LMNA knock-down affects differentiation and progression of human neuroblastoma cells.

Autor: Giovanna Maresca, Manuela Natoli, Marta Nardella, Ivan Arisi, Daniela Trisciuoglio, Marianna Desideri, Rossella Brandi, Simona D'Aguanno, Maria Rita Nicotra, Mara D'Onofrio, Andrea Urbani, Pier Giorgio Natali, Donatella Del Bufalo, Armando Felsani, Igea D'Agnano

Publikováno v: PLoS ONE, Vol 7, Iss 9, p e45513 (2012)

BackgroundNeuroblastoma (NB) is one of the most aggressive tumors that occur in childhood. Although genes, such as MYCN, have been shown to be involved in the aggressiveness of the disease, the identification of new biological markers is still desira

Externí odkaz: https://doaj.org/article/1083b3c8b24142498b9b0d57c958cd91

Circulating miRNAs in Small Extracellular Vesicles Secreted by a Human Melanoma Xenograft in Mouse Brains

Autor: Carlo Leonetti, Germana Falcone, Igea D'Agnano, Valentina Palmieri, Nicolò Panini, Carla Musa, Ingrid Cifola, Laura Vilardo, Ferdinando Scavizzi, Armando Felsani, Fabrizio Bonaventura, Ilaria Iannetti, Marta Nardella, Giulia Bolasco, Marcello Raspa, Beatrice Cardinali, Chiara Di Pietro, Loredana Guglielmi, Manuela Porru, Massimiliano Papi

Publikováno v: Cancers
Cancers, Vol 12, Iss 1635, p 1635 (2020)
Volume 12
Issue 6

The identification of liquid biomarkers remains a major challenge to improve the diagnosis of melanoma patients with brain metastases. Circulating miRNAs packaged into tumor-secreted small extracellular vesicles (sEVs) contribute to tumor progression

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0238d71eabc40228f231629865ff7e59
http://europepmc.org/articles/PMC7352810

Circulating miRNAs in Small Extracellular Vesicles Secreted by a Human Melanoma Xenograft in Mouse Brains

Autor: Loredana Guglielmi 1, Marta Nardella 2, Carla Musa 3, Ingrid Cifola 1, Manuela Porru 4, Beatrice Cardinali 3, Ilaria Iannetti 3, Chiara Di Pietro 3, Giulia Bolasco 5, Valentina Palmieri 6, 7, Laura Vilardo 1, Nicolò Panini 8, Fabrizio Bonaventura 3, Massimiliano Papi 6, Ferdinando Scavizzi 3, Marcello Raspa 3, Carlo Leonetti 4, Germana Falcone 3, Armando Felsani 9, and Igea D'Agnano 1

Publikováno v: Cancers (Basel) (2020).
info:cnr-pdr/source/autori:Loredana Guglielmi 1,+, Marta Nardella 2,+, Carla Musa 3,+, Ingrid Cifola 1,+, Manuela Porru 4, Beatrice Cardinali 3, Ilaria Iannetti 3, Chiara Di Pietro 3, Giulia Bolasco 5, Valentina Palmieri 6,7, Laura Vilardo 1, Nicolò Panini 8, Fabrizio Bonaventura 3, Massimiliano Papi 6,7, Ferdinando Scavizzi 3, Marcello Raspa 3, Carlo Leonetti 4,?, Germana Falcone 3,?, Armando Felsani 9,? and Igea D'Agnano 1,*,?/titolo:Circulating miRNAs in Small Extracellular Vesicles Secreted by a Human Melanoma Xenograft in Mouse Brains/doi:/rivista:Cancers (Basel)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume

The identification of liquid biomarkers remains a major challenge to improve the diagnosis of melanoma patients with brain metastases. Circulating miRNAs packaged into tumorsecreted small extracellular vesicles (sEVs) contribute to tumor progression.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::1fb15bb01db7349a35718b84ae406547
http://www.cnr.it/prodotto/i/424284

Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Autor: Marta Nardella, Adele D'Amico, Matteo Di Capua, Marina Trivisano, Nicola Specchio, Roberto Frusciante, Ginevra Zanni, José M. Fernández-Fernández, Lorena Travaglini, Emanuele Bellacchio, Raffaella Cusmai, Federico Vigevano, Massimiliano Valeriani, Enrico Bertini, Sabina Barresi, Alessandro Capuano, Silvia Morlino

Publikováno v: European Journal of Paediatric Neurology. 21:450-456

Background Mutations in the CACNA1A gene, encoding the pore-forming CaV2.1 (P/Q-type) channel α1A subunit, localized at presynaptic terminals of brain and cerebellar neurons, result in clinically variable neurological disorders including hemiplegic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d2ce5dc85c9e85cfbeb20c9c25be982
https://doi.org/10.1016/j.ejpn.2016.11.005

Correction to: Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital Ataxia

Autor: Marco Tartaglia, Marta Nardella, M Motta, Emanuele Bellacchio, Daniel Moreno-Andrés, P De Magistris, Hongqi Lue, Andrea Ciolfi, Antonella Sferra, Sabina Barresi, Enrico Bertini, Ginevra Zanni, Wolfram Antonin

Publikováno v: Cerebellum (London, England). 18(3)

The original version of this article unfortunately contained mistake in Fig. 3 image.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9061210119ecabc49d43a90f5ee9ca72
https://pubmed.ncbi.nlm.nih.gov/30741391