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Lauren W. Wang

Cleveland Clinic

22

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1157

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Proteolysis of fibrillin-2 microfibrils is essential for normal skeletal development

2021 bioRxiv
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Adamts10 inactivation in mice leads to persistence of ocular microfibrils subsequent to reduced fibrillin-2 cleavage

2019 Matrix Biology
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A disintegrin-like and metalloproteinase domain with thrombospondin type 1 motif 9 (ADAMTS9) regulates fibronectin fibrillogenesis and turnover

2019 Journal of Biological Chemistry
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Hedgehog Pathway Inhibition in Chondrosarcoma Using the Smoothened Inhibitor IPI-926 Directly Inhibits Sarcoma Cell Growth

2014 Molecular Cancer Therapeutics
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Time-resolved analysis of the matrix metalloproteinase 10 substrate degradome.

2014 Molecular & Cellular Proteomics
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ADAMTSL4, a Secreted Glycoprotein Widely Distributed in the Eye, Binds Fibrillin-1 Microfibrils and Accelerates Microfibril Biogenesis

2012 Investigative Ophthalmology & Visual Science
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A disintegrin-like and metalloprotease domain containing thrombospondin type 1 motif-like 5 (ADAMTSL5) is a novel fibrillin-1-, fibrillin-2-, and heparin-binding member of the ADAMTS superfamily containing a netrin-like module.

2012 Matrix Biology
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Mutations in the TGFβ Binding-Protein-Like Domain 5 of FBN1 Are Responsible for Acromicric and Geleophysic Dysplasias

2011 American Journal of Human Genetics
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An ADAMTSL2 Founder Mutation Causes Musladin-Lueke Syndrome, a Heritable Disorder of Beagle Dogs, Featuring Stiff Skin and Joint Contractures

2010 PLOS ONE
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Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani syndrome demonstrates a long-range effect on secretion of the full-length enzyme.

2008 Human Mutation
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Citations (39)