Regulation of the Mouse Treacher Collins Syndrome Homolog (Tcof1) Promoter Through Differential Repression of Constitutive Expression
Author:
Affiliation:
1. Department of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
Publisher
Mary Ann Liebert Inc
Subject
Cell Biology,Genetics,Molecular Biology,General Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/dna.2008.0766
Reference54 articles.
1. Xenopus cadherin-11 restrains cranial neural crest migration and influences neural crest specification
2. Genetic background has a major effect on the penetrance and severity of craniofacial defects in mice heterozygous for the gene encoding the nucleolar protein treacle
3. Identification of the complete coding sequence and genomic organization of the Treacher Collins syndrome gene.
4. Sequence Analysis, Identification of Evolutionary Conserved Motifs and Expression Analysis of Murine tcof1 Provide Further Evidence for a Potential Function for the Gene and Its Human Homologue, TCOF1
5. Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndrome
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1. The transcription of the main gene associated with Treacher–Collins syndrome (TCOF1) is regulated by G-quadruplexes and cellular nucleic acid binding protein (CNBP);Scientific Reports;2024-03-29
2. The transcription of TCOF1 , the main gene associated with Treacher-Collins syndrome, is regulated by G-quadruplexes and Cellular Nucleic acid Binding Protein (CNBP);2024-01-05
3. TCOF1 upregulation in triple-negative breast cancer promotes stemness and tumour growth and correlates with poor prognosis;British Journal of Cancer;2021-10-30
4. The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome;International Journal of Molecular Sciences;2021-03-01
5. Genome-wide DNase hypersensitivity, and occupancy of RUNX2 and CTCF reveal a highly dynamic gene regulome during MC3T3 pre-osteoblast differentiation;PLOS ONE;2017-11-27
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