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TGFBI gene
Known as:
Transforming Growth Factor, Beta-Induced, 68kDa Gene
, BIGH3
, TRANSFORMING GROWTH FACTOR, BETA-INDUCED, 68-KD
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This gene may play a role in cellular adhesion; however, this function has not been substantiated.
National Institutes of Health
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Related topics
Related topics
15 relations
Cell Adhesion
Cell Adhesion Inhibition
Cell Movement
Cell Proliferation
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TGFBI wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Serum proteins TGFBI, PCSK9, and CCL14 are potential biomarkers for different traditional Chinese medicine syndromes of multidrug‐resistant tuberculosis
Yu-ting Hu
,
Wen‐Jing Yi
,
+10 authors
Jicheng Li
The Anatomical Record
2020
Corpus ID: 210041307
Patients with multidrug‐resistant tuberculosis (MDR‐TB) tend to have a long course of anti‐TB treatment and severe side effects…
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Review
2015
Review
2015
Die revidierte neueste IC3D-Klassifikation der Hornhautdystrophien
B. Seitz
,
W. Lisch
,
J. Weiss
Klinische Monatsblätter für Augenheilkunde
2015
Corpus ID: 196213020
Zusammenfassung Ziele: Vorschlag, wie eine Hornhautdystrophie an der Spaltlampe diagnostiziert werden sollte und Darstellung der…
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2014
2014
TGFBI, CHST6, and GSN gene analysis in Mexican patients with stromal corneal dystrophies
J. González-Rodríguez
,
A. Ramirez-Miranda
,
S. Mota
,
J. Zenteno
Graefe's Archive for Clinical and Experimental…
2014
Corpus ID: 1419987
ObjectivesThe purpose of our study was to describe the results of molecular screening of TGFBI, CHST6, and GSN genes in a group…
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2013
2013
Chinese family with atypical granular corneal dystrophy type I caused by the typical R555W mutation in TGFBI.
Su-juan Zhao
,
Yanan Zhu
,
X. Shentu
,
Qi Miao
International Journal of Ophthalmology
2013
Corpus ID: 27234282
AIM To investigate the clinical features and genetic defects in four generations of a Chinese family affected with atypical…
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2011
2011
Heavy-Chain Amyloidosis in TGFBI-Negative and Gelsolin-Negative Atypical Lattice Corneal Dystrophy
Monika A Pradhan
,
R. Henderson
,
Dipika V. Patel
,
C. McGhee
,
A. Vincent
Cornea
2011
Corpus ID: 25146918
Purpose: An atypical case of late-onset lattice corneal dystrophy is described in a 61-year-old man without a family history of…
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2011
2011
Pathogenic mutations of TGFBI and CHST6 genes in Chinese patients with Avellino, lattice, and macular corneal dystrophies
Ya-nan Huo
,
Yu-feng Yao
,
P. Yu
Journal of Zhejiang University SCIENCE B
2011
Corpus ID: 21603465
ObjectiveTo investigate gene mutations associated with three different types of corneal dystrophies (CDs), and to establish a…
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2010
2010
The Effect of Oxytocin and an Oxytocin Antagonist on the Human Myometrial Proteome
Norbert C. J. de Wit
,
A. Heck
,
S. Thornton
Reproductive Sciences
2010
Corpus ID: 206803120
Objective: The immediate effects of oxytocin on myometrial signal transduction have been described. However, the longer term…
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2009
2009
Denaturation and solvent effect on the conformation and fibril formation of TGFBIp
H. Grothe
,
M. Little
,
Angela S. Cho
,
A. Huang
,
Ching Yuan
Molecular Vision
2009
Corpus ID: 8613921
Purpose Transforming growth factor beta-induced protein (TGFBIp) aggregates into the phenotypic amyloid fibrils and/or non…
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2007
2007
Reduced TGF-ß1 Expression and its Target Genes in Human Insulinomas
Anastasiya Nabokikh
,
A. Ilhan
,
+8 authors
L. Wagner
Experimental and clinical endocrinology…
2007
Corpus ID: 6203089
Aiming to identify signalling pathways relevant for ss-cell growth we performed an explorative micro-array analysis comparing the…
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2006
2006
Identification of cis and trans-acting transcriptional regulators in chondroinduced fibroblasts from the pre-phenotypic gene expression profile.
K. Yates
Gene
2006
Corpus ID: 40238445
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