The mouse notches up another success: understanding the causes of human vertebral malformation

FGF4 and FGF8 comprise the wavefront activity that controls somitogenesis

(2011) L. A. Naiche et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Tissue morphogenesis coupled with cell shape changes

(2010) Tadayoshi Watanabe et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Analysis of Ripply1/2-deficient mouse embryos reveals a mechanism underlying the rostro-caudal patterning within a somite

(2010) Jun Takahashi et al.   DEVELOPMENTAL BIOLOGY

Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis

(2010) Duncan B Sparrow et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Notch inhibition by the ligand Delta-Like 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis

(2010) Gavin Chapman et al.   HUMAN MOLECULAR GENETICS

Massively parallel sequencing and rare disease

(2010) S. B. Ng et al.   HUMAN MOLECULAR GENETICS

Rere controls retinoic acid signalling and somite bilateral symmetry

(2010) Gonçalo C. Vilhais-Neto et al.   NATURE

Clinical and radiological distinction between spondylothoracic dysostosis (Lavy-Moseley syndrome) and spondylocostal dysostosis (Jarcho-Levin syndrome)

(2010) Walter E. Berdon et al.   PEDIATRIC RADIOLOGY

The segmentation clock mechanism moves up a notch

(2010) Sarah Gibb et al.   TRENDS IN CELL BIOLOGY

The role of Notch in patterning the human vertebral column

(2009) Sally L Dunwoodie   CURRENT OPINION IN GENETICS & DEVELOPMENT

Effect of retinoic acid signaling on Wnt/β-catenin and FGF signaling during body axis extension

(2009) Xianling Zhao et al.   GENE EXPRESSION PATTERNS

Targeted capture and massively parallel sequencing of 12 human exomes

(2009) Sarah B. Ng et al.   NATURE

Posterior malformations in Dact1 mutant mice arise through misregulated Vangl2 at the primitive streak

(2009) Rowena Suriben et al.   NATURE GENETICS

Signaling Gradients during Paraxial Mesoderm Development

(2009) A. Aulehla et al.   Cold Spring Harbor Perspectives in Biology

Mutations in the MESP2 Gene Cause Spondylothoracic Dysostosis/Jarcho-Levin Syndrome

(2008) Alberto S. Cornier et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The vertebrate segmentation clock: the tip of the iceberg

(2008) Ertuğrul M Özbudak et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Generation and characterization ofEphA1receptor tyrosine kinase reporter knockout mice

(2008) Shannon L. Duffy et al.   GENESIS

Mutation of HAIRY-AND-ENHANCER-OF-SPLIT-7 in humans causes spondylocostal dysostosis

(2008) D. B. Sparrow et al.   HUMAN MOLECULAR GENETICS

Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome

(2008) May Tassabehji et al.   HUMAN MUTATION

Segmental patterning of the vertebrate embryonic axis

(2008) Mary-Lee Dequéant et al.   NATURE REVIEWS GENETICS