List of works - Chiara Vantaggiato

A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function.

scientific article published in July 2009

A novel nonsense mutation in the APTX gene associated with delayed DNA single-strand break removal fails to enhance sensitivity to different genotoxic agents

article

Antipsychotics Promote Metabolic Disorders Disrupting Cellular Lipid Metabolism and Trafficking

scientific article published on 01 February 2019

Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin.

scientific article published on 11 July 2009

Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study

scientific article

Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15

scientific article published on 11 September 2013

Drp1 overexpression induces desmin disassembling and drives kinesin-1 activation promoting mitochondrial trafficking in skeletal muscle

scientific article published on 10 February 2020

ERK1 and ERK2 mitogen-activated protein kinases affect Ras-dependent cell signaling differentially.

scientific article published on January 2006

Essential role for acid sphingomyelinase-inhibited autophagy in melanoma response to cisplatin

scientific article published on 14 April 2016

Further evidence supporting the role of GTDC1 in glycine metabolism and neurodevelopmental disorders

scientific article published in 2024

Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory

scientific article

Nitric oxide sustains long-term skeletal muscle regeneration by regulating fate of satellite cells via signaling pathways requiring Vangl2 and cyclic GMP.

scientific article

Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents

scientific article published on 31 October 2013

Past and ongoing adaptation of human cytomegalovirus to its host

scientific article published on 08 May 2020

Senataxin modulates neurite growth through fibroblast growth factor 8 signalling

scientific article

The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation

scientific article published on 04 April 2019

ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis

scientific article published on 13 September 2018

ZFYVE26/SPASTIZIN: a close link between complicated hereditary spastic paraparesis and autophagy

scientific article published on 26 November 2013

List of works by Chiara Vantaggiato

A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function.

A novel nonsense mutation in the APTX gene associated with delayed DNA single-strand break removal fails to enhance sensitivity to different genotoxic agents

Antipsychotics Promote Metabolic Disorders Disrupting Cellular Lipid Metabolism and Trafficking

Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin.

Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study

Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15

Drp1 overexpression induces desmin disassembling and drives kinesin-1 activation promoting mitochondrial trafficking in skeletal muscle

ERK1 and ERK2 mitogen-activated protein kinases affect Ras-dependent cell signaling differentially.

Essential role for acid sphingomyelinase-inhibited autophagy in melanoma response to cisplatin

Further evidence supporting the role of GTDC1 in glycine metabolism and neurodevelopmental disorders

Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory

Nitric oxide sustains long-term skeletal muscle regeneration by regulating fate of satellite cells via signaling pathways requiring Vangl2 and cyclic GMP.

Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents

Past and ongoing adaptation of human cytomegalovirus to its host

Senataxin modulates neurite growth through fibroblast growth factor 8 signalling

The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation

ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis

ZFYVE26/SPASTIZIN: a close link between complicated hereditary spastic paraparesis and autophagy