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Items: 1 to 20 of 89

1.

Calcium regulates cell death in cancer: roles of the mitochondria and mitochondria-associated membranes (MAMs).

Danese A, Patergnani S, Bonora M, Wieckowski MR, Previati M, Giorgi C, Pinton P.

Biochim Biophys Acta. 2017 Jan 10. pii: S0005-2728(17)30004-X. doi: 10.1016/j.bbabio.2017.01.003. [Epub ahead of print] Review.

PMID:
28087257
2.

Mitochondria in Multiple Sclerosis: Molecular Mechanisms of Pathogenesis.

Patergnani S, Fossati V, Bonora M, Giorgi C, Marchi S, Missiroli S, Rusielewicz T, Wieckowski MR, Pinton P.

Int Rev Cell Mol Biol. 2017;328:49-103. doi: 10.1016/bs.ircmb.2016.08.003.

PMID:
28069137
3.

Localization and Processing of the Amyloid-β Protein Precursor in Mitochondria-Associated Membranes.

Del Prete D, Suski JM, Oulès B, Debayle D, Gay AS, Lacas-Gervais S, Bussiere R, Bauer C, Pinton P, Paterlini-Bréchot P, Wieckowski MR, Checler F, Chami M.

J Alzheimers Dis. 2017;55(4):1549-1570. doi: 10.3233/JAD-160953.

4.

Carvedilol and antioxidant proteins in a type I diabetes animal model.

Diogo CV, Deus CM, Lebiedzinska-Arciszewska M, Wojtala A, Wieckowski MR, Oliveira PJ.

Eur J Clin Invest. 2017 Jan;47(1):19-29. doi: 10.1111/eci.12696.

PMID:
27805735
5.

Quantifying ROS levels using CM-H2DCFDA and HyPer.

Oparka M, Walczak J, Malinska D, van Oppen LM, Szczepanowska J, Koopman WJ, Wieckowski MR.

Methods. 2016 Oct 15;109:3-11. doi: 10.1016/j.ymeth.2016.06.008. Review.

PMID:
27302663
6.

Mitochondrial reactive oxygen species and inflammation: Molecular mechanisms, diseases and promising therapies.

Rimessi A, Previati M, Nigro F, Wieckowski MR, Pinton P.

Int J Biochem Cell Biol. 2016 Dec;81(Pt B):281-293. doi: 10.1016/j.biocel.2016.06.015.

PMID:
27373679
7.

Comprehensive analysis of mitochondrial permeability transition pore activity in living cells using fluorescence-imaging-based techniques.

Bonora M, Morganti C, Morciano G, Giorgi C, Wieckowski MR, Pinton P.

Nat Protoc. 2016 Jun;11(6):1067-80. doi: 10.1038/nprot.2016.064.

PMID:
27172167
8.

Alterations in Mitochondrial and Endoplasmic Reticulum Signaling by p53 Mutants.

Giorgi C, Bonora M, Missiroli S, Morganti C, Morciano G, Wieckowski MR, Pinton P.

Front Oncol. 2016 Feb 25;6:42. doi: 10.3389/fonc.2016.00042. Review.

9.

Measuring p66Shc Signaling Pathway Activation and Mitochondrial Translocation in Cultured Cells.

Wieckowski MR, Deus CM, Couto R, Oparka M, Lebiedzińska-Arciszewska M, Duszyński J, Oliveira PJ.

Curr Protoc Toxicol. 2015 Nov 2;66:25.6.1-21. doi: 10.1002/0471140856.tx2506s66.

PMID:
26523473
10.

p66Shc signaling is involved in stress responses elicited by anthracycline treatment of rat cardiomyoblasts.

Sampaio SF, Branco AF, Wojtala A, Vega-Naredo I, Wieckowski MR, Oliveira PJ.

Arch Toxicol. 2016 Jul;90(7):1669-84. doi: 10.1007/s00204-015-1583-9.

