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LTBP2 wt Allele

Known as: GLC3D, Latent Transforming Growth Factor Beta Binding Protein 2 wt Allele, C14orf141 
Human LTBP2 wild-type allele is located within 14q24 and is approximately 114 kb in length. This allele, which encodes latent transforming growth… 
National Institutes of Health

Papers overview

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2020
2020
Abstract Osteoarthritis (OA) is a common chronic joint disease affected by environmental and genetic factors. The LTBP3 gene may… 
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2020
2020
Glaucoma is the second most prominent cause of impaired vision in the world. Over 60 million individuals are presently affected… 
Review
2019
Review
2019
The latent transforming growth factor-beta-binding protein 3 (LTBP3), encoding extracellular matrix proteins, plays a role in… 
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2018
2018
The major diseases affecting the thoracic aorta are aneurysms and acute dissections, and pathogenic variants in 11 genes are… 
Highly Cited
2017
Highly Cited
2017
Though it is widely known that hepatitis B virus X protein (HBx) is involved in the progression of hepatocellular carcinoma (HCC… 
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2016
2016
Background Acromelic dysplasias are a group of disorders characterised by short stature, brachydactyly, limited joint extension… 
2015
2015
Inherited dental malformations constitute a clinically and genetically heterogeneous group of disorders. Here, we report on four… 
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Review
2011
Review
2011
Primary congenital glaucoma (PCG) is an autosomal recessive disorder in children due to the abnormal development of the… 
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Highly Cited
2009
Highly Cited
2009
We have identified a consanguineous Pakistani family where oligodontia is inherited along with short stature in an autosomal… 
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Highly Cited
2005
Highly Cited
2005
Traditional surgical methods for the reconstruction of cartilage defects rely on the transplantation of autologous and allogenous… 
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