Targeted disruption of the homeobox transcription factor Bapx1 results in lethal skeletal dysplasia with asplenia and gastroduodenal malformation
Open Access
- 1 June 2000
- journal article
- research article
- Published by Wiley in Genes to Cells
- Vol. 5 (6) , 499-513
- https://doi.org/10.1046/j.1365-2443.2000.00339.x
Abstract
Background NK homeobox genes have been shown to play important roles in cell‐type specification and organogenesis. Murine Bapx1, a member of NK homeobox gene family, is expressed in all the cartilag...Keywords
This publication has 38 references indexed in Scilit:
- Altered Cochlear Fibrocytes in a Mouse Model of DFN3 Nonsyndromic DeafnessScience, 1999
- Autosomal Dominant Postaxial Polydactyly, Nail Dystrophy, and Dental Abnormalities Map to Chromosome 4p16, in the Region Containing the Ellis–van Creveld Syndrome LocusAmerican Journal of Human Genetics, 1997
- Sequence and Chromosomal Assignment of HumanBAPX1, abagpipe-Related Gene, to 4p16.1: A Candidate Gene for Skeletal DysplasiaGenomics, 1997
- The Gene for the Ellis–van Creveld Syndrome Is Located on Chromosome 4p16Genomics, 1996
- Localization of craniosynostosis Adelaide type to 4p16Human Molecular Genetics, 1995
- Chromosome 4p16 and osteochondroplasiasNature Genetics, 1994
- Hox11 controls the genesis of the spleenNature, 1994
- Short rib-polydactyly syndrome and pericentric inversion of chromosome 4American Journal of Medical Genetics, 1994
- MFH‐1, a new member of the fork head domain family, is expressed in developing mesenchymeFEBS Letters, 1993
- Immunohistochemical localization of short chain cartilage collagen (type X) in avian tissues.The Journal of cell biology, 1985