Guaita-Esteruelas S - Search Results

1

Chk1- and claspin-dependent but ATR/ATM- and Rad17-independent DNA replication checkpoint response in HeLa cells.

Rodríguez-Bravo V, Guaita-Esteruelas S, Florensa R, Bachs O, Agell N. Rodríguez-Bravo V, et al. Cancer Res. 2006 Sep 1;66(17):8672-9. doi: 10.1158/0008-5472.CAN-05-4443. Cancer Res. 2006. PMID: 16951182

2

Different S/M checkpoint responses of tumor and non tumor cell lines to DNA replication inhibition.

Rodríguez-Bravo V, Guaita-Esteruelas S, Salvador N, Bachs O, Agell N. Rodríguez-Bravo V, et al. Cancer Res. 2007 Dec 15;67(24):11648-56. doi: 10.1158/0008-5472.CAN-07-3100. Cancer Res. 2007. PMID: 18089794

3

The stress-activated protein kinases p38α/β and JNK1/2 cooperate with Chk1 to inhibit mitotic entry upon DNA replication arrest.

Llopis A, Salvador N, Ercilla A, Guaita-Esteruelas S, Barrantes Idel B, Gupta J, Gaestel M, Davis RJ, Nebreda AR, Agell N. Llopis A, et al. Cell Cycle. 2012 Oct 1;11(19):3627-37. doi: 10.4161/cc.21917. Epub 2012 Aug 30. Cell Cycle. 2012. PMID: 22935704 Free PMC article.

4

OZF is a Claspin-interacting protein essential to maintain the replication fork progression rate under replication stress.

Feu S, Unzueta F, Llopis A, Semple JI, Ercilla A, Guaita-Esteruelas S, Jaumot M, Freire R, Agell N. Feu S, et al. Among authors: guaita esteruelas s. FASEB J. 2020 May;34(5):6907-6919. doi: 10.1096/fj.201901926R. Epub 2020 Apr 8. FASEB J. 2020. PMID: 32267586

5

Regulation of Snail transcription during epithelial to mesenchymal transition of tumor cells.

Barberà MJ, Puig I, Domínguez D, Julien-Grille S, Guaita-Esteruelas S, Peiró S, Baulida J, Francí C, Dedhar S, Larue L, García de Herreros A. Barberà MJ, et al. Oncogene. 2004 Sep 23;23(44):7345-54. doi: 10.1038/sj.onc.1207990. Oncogene. 2004. PMID: 15286702

6

Functional cooperation between Snail1 and twist in the regulation of ZEB1 expression during epithelial to mesenchymal transition.

Dave N, Guaita-Esteruelas S, Gutarra S, Frias À, Beltran M, Peiró S, de Herreros AG. Dave N, et al. J Biol Chem. 2011 Apr 8;286(14):12024-32. doi: 10.1074/jbc.M110.168625. Epub 2011 Feb 12. J Biol Chem. 2011. PMID: 21317430 Free PMC article.

7

FABP4 inhibitor BMS309403 decreases saturated-fatty-acid-induced endoplasmic reticulum stress-associated inflammation in skeletal muscle by reducing p38 MAPK activation.

Bosquet A, Girona J, Guaita-Esteruelas S, Heras M, Saavedra-García P, Martínez-Micaelo N, Masana L, Rodríguez-Calvo R. Bosquet A, et al. Among authors: guaita esteruelas s. Biochim Biophys Acta Mol Cell Biol Lipids. 2018 Jun;1863(6):604-613. doi: 10.1016/j.bbalip.2018.03.004. Epub 2018 Mar 15. Biochim Biophys Acta Mol Cell Biol Lipids. 2018. PMID: 29550588

8

Exogenous FABP4 induces endoplasmic reticulum stress in HepG2 liver cells.

Bosquet A, Guaita-Esteruelas S, Saavedra P, Rodríguez-Calvo R, Heras M, Girona J, Masana L. Bosquet A, et al. Atherosclerosis. 2016 Jun;249:191-9. doi: 10.1016/j.atherosclerosis.2016.04.012. Epub 2016 Apr 14. Atherosclerosis. 2016. PMID: 27155388

9

Extracellular FABP4 uptake by endothelial cells is dependent on cytokeratin 1 expression.

Martínez-Micaelo N, Rodríguez-Calvo R, Guaita-Esteruelas S, Heras M, Girona J, Masana L. Martínez-Micaelo N, et al. Among authors: guaita esteruelas s. Biochim Biophys Acta Mol Cell Biol Lipids. 2019 Mar;1864(3):234-244. doi: 10.1016/j.bbalip.2018.11.011. Epub 2018 Dec 3. Biochim Biophys Acta Mol Cell Biol Lipids. 2019. PMID: 30521939

10

Exogenous FABP4 increases breast cancer cell proliferation and activates the expression of fatty acid transport proteins.

Guaita-Esteruelas S, Bosquet A, Saavedra P, Gumà J, Girona J, Lam EW, Amillano K, Borràs J, Masana L. Guaita-Esteruelas S, et al. Mol Carcinog. 2017 Jan;56(1):208-217. doi: 10.1002/mc.22485. Epub 2016 Apr 6. Mol Carcinog. 2017. PMID: 27061264 Free article.

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