Pappalardo XG - Search Results

1

VDAC Genes Expression and Regulation in Mammals.

Zinghirino F, Pappalardo XG, Messina A, Nicosia G, De Pinto V, Guarino F. Zinghirino F, et al. Among authors: pappalardo xg. Front Physiol. 2021 Aug 5;12:708695. doi: 10.3389/fphys.2021.708695. eCollection 2021. Front Physiol. 2021. PMID: 34421651 Free PMC article. Review.

2

NRF-1 and HIF-1α contribute to modulation of human VDAC1 gene promoter during starvation and hypoxia in HeLa cells.

Guarino F, Zinghirino F, Mela L, Pappalardo XG, Ichas F, De Pinto V, Messina A. Guarino F, et al. Among authors: pappalardo xg. Biochim Biophys Acta Bioenerg. 2020 Dec 1;1861(12):148289. doi: 10.1016/j.bbabio.2020.148289. Epub 2020 Aug 15. Biochim Biophys Acta Bioenerg. 2020. PMID: 32810507 Free article.

3

Is the secret of VDAC Isoforms in their gene regulation? Characterization of human VDAC genes expression profile, promoter activity, and transcriptional regulators.

Zinghirino F, Pappalardo XG, Messina A, Guarino F, De Pinto V. Zinghirino F, et al. Among authors: pappalardo xg. Int J Mol Sci. 2020 Oct 7;21(19):7388. doi: 10.3390/ijms21197388. Int J Mol Sci. 2020. PMID: 33036380 Free PMC article.

4

Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia.

Pappalardo XG, Risiglione P, Zinghirino F, Ostuni A, Luciano D, Bisaccia F, De Pinto V, Guarino F, Messina A. Pappalardo XG, et al. Biol Res. 2023 Jun 22;56(1):33. doi: 10.1186/s40659-023-00446-1. Biol Res. 2023. PMID: 37344914 Free PMC article.

5

Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures.

Falsaperla R, Pappalardo XG, Romano C, Marino SD, Corsello G, Ruggieri M, Parano E, Pavone P. Falsaperla R, et al. Among authors: pappalardo xg. Front Pediatr. 2020 Sep 11;8:550. doi: 10.3389/fped.2020.00550. eCollection 2020. Front Pediatr. 2020. PMID: 33042910 Free PMC article.

6

Losing DNA methylation at repetitive elements and breaking bad.

Pappalardo XG, Barra V. Pappalardo XG, et al. Epigenetics Chromatin. 2021 Jun 3;14(1):25. doi: 10.1186/s13072-021-00400-z. Epigenetics Chromatin. 2021. PMID: 34082816 Free PMC article. Review.

7

Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions.

Pavone P, Pappalardo XG, Parano E, Falsaperla R, Marino SD, Fink JK, Ruggieri M. Pavone P, et al. Among authors: pappalardo xg. Front Pediatr. 2022 Apr 21;10:858945. doi: 10.3389/fped.2022.858945. eCollection 2022. Front Pediatr. 2022. PMID: 35529330 Free PMC article. Review.

8

Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review.

Pavone P, Striano P, Cacciaguerra G, Marino SD, Parano E, Pappalardo XG, Falsaperla R, Ruggieri M. Pavone P, et al. Among authors: pappalardo xg. Front Pediatr. 2023 Sep 8;11:1210272. doi: 10.3389/fped.2023.1210272. eCollection 2023. Front Pediatr. 2023. PMID: 37744437 Free PMC article.

9

Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity.

Parano E, Pappalardo XG, Pavone P, Ruggieri M, Cavallaro S. Parano E, et al. Among authors: pappalardo xg. Open Neurol J. 2016 Jun 30;10:30-1. doi: 10.2174/1874205X01610010030. eCollection 2016. Open Neurol J. 2016. PMID: 27499819 Free PMC article. No abstract available.

10

PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?

Pavone P, Corsello G, Cho SY, Pappalardo XG, Ruggieri M, Marino SD, Jin DK, Marino S, Falsaperla R. Pavone P, et al. Among authors: pappalardo xg. Ital J Pediatr. 2019 Dec 4;45(1):159. doi: 10.1186/s13052-019-0755-2. Ital J Pediatr. 2019. PMID: 31801583 Free PMC article. Review.

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