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Glassy dynamics of soft matter under 1D confinement: How irreversible adsorption affects molecular packing, mobility gradients and orientational polarization in thin films

The European physical journal. E, Soft matter and biological physics, 2013-06, Vol.36 (6), p.61-61, Article 61

2013

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Co-translational assembly of mammalian nuclear multisubunit complexes

Nature communications, 2019-04, Vol.10 (1), p.1740-1740, Article 1740

2019

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Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1

Human mutation, 2016-11, Vol.37 (11), p.1202-1208

2016

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Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population

Journal of the peripheral nervous system, 2014-12, Vol.19 (4), p.292-298

2014

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HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients

Journal of the peripheral nervous system, 2011-12, Vol.16 (4), p.287-294

2011

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Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation

Neuropathology, 2015-06, Vol.35 (3), p.254-259

2015

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Optimisation Strategies for the Design of Experiments in Materials Discovery

Capponi, Simona

2023

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Supercooled liquids with enhanced orientational order

Nature communications, 2012, Vol.3 (1), p.1233-1233, Article 1233

2012

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TNFα induces the expression of genes associated with endothelial dysfunction through p38MAPK-mediated down-regulation of miR-149

Biochemical and biophysical research communications, 2014-01, Vol.443 (1), p.246-251

2014

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Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations

Human mutation, 2017-05, Vol.38 (5), p.556-568

2017

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Polymer Brushes Grafted to “Passivated” Silicon Substrates Using Click Chemistry

Langmuir, 2008-03, Vol.24 (6), p.2732-2739

2008

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High Resolution Imaging Atomic Force Microscope Study of Interactions at the Membrane-Fluid Interface

Biophysical journal, 2016-02, Vol.110 (3), p.580a-581a

2016

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Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity

Human mutation, 2020-02, Vol.41 (2), p.449-464

2020

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Early onset Charcot‐Marie‐Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2‐related neuropathy

Journal of the peripheral nervous system, 2015-12, Vol.20 (4), p.415-418

2015

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A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot–Marie–Tooth disease

Journal of the neurological sciences, 2014-08, Vol.343 (1), p.183-186

2014

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Neuronal-specific microexon splicing of TAF1 mRNA is directly regulated by SRRM4/nSR100

RNA biology, 2020-01, Vol.17 (1), p.62-74

2020

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Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity

Human mutation, 2020-05, Vol.41 (5), p.1075-1075

2020

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Gain of glycosylation: A new pathomechanism of myelin protein zero mutations

Annals of neurology, 2012-03, Vol.71 (3), p.427-431

2012

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Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies

European journal of human genetics : EJHG, 2009-09, Vol.17 (9), p.1129-1134

2009

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Dissection of TAF1 neuronal splicing and implications for neurodegeneration in X-linked dystonia-parkinsonism

Brain communications, 2021-10, Vol.3 (4), p.fcab253-fcab253

2021

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A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family

Journal of the peripheral nervous system, 2012-09, Vol.17 (3), p.351-355

2012

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Dynamics in ultrathin liquid films studied by simultaneous dielectric spectroscopy (DRS) and organic molecular beam deposition (OMBD)

The European physical journal. ST, Special topics, 2010-10, Vol.189 (1), p.181-186

2010

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Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation

Neuropathology, 2015, Vol.35 (3), p.254-259

2015

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A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family

Journal of the Peripheral Nervous System, 2012, Vol.17 (3), p.351-355

2012

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Glassy dynamics of soft matter under 1D confinement: How irreversible adsorption affects molecular packing, mobility gradients and orientational polarization in thin films

Co-translational assembly of mammalian nuclear multisubunit complexes

Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1

Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population

HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients

Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation

Optimisation Strategies for the Design of Experiments in Materials Discovery

Supercooled liquids with enhanced orientational order

TNFα induces the expression of genes associated with endothelial dysfunction through p38MAPK-mediated down-regulation of miR-149

Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations

Polymer Brushes Grafted to “Passivated” Silicon Substrates Using Click Chemistry

High Resolution Imaging Atomic Force Microscope Study of Interactions at the Membrane-Fluid Interface

Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity

Early onset Charcot‐Marie‐Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2‐related neuropathy

A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot–Marie–Tooth disease

Neuronal-specific microexon splicing of TAF1 mRNA is directly regulated by SRRM4/nSR100

Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity

Gain of glycosylation: A new pathomechanism of myelin protein zero mutations

Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies

Dissection of TAF1 neuronal splicing and implications for neurodegeneration in X-linked dystonia-parkinsonism

A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family

Dynamics in ultrathin liquid films studied by simultaneous dielectric spectroscopy (DRS) and organic molecular beam deposition (OMBD)

Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation

A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family

Different Innate and Adaptive Immune Responses to SARS-CoV-2 Infection of Asymptomatic, Mild, and Severe Cases

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