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betaIG-H3 protein

Known as: beta IG-H3 protein, BIGH3 protein, transforming growth factor-beta induced protein 
National Institutes of Health

Related topics

Related topics

5 relations

Broader (2)

Extracellular Matrix ProteinsTransforming Growth Factor beta
TGFBI gene

Narrower (2)

TGFBI protein, humantgfbi protein, zebrafish

Papers overview

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Highly Cited
2011
Highly Cited
2011
Characterization of the cleavage plane in DESCemet's membrane endothelial keratoplasty.
Highly Cited
2008
Highly Cited
2008
Extracellular matrix protein betaig-h3/TGFBI promotes metastasis of colon cancer by enhancing cell extravasation.
Metastasis, the major cause of cancer death, is a multistep process that requires interactions between cancer cells and stromal… 
2002
2002
Induction and expression of betaig-h3 in pancreatic cancer cells.
betaig-h3 (TGFBI, keratoepithelin) was first identified as a transforming growth factor-beta1 (TGF-beta1)-inducible gene in a… 
Highly Cited
2000
Highly Cited
2000
Amyloid and Non-amyloid Forms of 5q31-linked Corneal Dystrophy Resulting from Kerato-epithelin Mutations at Arg-124 Are Associated with Abnormal Turnover of the Protein*
Mutations in kerato-epithelin are responsible for a group of hereditary cornea-specific deposition diseases, 5q31-linked corneal… 
Highly Cited
1999
Highly Cited
1999
On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies.
PURPOSE Recently, the authors identified a gene, BIGH3, in which different mutations cause a group of hereditary corneal… 
Highly Cited
1998
Highly Cited
1998
Two distinct kerato-epithelin mutations in Reis-Bücklers corneal dystrophy.
Highly Cited
1998
Highly Cited
1998
A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA.
1998
1998
A common beta ig-h3 gene mutation (delta f540) in a large cohort of Sardinian Reis Bücklers corneal dystrophy patients. Mutations in brief no. 180. Online.
Reis-Bücklers' corneal dystrophy (RBCD) is a relatively rare autosomal dominant disease originating in the Bowman's membrane… 
1998
1998
Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 --> Cys mutation in the kerato-epithelin gene. sgupta@ogh.on.ca.
Highly Cited
1997
Highly Cited
1997
Kerato-epithelin mutations in four 5q31-linked corneal dystrophies
Granular dystrophy Groenouw type I (CDGG1), Reis-Bücklers (CDRB), lattice type I (CDL1) and Avellino (ACD) are four 5q31-linked… 
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