-
1
-
-
0037205048
-
The phosphoinositide 3-kinase pathway
-
Cantley L.C. The phosphoinositide 3-kinase pathway. Science 2002, 296:1655-1657.
-
(2002)
Science
, vol.296
, pp. 1655-1657
-
-
Cantley, L.C.1
-
2
-
-
33749836234
-
Phosphoinositides in cell regulation and membrane dynamics
-
Di Paolo G., De Camilli P. Phosphoinositides in cell regulation and membrane dynamics. Nat. Rev. 2006, 443:651-657.
-
(2006)
Nat. Rev.
, vol.443
, pp. 651-657
-
-
Di Paolo, G.1
De Camilli, P.2
-
3
-
-
69249090082
-
Phosphoinositide signaling: new tools and insights
-
Balla T., Szentpetery Z., Kim Y.J. Phosphoinositide signaling: new tools and insights. Physiology 2009, 24:231-244.
-
(2009)
Physiology
, vol.24
, pp. 231-244
-
-
Balla, T.1
Szentpetery, Z.2
Kim, Y.J.3
-
4
-
-
0026451081
-
Intracellular signaling by hydrolysis of phospholipids and activation of protein kinase C
-
Nishizuka Y. Intracellular signaling by hydrolysis of phospholipids and activation of protein kinase C. Science 1992, 258:607-614.
-
(1992)
Science
, vol.258
, pp. 607-614
-
-
Nishizuka, Y.1
-
5
-
-
0029060391
-
Protein kinase C and lipid signaling for sustained cellular responses
-
Nishizuka Y. Protein kinase C and lipid signaling for sustained cellular responses. FASEB J. 1995, 9:484-496.
-
(1995)
FASEB J.
, vol.9
, pp. 484-496
-
-
Nishizuka, Y.1
-
6
-
-
0037463805
-
The newly synthesized linoleic acid derivative FR236924 induces a long-lasting facilitation of hippocampal neurotransmission by targeting nicotinic acetylcholine receptors
-
Tanaka A., Nishizaki T. The newly synthesized linoleic acid derivative FR236924 induces a long-lasting facilitation of hippocampal neurotransmission by targeting nicotinic acetylcholine receptors. Bioorg. Med. Chem. Lett. 2002, 13:1037-1040.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1037-1040
-
-
Tanaka, A.1
Nishizaki, T.2
-
7
-
-
33744828259
-
The linoleic acid derivative DCP-LA selectively activates PKC-e{open}, possibly binding to the phosphatidylserine binding site
-
Kanno T., Yamamoto H., Yaguchi T., Hi R., Mukasa T., Fujikawa H., Nagata T., Yamamoto S., Tanaka A., Nishizaki T. The linoleic acid derivative DCP-LA selectively activates PKC-e{open}, possibly binding to the phosphatidylserine binding site. J. Lipid Res. 2006, 47:1146-1156.
-
(2006)
J. Lipid Res.
, vol.47
, pp. 1146-1156
-
-
Kanno, T.1
Yamamoto, H.2
Yaguchi, T.3
Hi, R.4
Mukasa, T.5
Fujikawa, H.6
Nagata, T.7
Yamamoto, S.8
Tanaka, A.9
Nishizaki, T.10
-
8
-
-
79951633282
-
α,β-DCP-LA selectively activates PKC-e{open} and stimulates neurotransmitter release with the highest potency among 4 diastereomers
-
Shimizu T., Kanno T., Tanaka A., Nishizaki T. α,β-DCP-LA selectively activates PKC-e{open} and stimulates neurotransmitter release with the highest potency among 4 diastereomers. Cell. Physiol. Biochem. 2011, 27:149-158.
-
(2011)
Cell. Physiol. Biochem.
, vol.27
, pp. 149-158
-
-
Shimizu, T.1
Kanno, T.2
Tanaka, A.3
Nishizaki, T.4
-
9
-
-
84876077384
-
Effects of newly synthesized DCP-LA-phospholipids on protein kinase C and protein phosphatases
-
Kanno T., Tsuchiya A., Shimizu T., Nakao S., Tanaka A., Nishizaki T. Effects of newly synthesized DCP-LA-phospholipids on protein kinase C and protein phosphatases. Cell. Physiol. Biochem. 2013, 31:555-664.
-
(2013)
Cell. Physiol. Biochem.
