[cite web | title = Entrez Gene: SIX5 sine oculis homeobox homolog 5 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=147912| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Boucher CA, King SK, Carey N, "et al." |title=A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat. |journal=Hum. Mol. Genet. |volume=4 |issue= 10 |pages= 1919–25 |year= 1996 |pmid= 8595416 |doi=
*cite journal | author=Murakami Y, Ohto H, Ikeda U, "et al." |title=Promoter of mDMAHP/Six5: differential utilization of multiple transcription initiation sites and positive/negative regulatory elements. |journal=Hum. Mol. Genet. |volume=7 |issue= 13 |pages= 2103–12 |year= 1999 |pmid= 9817928 |doi=
*cite journal | author=Winchester CL, Ferrier RK, Sermoni A, "et al." |title=Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy. |journal=Hum. Mol. Genet. |volume=8 |issue= 3 |pages= 481–92 |year= 1999 |pmid= 9949207 |doi=
*cite journal | author=Ohto H, Kamada S, Tago K, "et al." |title=Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya. |journal=Mol. Cell. Biol. |volume=19 |issue= 10 |pages= 6815–24 |year= 2000 |pmid= 10490620 |doi=
*cite journal | author=Harris SE, Winchester CL, Johnson KJ |title=Functional analysis of the homeodomain protein SIX5. |journal=Nucleic Acids Res. |volume=28 |issue= 9 |pages= 1871–8 |year= 2000 |pmid= 10756185 |doi=
*cite journal | author=Winchester C, Robertson S, MacLeod T, "et al." |title=Expression of a homeobox gene (SIX5) in borderline ovarian tumours. |journal=J. Clin. Pathol. |volume=53 |issue= 3 |pages= 212–7 |year= 2000 |pmid= 10823141 |doi=
*cite journal | author=Dintilhac A, Bernués J |title=HMGB1 interacts with many apparently unrelated proteins by recognizing short amino acid sequences. |journal=J. Biol. Chem. |volume=277 |issue= 9 |pages= 7021–8 |year= 2002 |pmid= 11748221 |doi= 10.1074/jbc.M108417200
*cite journal | author=Sato S, Nakamura M, Cho DH, "et al." |title=Identification of transcriptional targets for Six5: implication for the pathogenesis of myotonic dystrophy type 1. |journal=Hum. Mol. Genet. |volume=11 |issue= 9 |pages= 1045–58 |year= 2002 |pmid= 11978764 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Fougerousse F, Durand M, Lopez S, "et al." |title=Six and Eya expression during human somitogenesis and MyoD gene family activation. |journal=J. Muscle Res. Cell. Motil. |volume=23 |issue= 3 |pages= 255–64 |year= 2003 |pmid= 12500905 |doi=
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Lim J, Hao T, Shaw C, "et al." |title=A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration. |journal=Cell |volume=125 |issue= 4 |pages= 801–14 |year= 2006 |pmid= 16713569 |doi= 10.1016/j.cell.2006.03.032
*cite journal | author=Hoskins BE, Cramer CH, Silvius D, "et al." |title=Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. |journal=Am. J. Hum. Genet. |volume=80 |issue= 4 |pages= 800–4 |year= 2007 |pmid= 17357085 |doi= 10.1086/513322
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