Marco Cammisa
Overview
Explore the profile of Marco Cammisa including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
295
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Recent Articles
1.
Theka I, Sottile F, Cammisa M, Bonnin S, Sanchez-Delgado M, Di Vicino U, et al.
Sci Rep
. 2019 Feb;
9(1):948.
PMID: 30700782
Mouse embryonic stem cells (mESCs) are pluripotent and can differentiate into cells belonging to the three germ layers of the embryo. However, mESC pluripotency and genome stability can be compromised...
2.
Meg3 Non-coding RNA Expression Controls Imprinting by Preventing Transcriptional Upregulation in cis
Sanli I, Lalevee S, Cammisa M, Perrin A, Rage F, Lleres D, et al.
Cell Rep
. 2018 Apr;
23(2):337-348.
PMID: 29641995
Although many long non-coding RNAs (lncRNAs) are imprinted, their roles often remain unknown. The Dlk1-Dio3 domain expresses the lncRNA Meg3 and multiple microRNAs and small nucleolar RNAs (snoRNAs) on the...
3.
Gatto S, Gagliardi M, Franzese M, Leppert S, Papa M, Cammisa M, et al.
Nucleic Acids Res
. 2017 Mar;
45(10):5739-5756.
PMID: 28334849
Hypomorphic mutations in DNA-methyltransferase DNMT3B cause majority of the rare disorder Immunodeficiency, Centromere instability and Facial anomalies syndrome cases (ICF1). By unspecified mechanisms, mutant-DNMT3B interferes with lymphoid-specific pathways resulting in...
4.
Citro V, Cammisa M, Liguori L, Cimmaruta C, Lukas J, Cubellis M, et al.
Int J Mol Sci
. 2016 Dec;
17(12).
PMID: 27916943
Fabry disease is caused by mutations in the gene and is characterized by a large genotypic and phenotypic spectrum. Missense mutations pose a special problem for graduating diagnosis and choosing...
5.
Riso V, Cammisa M, Kukreja H, Anvar Z, Verde G, Sparago A, et al.
Nucleic Acids Res
. 2016 Jun;
44(17):8165-78.
PMID: 27257070
ZFP57 is necessary for maintaining repressive epigenetic modifications at Imprinting control regions (ICRs). In mouse embryonic stem cells (ESCs), ZFP57 binds ICRs (ICRBS) and many other loci (non-ICRBS). To address...
6.
Anvar Z, Cammisa M, Riso V, Baglivo I, Kukreja H, Sparago A, et al.
Nucleic Acids Res
. 2015 Oct;
44(3):1118-32.
PMID: 26481358
Imprinting Control Regions (ICRs) need to maintain their parental allele-specific DNA methylation during early embryogenesis despite genome-wide demethylation and subsequent de novo methylation. ZFP57 and KAP1 are both required for...
7.
Cammisa M, Correra A, Andreotti G, Cubellis M
Orphanet J Rare Dis
. 2013 Jul;
8:111.
PMID: 23883437
Fabry_CEP is a user-friendly web-application designed to help clinicians Choose Eligible Patients for the therapy with pharmacological chaperones. It provides a database and a predictive tool to evaluate the responsiveness...
8.
Cammisa M, Correra A, Andreotti G, Cubellis M
BMC Bioinformatics
. 2013 Jul;
14 Suppl 7:S9.
PMID: 23815589
Background: The interaction between proteins and ligands occurs at pockets that are often lined by conserved amino acids. These pockets can represent the targets for low molecular weight drugs. In...
9.
Baglivo I, Esposito S, De Cesare L, Sparago A, Anvar Z, Riso V, et al.
FEBS Lett
. 2013 Mar;
587(10):1474-81.
PMID: 23499433
In the mouse, ZFP57 contains three classical Cys2His2 zinc finger domains (ZF) and recognizes the methylated TGC(met)CGC target sequence using the first and the second ZFs. In this study, we...
10.
Andreotti G, Citro V, De Crescenzo A, Orlando P, Cammisa M, Correra A, et al.
Orphanet J Rare Dis
. 2011 Oct;
6:66.
PMID: 22004918
Background: Fabry disease is a rare disorder caused by a large variety of mutations in the gene encoding lysosomal alpha-galactosidase. Many of these mutations are unique to individual families. Fabry...