Pinotti M - Search Results

1

A naturally occurring mutation in ATP synthase subunit c is associated with increased damage following hypoxia/reoxygenation in STEMI patients.

Morciano G, Pedriali G, Bonora M, Pavasini R, Mikus E, Calvi S, Bovolenta M, Lebiedzinska-Arciszewska M, Pinotti M, Albertini A, Wieckowski MR, Giorgi C, Ferrari R, Galluzzi L, Campo G, Pinton P. Morciano G, et al. Among authors: pinotti m. Cell Rep. 2021 Apr 13;35(2):108983. doi: 10.1016/j.celrep.2021.108983. Cell Rep. 2021. PMID: 33852870 Free article.

2

Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.

Pinotti M, Rizzotto L, Pinton P, Ferraresi P, Chuansumrit A, Charoenkwan P, Marchetti G, Rizzuto R, Mariani G, Bernardi F; International Factor VII Deficiency Study Group. Pinotti M, et al. J Thromb Haemost. 2006 Jun;4(6):1308-14. doi: 10.1111/j.1538-7836.2006.01915.x. J Thromb Haemost. 2006. PMID: 16706976 Free article.

3

Intracellular evaluation of ER targeting elucidates a mild form of inherited coagulation deficiency.

Rizzotto L, Pinotti M, Pinton P, Rizzuto R, Bernardi F. Rizzotto L, et al. Among authors: pinotti m. Mol Med. 2006 Jul-Aug;12(7-8):137-42. doi: 10.2119/2005-00040.Rizzotto. Mol Med. 2006. PMID: 17088945 Free PMC article.

4

Mcl-1 involvement in mitochondrial dynamics is associated with apoptotic cell death.

Morciano G, Giorgi C, Balestra D, Marchi S, Perrone D, Pinotti M, Pinton P. Morciano G, et al. Among authors: pinotti m. Mol Biol Cell. 2016 Jan 1;27(1):20-34. doi: 10.1091/mbc.E15-01-0028. Epub 2015 Nov 4. Mol Biol Cell. 2016. PMID: 26538029 Free PMC article.

5

An engineered tale-transcription factor rescues transcription of factor VII impaired by promoter mutations and enhances its endogenous expression in hepatocytes.

Barbon E, Pignani S, Branchini A, Bernardi F, Pinotti M, Bovolenta M. Barbon E, et al. Among authors: pinotti m. Sci Rep. 2016 Jun 24;6:28304. doi: 10.1038/srep28304. Sci Rep. 2016. PMID: 27341548 Free PMC article.

6

Fo ATP synthase C subunit serum levels in patients with ST-segment Elevation Myocardial Infarction: Preliminary findings.

Campo G, Morciano G, Pavasini R, Bonora M, Sbano L, Biscaglia S, Bovolenta M, Pinotti M, Punzetti S, Rizzo P, Aquila G, Giorgi C, Ferrari R, Pinton P. Campo G, et al. Among authors: pinotti m. Int J Cardiol. 2016 Oct 15;221:993-7. doi: 10.1016/j.ijcard.2016.07.125. Epub 2016 Jul 9. Int J Cardiol. 2016. PMID: 27441480

7

Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy.

Scalet D, Balestra D, Rohban S, Bovolenta M, Perrone D, Bernardi F, Campaner S, Pinotti M. Scalet D, et al. Among authors: pinotti m. Biochim Biophys Acta Mol Basis Dis. 2017 Jan;1863(1):15-20. doi: 10.1016/j.bbadis.2016.09.011. Epub 2016 Sep 14. Biochim Biophys Acta Mol Basis Dis. 2017. PMID: 27639833 Free article.

8

The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutation.

Pignani S, Todaro A, Ferrarese M, Marchi S, Lombardi S, Balestra D, Pinton P, Bernardi F, Pinotti M, Branchini A. Pignani S, et al. Among authors: pinotti m. J Thromb Haemost. 2018 Oct;16(10):2035-2043. doi: 10.1111/jth.14236. Epub 2018 Aug 9. J Thromb Haemost. 2018. PMID: 29993188 Free article.

9

Akt-mediated phosphorylation of MICU1 regulates mitochondrial Ca²⁺ levels and tumor growth.

Marchi S, Corricelli M, Branchini A, Vitto VAM, Missiroli S, Morciano G, Perrone M, Ferrarese M, Giorgi C, Pinotti M, Galluzzi L, Kroemer G, Pinton P. Marchi S, et al. Among authors: pinotti m. EMBO J. 2019 Jan 15;38(2):e99435. doi: 10.15252/embj.201899435. Epub 2018 Nov 30. EMBO J. 2019. PMID: 30504268 Free PMC article.

10

Tailoring the CRISPR system to transactivate coagulation gene promoters in normal and mutated contexts.

Pignani S, Zappaterra F, Barbon E, Follenzi A, Bovolenta M, Bernardi F, Branchini A, Pinotti M. Pignani S, et al. Among authors: pinotti m. Biochim Biophys Acta Gene Regul Mech. 2019 Jun;1862(6):619-624. doi: 10.1016/j.bbagrm.2019.04.002. Epub 2019 Apr 18. Biochim Biophys Acta Gene Regul Mech. 2019. PMID: 31005673

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