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Summary Expression Phenotypes Gene Literature (14) GO Terms (3) Nucleotides (245) Proteins (46) Interactants (123) Wiki
XB-GENEPAGE-944182

Papers associated with map2k6



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E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE, Baker JC., Dev Cell. February 9, 2015; 32 (3): 345-57.                  

Osmostress-induced apoptosis in Xenopus oocytes: role of stress protein kinases, calpains and Smac/DIABLO., Ben Messaoud N, Yue J, Valent D, Katzarova I, López JM., PLoS One. January 1, 2015; 10 (4): e0124482.            

Neural ectoderm-secreted FGF initiates the expression of Nkx2.5 in cardiac progenitors via a p38 MAPK/CREB pathway., Keren-Politansky A, Keren A, Bengal E., Dev Biol. November 15, 2009; 335 (2): 374-84.            

Vg1RBP phosphorylation by Erk2 MAP kinase correlates with the cortical release of Vg1 mRNA during meiotic maturation of Xenopus oocytes., Git A, Allison R, Perdiguero E, Nebreda AR, Houliston E, Standart N., RNA. June 1, 2009; 15 (6): 1121-33.

The extracellular signal-regulated kinase-mitogen-activated protein kinase pathway phosphorylates and targets Cdc25A for SCF beta-TrCP-dependent degradation for cell cycle arrest., Isoda M, Kanemori Y, Nakajo N, Uchida S, Yamashita K, Ueno H, Sagata N., Mol Biol Cell. April 1, 2009; 20 (8): 2186-95.              

A p38 MAPK-CREB pathway functions to pattern mesoderm in Xenopus., Keren A, Keren-Politansky A, Bengal E., Dev Biol. October 1, 2008; 322 (1): 86-94.        

p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development., Keren A, Bengal E, Frank D., Dev Biol. December 1, 2005; 288 (1): 73-86.              

Xp38gamma/SAPK3 promotes meiotic G(2)/M transition in Xenopus oocytes and activates Cdc25C., Perdiguero E, Pillaire MJ, Bodart JF, Hennersdorf F, Frödin M, Duesbery NS, Alonso G, Nebreda AR., EMBO J. November 3, 2003; 22 (21): 5746-56.

Anthrax lethal factor proteolysis and inactivation of MAPK kinase., Chopra AP, Boone SA, Liang X, Duesbery NS., J Biol Chem. March 14, 2003; 278 (11): 9402-6.

Differential activation of p38 mitogen-activated protein kinase isoforms depending on signal strength., Alonso G, Ambrosino C, Jones M, Nebreda AR., J Biol Chem. December 22, 2000; 275 (51): 40641-8.

Concentration-dependent positive and negative regulation of a MAP kinase by a MAP kinase kinase., Kieran MW, Katz S, Vail B, Zon LI, Mayer BJ., Oncogene. November 18, 1999; 18 (48): 6647-57.

Distinct domains of mouse dishevelled are responsible for the c-Jun N-terminal kinase/stress-activated protein kinase activation and the axis formation in vertebrates., Moriguchi T, Kawachi K, Kamakura S, Masuyama N, Yamanaka H, Matsumoto K, Kikuchi A, Nishida E., J Biol Chem. October 22, 1999; 274 (43): 30957-62.        

Activation of the novel stress-activated protein kinase SAPK4 by cytokines and cellular stresses is mediated by SKK3 (MKK6); comparison of its substrate specificity with that of other SAP kinases., Goedert M, Cuenda A, Craxton M, Jakes R, Cohen P., EMBO J. June 16, 1997; 16 (12): 3563-71.

Activation of stress-activated protein kinase-3 (SAPK3) by cytokines and cellular stresses is mediated via SAPKK3 (MKK6); comparison of the specificities of SAPK3 and SAPK2 (RK/p38)., Cuenda A, Cohen P, Buée-Scherrer V, Goedert M., EMBO J. January 15, 1997; 16 (2): 295-305.

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