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LTBP2 gene

Known as: latent transforming growth factor beta binding protein 2, Latent Transforming Growth Factor Beta Binding Protein 2 Gene, LATENT TRANSFORMING GROWTH FACTOR-BETA-BINDING PROTEIN 2 
This gene is involved in extracellular matrix interactions and in cellular adhesion.
National Institutes of Health

Related topics

Related topics

5 relations
Intercellular Communication ProcessLTBP2 protein, humanLigand Bindingmelanoma

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Genetic mapping of autosomal recessive microspherophakia to chromosome 14q24.3 in a consanguineous Pakistani family and screening of exon 36 of LTBP2 gene.
Latent transforming growth factor beta binding protein 2 (LTBP2) plays a critical role in the development of connective tissue… 
2017
2017
Down-regulation of LTBP 2 suppresses the proliferation , migration and invasion in human prostate cancer cells
Latent transforming growth factor-beta binding protein 2 (LTBP2) is a member of the LTBPs family. It is dysregulated in many… 
2016
2016
Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Purpose To identify deleterious mutations in the latent transforming growth factor-β–binding protein 2 (LTBP2) gene in sporadic… 
2016
2016
Correction: A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
[This corrects the article DOI: 10.1371/journal.pone.0154412.]. 
Review
2015
Review
2015
Glaucoma in Iran and Contributions of Studies in Iran to the Understanding of the Etiology of Glaucoma
Epidemiologic and genetic/molecular research on glaucoma in Iran started within the past decade. A population-based study on the… 
2014
2014
Extracellular matrix protein, LTBP2, regulates the nuclear trafficking of canonical NF-kB p65 to mediate tumor suppressive effect in NPC
2013
2013
Characterization of a novel missense mutation in the prodomain of GDF5, which underlies brachydactyly type C and mild Grebe type chondrodysplasia in a large Pakistani family
All TGF-beta family members have a prodomain that is important for secretion. Lack of secretion of a TGF-beta family member GDF5… 
2010
2010
Novel Gene Mutations Causing Primary Congenital Glaucoma
P r i m a r y c o n g e n i t a l g l a u c o m a ( P C G ) i s characterized by an anatomical defect in the trabecular meshwork… 
2004
2004
Mapping of human and murine genes for latent TGF-β binding protein-2 (LTBP2)
A novel gene, isolated because of structural similarities to fibrillin, was called LTBP2 when its 4.6-kb transcript was found to… 
1995
1995
Mapping of human and murine genes for latent TGF-beta binding protein-2 (LTBP2).
A novel gene, isolated because of structural similarities to fibrillin, was called LTBP2 when its 4.6-kb transcript was found to… 
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