Cieslar-Pobuda A - Search Results

1

NADPH Oxidases: Insights into Selected Functions and Mechanisms of Action in Cancer and Stem Cells.

Skonieczna M, Hejmo T, Poterala-Hejmo A, Cieslar-Pobuda A, Buldak RJ. Skonieczna M, et al. Oxid Med Cell Longev. 2017;2017:9420539. doi: 10.1155/2017/9420539. Epub 2017 May 23. Oxid Med Cell Longev. 2017. PMID: 28626501 Free PMC article. Review.

2

ROS and Oxidative Stress in Stem Cells.

Cieślar-Pobuda A, Yue J, Lee HC, Skonieczna M, Wei YH. Cieślar-Pobuda A, et al. Oxid Med Cell Longev. 2017;2017:5047168. doi: 10.1155/2017/5047168. Epub 2017 Sep 6. Oxid Med Cell Longev. 2017. PMID: 29018510 Free PMC article. No abstract available.

3

Changes of reactive oxygen and nitrogen species and mitochondrial functioning in human K562 and HL60 cells exposed to ionizing radiation.

Saenko Y, Cieslar-Pobuda A, Skonieczna M, Rzeszowska-Wolny J. Saenko Y, et al. Radiat Res. 2013 Oct;180(4):360-6. doi: 10.1667/RR3247.1. Epub 2013 Sep 13. Radiat Res. 2013. PMID: 24033192

4

MicroRNAs and reactive oxygen species: are they in the same regulatory circuit?

Jaksik R, Lalik A, Skonieczna M, Cieslar-Pobuda A, Student S, Rzeszowska-Wolny J. Jaksik R, et al. Mutat Res Genet Toxicol Environ Mutagen. 2014 Apr;764-765:64-71. doi: 10.1016/j.mrgentox.2013.09.003. Epub 2013 Sep 16. Mutat Res Genet Toxicol Environ Mutagen. 2014. PMID: 24051449

5

The Impact of DIDS-Induced Inhibition of Voltage-Dependent Anion Channels (VDAC) on Cellular Response of Lymphoblastoid Cells to Ionizing Radiation.

Skonieczna M, Cieslar-Pobuda A, Saenko Y, Foksinski M, Olinski R, Rzeszowska-Wolny J, Wiechec E. Skonieczna M, et al. Med Chem. 2017;13(5):477-483. doi: 10.2174/1573406413666170421102353. Med Chem. 2017. PMID: 28427245 Free article.

6

Human induced pluripotent stem cell differentiation and direct transdifferentiation into corneal epithelial-like cells.

Cieślar-Pobuda A, Rafat M, Knoflach V, Skonieczna M, Hudecki A, Małecki A, Urasińska E, Ghavami S, Łos MJ. Cieślar-Pobuda A, et al. Oncotarget. 2016 Jul 5;7(27):42314-42329. doi: 10.18632/oncotarget.9791. Oncotarget. 2016. PMID: 27275539 Free PMC article.

7

Bystander normal human fibroblasts reduce damage response in radiation targeted cancer cells through intercellular ROS level modulation.

Widel M, Przybyszewski WM, Cieslar-Pobuda A, Saenko YV, Rzeszowska-Wolny J. Widel M, et al. Mutat Res. 2012 Mar 1;731(1-2):117-24. doi: 10.1016/j.mrfmmm.2011.12.007. Epub 2011 Dec 21. Mutat Res. 2012. PMID: 22210495

8

PARP-1 inhibition induces a late increase in the level of reactive oxygen species in cells after ionizing radiation.

Cieślar-Pobuda A, Saenko Y, Rzeszowska-Wolny J. Cieślar-Pobuda A, et al. Mutat Res. 2012 Apr 1;732(1-2):9-15. doi: 10.1016/j.mrfmmm.2012.01.005. Epub 2012 Feb 2. Mutat Res. 2012. PMID: 22321899

9

Could drugs inhibiting the mevalonate pathway also target cancer stem cells?

Likus W, Siemianowicz K, Bieńk K, Pakuła M, Pathak H, Dutta C, Wang Q, Shojaei S, Assaraf YG, Ghavami S, Cieślar-Pobuda A, Łos MJ. Likus W, et al. Drug Resist Updat. 2016 Mar;25:13-25. doi: 10.1016/j.drup.2016.02.001. Epub 2016 Feb 20. Drug Resist Updat. 2016. PMID: 27155373 Free article. Review.

10

Role of ion channels in regulating Ca²⁺ homeostasis during the interplay between immune and cancer cells.

Bose T, Cieślar-Pobuda A, Wiechec E. Bose T, et al. Cell Death Dis. 2015 Feb 19;6(2):e1648. doi: 10.1038/cddis.2015.23. Cell Death Dis. 2015. PMID: 25695601 Free PMC article. Review.

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