Molecular characterization of a new human T-box gene (TBX22) located in Xq21.1 encoding a protein containing a truncated T-domain
- 1 September 2000
- Vol. 255 (2) , 289-296
- https://doi.org/10.1016/s0378-1119(00)00326-7
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Transcript map of the human chromosome Xq11–Xq21 region: localization of 33 novel genes and one pseudogeneGene, 1999
- Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeNature Genetics, 1997
- Isolation and Regional Mapping of cDNAs Expressed during Early Human DevelopmentGenomics, 1997
- Mutations in human cause limb and cardiac malformation in Holt-Oram syndromeNature Genetics, 1997
- Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyNature Genetics, 1997
- The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27.Genome Research, 1996
- An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locusNature Genetics, 1994
- Expression of a xenopus homolog of Brachyury (T) is an immediate-early response to mesoderm inductionCell, 1991
- Expression pattern of the mouse T gene and its role in mesoderm formationNature, 1990
- Cloning of the T gene required in mesoderm formation in the mouseNature, 1990