[HTML][HTML] Ion channels and bacterial infection: the case of β-barrel pore-forming protein toxins of Staphylococcus aureus

…, G Viero, S Werner, DA Colin, H Monteil, G Prevost - FEBS letters, 2003 - Elsevier
Staphylococcus aureus strains causing human pathologies produce several toxins,
including a pore-forming protein family formed by the single-component α-hemolysin and the …

Molecular mechanism of pore formation by actinoporins

…, G Viero, M Dalla Serra, P Maček, G Anderluh - Toxicon, 2009 - Elsevier
Actinoporins are effective pore-forming toxins produced by sea anemones. These extremely
potent, basic 20kDa proteins readily form pores in membranes that contain sphingomyelin. …

Integration of mitigation and adaptation in urban climate change action plans in Europe: A systematic assessment

S Grafakos, G Viero, D Reckien, K Trigg… - … and Sustainable Energy …, 2020 - Elsevier
Cities are major drivers of energy consumption and greenhouse gas emissions--the
sources of anthropocentric climate change, whilst also concentrating people, buildings, and …

[HTML][HTML] A novel mechanism of pore formation: membrane penetration by the N-terminal amphipathic region of equinatoxin

P Malovrh, G Viero, M Dalla Serra, Z Podlesek… - Journal of Biological …, 2003 - ASBMB
Equinatoxin II is a representative of actinoporins, eukaryotic pore-forming toxins from sea
anemones. It creates pores in natural and artificial lipid membranes by an association of three …

[HTML][HTML] riboWaltz: optimization of ribosome P-site positioning in ribosome profiling data

…, EJN Groen, TH Gillingwater, G Viero - PLoS computational …, 2018 - journals.plos.org
Ribosome profiling is a powerful technique used to study translation at the genome-wide
level, generating unique information concerning ribosome positions along RNAs. Optimal …

[HTML][HTML] Widespread uncoupling between transcriptome and translatome variations after a stimulus in mammalian cells

T Tebaldi, A Re, G Viero, I Pegoretti, A Passerini… - BMC genomics, 2012 - Springer
… percentages are displayed following the same colour scheme adopted in the rest of the
figure (FG) Scatterplot showing correlation between transcriptome (F) and translatome (G) log2 …

[PDF][PDF] m6A modification prevents formation of endogenous double-stranded RNAs and deleterious innate immune responses during hematopoietic development

…, X Fu, X Wang, P Joshi, V Lee, B Dura, G Viero… - Immunity, 2020 - cell.com
N 6 -methyladenosine (m 6 A) is the most abundant RNA modification, but little is known
about its role in mammalian hematopoietic development. Here, we show that conditional …

[HTML][HTML] Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures

G Anderluh, M Dalla Serra, G Viero, G Guella… - Journal of Biological …, 2003 - ASBMB
Pore formation in the target cell membranes is a common mechanism used by many toxins
in order to kill cells. Among various described mechanisms, a toroidal pore concept was …

[PDF][PDF] In vivo translatome profiling in spinal muscular atrophy reveals a role for SMN protein in ribosome biology

…, F Muntoni, A Quattrone, TH Gillingwater, G Viero - Cell reports, 2017 - cell.com
… (F and G) Comparison between the fraction of ribosomes in polysomes (FRP) in CTRL
and SMA mouse brains (F) and spinal cords (G) at three stages of disease (brain: pre-symptomatic…

[HTML][HTML] The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration

…, P Zuccotti, G Viero, A Quattrone, S Barlati, G De Petro… - PloS one, 2011 - journals.plos.org
CDK5R1 encodes p35, a specific activator of the serine/threonine kinase CDK5, which plays
crucial roles in CNS development and maintenance. CDK5 activity strongly depends on …