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betaIG-H3 protein
Known as:
beta IG-H3 protein
, BIGH3 protein
, transforming growth factor-beta induced protein
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National Institutes of Health
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Related topics
Related topics
5 relations
Broader (2)
Extracellular Matrix Proteins
Transforming Growth Factor beta
TGFBI gene
Narrower (2)
TGFBI protein, human
tgfbi protein, zebrafish
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
Characterization of the cleavage plane in DESCemet's membrane endothelial keratoplasty.
U. Schlötzer-Schrehardt
,
B. Bachmann
,
K. Laaser
,
C. Cursiefen
,
F. Kruse
Ophthalmology
2011
Corpus ID: 25687341
PURPOSE To define the cleavage plane between Descemet's membrane (DM) and posterior corneal stroma in Descemet's membrane…
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Highly Cited
2008
Highly Cited
2008
Extracellular matrix protein betaig-h3/TGFBI promotes metastasis of colon cancer by enhancing cell extravasation.
C. Ma
,
Y. Rong
,
+8 authors
X. Wang
Genes & development
2008
Corpus ID: 46398489
Metastasis, the major cause of cancer death, is a multistep process that requires interactions between cancer cells and stromal…
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Highly Cited
2005
Highly Cited
2005
Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.
B. Stix
,
M. Leber
,
+8 authors
C. Röcken
Investigative ophthalmology & visual science
2005
Corpus ID: 29516129
PURPOSE To investigate the molecular basis of hereditary lattice corneal dystrophy (LCD) type IIIA associated with corneal…
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2002
2002
Induction and expression of betaig-h3 in pancreatic cancer cells.
D. Schneider
,
J. Kleeff
,
+4 authors
M. Büchler
Biochimica et biophysica acta
2002
Corpus ID: 29097425
betaig-h3 (TGFBI, keratoepithelin) was first identified as a transforming growth factor-beta1 (TGF-beta1)-inducible gene in a…
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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*
E. Korvatska
,
H. Henry
,
+4 authors
D. Schorderet
The Journal of Biological Chemistry
2000
Corpus ID: 476798
Mutations in kerato-epithelin are responsible for a group of hereditary cornea-specific deposition diseases, 5q31-linked corneal…
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Highly Cited
1999
Highly Cited
1999
On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies.
E. Korvatska
,
F. Munier
,
+6 authors
D. Schorderet
Investigative ophthalmology & visual science
1999
Corpus ID: 16570390
PURPOSE Recently, the authors identified a gene, BIGH3, in which different mutations cause a group of hereditary corneal…
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Highly Cited
1998
Highly Cited
1998
A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA.
S. Yamamoto
,
M. Okada
,
+9 authors
Y. Tano
American journal of human genetics
1998
Corpus ID: 45824396
Highly Cited
1998
Highly Cited
1998
Two distinct kerato-epithelin mutations in Reis-Bücklers corneal dystrophy.
M. Okada
,
S. Yamamoto
,
+8 authors
Y. Tano
American journal of ophthalmology
1998
Corpus ID: 30919853
PURPOSE Two patients were diagnosed with Reis-Bücklers corneal dystrophy (RBCD), although the pattern and severity of corneal…
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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.
C. Rozzo
,
M. Fossarello
,
+5 authors
M. Pirastu
Human mutation
1998
Corpus ID: 24535490
Reis-Bücklers' corneal dystrophy (RBCD) is a relatively rare autosomal dominant disease originating in the Bowman's membrane…
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Highly Cited
1997
Highly Cited
1997
Kerato-epithelin mutations in four 5q31-linked corneal dystrophies
F. Munier
,
E. Korvatska
,
+4 authors
D. Schorderet
Nature Genetics
1997
Corpus ID: 19284412
Granular dystrophy Groenouw type I (CDGG1), Reis-Bücklers (CDRB), lattice type I (CDL1) and Avellino (ACD) are four 5q31-linked…
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