, vol.31
, pp. 555-664
-
-
Kanno, T.1
Tsuchiya, A.2
Shimizu, T.3
Nakao, S.4
Tanaka, A.5
Nishizaki, T.6
-
10
-
-
84870313599
-
Indomethacin serves as a potential inhibitor of protein phosphatases
-
Kanno T., Tsuchiya A., Shimizu T., Tanaka A., Nishizaki T. Indomethacin serves as a potential inhibitor of protein phosphatases. Cell. Physiol. Biochem. 2012, 30:1014-1022.
-
(2012)
Cell. Physiol. Biochem.
, vol.30
, pp. 1014-1022
-
-
Kanno, T.1
Tsuchiya, A.2
Shimizu, T.3
Tanaka, A.4
Nishizaki, T.5
-
11
-
-
84860352065
-
Intracellularly transported adenosine induces apoptosis in MCF-7 human breast cancer cells by accumulating AMID in the nucleus
-
Tsuchiya A., Kanno T., Saito M., Miyoshi Y., Gotoh A., Nakano T., Nishizaki T. Intracellularly transported adenosine induces apoptosis in MCF-7 human breast cancer cells by accumulating AMID in the nucleus. Cancer Lett. 2012, 321:65-72.
-
(2012)
Cancer Lett.
, vol.321
, pp. 65-72
-
-
Tsuchiya, A.1
Kanno, T.2
Saito, M.3
Miyoshi, Y.4
Gotoh, A.5
Nakano, T.6
Nishizaki, T.7
-
12
-
-
84878431342
-
Phosphatase: PP2A structural importance, regulation and its aberrant expression in cancer
-
Seshacharyulu P., Pandey P., Datta K., Batra S.K. Phosphatase: PP2A structural importance, regulation and its aberrant expression in cancer. Cancer Lett. 2013, 335:9-18.
-
(2013)
Cancer Lett.
, vol.335
, pp. 9-18
-
-
Seshacharyulu, P.1
Pandey, P.2
Datta, K.3
Batra, S.K.4
-
13
-
-
84880497002
-
PP2A counterbalances phosphorylation of pRB and mitotic proteins by multiple CDKs: Potential implications for PP2A disruption in cancer
-
Kurimchak A., Graña X. PP2A counterbalances phosphorylation of pRB and mitotic proteins by multiple CDKs: Potential implications for PP2A disruption in cancer. Genes Cancer 2012, 3:739-748.
-
(2012)
Genes Cancer
, vol.3
, pp. 739-748
-
-
Kurimchak, A.1
Graña, X.2
-
14
-
-
84866604619
-
Phosphatases: the new brakes for cancer development?
-
Zhang Q., Claret F.X. Phosphatases: the new brakes for cancer development?. Enzyme Res. 2012, 659649. 10.1155/2012/659649.
-
(2012)
Enzyme Res.
, pp. 659649
-
-
Zhang, Q.1
Claret, F.X.2
-
15
-
-
84857133852
-
The role and therapeutic potential of Ser/Thr phosphatase PP2A in apoptotic signalling networks in human cancer cells
-
Janssens V., Rebollo A. The role and therapeutic potential of Ser/Thr phosphatase PP2A in apoptotic signalling networks in human cancer cells. Curr. Mol. Med. 2012, 12:268-287.
-
(2012)
Curr. Mol. Med.
, vol.12
, pp. 268-287
-
-
Janssens, V.1
Rebollo, A.2
-
16
-
-
84876990097
-
Protein phosphatase 2A: a target for anticancer therapy
-
Perrotti D., Neviani P. Protein phosphatase 2A: a target for anticancer therapy. Lancet Oncol. 2013, 14:e229-38. 10.1016/S1470-2045(12)70558-2.
-
(2013)
Lancet Oncol.
, vol.14
-
-
Perrotti, D.1
Neviani, P.2
-
17
-
-
77949464718
-
From basic research to clinical development of MEK1/2 inhibitors for cancer therapy
-
Frémin C., Meloche S. From basic research to clinical development of MEK1/2 inhibitors for cancer therapy. J. Hematol. Oncol. 2010, 3:8. 10.1186/1756-8722-3-8.
-
(2010)
J. Hematol. Oncol.
, vol.3
, pp. 8
-
-
Frémin, C.1
Meloche, S.2
|