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Items: 1 to 20 of 78

1.

The Paired-box protein PAX-3 regulates the choice between lateral and ventral epidermal cell fates in C. elegans.

Thompson KW, Joshi P, Dymond JS, Gorrepati L, Smith HE, Krause MW, Eisenmann DM.

Dev Biol. 2016 Apr 15;412(2):191-207. doi: 10.1016/j.ydbio.2016.03.002.

PMID:
26953187
2.

Homeodomain proteins: an update.

Bürglin TR, Affolter M.

Chromosoma. 2016 Jun;125(3):497-521. doi: 10.1007/s00412-015-0543-8. Review.

3.

Pax2/5/8 and Pax6 alternative splicing events in basal chordates and vertebrates: a focus on paired box domain.

Fabian P, Kozmikova I, Kozmik Z, Pantzartzi CN.

Front Genet. 2015 Jul 2;6:228. doi: 10.3389/fgene.2015.00228.

4.

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.

5.

Evidence for intermediate mesoderm and kidney progenitor cell specification by Pax2 and PTIP dependent mechanisms.

Ranghini EJ, Dressler GR.

Dev Biol. 2015 Mar 15;399(2):296-305. doi: 10.1016/j.ydbio.2015.01.005.

6.

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.

7.

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.

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.

Pax3 and Tbx5 specify whether PDGFRα+ cells assume skeletal or cardiac muscle fate in differentiating embryonic stem cells.

Magli A, Schnettler E, Swanson SA, Borges L, Hoffman K, Stewart R, Thomson JA, Keirstead SA, Perlingeiro RC.

Stem Cells. 2014 Aug;32(8):2072-83. doi: 10.1002/stem.1713.

10.

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.

11.

Mutation analysis of paired box 6 gene in inherited aniridia in northern China.

Chen P, Zang X, Sun D, Wang Y, Wang Y, Zhao X, Zhang M, Xie L.

Mol Vis. 2013 May 30;19:1169-77.

12.

SUMOylation of Pax7 is essential for neural crest and muscle development.

Luan Z, Liu Y, Stuhlmiller TJ, Marquez J, García-Castro MI.

Cell Mol Life Sci. 2013 May;70(10):1793-806. doi: 10.1007/s00018-012-1220-1.

13.

Functional dissection of Pax3 in paraxial mesoderm development and myogenesis.

Magli A, Schnettler E, Rinaldi F, Bremer P, Perlingeiro RC.

Stem Cells. 2013 Jan;31(1):59-70. doi: 10.1002/stem.1254.

14.

Crystal structure of the human NKX2.5 homeodomain in complex with DNA target.

Pradhan L, Genis C, Scone P, Weinberg EO, Kasahara H, Nam HJ.

Biochemistry. 2012 Aug 14;51(32):6312-9.

15.

The B-cell identity factor Pax5 regulates distinct transcriptional programmes in early and late B lymphopoiesis.

Revilla-I-Domingo R, Bilic I, Vilagos B, Tagoh H, Ebert A, Tamir IM, Smeenk L, Trupke J, Sommer A, Jaritz M, Busslinger M.

EMBO J. 2012 Jun 5;31(14):3130-46. doi: 10.1038/emboj.2012.155.

16.
17.

Functional redundancy of two Pax-like proteins in transcriptional activation of cyst wall protein genes in Giardia lamblia.

Chuang SF, Su LH, Cho CC, Pan YJ, Sun CH.

PLoS One. 2012;7(2):e30614. doi: 10.1371/journal.pone.0030614.

18.

Soluble expression, purification and characterization of the full length IS2 Transposase.

Lewis LA, Astatke M, Umekubo PT, Alvi S, Saby R, Afrose J.

Mob DNA. 2011 Oct 27;2:14. doi: 10.1186/1759-8753-2-14.

19.

Molecular genetics of familial nystagmus complicated with cataract and iris anomalies.

Yan N, Zhao Y, Wang Y, Xie A, Huang H, Yu W, Liu X, Cai SP.

Mol Vis. 2011;17:2612-7.

20.

Dominant-negative mechanism of leukemogenic PAX5 fusions.

Kawamata N, Pennella MA, Woo JL, Berk AJ, Koeffler HP.

Oncogene. 2012 Feb 23;31(8):966-77. doi: 10.1038/onc.2011.291.

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