Loredana Poeta
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Explore the profile of Loredana Poeta including associated specialties, affiliations and a list of published articles.
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9
Citations
90
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Recent Articles
1.
Sannino A, Scarfi M, Dufossee M, Romeo S, Poeta L, Prouzet-Mauleon V, et al.
Int J Mol Sci
. 2022 Aug;
23(15).
PMID: 35955556
In the last years, radiofrequency (RF) has demonstrated that it can reduce DNA damage induced by a subsequent treatment with chemical or physical agents in different cell types, resembling the...
2.
Poeta L, Malacarne M, Padula A, Drongitis D, Verrillo L, Lioi M, et al.
Int J Mol Sci
. 2022 Mar;
23(6).
PMID: 35328505
The X-linked gene encoding aristaless-related homeobox () is a bi-functional transcription factor capable of activating or repressing gene transcription, whose mutations have been found in a wide spectrum of neurodevelopmental...
3.
Romeo S, Zeni O, Scarfi M, Poeta L, Lioi M, Sannino A
Int J Mol Sci
. 2022 Feb;
23(4).
PMID: 35216437
In the last decades, experimental studies have been carried out to investigate the effects of radiofrequency (RF, 100 kHz-300 GHz) electromagnetic fields (EMF) exposure on the apoptotic process. As evidence-based...
4.
Drongitis D, Caterino M, Verrillo L, Santonicola P, Costanzo M, Poeta L, et al.
Hum Mol Genet
. 2022 Jan;
31(11):1884-1908.
PMID: 35094084
X-linked lissencephaly with abnormal genitalia (XLAG) and developmental epileptic encephalopathy-1 (DEE1) are caused by mutations in the Aristaless-related homeobox (ARX) gene, which encodes a transcription factor responsible for brain development....
5.
Poeta L, Padula A, Lioi M, van Bokhoven H, Miano M
Genes (Basel)
. 2021 Aug;
12(7).
PMID: 34356104
Dysregulation of transcriptional pathways is observed in multiple forms of neurodevelopmental disorders (NDDs), such as intellectual disability (ID), epilepsy and autism spectrum disorder (ASD). We previously demonstrated that the NDD...
6.
Poeta L, Drongitis D, Verrillo L, Miano M
Genes (Basel)
. 2020 Jun;
11(6).
PMID: 32580525
Unstable repeat disorders comprise a variable group of incurable human neurological and neuromuscular diseases caused by an increase in the copy number of tandem repeats located in various regions of...
7.
Poeta L, Padula A, Attianese B, Valentino M, Verrillo L, Filosa S, et al.
Hum Mol Genet
. 2019 Nov;
28(24):4089-4102.
PMID: 31691806
A disproportional large number of neurodevelopmental disorders (NDDs) is caused by variants in genes encoding transcription factors and chromatin modifiers. However, the functional interactions between the corresponding proteins are only...
8.
Poeta L, Fusco F, Drongitis D, Shoubridge C, Manganelli G, Filosa S, et al.
Am J Hum Genet
. 2012 Dec;
92(1):114-25.
PMID: 23246292
Intellectual disability (ID) and epilepsy often occur together and have a dramatic impact on the development and quality of life of the affected children. Polyalanine (polyA)-expansion-encoding mutations of aristaless-related homeobox...
9.
Fusco F, Paciolla M, Chen E, Li X, Genesio R, Conti A, et al.
Hum Reprod
. 2011 Aug;
26(11):3186-96.
PMID: 21859812
Background: Diminished ovarian reserve (DOR) is a heterogeneous disorder causing infertility, characterized by a decreased number of oocytes, the genetic cause of which is still unknown. Methods And Results: We...