Cartilage ultrastructure in proteoglycan-deficient zebrafish mutants brings to light new candidate genes for human skeletal disorders

UDP xylose synthase 1 is required for morphogenesis and histogenesis of the craniofacial skeleton

(2010) B. Frank Eames et al.   DEVELOPMENTAL BIOLOGY

Zebrafish models of collagen VI-related myopathies

(2010) W.R. Telfer et al.   HUMAN MOLECULAR GENETICS

Primary cilia organization reflects polarity in the growth plate and implies loss of polarity and mosaicism in osteochondroma

(2010) Carlos E de Andrea et al.   LABORATORY INVESTIGATION

Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia

(2009) Ana Belinda Campos-Xavier et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Craniofacial skeletal defects of adult zebrafishGlypican 4 (knypek)mutants

(2009) Elizabeth E. LeClair et al.   DEVELOPMENTAL DYNAMICS

A Zebrafish Model for the Shwachman-Diamond Syndrome (SDS)

(2009) Narayanan Venkatasubramani et al.   PEDIATRIC RESEARCH

Molecular Mechanisms of Paraptosis Induction: Implications for a Non-Genetically Modified Tumor Vaccine

(2009) Neil Hoa et al.   PLoS One

Running GAGs: myxoid matrix in tumor pathology revisited

(2009) Stefan M. Willems et al.   VIRCHOWS ARCHIV

Congenital Joint Dislocations Caused by Carbohydrate Sulfotransferase 3 Deficiency in Recessive Larsen Syndrome and Humero-Spinal Dysostosis

(2008) Pia Hermanns et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Multiple osteochondromas

(2008) Judith VMG Bovée   Orphanet Journal of Rare Diseases

Regulation of Zebrafish Skeletogenesis by ext2/dackel and papst1/pinscher

(2008) Aurélie Clément et al.   PLoS Genetics