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Results: 1 to 20 of 71

Cited In for PubMed (Select 10346815)

1.

Pioneer transcription factors target partial DNA motifs on nucleosomes to initiate reprogramming.

Soufi A, Garcia MF, Jaroszewicz A, Osman N, Pellegrini M, Zaret KS.

Cell. 2015 Apr 23;161(3):555-68. doi: 10.1016/j.cell.2015.03.017. Epub 2015 Apr 16.

PMID:
25892221
2.

Regulation of cerebral cortical neurogenesis by the Pax6 transcription factor.

Manuel MN, Mi D, Mason JO, Price DJ.

Front Cell Neurosci. 2015 Mar 10;9:70. doi: 10.3389/fncel.2015.00070. eCollection 2015.

3.

The RED domain of Paired is specifically required for Drosophila accessory gland maturation.

Li L, Li P, Xue L.

Open Biol. 2015 Feb;5(2):140179. doi: 10.1098/rsob.140179.

4.

DNA-mediated cooperativity facilitates the co-selection of cryptic enhancer sequences by SOX2 and PAX6 transcription factors.

Narasimhan K, Pillay S, Huang YH, Jayabal S, Udayasuryan B, Veerapandian V, Kolatkar P, Cojocaru V, Pervushin K, Jauch R.

Nucleic Acids Res. 2015 Feb 18;43(3):1513-28. doi: 10.1093/nar/gku1390. Epub 2015 Jan 10.

5.

Search by proteins for their DNA target site: 2. The effect of DNA conformation on the dynamics of multidomain proteins.

Bhattacherjee A, Levy Y.

Nucleic Acids Res. 2014 Nov 10;42(20):12415-24. doi: 10.1093/nar/gku933. Epub 2014 Oct 16.

6.

The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function.

Tanaka-Matakatsu M, Miller J, Du W.

Protein Cell. 2015 Jan;6(1):68-78. doi: 10.1007/s13238-014-0101-9. Epub 2014 Sep 20.

7.

Whole exome sequence analysis of Peters anomaly.

Weh E, Reis LM, Happ HC, Levin AV, Wheeler PG, David KL, Carney E, Angle B, Hauser N, Semina EV.

Hum Genet. 2014 Dec;133(12):1497-511. doi: 10.1007/s00439-014-1481-x. Epub 2014 Sep 3.

PMID:
25182519
8.

Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism.

Vincenzi M, Camilot M, Ferrarini E, Teofoli F, Venturi G, Gaudino R, Cavarzere P, De Marco G, Agretti P, Dimida A, Tonacchera M, Boner A, Antoniazzi F.

BMC Endocr Disord. 2014 Aug 22;14:69. doi: 10.1186/1472-6823-14-69.

9.

Daughterless homodimer synergizes with Eyeless to induce Atonal expression and retinal neuron differentiation.

Tanaka-Matakatsu M, Miller J, Borger D, Tang WJ, Du W.

Dev Biol. 2014 Aug 15;392(2):256-65. doi: 10.1016/j.ydbio.2014.05.019. Epub 2014 Jun 2.

PMID:
24886829
10.

Gene regulation by PAX6: structural-functional correlations of missense mutants and transcriptional control of Trpm3/miR-204.

Xie Q, Ung D, Khafizov K, Fiser A, Cvekl A.

Mol Vis. 2014 Mar 6;20:270-82. eCollection 2014.

11.

Disruption of autoregulatory feedback by a mutation in a remote, ultraconserved PAX6 enhancer causes aniridia.

Bhatia S, Bengani H, Fish M, Brown A, Divizia MT, de Marco R, Damante G, Grainger R, van Heyningen V, Kleinjan DA.

Am J Hum Genet. 2013 Dec 5;93(6):1126-34. doi: 10.1016/j.ajhg.2013.10.028. Epub 2013 Nov 27. Review.

12.

Distinct regulatory mechanisms act to establish and maintain Pax3 expression in the developing neural tube.

Moore S, Ribes V, Terriente J, Wilkinson D, Relaix F, Briscoe J.

PLoS Genet. 2013;9(10):e1003811. doi: 10.1371/journal.pgen.1003811. Epub 2013 Oct 3.

13.

Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation.

Thomas S, Thomas MG, Andrews C, Chan WM, Proudlock FA, McLean RJ, Pradeep A, Engle EC, Gottlob I.

Eur J Hum Genet. 2014 Mar;22(3):344-9. doi: 10.1038/ejhg.2013.162. Epub 2013 Aug 14.

14.

Cancer missense mutations alter binding properties of proteins and their interaction networks.

Nishi H, Tyagi M, Teng S, Shoemaker BA, Hashimoto K, Alexov E, Wuchty S, Panchenko AR.

PLoS One. 2013 Jun 14;8(6):e66273. doi: 10.1371/journal.pone.0066273. Print 2013.

15.

High efficiency TALENs enable F0 functional analysis by targeted gene disruption in Xenopus laevis embryos.

Suzuki KT, Isoyama Y, Kashiwagi K, Sakuma T, Ochiai H, Sakamoto N, Furuno N, Kashiwagi A, Yamamoto T.

Biol Open. 2013 Mar 4;2(5):448-52. doi: 10.1242/bio.20133855. Print 2013 May 15.

16.

Functional dissection of the paired domain of Pax6 reveals molecular mechanisms of coordinating neurogenesis and proliferation.

Walcher T, Xie Q, Sun J, Irmler M, Beckers J, Öztürk T, Niessing D, Stoykova A, Cvekl A, Ninkovic J, Götz M.

Development. 2013 Mar;140(5):1123-36. doi: 10.1242/dev.082875.

17.

Pax6 interactions with chromatin and identification of its novel direct target genes in lens and forebrain.

Xie Q, Yang Y, Huang J, Ninkovic J, Walcher T, Wolf L, Vitenzon A, Zheng D, Götz M, Beebe DC, Zavadil J, Cvekl A.

PLoS One. 2013;8(1):e54507. doi: 10.1371/journal.pone.0054507. Epub 2013 Jan 14.

18.

Solution properties of the archaeal CRISPR DNA repeat-binding homeodomain protein Cbp2.

Kenchappa CS, Heidarsson PO, Kragelund BB, Garrett RA, Poulsen FM.

Nucleic Acids Res. 2013 Mar 1;41(5):3424-35. doi: 10.1093/nar/gks1465. Epub 2013 Jan 15.

19.

Linkers in the structural biology of protein-protein interactions.

Reddy Chichili VP, Kumar V, Sivaraman J.

Protein Sci. 2013 Feb;22(2):153-67. doi: 10.1002/pro.2206. Epub 2013 Jan 8. Review.

20.

Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses.

Hauswirth R, Haase B, Blatter M, Brooks SA, Burger D, Drögemüller C, Gerber V, Henke D, Janda J, Jude R, Magdesian KG, Matthews JM, Poncet PA, Svansson V, Tozaki T, Wilkinson-White L, Penedo MC, Rieder S, Leeb T.

PLoS Genet. 2012;8(4):e1002653. doi: 10.1371/journal.pgen.1002653. Epub 2012 Apr 12.

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