Andrea Micaloni
Overview
Explore the profile of Andrea Micaloni including associated specialties, affiliations and a list of published articles.
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5
Citations
83
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Recent Articles
1.
Garibaldi M, Fattori F, Pennisi E, Merlonghi G, Fionda L, Vanoli F, et al.
Neuromuscul Disord
. 2021 Jan;
31(2):139-148.
PMID: 33384202
ACTA1 gene encodes the skeletal muscle alpha-actin, the core of thin filaments of the sarcomere. ACTA1 mutations are responsible of several muscle disorders including nemaline, cores, actin aggregate myopathies and...
2.
Forte M, Bianchi F, Cotugno M, Marchitti S, De Falco E, Raffa S, et al.
Autophagy
. 2019 Nov;
16(8):1468-1481.
PMID: 31679456
Abbreviations: 10 VSMCs: aortic vascular smooth muscle cells; COX4I1/COX IV: cytochrome c oxidase subunit 4I1; ECs: endothelial cells; EPCs: endothelial progenitor cells; JD: Japanese-style diet; MAP1LC3/LC3: microtubule-associated protein 1 light...
3.
Raffa S, Chin X, Stanzione R, Forte M, Bianchi F, Cotugno M, et al.
Int J Cardiol
. 2019 Feb;
286:127-133.
PMID: 30808603
Background: Deficiency of NADH dehydrogenase [ubiquinone], the mitochondrial complex I, represents an emerging mechanism of cardiovascular diseases. Ndufc2, a subunit of mitochondrial complex I, is involved in stroke development. We...
4.
Coluccia R, Raffa S, Ranieri D, Micaloni A, Valente S, Salerno G, et al.
Oncotarget
. 2018 Nov;
9(80):35028-35040.
PMID: 30416677
Oxidative stress is currently viewed as a key factor in the genesis and progression of Heart Failure (HF). The aim of this study was to characterize the mitochondrial changes linked...
5.
Raffa S, Scrofani C, Valente S, Micaloni A, Forte M, Bianchi F, et al.
Hum Mol Genet
. 2017 Oct;
26(23):4541-4555.
PMID: 28973657
Ndufc2, a subunit of the NADH: ubiquinone oxidoreductase, plays a key role in the assembly and activity of complex I within the mitochondrial OXPHOS chain. Its deficiency has been shown...