Valentina Achille
Overview
Explore the profile of Valentina Achille including associated specialties, affiliations and a list of published articles.
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7
Citations
43
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0
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Recent Articles
1.
Rotta G, Achille V, Bornheimer S, Duenas M, Fernandez M, Gatti A, et al.
STAR Protoc
. 2024 Dec;
6(1):103343.
PMID: 39705144
Flow cytometry characterization of antigen-specific polyfunctional T cells is a valuable tool to study adaptive immunity. Here, we present a protocol for flow cytometry immunophenotyping of human antigen-specific T cells...
2.
Bettio D, Capalbo A, Albani E, Rienzi L, Achille V, Venci A, et al.
Reprod Biol Endocrinol
. 2016 Sep;
14(1):55.
PMID: 27600956
Background: Preimplantation genetic screening (PGS) provides an opportunity to eliminate a potential implantation failure due to aneuploidy in infertile couples. Some studies clearly show that twins following single embryo transfer...
3.
Bettio D, Venci A, Achille V, Alloisio M, Santoro A
Exp Ther Med
. 2016 Feb;
11(1):98-100.
PMID: 26889224
The pathogenesis of lung cancer has not been fully elucidated and biological markers acting as predictors of tumor evolution and aggressiveness remain unidentified. The multi-step hypothesis, suggesting a progression from...
4.
Borghesi A, Avanzini M, Novara F, Mantelli M, Lenta E, Achille V, et al.
Cytotherapy
. 2013 Oct;
15(11):1362-73.
PMID: 24094488
Background Aims: The umbilical cord (UC) is a promising source of mesenchymal stromal cells (MSCs). UC-MSCs display very similar in vitro characteristics to bone marrow-MSCs and could represent a valuable...
5.
Novara F, Rizzo A, Bedini G, Girgenti V, Esposito S, Pantaleoni C, et al.
Eur J Med Genet
. 2013 Feb;
56(5):260-5.
PMID: 23402836
5q14.3 deletions including the MEF2C gene have been identified to date using genomic arrays in patients with severe developmental delay or intellectual disability, stereotypic behavior, epilepsy, cerebral malformations and a...
6.
Novara F, Alfei E, DArrigo S, Pantaleoni C, Beri S, Achille V, et al.
Eur J Med Genet
. 2012 Oct;
56(1):54-8.
PMID: 23085304
Chromosome 5p13 duplication syndrome (OMIM #613174), a contiguous gene syndrome involving duplication of several genes on chromosome 5p13 including NIPBL (OMIM 608667), has been described in rare patients with developmental...
7.
Achille V, Mantelli M, Arrigo G, Novara F, Avanzini M, Bernardo M, et al.
J Cell Biochem
. 2011 Mar;
112(7):1817-21.
PMID: 21400572
Human mesenchymal stromal cells (MSCs) expanded in vitro for cell therapy approaches need to be carefully investigated for genetic stability, by employing both molecular and conventional karyotyping. Reliability of cytogenetic...