Exostosin-2

Known as: EC 2.4.1.225, Putative Tumor Suppressor Protein EXT2, EXT2 
Exostosin-2 (718 aa, ~82 kDa) is encoded by the human EXT2 gene. This protein plays a role in both bone formation and glycosaminoglycan synthesis.

Topic mentions per year

Topic mentions per year

1995-2018
02419952018

Papers overview

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2013
2013
Multiple osteochondromas is an autosomal dominant skeletal disorder characterized by the formation of multiple cartilage-capped… (More)
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2004
2004
Multiple hereditary exostoses (HME) is an autosomal dominant developmental disorder exhibiting multiple osteocartilaginous bone… (More)
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2002
2002
Hereditary multiple exostoses (HME) is an autosomal dominant disorder characterized by growth of benign bone tumors. This… (More)
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2001
2001
Hereditary multiple exostoses (HME), a dominantly inherited genetic disorder characterized by multiple cartilaginous tumors, is… (More)
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Highly Cited
2000
Highly Cited
2000
Hereditary multiple exostoses, a dominantly inherited genetic disorder characterized by multiple cartilaginous tumors, is caused… (More)
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2000
2000
We prepared the specific antibodies for EXT1 and EXT2, hereditary multiple exostoses (HME) gene products, and characterized their… (More)
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2000
2000
The D-glucuronyltransferase and N-acetyl-D-glucosaminyltransferase reactions in heparan sulfate biosynthesis have been associated… (More)
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1998
1998
Hereditary multiple exostoses (EXT) is an autosomal dominant disorder that is characterized by the appearance of multiple… (More)
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1997
1997
Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by the presence of multiple cartilage-capped… (More)
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Highly Cited
1996
Highly Cited
1996
Hereditary multiple exostosis (EXT) is an autosomal dominant condition mainly characterized by the presence of multiple exostoses… (More)
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