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ADAMTS17 gene

Known as: ADAMTS17, ADAM metallopeptidase with thrombospondin type 1 motif 17, FLJ32769 
National Institutes of Health

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ADAMTS16 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrix.
Weill-Marchesani syndrome (WMS) is a rare genetic disorder that affects the musculoskeletal system, the eye, and the… Expand
2017
2017
Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease
Secreted metalloproteases have diverse roles in the formation, remodeling, and the destruction of extracellular matrix. Recessive… Expand
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2016
2016
Preconditioning mesenchymal stem cells with the mood stabilizers lithium and valproic acid enhances therapeutic efficacy in a mouse model of Huntington's disease
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by CAG repeat expansions in the huntingtin gene. Although… Expand
Review
2015
Review
2015
Genetics of Canine Primary Glaucomas.
Primary glaucomas are a leading cause of incurable vision loss in dogs. Based on their specific breed predilection, a genetic… Expand
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2014
2014
Sp1 Is Necessary for Gene Activation of Adamts17 by Estrogen
Adamts17 is a member of a family of secreted metalloproteinases. In this report, we show that knockdown of Adamts17 expression… Expand
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