Citations for
1BOR2, SIX5
Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome.
Hoskins BE, Cramer CH, Silvius D, Zou D, Raymond RM, Orten DJ, Kimberling WJ, Smith RJ, Weil D, Petit C, Otto EA, Xu PX, Hildebrandt F.
Am J Hum Genet 80(4):800-4. Epub 2007 Feb 22. 2007
2SIX5
Six5 is required for spermatogenic cell survival and spermiogenesis.
Sarkar PS, Paul S, Han J, Reddy S.
Hum Mol Genet 13(14):1421-31. Epub 2004 May 26. 2004
3ACTN4, AURKC, CKM, CYP2B6, CYTH2, DMPK, FOSB, IRF3, ITPKC, MIA, SIX5, VASP
The telomeric region of BTA18 containing a potential QTL region for health in cattle exhibits high similarity to the HSA19q region in humans small star, filled
Brunner RM, Sanftleben H, Goldammer T, Kuhn C, Weikard R, Kata SR, Womack JE, Schwerin M.
Genomics 81(3):270-8. 2003
4IGFBP5, SIX5
Identification of transcriptional targets for Six5: implication for the pathogenesis of myotonic dystrophy type 1.
Sato S, Nakamura M, Cho DH, Tapscott SJ, Ozaki H, Kawakami K.
Hum Mol Genet 11(9):1045-58. 2002
5SIX5
Drosophila homolog of the myotonic dystrophy-associated gene, SIX5, is required for muscle and gonad development.
Kirby RJ, Hamilton GM, Finnegan DJ, Johnson KJ, Jarman AP.
Curr Biol 11(13):1044-9. 2001
6SIX5
Functional analysis of the homeodomain protein SIX5.
Harris SE, Winchester CL, Johnson KJ.
Nucleic Acids Res 28(9):1871-8. 2000
7SIX5
Reduced expression of DMAHP/SIX5 gene in myotonic dystrophy muscle.
Inukai A, Doyu M, Kato T, Liang Y, Kuru S, Yamamoto M, Kobayashi Y, Sobue G.
Muscle Nerve 23(9):1421-6. 2000
8DMPK, SIX5
Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy.
Winchester CL, Ferrier RK, Sermoni A, Clark BJ, Johnson KJ.
Hum Mol Genet 8 : 481-492. 1999
9DM1, DMPK, SIX5
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression.
Korade-Mirnics Z, et al.
Hum Mol Genet 8(6):1017-23. 1999
10DMWD, SIX5
Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but notDMAHP levels.
Eriksson M, et al.
Hum Mol Genet 8(6):1053-60. 1999
11SIX5
Promoter of mDMAHP/Six5 : differential utilization of multiple transcription initiation sites and positive/negative regulatory elements.
Murakami Y, et al.
Hum Mol Genet 7 : 2103-2112. 1998
12DM1, DMPK, DMWD, SIX5
Myotonic dystrophy: molecular windows on a complex etiology.
Korade-Mirnics Z, Babitzke P, Hoffman E.
Nucleic Acids Res 26(6):1363-8. Review 1998
13SIX5, DM1
Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP.
Klesert TR, Otten AD, Bird TD, Tapscott SJ.
Nat Genet 16(4):402-6. 1997
14SIX5
Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene.
Thornton CA, Wymer JP, Simmons Z, McClain C, Moxley RT 3rd.
Nat Genet 16(4):407-9. 1997
15DM1, SIX5, DMPK
A novel homeo domain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat.
Boucher CA, King SK, Carey N, Krahe R, Winchester CL, Rahman S, Creavin T, Meghji P, Bailey ME, Chartier FL, et al.
Hum Mol Genet 4(10):1919-25. 1995