Pubblicazioni

Two new RHD alleles with deletions spanning multiple exons

2021 - TRANSFUSION

Matteocci, A; Monge-Ruiz, J; Stef, M; Apraiz, ; I., Herrera-del-Val L; Mancuso, T; Fennell, K; Lopez, M; Larizgoitia-Martin, Y; Nespoli, G; Rubia-Tejero, M; Collaretti, A; Pierelli, L; Ochoa-Garay, G.

Developmental up-regulation of NMDA receptors in the prefrontal cortex and hippocampus of mGlu5 receptor knock-out mice

2021 - MOLECULAR BRAIN

Imbriglio, T.; Verhaeghe, R.; Antenucci, N.; Maccari, S.; Battaglia, G.; Nicoletti, F.; Cannella, M.

A novel CDKN2A in-frame deletion associated with pancreatic cancer-melanoma syndrome

2020 - DERMATOLOGY ONLINE JOURNAL

Bottillo, Irene; Valiante, Michele; Menale, Lucia; Paiardini, Alessandro; Papi, Laura; Janson, Giacomo; Sestini, Roberta; Iorio, Alessandra; De Simone, Paola; Frascione, Pasquale; Grammatico, Paola

Posttranscriptional regulation of colonic epithelial repair by RNA binding protein IMP1/IGF2BP1

2019 - EMBO REPORTS

Chatterji, P.; Williams, P. A.; Whelan, K. A.; Samper, F. C.; Andres, S. F.; Simon, L. A.; Parham, L. R.; Mizuno, R.; Lundsmith, E. T.; Lee, D. S. M.; Liang, S.; Wijeratne, H. R. S.; Marti, S.; Chau, L.; Giroux, V.; Wilkins, B. J.; Wu, G. D.; Shah, P.; Tartaglia, G. G.; Hamilton, K. E.

A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3

2019 - PARKINSONISM & RELATED DISORDERS

Mastrangelo, M.; Mei, D.; Cesario, S.; Fioriello, F.; Bernardini, L.; Brinciotti, M.; Guerrini, R.; Leuzzi, V.

Deletion of the endogenous TrkB.T1 receptor isoform restores the number of hippocampal CA1 parvalbumin-positive neurons and rescues long-term potentiation in pre-symptomatic mSOD1(G93A) ALS mice

2018 - MOLECULAR AND CELLULAR NEUROSCIENCES

Quarta, Eros; Fulgenzi, Gianluca; Bravi, Riccardo; Cohen, Erez James; Yanpallewar, Sudhirkumar; Tessarollo, Lino; Minciacchi, Diego

Plasmids carrying blaCMY -2/4 in Escherichia coli from poultry, poultry meat, and humans belong to a novel IncK subgroup designated IncK2

2017 - FRONTIERS IN MICROBIOLOGY

Seiffert, Sn; Carattoli, A; Schwendener, S; Collaud, A; Endimiani, A; Perreten, V.

COG7 deficiency in Drosophila generates multifaceted developmental, behavioral and protein glycosylation phenotypes

2017 - JOURNAL OF CELL SCIENCE

Frappaolo, A.; Sechi, S.; Kumagai, T.; Robinson, S.; Fraschini, R.; Karimpour-Ghahnavieh, A.; Belloni, G.; Piergentili, R.; Tiemeyer, K. H.; Tiemeyer, M.; Giansanti, M. G.

Careful with that axe, gene, genome perturbation after a PEG-mediated protoplast transformation in Fusarium verticillioides

2017 - TOXINS

Scala, Valeria; Grottoli, Alessandro; Cigliano, Riccardo Aiese; Anzar, Irantzu; Beccaccioli, Marzia; Fanelli, Corrado; DallÃ¢ÂÂasta, Chiara; Battilani, Paola; Reverberi, Massimo; Sanseverino, Walter

Woodchuck hepatitis virus core gene deletions and proliferative responses of peripheral blood mononuclear cells stimulated by an immunodominant epitope: a viral immune escape in the woodchuck model of chronic hepatitis B?

2015 - ARCHIVES OF VIROLOGY

Taffon, Stefania; Kondili, Loreta A.; Giuseppetti, Roberto; Ciccaglione, Anna Rita; Pulimanti, Barbara; Attili, Adolfo Francesco; Rapicetta, Maria; DâUgo, Emilio

A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report

2015 - BMC GASTROENTEROLOGY

Kelsen, Judith R; Dawany, Noor; Martinez, Alejandro; Martinez, Alejuandro; Grochowski, Christopher M; Maurer, Kelly; Rappaport, Eric; Piccoli, David A; Baldassano, Robert N; Mamula, Petar; Sullivan, Kathleen E; Devoto, Marcella