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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2001 | 1 |
2004 | 1 |
2010 | 1 |
2012 | 1 |
2024 | 0 |
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Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome.
Hum Mol Genet. 2001 Nov 15;10(24):2775-81. doi: 10.1093/hmg/10.24.2775.
Hum Mol Genet. 2001.
PMID: 11734542
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
Ruf RG, Xu PX, Silvius D, Otto EA, Beekmann F, Muerb UT, Kumar S, Neuhaus TJ, Kemper MJ, Raymond RM Jr, Brophy PD, Berkman J, Gattas M, Hyland V, Ruf EM, Schwartz C, Chang EH, Smith RJ, Stratakis CA, Weil D, Petit C, Hildebrandt F.
Ruf RG, et al.
Proc Natl Acad Sci U S A. 2004 May 25;101(21):8090-5. doi: 10.1073/pnas.0308475101. Epub 2004 May 12.
Proc Natl Acad Sci U S A. 2004.
PMID: 15141091
Free PMC article.
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Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development.
Landgraf K, Bollig F, Trowe MO, Besenbeck B, Ebert C, Kruspe D, Kispert A, Hänel F, Englert C.
Landgraf K, et al.
Mol Cell Biol. 2010 Dec;30(24):5764-75. doi: 10.1128/MCB.01645-09. Epub 2010 Oct 18.
Mol Cell Biol. 2010.
PMID: 20956555
Free PMC article.
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EYA1 and SIX1 drive the neuronal developmental program in cooperation with the SWI/SNF chromatin-remodeling complex and SOX2 in the mammalian inner ear.
Ahmed M, Xu J, Xu PX.
Ahmed M, et al.
Development. 2012 Jun;139(11):1965-77. doi: 10.1242/dev.071670. Epub 2012 Apr 18.
Development. 2012.
PMID: 22513373
Free PMC article.
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