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NFAT3/c4-mediated excitotoxicity in hippocampal apoptosis during radiation-induced brain injury.

Xu M, Fan Q, Zhang J, Chen Y, Xu R, Chen L, Zhao P, Tian Y.

J Radiat Res. 2017 Nov 1;58(6):827-833. doi: 10.1093/jrr/rrx041.


STIM1 Ca2+ Sensor Control of L-type Ca2+-Channel-Dependent Dendritic Spine Structural Plasticity and Nuclear Signaling.

Dittmer PJ, Wild AR, Dell'Acqua ML, Sather WA.

Cell Rep. 2017 Apr 11;19(2):321-334. doi: 10.1016/j.celrep.2017.03.056.


Nerve growth factor (NGF) regulates activity of nuclear factor of activated T-cells (NFAT) in neurons via the phosphatidylinositol 3-kinase (PI3K)-Akt-glycogen synthase kinase 3β (GSK3β) pathway.

Kim MS, Shutov LP, Gnanasekaran A, Lin Z, Rysted JE, Ulrich JD, Usachev YM.

J Biol Chem. 2014 Nov 7;289(45):31349-60. doi: 10.1074/jbc.M114.587188. Epub 2014 Sep 17.


NFATc3 pathway participates in the process that 15-LO/15-HETE protects pulmonary artery smooth muscle cells against apoptosis during hypoxia.

Ran Y, Wu H, Wei L, Yu X, Chen J, Li S, Zhang L, Lou J, Zhu D.

J Recept Signal Transduct Res. 2014 Aug;34(4):270-82. doi: 10.3109/10799893.2014.917322. Epub 2014 May 22.


Calcineurin/nuclear factor of activated T cells-coupled vanilliod transient receptor potential channel 4 ca2+ sparklets stimulate airway smooth muscle cell proliferation.

Zhao L, Sullivan MN, Chase M, Gonzales AL, Earley S.

Am J Respir Cell Mol Biol. 2014 Jun;50(6):1064-75. doi: 10.1165/rcmb.2013-0416OC.


Differential effect of traumatic brain injury on the nuclear factor of activated T Cells C3 and C4 isoforms in the rat hippocampus.

Yan HQ, Shin SS, Ma X, Li Y, Dixon CE.

Brain Res. 2014 Feb 22;1548:63-72. doi: 10.1016/j.brainres.2013.12.028. Epub 2013 Dec 31.


A new role for the calcineurin/NFAT pathway in neonatal myosin heavy chain expression via the NFATc2/MyoD complex during mouse myogenesis.

Daou N, Lecolle S, Lefebvre S, della Gaspera B, Charbonnier F, Chanoine C, Armand AS.

Development. 2013 Dec;140(24):4914-25. doi: 10.1242/dev.097428.


COX-2 is involved in ET-1-induced hypertrophy of neonatal rat cardiomyocytes: role of NFATc3.

Li H, Gao S, Ye J, Feng X, Cai Y, Liu Z, Lu J, Li Q, Huang X, Chen S, Liu P.

Mol Cell Endocrinol. 2014 Feb 15;382(2):998-1006. doi: 10.1016/j.mce.2013.11.012. Epub 2013 Nov 26.


MicroRNA-124 suppresses the transactivation of nuclear factor of activated T cells by targeting multiple genes and inhibits the proliferation of pulmonary artery smooth muscle cells.

Kang K, Peng X, Zhang X, Wang Y, Zhang L, Gao L, Weng T, Zhang H, Ramchandran R, Raj JU, Gou D, Liu L.

J Biol Chem. 2013 Aug 30;288(35):25414-27. doi: 10.1074/jbc.M113.460287. Epub 2013 Jul 12.


MicroRNA-26 governs profibrillatory inward-rectifier potassium current changes in atrial fibrillation.

Luo X, Pan Z, Shan H, Xiao J, Sun X, Wang N, Lin H, Xiao L, Maguy A, Qi XY, Li Y, Gao X, Dong D, Zhang Y, Bai Y, Ai J, Sun L, Lu H, Luo XY, Wang Z, Lu Y, Yang B, Nattel S.

J Clin Invest. 2013 May;123(5):1939-51. doi: 10.1172/JCI62185. Epub 2013 Apr 1.


Silencing of STIM1 attenuates hypoxia-induced PASMCs proliferation via inhibition of the SOC/Ca2+/NFAT pathway.

Hou X, Chen J, Luo Y, Liu F, Xu G, Gao Y.

Respir Res. 2013 Jan 5;14:2. doi: 10.1186/1465-9921-14-2.


IGF-1 induces IP3 -dependent calcium signal involved in the regulation of myostatin gene expression mediated by NFAT during myoblast differentiation.

Valdés JA, Flores S, Fuentes EN, Osorio-Fuentealba C, Jaimovich E, Molina A.

J Cell Physiol. 2013 Jul;228(7):1452-63. doi: 10.1002/jcp.24298. Erratum in: J Cell Physiol. 2015 May;230(5):1158-9.


Dynamic response diversity of NFAT isoforms in individual living cells.

Yissachar N, Sharar Fischler T, Cohen AA, Reich-Zeliger S, Russ D, Shifrut E, Porat Z, Friedman N.

Mol Cell. 2013 Jan 24;49(2):322-30. doi: 10.1016/j.molcel.2012.11.003. Epub 2012 Dec 6.


Positive feedback control between STIM1 and NFATc3 is required for C2C12 myoblast differentiation.

Phuong TT, Yun YH, Kim SJ, Kang TM.

Biochem Biophys Res Commun. 2013 Jan 11;430(2):722-8. doi: 10.1016/j.bbrc.2012.11.082. Epub 2012 Dec 1.


Distinct activation properties of the nuclear factor of activated T-cells (NFAT) isoforms NFATc3 and NFATc4 in neurons.

Ulrich JD, Kim MS, Houlihan PR, Shutov LP, Mohapatra DP, Strack S, Usachev YM.

J Biol Chem. 2012 Nov 2;287(45):37594-609. doi: 10.1074/jbc.M112.365197. Epub 2012 Sep 12.


Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.

Gaudet P, Livstone MS, Lewis SE, Thomas PD.

Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.


Opposing roles of FoxP1 and Nfat3 in transcriptional control of cardiomyocyte hypertrophy.

Bai S, Kerppola TK.

Mol Cell Biol. 2011 Jul;31(14):3068-80. doi: 10.1128/MCB.00925-10. Epub 2011 May 23.


High extracellular calcium-induced NFATc3 regulates the expression of receptor activator of NF-κB ligand in osteoblasts.

Lee HL, Bae OY, Baek KH, Kwon A, Hwang HR, Qadir AS, Park HJ, Woo KM, Ryoo HM, Baek JH.

Bone. 2011 Aug;49(2):242-9. doi: 10.1016/j.bone.2011.04.006. Epub 2011 Apr 14.


NFAT/Fas signaling mediates the neuronal apoptosis and motor side effects of GSK-3 inhibition in a mouse model of lithium therapy.

Gómez-Sintes R, Lucas JJ.

J Clin Invest. 2010 Jul;120(7):2432-45. doi: 10.1172/JCI37873. Epub 2010 Jun 7.


miR-9 and NFATc3 regulate myocardin in cardiac hypertrophy.

Wang K, Long B, Zhou J, Li PF.

J Biol Chem. 2010 Apr 16;285(16):11903-12. doi: 10.1074/jbc.M109.098004. Epub 2010 Feb 21.

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