Enrico Ginelli
Overview
Explore the profile of Enrico Ginelli including associated specialties, affiliations and a list of published articles.
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10
Citations
435
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Recent Articles
1.
Isayeva U, Paribello P, Ginelli E, Pisanu C, Comai S, Carpiniello B, et al.
Psychiatr Genet
. 2024 Nov;
35(1):1-11.
PMID: 39560176
The role of genetic factors in cluster headache etiology, suggested by familial and twin studies, remains ill-defined, with the exact pathophysiological mechanisms still largely elusive. This systematic review aims to...
2.
Colangelo V, Francois S, Solda G, Picco R, Roma F, Ginelli E, et al.
PLoS One
. 2014 Oct;
9(10):e108411.
PMID: 25285664
Emerging evidence has demonstrated that miRNA sequences can regulate skeletal myogenesis by controlling the process of myoblast proliferation and differentiation. However, at present a deep analysis of miRNA expression in...
3.
Giussani M, Cardone M, Bodega B, Ginelli E, Meneveri R
Genomics
. 2012 Jul;
100(5):289-96.
PMID: 22824653
We performed a detailed genomic investigation of the chimpanzee locus syntenic to human chromosome 4q35.2, associated to the facioscapulohumeral dystrophy. Two contigs of approximately 150 kb and 200 kb were...
4.
Cabianca D, Casa V, Bodega B, Xynos A, Ginelli E, Tanaka Y, et al.
Cell
. 2012 May;
149(4):819-31.
PMID: 22541069
Repetitive sequences account for more than 50% of the human genome. Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal-dominant disease associated with reduction in the copy number of the D4Z4 repeat...
5.
Cheli S, Francois S, Bodega B, Ferrari F, Tenedini E, Roncaglia E, et al.
PLoS One
. 2011 Jun;
6(6):e20966.
PMID: 21695143
Background: Determine global gene dysregulation affecting 4q-linked (FSHD-1) and non 4q-linked (FSHD-2) cells during early stages of myogenic differentiation. This approach has been never applied to FSHD pathogenesis. Methodology/principal Findings:...
6.
Zibetti C, Adamo A, Binda C, Forneris F, Toffolo E, Verpelli C, et al.
J Neurosci
. 2010 Feb;
30(7):2521-32.
PMID: 20164337
A variety of chromatin remodeling complexes are thought to orchestrate transcriptional programs that lead neuronal precursors from earliest commitment to terminal differentiation. Here we show that mammalian neurons have a...
7.
Bodega B, Ramirez G, Grasser F, Cheli S, Brunelli S, Mora M, et al.
BMC Biol
. 2009 Jul;
7:41.
PMID: 19607661
Background: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder associated with the partial deletion of integral numbers of 3.3 kb D4Z4 DNA repeats within the subtelomere of chromosome...
8.
Bodega B, Cardone M, Muller S, Neusser M, Orzan F, Rossi E, et al.
BMC Evol Biol
. 2007 Mar;
7:39.
PMID: 17359533
Background: In order to obtain insights into the functionality of the human 4q35.2 domain harbouring the facioscapulohumeral muscular dystrophy (FSHD) locus, we investigated in African apes genomic and chromatin organisations,...
9.
Rossi E, Picozzi P, Bodega B, Lavazza C, Carlo-Stella C, Marozzi A, et al.
Cancer Biol Ther
. 2007 Jan;
6(2):238-44.
PMID: 17218779
The constitutive over-expression of the retinol dehydrogenase 10 (RDH10) gene, involved in retinoic acid (RA) biosynthesis, produced in HepG2 cells a significant antiproliferative response, but not signs of apoptosis. An...
10.
Sabbadini M, Barisani D, Conforti E, Marozzi A, Ginelli E, Miserocchi G, et al.
Biochim Biophys Acta
. 2003 Jul;
1638(2):149-56.
PMID: 12853120
To investigate the molecular events taking place during the development of hydraulic interstitial edema, we analyzed by microarray and conventional molecular techniques the variation of gene expression in lung from...