Publications by authors named "Denise Ferrera"

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Cryopyrin-associated Periodic Syndromes in Italian Patients: Evaluation of the Rate of Somatic NLRP3 Mosaicism and Phenotypic Characterization.
Denise Lasigliè, Anna Mensa-Vilaro, Denise Ferrera, Roberta Caorsi, Federica Penco

J Rheumatol· November 2017

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Gene expression profile in TNF receptor-associated periodic syndrome reveals constitutively enhanced pathways and new players in the underlying inflammation.
Silvia Borghini, Denise Ferrera, Ignazia Prigione, Michele Fiore, Chiara Ferraris

Clin Exp Rheumatol· February 2017

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A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD).
Elisa Giorgio, Daniel Robyr, Malte Spielmann, Enza Ferrero, Eleonora Di Gregorio, Denise Ferrera

Hum Mol Genet· June 2015

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Resting microglia react to Aβ42 fibrils but do not detect oligomers or oligomer-induced neuronal damage.
Denise Ferrera, Nadia Mazzaro, Claudio Canale, Laura Gasparini

Neurobiol Aging· November 2014

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Lamin B1 overexpression increases nuclear rigidity in autosomal dominant leukodystrophy fibroblasts.
Denise Ferrera, Claudio Canale, Roberto Marotta, Nadia Mazzaro, Marta Gritti

FASEB J· September 2014

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Recombinase-deficient T cell development by selective accumulation of CD3 into lipid rafts.
Denise Ferrera, Maddalena Panigada, Simona Porcellini, Fabio Grassi

Eur J Immunol· April 2008

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Regulation of peripheral T cell activation by calreticulin.
Simona Porcellini, Elisabetta Traggiai, Ursula Schenk, Denise Ferrera, Michela Matteoli

J Exp Med· February 2006

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Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion.
Tiziana Bonaldi, Fabio Talamo, Paola Scaffidi, Denise Ferrera, Annalisa Porto

EMBO J· October 2003

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The nuclear protein HMGB1 is secreted by monocytes via a non-classical, vesicle-mediated secretory pathway.
Stefania Gardella, Cristina Andrei, Denise Ferrera, Lavinia V Lotti, Maria R Torrisi

EMBO Rep· October 2002

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