PMID:
26318906
11.

Mitochondrial Ca(2+) Remodeling is a Prime Factor in Oncogenic Behavior.

Rimessi A, Patergnani S, Bonora M, Wieckowski MR, Pinton P.

Front Oncol. 2015 Jun 25;5:143. doi: 10.3389/fonc.2015.00143. Review.

12.

p53 at the endoplasmic reticulum regulates apoptosis in a Ca2+-dependent manner.

Giorgi C, Bonora M, Sorrentino G, Missiroli S, Poletti F, Suski JM, Galindo Ramirez F, Rizzuto R, Di Virgilio F, Zito E, Pandolfi PP, Wieckowski MR, Mammano F, Del Sal G, Pinton P.

Proc Natl Acad Sci U S A. 2015 Feb 10;112(6):1779-84. doi: 10.1073/pnas.1410723112.

13.

Mitochondria-associated membranes: composition, molecular mechanisms, and physiopathological implications.

Giorgi C, Missiroli S, Patergnani S, Duszynski J, Wieckowski MR, Pinton P.

Antioxid Redox Signal. 2015 Apr 20;22(12):995-1019. doi: 10.1089/ars.2014.6223. Review.

PMID:
25557408
14.

Mitochondrial dysfunction in primary human fibroblasts triggers an adaptive cell survival program that requires AMPK-α.

Distelmaier F, Valsecchi F, Liemburg-Apers DC, Lebiedzinska M, Rodenburg RJ, Heil S, Keijer J, Fransen J, Imamura H, Danhauser K, Seibt A, Viollet B, Gellerich FN, Smeitink JA, Wieckowski MR, Willems PH, Koopman WJ.

Biochim Biophys Acta. 2015 Mar;1852(3):529-40. doi: 10.1016/j.bbadis.2014.12.012.

15.

The interplay between p66Shc, reactive oxygen species and cancer cell metabolism.

Lebiedzinska-Arciszewska M, Oparka M, Vega-Naredo I, Karkucinska-Wieckowska A, Pinton P, Duszynski J, Wieckowski MR.

Eur J Clin Invest. 2015 Jan;45 Suppl 1:25-31. doi: 10.1111/eci.12364. Review.

PMID:
25524583
16.

Histoenzymatic methods for visualization of the activity of individual mitochondrial respiratory chain complexes in the muscle biopsies from patients with mitochondrial defects.

Karkucinska-Wieckowska A, Pronicki M, Wieckowski MR.

Methods Mol Biol. 2015;1241:85-93. doi: 10.1007/978-1-4939-1875-1_8.

PMID:
25308490
17.

Isolation of crude mitochondrial fraction from cells.

Wieckowski MR, Wojtczak L.

Methods Mol Biol. 2015;1241:1-8. doi: 10.1007/978-1-4939-1875-1_1.

PMID:
25308483
18.

Molecular identity of the mitochondrial permeability transition pore and its role in ischemia-reperfusion injury.

Morciano G, Giorgi C, Bonora M, Punzetti S, Pavasini R, Wieckowski MR, Campo G, Pinton P.

J Mol Cell Cardiol. 2015 Jan;78:142-53. doi: 10.1016/j.yjmcc.2014.08.015. Review.

PMID:
25172387
19.

STAT3 Activities and Energy Metabolism: Dangerous Liaisons.

Camporeale A, Demaria M, Monteleone E, Giorgi C, Wieckowski MR, Pinton P, Poli V.

Cancers (Basel). 2014 Jul 31;6(3):1579-96. doi: 10.3390/cancers6031579.

20.

Methods to monitor and compare mitochondrial and glycolytic ATP production.

Patergnani S, Baldassari F, De Marchi E, Karkucinska-Wieckowska A, Wieckowski MR, Pinton P.

Methods Enzymol. 2014;542:313-32. doi: 10.1016/B978-0-12-416618-9.00016-9.

PMID:
24862273
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