FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

about

Ocular surface development and gene expression.Reply to Chakrabarti et al.: Corneal angiogenesis in patients with null FOXC1 variants.

P2860

Q41204566-AE93CEF3-18C5-4679-8189-DDBF902763BE Q46144805-4A2B004B-4C2F-4D6E-85E6-FA2F409AFFD1

P2860

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

Item

http://www.wikidata.org/entity/Q43208874

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年学术文章

@wuu

2012年学术文章

@zh

2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

@zh-hant

name

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

@en

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

@nl

type

Item

label

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

@en

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

@nl

prefLabel

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

@en

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

@nl

P1476

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

@en

P2093

Inderjeet Kaur

http://www.w3.org/2001/XMLSchema#string

Muralidhar Ramappa

http://www.w3.org/2001/XMLSchema#string

Subhabrata Chakrabarti

http://www.w3.org/2001/XMLSchema#string

Sunita Chaurasia

http://www.w3.org/2001/XMLSchema#string

P2860

Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth

Chromosome abnormalities and the genetics of congenital corneal opacification.

The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma.

Sclerocornea associated with the chromosome 22q11.2 deletion syndrome.

P304

E1509; author reply E1510

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1073/PNAS.1204423109

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

109

http://www.w3.org/2001/XMLSchema#string

P50

Anil Kumar Mandal

P577

2012-05-11T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

224946933

http://www.w3.org/2001/XMLSchema#string

P698

22582167

http://www.w3.org/2001/XMLSchema#string

P921

neovascularization

P932

3386115

http://www.w3.org/2001/XMLSchema#string

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

about

P2860

P2860

FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P921

P932