Microform Holoprosencephaly in Mice that Lack the Ig Superfamily Member Cdon
- 1 March 2003
- journal article
- Published by Elsevier in Current Biology
- Vol. 13 (5) , 411-415
- https://doi.org/10.1016/s0960-9822(03)00088-5
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Multiple Hits during Early Embryonic Development: Digenic Diseases and HoloprosencephalyAmerican Journal of Human Genetics, 2002
- BOC, an Ig superfamily member, associates with CDO to positively regulate myogenic differentiationThe EMBO Journal, 2002
- Mutations in holoprosencephalyHuman Mutation, 2000
- Developmental expression pattern of thecdo geneDevelopmental Dynamics, 2000
- Genetics of ventral forebrain development and holoprosencephalyCurrent Opinion in Genetics & Development, 2000
- CDO, A Robo-related Cell Surface Protein that Mediates Myogenic DifferentiationThe Journal of cell biology, 1998
- Holoprosencephaly: from Homer to HedgehogClinical Genetics, 1998
- CDO: An Oncogene-, Serum-, and Anchorage-regulated Member of the Ig/Fibronectin Type III Repeat FamilyThe Journal of cell biology, 1997
- Sonic hedgehogParticipates in Craniofacial Morphogenesis and Is Down-regulated by Teratogenic Doses of Retinoic AcidDevelopmental Biology, 1997
- The contribution of both forebrain and midbrain crest cells to the mesenchyme in the frontonasal mass of mouse embryosDevelopmental Biology, 1994