Maria Giuseppina Miano - Search Results

Year	Number of Results
2002	1
2003	1
2004	1
2005	1
2006	2
2007	2
2008	1
2009	1
2010	1
2011	2
2012	3
2013	2
2014	1
2019	1
2020	3
2021	2
2022	5
2023	3
2024	0

1

Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability.

Poeta L, Malacarne M, Padula A, Drongitis D, Verrillo L, Lioi MB, Chiariello AM, Bianco S, Nicodemi M, Piccione M, Salzano E, Coviello D, Miano MG. Poeta L, et al. Among authors: miano mg. Int J Mol Sci. 2022 Mar 13;23(6):3084. doi: 10.3390/ijms23063084. Int J Mol Sci. 2022. PMID: 35328505 Free PMC article. Review.

2

Suberoylanilide Hydroxamic Acid (SAHA) Is a Driver Molecule of Neuroplasticity: Implication for Neurological Diseases.

Verrillo L, Di Palma R, de Bellis A, Drongitis D, Miano MG. Verrillo L, et al. Among authors: miano mg. Biomolecules. 2023 Aug 24;13(9):1301. doi: 10.3390/biom13091301. Biomolecules. 2023. PMID: 37759701 Free PMC article. Review.

3

Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants.

Leonardi E, Aspromonte MC, Drongitis D, Bettella E, Verrillo L, Polli R, McEntagart M, Licchetta L, Dilena R, D'Arrigo S, Ciaccio C, Esposito S, Leuzzi V, Torella A, Baldo D, Lonardo F, Bonato G, Pellegrin S, Stanzial F, Posmyk R, Kaczorowska E, Carecchio M, Gos M, Rzońca-Niewczas S, Miano MG, Murgia A. Leonardi E, et al. Among authors: miano mg. Eur J Hum Genet. 2023 Feb;31(2):202-215. doi: 10.1038/s41431-022-01233-4. Epub 2022 Nov 25. Eur J Hum Genet. 2023. PMID: 36434256 Free PMC article.

4

DNA Hypermethylation and Unstable Repeat Diseases: A Paradigm of Transcriptional Silencing to Decipher the Basis of Pathogenic Mechanisms.

Poeta L, Drongitis D, Verrillo L, Miano MG. Poeta L, et al. Among authors: miano mg. Genes (Basel). 2020 Jun 22;11(6):684. doi: 10.3390/genes11060684. Genes (Basel). 2020. PMID: 32580525 Free PMC article. Review.

5

Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy.

Drongitis D, Caterino M, Verrillo L, Santonicola P, Costanzo M, Poeta L, Attianese B, Barra A, Terrone G, Lioi MB, Paladino S, Di Schiavi E, Costa V, Ruoppolo M, Miano MG. Drongitis D, et al. Among authors: miano mg. Hum Mol Genet. 2022 Jun 4;31(11):1884-1908. doi: 10.1093/hmg/ddac028. Hum Mol Genet. 2022. PMID: 35094084 Free PMC article.

6

The Chromatin-Oxygen Sensor Gene KDM5C Associates with Novel Hypoxia-Related Signatures in Glioblastoma Multiforme.

Drongitis D, Verrillo L, De Marinis P, Orabona P, Caiola A, Turitto G, Alfieri A, Bruscella S, Gentile M, Moriello V, Sannino E, Di Muccio I, Costa V, Miano MG, de Bellis A. Drongitis D, et al. Among authors: miano mg. Int J Mol Sci. 2022 Sep 6;23(18):10250. doi: 10.3390/ijms231810250. Int J Mol Sci. 2022. PMID: 36142158 Free PMC article.

7

A reliable strategy for single-cell RNA sequencing analysis using cryoconserved primary cortical cells.

Verrillo L, Mangano E, Drongitis D, Merelli I, Pischedda F, Piccoli G, Consolandi C, Bordoni R, Miano MG. Verrillo L, et al. Among authors: miano mg. J Neurosci Methods. 2021 Jan 1;347:108960. doi: 10.1016/j.jneumeth.2020.108960. Epub 2020 Sep 25. J Neurosci Methods. 2021. PMID: 32987100 Free article.

8

[Human Papilloma Virus (HPV), cervical cancer incidence and screening uptake: differences among Northern, Central and Southern Italy].

Giorgi Rossi P, Chini F, Borgia P, Guasticchi G, Carozzi FM, Confortini M, Angeloni C, Buzzoni C, Buonaguro FM; Gruppo di lavoro HPV Prevalenza. Giorgi Rossi P, et al. Epidemiol Prev. 2012 Mar-Apr;36(2):108-19. Epidemiol Prev. 2012. PMID: 22706361 Review. Italian.

9

Preservation of neurons in an AD 79 vitrified human brain.

Petrone P, Giordano G, Vezzoli E, Pensa A, Castaldo G, Graziano V, Sirano F, Capasso E, Quaremba G, Vona A, Miano MG, Savino S, Niola M. Petrone P, et al. Among authors: miano mg. PLoS One. 2020 Oct 6;15(10):e0240017. doi: 10.1371/journal.pone.0240017. eCollection 2020. PLoS One. 2020. PMID: 33022024 Free PMC article.

10

Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures.

Poeta L, Padula A, Lioi MB, van Bokhoven H, Miano MG. Poeta L, et al. Among authors: miano mg. Genes (Basel). 2021 Jul 18;12(7):1088. doi: 10.3390/genes12071088. Genes (Basel). 2021. PMID: 34356104 Free PMC article.

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