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Items: 1 to 20 of 111

1.

TGF-β1 enhances tumor-induced angiogenesis via JNK pathway and macrophage infiltration in an improved zebrafish embryo/xenograft glioma model.

Yang XJ, Chen GL, Yu SC, Xu C, Xin YH, Li TT, Shi Y, Gu A, Duan JJ, Qian C, Cui YH, Zhang X, Bian XW.

Int Immunopharmacol. 2013 Feb;15(2):191-8. doi: 10.1016/j.intimp.2012.12.002. Epub 2012 Dec 21.

PMID:
23261760
2.

C-Jun-NH2-terminal kinase mediates expression of connective tissue growth factor induced by transforming growth factor-beta1 in human lung fibroblasts.

Utsugi M, Dobashi K, Ishizuka T, Masubuchi K, Shimizu Y, Nakazawa T, Mori M.

Am J Respir Cell Mol Biol. 2003 Jun;28(6):754-61.

PMID:
12760970
3.

Andrographolide acts through inhibition of ERK1/2 and Akt phosphorylation to suppress chemotactic migration.

Tsai HR, Yang LM, Tsai WJ, Chiou WF.

Eur J Pharmacol. 2004 Sep 13;498(1-3):45-52.

PMID:
15363974
4.

Specific inhibition of basal mitogen-activated protein kinases and phosphatidylinositol 3 kinase activities in leukemia cells: a possible therapeutic role for the kinase inhibitors.

Champelovier P, El Atifi M, Pautre V, Rostaing B, Berger F, Seigneurin D.

Exp Hematol. 2008 Jan;36(1):28-36. Epub 2007 Oct 18.

PMID:
17949889
5.

[Transforming growth factor-beta1 induced phenotypic differentiation of human lung fibroblasts through mitogen activated protein kinase-dependent pathway].

Hu YB, Feng DY, Peng JW, Chu L, Lin Z, Zeng QF.

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2005 Apr;23(2):109-12. Chinese.

PMID:
16105451
7.

Beta-sitosterol-induced-apoptosis is mediated by the activation of ERK and the downregulation of Akt in MCA-102 murine fibrosarcoma cells.

Moon DO, Lee KJ, Choi YH, Kim GY.

Int Immunopharmacol. 2007 Aug;7(8):1044-53. Epub 2007 Apr 26.

PMID:
17570321
9.
10.

EGCG blocks TGFβ1-induced CCN2 by suppressing JNK and p38 in buccal fibroblasts.

Chang JZ, Yang WH, Deng YT, Chen HM, Kuo MY.

Clin Oral Investig. 2013 Mar;17(2):455-61. doi: 10.1007/s00784-012-0713-5. Epub 2012 Mar 15.

PMID:
22415218
11.

Glucose-potentiated chemotaxis in human vascular smooth muscle is dependent on cross-talk between the PI3K and MAPK signaling pathways.

Campbell M, Allen WE, Sawyer C, Vanhaesebroeck B, Trimble ER.

Circ Res. 2004 Aug 20;95(4):380-8. Epub 2004 Jul 8.

12.

Porphyromonas gingivalis-related cardiac cell apoptosis was majorly co-activated by p38 and extracellular signal-regulated kinase pathways.

Lee SD, Wu CC, Kuo WW, Lin JA, Hwang JM, Lu MC, Chen LM, Hsu HH, Wang CK, Chang SH, Huang CY.

J Periodontal Res. 2006 Feb;41(1):39-46.

PMID:
16409254
14.

Mammalian tumor xenografts induce neovascularization in zebrafish embryos.

Nicoli S, Ribatti D, Cotelli F, Presta M.

Cancer Res. 2007 Apr 1;67(7):2927-31.

17.

Molecular requirements for induction of CTGF expression by TGF-beta1 in primary osteoblasts.

Arnott JA, Zhang X, Sanjay A, Owen TA, Smock SL, Rehman S, DeLong WG, Safadi FF, Popoff SN.

Bone. 2008 May;42(5):871-85. doi: 10.1016/j.bone.2008.01.006. Epub 2008 Jan 26.

18.

Ghrelin stimulates angiogenesis via GHSR1a-dependent MEK/ERK and PI3K/Akt signal pathways in rat cardiac microvascular endothelial cells.

Wang L, Chen Q, Li G, Ke D.

Peptides. 2012 Jan;33(1):92-100. doi: 10.1016/j.peptides.2011.11.001. Epub 2011 Nov 7.

PMID:
22100225
19.

Identification of phosphorylase kinase as a novel therapeutic target through high-throughput screening for anti-angiogenesis compounds in zebrafish.

Camus S, Quevedo C, Menéndez S, Paramonov I, Stouten PF, Janssen RA, Rueb S, He S, Snaar-Jagalska BE, Laricchia-Robbio L, Izpisua Belmonte JC.

Oncogene. 2012 Sep 27;31(39):4333-42. doi: 10.1038/onc.2011.594. Epub 2011 Dec 19.

PMID:
22179836
20.

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