Biology:SIX5
From HandWiki
Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
Homeobox protein SIX5 is a protein that in humans is encoded by the SIX5 gene.[1][2]
References
- ↑ "A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat". Hum Mol Genet 4 (10): 1919–25. Apr 1996. doi:10.1093/hmg/4.10.1919. PMID 8595416.
- ↑ "Entrez Gene: SIX5 sine oculis homeobox homolog 5 (Drosophila)". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=147912.
Further reading
- "Promoter of mDMAHP/Six5: differential utilization of multiple transcription initiation sites and positive/negative regulatory elements". Hum. Mol. Genet. 7 (13): 2103–12. 1999. doi:10.1093/hmg/7.13.2103. PMID 9817928.
- "Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy". Hum. Mol. Genet. 8 (3): 481–92. 1999. doi:10.1093/hmg/8.3.481. PMID 9949207.
- "Cooperation of Six and Eya in Activation of Their Target Genes through Nuclear Translocation of Eya". Mol. Cell. Biol. 19 (10): 6815–24. 2000. doi:10.1128/mcb.19.10.6815. PMID 10490620.
- "Functional analysis of the homeodomain protein SIX5". Nucleic Acids Res. 28 (9): 1871–8. 2000. doi:10.1093/nar/28.9.1871. PMID 10756185.
- "Expression of a homeobox gene (SIX5) in borderline ovarian tumours". J. Clin. Pathol. 53 (3): 212–7. 2000. doi:10.1136/jcp.53.3.212. PMID 10823141.
- "HMGB1 interacts with many apparently unrelated proteins by recognizing short amino acid sequences". J. Biol. Chem. 277 (9): 7021–8. 2002. doi:10.1074/jbc.M108417200. PMID 11748221.
- "Identification of transcriptional targets for Six5: implication for the pathogenesis of myotonic dystrophy type 1". Hum. Mol. Genet. 11 (9): 1045–58. 2002. doi:10.1093/hmg/11.9.1045. PMID 11978764.
- "Six and Eya expression during human somitogenesis and MyoD gene family activation". J. Muscle Res. Cell. Motil. 23 (3): 255–64. 2003. doi:10.1023/A:1020990825644. PMID 12500905.
- "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell 125 (4): 801–14. 2006. doi:10.1016/j.cell.2006.03.032. PMID 16713569.
- "Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome". Am. J. Hum. Genet. 80 (4): 800–4. 2007. doi:10.1086/513322. PMID 17357085.
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