4.3 Article

Multiple hereditary exostoses (MHE): elucidating the pathogenesis of a rare skeletal disorder through interdisciplinary research

Related references

Note: Only part of the references are listed.
Article Cell Biology

Development of the Endochondral Skeleton

Fanxin Long et al.

COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2013)

Article Pathology

No Haploinsufficiency but Loss of Heterozygosity for EXT in Multiple Osteochondromas

Christianne M. A. Reijnders et al.

AMERICAN JOURNAL OF PATHOLOGY (2010)

Article Multidisciplinary Sciences

A mouse model of osteochondromagenesis from clonal inactivation of Ext1 in chondrocytes

Kevin B. Jones et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Multidisciplinary Sciences

A mouse model of chondrocyte-specific somatic mutation reveals a role for Ext1 loss of heterozygosity in multiple hereditary exostoses

Kazu Matsumoto et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Pathology

The molecular and cellular basis of exostosis formation in hereditary multiple exostoses

Meirav Trebicz-Geffen et al.

INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY (2008)

Article Orthopedics

Clinical outcome and genotype in patients with hereditary multiple exostoses

Marcus Jaerger et al.

JOURNAL OF ORTHOPAEDIC RESEARCH (2007)

Article Cell Biology

Heparanase is expressed in osteoblastic cells and stimulates bone formation and bone mass

V Kram et al.

JOURNAL OF CELLULAR PHYSIOLOGY (2006)

Article Developmental Biology

Mice deficient in Ext2 lack heparan sulfate and develop exostoses

D Stickens et al.

DEVELOPMENT (2005)

Article Developmental Biology

Sequential roles of Hedgehog and Wnt signaling in osteoblast development

HL Hu et al.

DEVELOPMENT (2005)

Review Multidisciplinary Sciences

Developmental regulation of the growth plate

HM Kronenberg

NATURE (2003)

Article Genetics & Heredity

Genotype-phenotype correlation in hereditary multiple exostoses

C Francannet et al.

JOURNAL OF MEDICAL GENETICS (2001)

Article Developmental Biology

Disruption of gastrulation and heparan sulfate biosynthesis in EXT1-deficient mice

X Lin et al.

DEVELOPMENTAL BIOLOGY (2000)

Article Multidisciplinary Sciences

The putative tumor suppressors EXT1 and EXT2 form a stable complex that accumulates in the Golgi apparatus and catalyzes the synthesis of heparan sulfate

C McCormick et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)