Andrea Masotti

Dr. Andrea Masotti

Bambino Gesù Children's Hospital, IRCCS, Research Laboratories, V.le di San Paolo 15, 00146 Rome, Italy
orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2011 in Laboratory Investigation
Verified
Journal Article
Closed access
Anna AlisiAnna Alisi
Anna Alisi
LSLetizia Da Sacco
Letizia Da Sacco
GBGiovannella Bruscalupi
Giovannella Bruscalupi
FPFiorella Piemonte
Fiorella Piemonte
NPNadia Panera
Nadia Panera
VNValerio Nobili
Valerio Nobili

1 February 2009 in Colloids and Surfaces B: Biointerfaces
Verified
Journal Article
Closed access
Andrea MasottiAndrea Masotti
Andrea Masotti
GMG. Mossa
G. Mossa
Cesare CamettiCesare Cametti
Cesare Cametti
GOG. Ortaggi
G. Ortaggi
ABA. Bianco
A. Bianco
CEC. Esposito
C. Esposito

1 February 2015 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
Andrea MasottiAndrea Masotti
Andrea Masotti
PUPaolo Uva
Paolo Uva
LDLaura Davis-Keppen
Laura Davis-Keppen
LSLina Basel Salmon
Lina Basel Salmon
LCLior Cohen
Lior Cohen
BDBruno Dallapiccola
Bruno Dallapiccola

1 November 2008 in Current Medicinal Chemistry
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Journal Article
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PVPaola Vicennati
Paola Vicennati
AGAntonella Giuliano
Antonella Giuliano
GOGiancarlo Ortaggi
Giancarlo Ortaggi
Andrea MasottiAndrea Masotti
Andrea Masotti
Polyethylenimine (PEI), an organic branched or linear polyamine polymer, has been successfully used in the past for DNA complexation and transfection in vitro and in vivo into several cell lines and tissues. PEI was also applied in different fields from gene therapy and several studies have emphasized the importance of this polymer in medicinal chemistry. In this brief critical review the uses and applications of this versatile polymeric molecule will be discussed.

7 January 2014 in Epigenetics & Chromatin
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Journal Article
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CSCecilia Surace
Cecilia Surace
Francesco BerardinelliFrancesco Berardinelli
Francesco Berardinelli
Andrea MasottiAndrea Masotti
Andrea Masotti
MRMaria Cristina Roberti
Maria Cristina Roberti
LSLetizia Da Sacco
Letizia Da Sacco
AAAdriano Angioni
Adriano Angioni
Ring chromosome 17 syndrome is a rare disease that arises from the breakage and reunion of the short and long arms of chromosome 17. Usually this abnormality results in deletion of genetic material, which explains the clinical features of the syndrome. Moreover, similar phenotypic features have been observed in cases with complete or partial loss of the telomeric repeats and conservation of the euchromatic regions. We studied two different cases of ring 17 syndrome, firstly, to clarify, by analyzing gene expression analysis using real-time qPCR, the role of the telomere absence in relationship with the clinical symptoms, and secondly, to look for a new model of the mechanism of ring chromosome transmission in a rare case of familial mosaicism, through cytomolecular and quantitative fluorescence in-situ hybridization (Q-FISH) investigations.

2 September 2015 in PLOS ONE
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Journal Article
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FCFederica Del Chierico
Federica Del Chierico
PVPamela Vernocchi
Pamela Vernocchi
APAndrea Petrucca
Andrea Petrucca
PPPaola Paci
Paola Paci
SFSusana Fuentes
Susana Fuentes
LPLorenza Putignani
Lorenza Putignani
The colonization and development of gut microbiota immediately after birth is highly variable and depends on several factors, such as delivery mode and modality of feeding during the first months of life. A cohort of 31 mother and neonate pairs, including 25 at-term caesarean (CS) and 6 vaginally (V) delivered neonates (DNs), were included in this study and 121 meconium/faecal samples were collected at days 1 through 30 following birth. Operational taxonomic units (OTUs) were assessed in 69 stool samples by phylogenetic microarray HITChip and inter- and intra-individual distributions were established by inter-OTUs correlation matrices and OTUs co-occurrence or co-exclusion networks. 1H-NMR metabolites were determined in 70 stool samples, PCA analysis was performed on 55 CS DNs samples, and metabolome/OTUs co-correlations were assessed in 45 CS samples, providing an integrated map of the early microbiota OTUs-metabolome. A microbiota “core” of OTUs was identified that was independent of delivery mode and lactation stage, suggesting highly specialized communities that act as seminal colonizers of microbial networks. Correlations among OTUs, metabolites, and OTUs-metabolites revealed metabolic profiles associated with early microbial ecological dynamics, maturation of milk components, and host physiology.