Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Frontiers in Cellular and Infection Microbiology|April 10, 2026
Host transcriptomic analysis reveals a defective intracellular environment that limits SARS-CoV-2 replication in CFTR-deficient airway epitheliumAnna Lagni, Virginia Lotti, Riccardo Cecchetto, et al.
G3 (Bethesda, Md.)|September 3, 2025
Chromosomal-level assembly of Magnusiomyces clavatus: novel genetic insights on an emerging fungal pathogenEmil Tonon, Riccardo Cecchetto, Maya Carrera, et al.
Journal of Human Genetics|October 11, 2013
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patientsSilvia Ferronato, Macarena Gomez-Lira, Marta Menegazzi, et al.
Archives of Neurology|July 16, 2008
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsyPasquale Striano, Arturo de Falco, Erica Diani, et al.
Microorganisms|October 28, 2023
Detection of SARS-CoV-2 Δ426 ORF8 Deletion Mutant Cluster in NGS ScreeningRiccardo Cecchetto, Emil Tonon, Nicoletta Medaina, et al.
Scientific Reports|February 2, 2017
M48U1 and Tenofovir combination synergistically inhibits HIV infection in activated PBMCs and human cervicovaginal histoculturesGiuseppina Musumeci, Isabella Bon, David Lembo, et al.
Heliyon|December 17, 2019
Interferon gamma inducible protein 16 (IFI16) expression is reduced in mantle cell lymphomaPier Paolo Piccaluga, Mohsen Navari, Axel Visani, et al.
Epilepsia|April 21, 2011
Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsyCarlo Di Bonaventura, Francesca F Operto, Giorgia Busolin, et al.
Epilepsia|June 26, 2009
Drug resistant ADLTE and recurrent partial status epilepticus with dysphasic features in a family with a novel LGI1mutation: electroclinical, genetic, and EEG/fMRI findingsCarlo Di Bonaventura, Marco Carni, Erica Diani, et al.
Frontiers in Neurology|October 10, 2018
HIV-1-Associated Neurocognitive Disorders: Is HLA-C Binding Stability to β2-Microglobulin a Missing Piece of the Pathogenetic Puzzle?Donato Zipeto, Michela Serena, Simona Mutascio, et al.
Pageof 5