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Items: 1 to 20 of 85


Regulation of the MEX-5 gradient by a spatially segregated kinase/phosphatase cycle.

Griffin EE, Odde DJ, Seydoux G.

Cell. 2011 Sep 16;146(6):955-68. doi: 10.1016/j.cell.2011.08.012.


The RNA binding protein MEX-3 retains asymmetric activity in the early Caenorhabditis elegans embryo in the absence of asymmetric protein localization.

Huang NN, Hunter CP.

Gene. 2015 Jan 10;554(2):160-73. doi: 10.1016/j.gene.2014.10.042. Epub 2014 Oct 28.


MEX-5 enrichment in the C. elegans early embryo mediated by differential diffusion.

Daniels BR, Dobrowsky TM, Perkins EM, Sun SX, Wirtz D.

Development. 2010 Aug 1;137(15):2579-85. doi: 10.1242/dev.051326.


MEX-3 interacting proteins link cell polarity to asymmetric gene expression in Caenorhabditis elegans.

Huang NN, Mootz DE, Walhout AJ, Vidal M, Hunter CP.

Development. 2002 Feb;129(3):747-59.


MEX-5 asymmetry in one-cell C. elegans embryos requires PAR-4- and PAR-1-dependent phosphorylation.

Tenlen JR, Molk JN, London N, Page BD, Priess JR.

Development. 2008 Nov;135(22):3665-75. doi: 10.1242/dev.027060. Epub 2008 Oct 8.


Polo kinases regulate C. elegans embryonic polarity via binding to DYRK2-primed MEX-5 and MEX-6.

Nishi Y, Rogers E, Robertson SM, Lin R.

Development. 2008 Feb;135(4):687-97. doi: 10.1242/dev.013425. Epub 2008 Jan 16.


PAR proteins direct asymmetry of the cell cycle regulators Polo-like kinase and Cdc25.

Rivers DM, Moreno S, Abraham M, Ahringer J.

J Cell Biol. 2008 Mar 10;180(5):877-85. doi: 10.1083/jcb.200710018. Epub 2008 Mar 3.


Polarization of the C. elegans zygote proceeds via distinct establishment and maintenance phases.

Cuenca AA, Schetter A, Aceto D, Kemphues K, Seydoux G.

Development. 2003 Apr;130(7):1255-65.


Coupling between cytoplasmic concentration gradients through local control of protein mobility in the Caenorhabditis elegans zygote.

Wu Y, Zhang H, Griffin EE.

Mol Biol Cell. 2015 Sep 1;26(17):2963-70. doi: 10.1091/mbc.E15-05-0302. Epub 2015 Jul 8.


Asymmetric enrichment of PIE-1 in the Caenorhabditis elegans zygote mediated by binary counterdiffusion.

Daniels BR, Perkins EM, Dobrowsky TM, Sun SX, Wirtz D.

J Cell Biol. 2009 Feb 23;184(4):473-9. doi: 10.1083/jcb.200809077. Epub 2009 Feb 16.


Multiple RNA-binding proteins function combinatorially to control the soma-restricted expression pattern of the E3 ligase subunit ZIF-1.

Oldenbroek M, Robertson SM, Guven-Ozkan T, Gore S, Nishi Y, Lin R.

Dev Biol. 2012 Mar 15;363(2):388-98. doi: 10.1016/j.ydbio.2012.01.002. Epub 2012 Jan 12.


MEX-5 and MEX-6 function to establish soma/germline asymmetry in early C. elegans embryos.

Schubert CM, Lin R, de Vries CJ, Plasterk RH, Priess JR.

Mol Cell. 2000 Apr;5(4):671-82.


MEX-3 is a KH domain protein that regulates blastomere identity in early C. elegans embryos.

Draper BW, Mello CC, Bowerman B, Hardin J, Priess JR.

Cell. 1996 Oct 18;87(2):205-16.


The Caenorhabditis elegans par-5 gene encodes a 14-3-3 protein required for cellular asymmetry in the early embryo.

Morton DG, Shakes DC, Nugent S, Dichoso D, Wang W, Golden A, Kemphues KJ.

Dev Biol. 2002 Jan 1;241(1):47-58.


PP2A phosphatase acts upon SAS-5 to ensure centriole formation in C. elegans embryos.

Kitagawa D, Flückiger I, Polanowska J, Keller D, Reboul J, Gönczy P.

Dev Cell. 2011 Apr 19;20(4):550-62. doi: 10.1016/j.devcel.2011.02.005.


Exclusion of germ plasm proteins from somatic lineages by cullin-dependent degradation.

DeRenzo C, Reese KJ, Seydoux G.

Nature. 2003 Aug 7;424(6949):685-9. Epub 2003 Jul 23.


Modulation of KSR activity in Caenorhabditis elegans by Zn ions, PAR-1 kinase and PP2A phosphatase.

Yoder JH, Chong H, Guan KL, Han M.

EMBO J. 2004 Jan 14;23(1):111-9. Epub 2003 Dec 11.

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