| scholarly article | Q13442814 |
| P2093 | author name string | Yu Zhang | |
| Guixing Qiu | |||
| Zuchao Gu | |||
| P2860 | cites work | Hes7: a bHLH-type repressor gene regulated by Notch and expressed in the presomitic mesoderm | Q24290956 |
| Mutations in the human Jagged1 gene are responsible for Alagille syndrome | Q24314702 | ||
| Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1 | Q24314766 | ||
| Mutated MESP2 causes spondylocostal dysostosis in humans | Q24534025 | ||
| Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype | Q24540500 | ||
| Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis | Q24677244 | ||
| Wnt-3a regulates somite and tailbud formation in the mouse embryo | Q28504870 | ||
| The Mesp2 transcription factor establishes segmental borders by suppressing Notch activity | Q28505901 | ||
| Periodic repression by the bHLH factor Hes7 is an essential mechanism for the somite segmentation clock | Q28585491 | ||
| Dynamic expression and essential functions of Hes7 in somite segmentation | Q28593057 | ||
| Mutation of Hairy-and-Enhancer-of-Split-7 in humans causes spondylocostal dysostosis | Q28593626 | ||
| Congenital and idiopathic scoliosis: clinical and genetic aspects. | Q33723361 | ||
| The role of Pax-1 in axial skeleton development. | Q34329886 | ||
| New mutant mouse with skeletal deformities caused by mutation in delta like 3 (Dll3) gene | Q44903445 | ||
| Defects in somite formation in lunatic fringe-deficient mice | Q47741558 | ||
| P433 | issue | 9 | |
| P921 | main subject | scoliosis | Q174857 |
| congenital disorder | Q727096 | ||
| P304 | page(s) | 16714-16718 | |
| P577 | publication date | 2015-09-15 | |
| P1433 | published in | International Journal of Clinical and Experimental Medicine | Q6051338 |
| P1476 | title | Genetic association analysis between polymorphisms of HAIRY-AND-ENHANCER-OF SPLIT-7 and congenital scoliosis | |
| P478 | volume | 8 |
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