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ADAMTS17 gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Weill-Marchesani syndrome (WMS) is a rare genetic disorder that affects the musculoskeletal system, the eye, and the… Expand
2017
2017
Secreted metalloproteases have diverse roles in the formation, remodeling, and the destruction of extracellular matrix. Recessive… Expand
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2016
2016
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by CAG repeat expansions in the huntingtin gene. Although… Expand
Review
2015
Review
2015
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
Adamts17 is a member of a family of secreted metalloproteinases. In this report, we show that knockdown of Adamts17 expression… Expand