Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia
Open Access
- 1 May 1997
- journal article
- research article
- Published by Elsevier BV in Cell
- Vol. 89 (5), 773-779
- https://doi.org/10.1016/s0092-8674(00)80260-3
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- The Tissue-Specific Nuclear Matrix Protein, NMP-2, Is a Member of the AML/PEBP2/Runt Domain Transcription Factor Family: Interactions with the Osteocalcin Gene PromoterBiochemistry, 1995
- Alternative splicing and genomic structure of theAML1gene involved in acute myeloid leukemiaNucleic Acids Research, 1995
- Toward a molecular understanding of skeletal developmentCell, 1995
- AML1, AML2, and AML3, the Human Members of the runt domain Gene-Family: cDNA Structure, Expression, and Chromosomal LocalizationGenomics, 1994
- PEBP2 alpha B/mouse AML1 consists of multiple isoforms that possess differential transactivation potentials.Molecular and Cellular Biology, 1994
- A new bacteriophage P1–derived vector for the propagation of large human DNA fragmentsNature Genetics, 1994
- Fusion Between Transcription Factor CBFβ/PEBP2β and a Myosin Heavy Chain in Acute Myeloid LeukemiaScience, 1993
- Chromosomal assignment of human YAC clones by fluorescence in Situ hybridization: Use of single-yeast-colony PCR and multiple labelingGenomics, 1992
- Linkage mapping and fluorescence in situ hybridization of TCTE1 on human chromosome 6p: Analysis of dinucleotide polymorphisms on native gelsGenomics, 1991
- The Drosophila segmentation gene runt encodes a novel nuclear regulatory protein that is also expressed in the developing nervous system.Journal of Bone and Joint Surgery, 1990