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Article

The link between heparan sulfate and hereditary bone disease: finding a function for the EXT family of putative tumor suppressor proteins.

The Journal of clinical investigation - 1 Aug 2001

Duncan G, McCormick C, Tufaro F

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Share to Acetylglucosamine
Share to Exostoses, Multiple Hereditary
Share to Exostosin 1
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Receptor, Parathyroid Hormone, Type 1

Source

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Identifiers

PMID: 11518722
DOI: 10.1172/JCI13737
PMCID: PMC209410

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The link between heparan sulfate and hereditary bone disease: finding a function for the EXT family of putative tumor suppressor proteins.PMID 11518722Read ↗

New perspectives on the molecular basis of hereditary bone tumours.Semantic proximity Read ↗

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Hereditary Multiple Exostoses—A Review of the Molecular Background, Diagnostics, and Potential Therapeutic StrategiesSemantic proximity Read ↗

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Heparan sulfate as a regulator of endochondral ossification and osteochondroma developmentSemantic proximity Read ↗

A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfateSemantic proximity Read ↗

Insights into the molecular regulatory network of pathomechanisms in osteochondromaSemantic proximity Read ↗

Novel EXT1 mutation identified in a pedigree with hereditary multiple exostoses.Semantic proximity Read ↗

Heparan sulfate in skeletal development, growth, and pathology: The case of hereditary multiple exostosesSemantic proximity Read ↗

Hereditary Multiple Exostoses: New Insights into Pathogenesis, Clinical Complications, and Potential Treatments.Semantic proximity Read ↗

Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies.Semantic proximity Read ↗

Heparan Sulphate Biosynthesis and DiseaseSemantic proximity Read ↗

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