment

1 reference

12 December 2020

Unique and redundant connexin contributions to lens development

1 reference

12 December 2020

Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney

1 reference

12 December 2020

Genetic factors influence cataract formation in alpha 3 connexin knockout mice

1 reference

12 December 2020

Spatial and temporal patterns of distribution of the gap junction protein connexin43 during mouse gastrulation and organogenesis

1 reference

12 December 2020

Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8.

1 reference

12 December 2020