Association of EPHA2 polymorphisms and age-related cortical cataract in a Han Chinese population (Q35047331)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21686326%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

title

Association of EPHA2 polymorphisms and age-related cortical cataract in a Han Chinese population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21686326%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

author name string

Wei Tan

1

1 reference

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5 February 2020

Shengping Hou

2

1 reference

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5 February 2020

Zhengxuan Jiang

3

1 reference

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5 February 2020

Zheng Hu

4

1 reference

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5 February 2020

Peizeng Yang

5

1 reference

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5 February 2020

Jian Ye

6

1 reference

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5 February 2020

publication date

9 June 2011

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5 February 2020

1 reference

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5 February 2020

volume

17

1 reference

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5 February 2020

page(s)

1553-1558

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21686326%20AND%20SRC:MED&resulttype=core&format=json

Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study.

5 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Polymorphisms in two DNA repair genes (XPD and XRCC1)--association with age related cataracts

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

First mutation in the βA2-crystallin encoding gene is associated with small lenses and age-related cataracts

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Alterations of the 5'untranslated region of SLC16A12 lead to age-related cataract

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

A novel mutation (F71L) in alphaA-crystallin with defective chaperone-like function associated with age-related cataract

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Mutation screening of HSF4 in 150 age-related cataract patients

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Eph-ephrin bidirectional signaling in physiology and disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Cell-cell signaling via Eph receptors and ephrins

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Bidirectional Eph-ephrin signaling during axon guidance

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Eph receptor signalling casts a wide net on cell behaviour

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Identification of a major locus for age-related cortical cataract on chromosome 6p12-q12 in the Beaver Dam Eye Study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Important Causes of Visual Impairment in the World Today

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Eph signaling: a structural view

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Cataract blindness--challenges for the 21st century

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Multiple roles of EPH receptors and ephrins in neural development

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Topographic guidance labels in a sensory projection to the forebrain

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Prevalence of age-related cataract in high-selenium areas of China

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3115745

Lens opacities classification system II (LOCS II)

25 October 2018

1 reference

12 December 2020

The Lens Opacities Case-Control Study. Risk factors for cataract

1 reference

12 December 2020

Prevalence of age-related lens opacities in a population. The Beaver Dam Eye Study

1 reference

12 December 2020

Familial aggregation of lens opacities: the Framingham Eye Study and the Framingham Offspring Eye Study

1 reference

12 December 2020

Incidence and progression of cortical, nuclear, and posterior subcapsular cataracts. The Italian-American Cataract Study Group

1 reference

12 December 2020

Evidence for a major gene for cortical cataract

1 reference

12 December 2020

Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36

1 reference

12 December 2020

A locus for autosomal dominant posterior polar cataract on chromosome 1p

1 reference

12 December 2020

SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21686326%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

PubMed publication ID

21686326

1 reference