Pfaff D - Search Results

1

T-cadherin promotes autophagy and survival in vascular smooth muscle cells through MEK1/2/Erk1/2 axis activation.

Kyriakakis E, Frismantiene A, Dasen B, Pfaff D, Rivero O, Lesch KP, Erne P, Resink TJ, Philippova M. Kyriakakis E, et al. Among authors: pfaff d. Cell Signal. 2017 Jul;35:163-175. doi: 10.1016/j.cellsig.2017.04.004. Epub 2017 Apr 6. Cell Signal. 2017. PMID: 28392425

2

A guide and guard: the many faces of T-cadherin.

Philippova M, Joshi MB, Kyriakakis E, Pfaff D, Erne P, Resink TJ. Philippova M, et al. Among authors: pfaff d. Cell Signal. 2009 Jul;21(7):1035-44. doi: 10.1016/j.cellsig.2009.01.035. Cell Signal. 2009. PMID: 19399994 Review.

3

T-cadherin attenuates the PERK branch of the unfolded protein response and protects vascular endothelial cells from endoplasmic reticulum stress-induced apoptosis.

Kyriakakis E, Philippova M, Joshi MB, Pfaff D, Bochkov V, Afonyushkin T, Erne P, Resink TJ. Kyriakakis E, et al. Among authors: pfaff d. Cell Signal. 2010 Sep;22(9):1308-16. doi: 10.1016/j.cellsig.2010.04.008. Epub 2010 May 8. Cell Signal. 2010. PMID: 20457250

4

T-cadherin attenuates insulin-dependent signalling, eNOS activation, and angiogenesis in vascular endothelial cells.

Philippova M, Joshi MB, Pfaff D, Kyriakakis E, Maslova K, Erne P, Resink TJ. Philippova M, et al. Among authors: pfaff d. Cardiovasc Res. 2012 Mar 1;93(3):498-507. doi: 10.1093/cvr/cvs004. Epub 2012 Jan 10. Cardiovasc Res. 2012. PMID: 22235028

5

Cross-talk between EGFR and T-cadherin: EGFR activation promotes T-cadherin localization to intercellular contacts.

Kyriakakis E, Maslova K, Frachet A, Ferri N, Contini A, Pfaff D, Erne P, Resink TJ, Philippova M. Kyriakakis E, et al. Among authors: pfaff d. Cell Signal. 2013 May;25(5):1044-53. doi: 10.1016/j.cellsig.2013.02.001. Epub 2013 Feb 11. Cell Signal. 2013. PMID: 23411345

6

Regulation of contractile signaling and matrix remodeling by T-cadherin in vascular smooth muscle cells: constitutive and insulin-dependent effects.

Frismantiene A, Pfaff D, Frachet A, Coen M, Joshi MB, Maslova K, Bochaton-Piallat ML, Erne P, Resink TJ, Philippova M. Frismantiene A, et al. Among authors: pfaff d. Cell Signal. 2014 Sep;26(9):1897-908. doi: 10.1016/j.cellsig.2014.05.001. Epub 2014 May 9. Cell Signal. 2014. PMID: 24815187

7

T-cadherin promotes vascular smooth muscle cell dedifferentiation via a GSK3β-inactivation dependent mechanism.

Frismantiene A, Dasen B, Pfaff D, Erne P, Resink TJ, Philippova M. Frismantiene A, et al. Among authors: pfaff d. Cell Signal. 2016 May;28(5):516-530. doi: 10.1016/j.cellsig.2016.02.014. Epub 2016 Feb 22. Cell Signal. 2016. PMID: 26907733

8

T-cadherin loss induces an invasive phenotype in human keratinocytes and squamous cell carcinoma (SCC) cells in vitro and is associated with malignant transformation of cutaneous SCC in vivo.

Pfaff D, Philippova M, Buechner SA, Maslova K, Mathys T, Erne P, Resink TJ. Pfaff D, et al. Br J Dermatol. 2010 Aug;163(2):353-63. doi: 10.1111/j.1365-2133.2010.09801.x. Epub 2010 Apr 12. Br J Dermatol. 2010. PMID: 20394625

9

Extracellular cadherin repeat domains EC1 and EC5 of T-cadherin are essential for its ability to stimulate angiogenic behavior of endothelial cells.

Joshi MB, Kyriakakis E, Pfaff D, Rupp K, Philippova M, Erne P, Resink TJ. Joshi MB, et al. Among authors: pfaff d. FASEB J. 2009 Nov;23(11):4011-21. doi: 10.1096/fj.09-133611. Epub 2009 Jul 28. FASEB J. 2009. PMID: 19638398

10

Paradoxical effects of T-cadherin on squamous cell carcinoma: up- and down-regulation increase xenograft growth by distinct mechanisms.

Pfaff D, Philippova M, Kyriakakis E, Maslova K, Rupp K, Buechner SA, Iezzi G, Spagnoli GC, Erne P, Resink TJ. Pfaff D, et al. J Pathol. 2011 Dec;225(4):512-24. doi: 10.1002/path.2900. Epub 2011 Jul 15. J Pathol. 2011. PMID: 21766307

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