Antonella Marte
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Explore the profile of Antonella Marte including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
580
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Recent Articles
1.
Pepe S, Aprile D, Castroflorio E, Marte A, Giubbolini S, Hopestone S, et al.
iScience
. 2025 Jan;
28(1):111515.
PMID: 39758816
The vacuolar ATPase (v-ATPase) is essential for acidification of intracellular organelles, including synaptic vesicles. Its activity is controlled by cycles of association and dissociation of the ATP hydrolysis (V) and...
2.
Parisi B, Esposito A, Castroflorio E, Bramini M, Pepe S, Marte A, et al.
Cell Mol Life Sci
. 2024 Oct;
81(1):416.
PMID: 39367928
Neurons are dependent on efficient quality control mechanisms to maintain cellular homeostasis and function due to their polarization and long-life span. Autophagy is a lysosomal degradative pathway that provides nutrients...
3.
Casazza A, Capraro M, Pedrazzi M, DAgostino G, Onofri F, Marte A, et al.
Int J Mol Sci
. 2024 Jan;
25(2).
PMID: 38255981
High-pressure and temperature extraction (HPTE) can effectively recover bioactive compounds from olive pomace (OP). HPTE extract obtained by extracting OP with ethanol and water (50:50 /) at 180 °C for...
4.
Sterlini B, Franchi F, Morinelli L, Corradi B, Parodi C, Albini M, et al.
Neurobiol Dis
. 2023 Jun;
183:106177.
PMID: 37271286
PRRT2 is a neuronal protein that controls neuronal excitability and network stability by modulating voltage-gated Na channel (Nav). PRRT2 pathogenic variants cause pleiotropic syndromes including epilepsy, paroxysmal kinesigenic dyskinesia and...
5.
Franchi F, Marte A, Corradi B, Sterlini B, Alberini G, Romei A, et al.
J Biol Chem
. 2023 Mar;
299(5):104632.
PMID: 36958475
Proline-rich transmembrane protein 2 (PRRT2) is the single causative gene for pleiotropic paroxysmal syndromes, including epilepsy, kinesigenic dyskinesia, episodic ataxia, and migraine. PRRT2 is a neuron-specific type-2 membrane protein with...
6.
Centonze E, Marte A, Albini M, Rocchi A, Cesca F, Chiacchiaretta M, et al.
J Neurochem
. 2023 Jan;
165(5):701-721.
PMID: 36636908
Neuron-restrictive silencer factor/repressor element 1 (RE1)-silencing transcription factor (NRSF/REST) is a transcriptional repressor of a large cluster of neural genes containing RE1 motifs in their promoter region. NRSF/REST is ubiquitously...
7.
Valente P, Marte A, Franchi F, Sterlini B, Casagrande S, Corradi A, et al.
Mol Neurobiol
. 2022 Nov;
60(3):1281-1296.
PMID: 36441479
Proline-rich transmembrane protein 2 (PRRT2) is a neuron-specific protein implicated in the control of neurotransmitter release and neural network stability. Accordingly, PRRT2 loss-of-function mutations associate with pleiotropic paroxysmal neurological disorders,...
8.
Iovino L, Giusti V, Pischedda F, Giusto E, Plotegher N, Marte A, et al.
Acta Neuropathol
. 2022 May;
144(1):81-106.
PMID: 35596783
The Excitatory Amino Acid Transporter 2 (EAAT2) accounts for 80% of brain glutamate clearance and is mainly expressed in astrocytic perisynaptic processes. EAAT2 function is finely regulated by endocytic events,...
9.
Prestigio C, Ferrante D, Marte A, Romei A, Lignani G, Onofri F, et al.
Elife
. 2021 Dec;
10.
PMID: 34855580
The repressor-element 1-silencing transcription/neuron-restrictive silencer factor (REST/NRSF) controls hundreds of neuron-specific genes. We showed that REST/NRSF downregulates glutamatergic transmission in response to hyperactivity, thus contributing to neuronal homeostasis. However, whether...
10.
Ferrante D, Sterlini B, Prestigio C, Marte A, Corradi A, Onofri F, et al.
Cell Rep
. 2021 Jun;
35(11):109248.
PMID: 34133925
Loss-of-function mutations in proline-rich transmembrane protein-2 (PRRT2) cause paroxysmal disorders associated with defective Ca dependence of glutamatergic transmission. We find that either acute or constitutive PRRT2 deletion induces a significant...