Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Matteo Esposito"'
Autor:
Matteo Esposito, Antonella Migliaccio, Sara Carmela Credendino, Rufina Maturi, Nella Prevete, Gabriella De Vita
Publikováno v:
Cell Death Discovery, Vol 10, Iss 1, Pp 1-12 (2024)
Abstract KLHL14 is a substrate-binding subunit of Cullin-RING ligase 3 ubiquitin ligase complex, highly enriched in thyroid since early embryonic development, together with its antisense RNA KLHL14-AS. We have previously demonstrated that Klhl14-AS i
Externí odkaz:
https://doaj.org/article/b6f45d7c980a4d419cfaade21ceada2b
Autor:
Sara C. Credendino, Marta De Menna, Irene Cantone, Carmen Moccia, Matteo Esposito, Luigi Di Guida, Mario De Felice, Gabriella De Vita
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 14, p 7666 (2021)
Forkhead box E1 (FOXE1) is a lineage-restricted transcription factor involved in thyroid cancer susceptibility. Cancer-associated polymorphisms map in regulatory regions, thus affecting the extent of gene expression. We have recently shown that genet
Externí odkaz:
https://doaj.org/article/cc0850c4868d4361bcf67e88962468b6
Autor:
Nunzia Mollo, Matteo Esposito, Miriam Aurilia, Roberta Scognamiglio, Rossella Accarino, Ferdinando Bonfiglio, Rita Cicatiello, Maria Charalambous, Claudio Procaccini, Teresa Micillo, Rita Genesio, Gaetano Calì, Agnese Secondo, Simona Paladino, Giuseppe Matarese, Gabriella De Vita, Anna Conti, Lucio Nitsch, Antonella Izzo
Publikováno v:
Biology, Vol 10, Iss 7, p 609 (2021)
Background: The presence of mitochondrial alterations in Down syndrome suggests that it might affect neuronal differentiation. We established a model of trisomic iPSCs, differentiating into neural precursor cells (NPCs) to monitor the occurrence of d
Externí odkaz:
https://doaj.org/article/e283770a81d44bdaa3143288d2f1f94a
Autor:
Paolo, Gallo, Francesca, Terracciani, Giulia, Di Pasquale, Matteo, Esposito, Antonio, Picardi, Umberto, Vespasiani-Gentilucci
Publikováno v:
World Journal of Gastroenterology. 28:4061-4074
Chronic liver disease is characterized by several hematological derangements resulting in a complex and barely rebalanced haemostatic environment. Thrombocytopenia is the most common abnormality observed in these patients and recent advances have led
Autor:
Davide Falessi, Simone Mesiano Laureani, Jonida Çarka, Matteo Esposito, Daniel Alencar da Costa
Publikováno v:
Empirical Software Engineering. 28
Context Defect prediction can help at prioritizing testing tasks by, for instance, ranking a list of items (methods and classes) according to their likelihood to be defective. While many studies investigated how to predict the defectiveness of commit
Publikováno v:
Empirical Software Engineering. 27
ContextAdvances in defect prediction models, aka classifiers, have been validated via accuracy metrics. Effort-aware metrics (EAMs) relate to benefits provided by a classifier in accurately ranking defective entities such as classes or methods. PofB
Publikováno v:
Cortex, 141, 421-435. ELSEVIER MASSON, CORPORATION OFFICE
Recent studies in humans and animal models suggest a primary role of the basal ganglia in the extraction of stimulus-value regularities, then exploited to orient attentional shift and build up sensorimotor memories. The tail of the caudate and the po
We present an analysis aimed at combining cosmological constraints from number counts of galaxy clusters identified through the Sunyaev-Zeldovich effect, obtained with the South Pole Telescope (SPT), and from Lyman-$\alpha$ spectra obtained with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c29276be7fcb04858b5e21533429ac94
Autor:
Massimiliano Scalvenzi, Alessandro Testori, Michiel Vermeulen, Annalaura Montella, Nicola Zambrano, Marijke P. Baltissen, Vito Alessandro Lasorsa, Marianna Avitabile, Kevin M. Brown, Sueva Cantalupo, Flora Cimmino, Antonella Cardinale, Mai Xu, Mark M. Iles, Achille Iolascon, Paola Ghiorzo, Fabrizio Ayala, Ferdinando Bonfiglio, Mariangela Succoio, Matthew Law, Daniela Formicola, Matteo Esposito, Mario Capasso
Publikováno v:
Human Molecular Genetics, 31, 863-874
Hum Mol Genet
Human Molecular Genetics, 31, 6, pp. 863-874
Hum Mol Genet
Human Molecular Genetics, 31, 6, pp. 863-874
The 10q24.33 locus is known to be associated with susceptibility to cutaneous malignant melanoma (CMM), but the mechanisms underlying this association have been not extensively investigated. We carried out an integrative genomic analysis of 10q24.33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fdb5f2d344407fe0b72d1c0a3be378e
http://hdl.handle.net/2066/250105
http://hdl.handle.net/2066/250105
Autor:
Miriam Aurilia, Matteo Esposito, Giuseppe Matarese, Teresa Micillo, Agnese Secondo, Lucio Nitsch, Rita Genesio, Simona Paladino, Maria Charalambous, Anna Conti, Nunzia Mollo, Roberta Scognamiglio, Antonella Izzo, Gabriella De Vita, Rita Cicatiello, Gaetano Calì, Rossella Accarino, Claudio Procaccini, Ferdinando Bonfiglio
Publikováno v:
Biology
Biology, Vol 10, Iss 609, p 609 (2021)
Volume 10
Issue 7
Biology (Basel)
Biology, Vol 10, Iss 609, p 609 (2021)
Volume 10
Issue 7
Biology (Basel)
Simple Summary Down Syndrome, which is due to the presence of three copies of chromosome 21, always presents with mental retardation, possibly caused by defects in the development of neurons. In recent years, it has been shown that cells and tissues