Citations for
1CA8, PRKCG
Carbonic Anhydrase 8 Expression in Purkinje Cells Is Controlled by PKCγ Activity and Regulates Purkinje Cell Dendritic Growth.
Shimobayashi E, Wagner W, Kapfhammer JP.
Mol Neurobiol ol Neurobiol. 2015 Sep 23. [Epub ahead of print] 2015
2HINT1, PRKCG
Hint1 knockout results in a compromised activation of protein kinase C gamma in the brain.
Zhang F, Fang Z, Wang JB.
Brain Res 1622:196-203. doi: 10.1016/j.brainres.2015.06.029. Epub 2015 Jun 29. 2015
3PRKCG
Single-nucleotide polymorphisms of the PRKCG gene and osteosarcoma susceptibility.
Zhang Y, Hu X, Wang HK, Shen WW, Liao TQ, Chen P, Chu TW.
Tumour Biol 35(12):12671-7. doi: 10.1007/s13277-014-2591-8. Epub 2014 Sep 25. 2014
4PRKCG, SCA14
Increased protein kinase C gamma activity induces Purkinje cell pathology in a mouse model of spinocerebellar ataxia 14.
Ji J, Hassler ML, Shimobayashi E, Paka N, Streit R, Kapfhammer JP.
Neurobiol Dis 70:1-11. doi: 10.1016/j.nbd.2014.06.002. Epub 2014 Jun 14. 2014
5PRKCG, SCA14
Deregulation of the actin cytoskeleton and macropinocytosis in response to phorbol ester by the mutant protein kinase C gamma that causes spinocerebellar ataxia type 14.
Yamamoto K, Seki T, Yamamoto H, Adachi N, Tanaka S, Hide I, Saito N, Sakai N.
Front Physiol 5:126. doi: 10.3389/fphys.2014.00126. eCollection 2014. 2014
6ARNTL, PRKCG
PKCγ participates in food entrainment by regulating BMAL1.
Zhang L, Abraham D, Lin ST, Oster H, Eichele G, Fu YH, Ptáček LJ.
Proc Natl Acad Sci U S A 109(50):20679-84. doi: 10.1073/pnas.1218699110. Epub 2012 Nov 26. 2012
7PRKCG, SCA14
Mutant PKCγ in spinocerebellar ataxia type 14 disrupts synapse elimination and long-term depression in Purkinje cells in vivo.
Shuvaev AN, Horiuchi H, Seki T, Goenawan H, Irie T, Iizuka A, Sakai N, Hirai H.
J Neurosci 31(40):14324-34. doi: 10.1523/JNEUROSCI.5530-10.2011. 2011
8PRKCG
Effect of perinatal thyroid hormone deficiency on expression of rat hippocampal conventional protein kinase C isozymes.
Zhang HM, Lin N, Dong Y, Su Q, Luo M.
Mol Cell Biochem 353(1-2):65-71. doi: 10.1007/s11010-011-0775-8. Epub 2011 Mar 22. 2011
9GRIN1, PRKCG
Involvement of the spinal NMDA receptor/PKCγ signaling pathway in the development of bone cancer pain.
Xiaoping G, Xiaofang Z, Yaguo Z, Juan Z, Junhua W, Zhengliang M.
Brain Res 1335:83-90. doi: 10.1016/j.brainres.2010.03.083. Epub 2010 Apr 1. 2010
10PRKCG, SLC6A1
Gamma-aminobutyric acid transporter 1 negatively regulates T cell activation and survival through protein kinase C-dependent signaling pathways.
Wang Y, Luo Q, Xu Y, Feng D, Fei J, Cheng Q, Xu L.
J Immunol 183(5):3488-95. doi: 10.4049/jimmunol.0900767. Epub 2009 Aug 10. 2009
11PRKCG, SCA14
Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin.
Asai H, Hirano M, Shimada K, Kiriyama T, Furiya Y, Ikeda M, Iwamoto T, Mori T, Nishinaka K, Konishi N, Udaka F, Ueno S.
Hum Mol Genet 18(19):3533-43. doi: 10.1093/hmg/ddp298. Epub 2009 Jun 26. 2009
12PRKCG
Activation of mutant protein kinase Cgamma leads to aberrant sequestration and impairment of its cellular function.
Doran G, Davies KE, Talbot K.
Biochem Biophys Res Commun 372(3):447-53. doi: 10.1016/j.bbrc.2008.05.072. Epub 2008 May 27. 2008
13PRKCG
Synergistic control of protein kinase Cgamma activity by ionotropic and metabotropic glutamate receptor inputs in hippocampal neurons.
Codazzi F, Di Cesare A, Chiulli N, Albanese A, Meyer T, Zacchetti D, Grohovaz F.
J Neurosci 26(13):3404-11. 2006
14SCA14, PRKCG
The clinical and genetic spectrum of spinocerebellar ataxia 14.
Chen DH, Cimino PJ, Ranum LP, Zoghbi HY, Yabe I, Schut L, Margolis RL, Lipe HP, Feleke A, Matsushita M, Wolff J, Morgan C, Lau D, Fernandez M, Sasaki H, Raskind WH, Bird TD.
Neurology 64(7):1258-60. 2005
15PRKCG,SCA14
A novel H101Q mutation causes PKCgamma loss in spinocerebellar ataxia type 14.
Alonso I, Costa C, Gomes A, Ferro A, Seixas AI, Silva S, Cruz VT, Coutinho P, Sequeiros J, Silveira I.
J Hum Genet 50(10):523-9. Epub 2005 Sep 28. 2005
16SCA14, PRKCG
Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
Stevanin G, Hahn V, Lohmann E, Bouslam N, Gouttard M, Soumphonphakdy C, Welter ML, Ollagnon-Roman E, Lemainque A, Ruberg M, Brice A, Durr A.
Arch Neurol 61(8):1242-8. 2004
17GJA3, GJA8, PRKCG
Differential phosphorylation of connexin46 and connexin50 by H2O2 activation of protein kinase Cgamma.
Lin D, Lobell S, Jewell A, Takemoto DJ.
Mol Vis 10:688-95. 2004
18PRKCG, SCA14
Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
Chen DH, Brkanac Z, Verlinde CL, Tan XJ, Bylenok L, Nochlin D, Matsushita M, Lipe H, Wolff J, Fernandez M, Cimino PJ, Bird TD, Raskind WH.
Am J Hum Genet 72(4):839-49. Epub 2003 Mar 17. 2003
19CA8, PRKCG
Altered dendritic development of cerebellar Purkinje cells in slice cultures from protein kinase Cgamma-deficient mice.
Schrenk K, Kapfhammer JP, Metzger F.
Neuroscience 110(4):675-89. 2002
20PRKCG, RP11
Segregation of a PRKCG mutation in two RP11 families.
Al-Maghtheh M, et al.
Am J Hum Genet 62 : 1248-1252. 1998
21PRKCG
Linkage relationships of the protein kinase C gamma gene exclude it as a candidate for myotonic dystrophy.
Johnson KJ, et al.
Cytogenet Cell Genet 48 : 13-15. 1988
22PRKCA, IGF1R, PRKCG
Chromosomal mapping of genes involved in growth control.
Francke U, et al.
Cold Spring Harbor Symp Quant Biol 51 : 855-866. 1986
23PRKCA, PRKCB, PRKCG
The complete primary structure of protein kinase C : the major phobol ester receptor.
Parker PJ, et al.
Science 233 : 853-859. 1986
24PRKCA, PRKCB, PRKCG
Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways.
Coussens L, et al.
Science 233 : 859-866. 1986