Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dominant genetic condition that is characterized by the formation of cartilaginous bone tumours (osteochondromas) at multiple sites in the skeleton, secondary bursa formation and impingement of nerves, tendons and vessels, bone curving, and short stature. MO is also known to be associated with arthritis, general pain, scarring and occasional malignant transformation of osteochondroma into secondary peripheral chondrosarcoma. MO patients present additional complains but the relevance of those in relation to the syndromal background needs validation. Mutations in two enzymes that are required during heparan sulphate synthesis (EXT1 or EXT2) are kn...
The zebrafish has emerged as an important model for vertebrate development as it relates to human he...
Introduction: Animal models for OI have proved indispensable for unraveling molecular mechanisms in ...
In a large-scale screen for mutations affecting embryogenesis in zebrafish, we identified 48 mutatio...
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dom...
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dom...
development of osteochondroma, an isolated/sporadic- or a multifocal/hereditary cartilaginous bone t...
Osteogenesis imperfecta (OI) is a hereditary brittle bone disorder that is mostly (>90%) caused by d...
Osteogenesis imperfecta (OI) is a hereditary brittle bone disorder that is mostly (>90%) caused by d...
Mutations in human Exostosin genes (EXTs) confer a disease called Hereditary Multiple Exostoses (HME...
Fragile bone disorders (FBD) are characterized by increased fracture risks due to insufficient or fr...
Zebrafish are increasingly becoming an important model organism for studying the pathophysiological ...
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in...
Bruck syndrome, a disorder caused by recessive mutations in either PLOD2 or FKBP10, is characterized...
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in...
The capacity to fully replace teeth continuously makes zebrafish an attractive model to explore rege...
The zebrafish has emerged as an important model for vertebrate development as it relates to human he...
Introduction: Animal models for OI have proved indispensable for unraveling molecular mechanisms in ...
In a large-scale screen for mutations affecting embryogenesis in zebrafish, we identified 48 mutatio...
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dom...
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dom...
development of osteochondroma, an isolated/sporadic- or a multifocal/hereditary cartilaginous bone t...
Osteogenesis imperfecta (OI) is a hereditary brittle bone disorder that is mostly (>90%) caused by d...
Osteogenesis imperfecta (OI) is a hereditary brittle bone disorder that is mostly (>90%) caused by d...
Mutations in human Exostosin genes (EXTs) confer a disease called Hereditary Multiple Exostoses (HME...
Fragile bone disorders (FBD) are characterized by increased fracture risks due to insufficient or fr...
Zebrafish are increasingly becoming an important model organism for studying the pathophysiological ...
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in...
Bruck syndrome, a disorder caused by recessive mutations in either PLOD2 or FKBP10, is characterized...
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in...
The capacity to fully replace teeth continuously makes zebrafish an attractive model to explore rege...
The zebrafish has emerged as an important model for vertebrate development as it relates to human he...
Introduction: Animal models for OI have proved indispensable for unraveling molecular mechanisms in ...
In a large-scale screen for mutations affecting embryogenesis in zebrafish, we identified 48 mutatio...