Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Luisa M. R. Napolitano"'
Autor:
Elisa De Piante, Federica D’Aria, Luisa M. R. Napolitano, Jussara Amato, Simone Pirrello, Silvia Onesti, Concetta Giancola
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Despite numerous reports on the interactions of G-quadruplexes (G4s) with helicases, systematic analysis addressing the selectivity and specificity of each helicase towards a variety of G4 topologies are scarce. Among the helicases able to u
Externí odkaz:
https://doaj.org/article/bf1b7cfb418447afa685ce50eff0faba
Autor:
Monica Mazzolini, Manuel Arcangeletti, Arin Marchesi, Luisa M. R. Napolitano, Debora Grosa, Sourav Maity, Claudio Anselmi, Vincent Torre
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-15 (2018)
Abstract Cyclic nucleotide-gated (CNG) channels mediate transduction in several sensory neurons. These channels use the free energy of CNs’ binding to open the pore, a process referred to as gating. CNG channels belong to the superfamily of voltage
Externí odkaz:
https://doaj.org/article/60a94f99df51492fb6ad132b1af0b964
Autor:
Luisa M R Napolitano, Arin Marchesi, Alex Rodriguez, Matteo De March, Silvia Onesti, Alessandro Laio, Vincent Torre
Publikováno v:
PLoS Computational Biology, Vol 14, Iss 8, p e1006295 (2018)
Several channels, ranging from TRP receptors to Gap junctions, allow the exchange of small organic solute across cell membrane. However, very little is known about the molecular mechanism of their permeation. Cyclic Nucleotide Gated (CNG) channels, d
Externí odkaz:
https://doaj.org/article/8c4debab477b416eb1a1011324205d57
Autor:
Simone Mortal, Federico Iseppon, Andrea Perissinotto, Elisa D'Este, Dan Cojoc, Luisa M. R. Napolitano, Vincent Torre
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 11 (2017)
During neurite development, Actin Waves (AWs) emerge at the neurite base and move up to its tip, causing a transient retraction of the Growth Cone (GC). Many studies have shown that AWs are linked to outbursts of neurite growth and, therefore, contri
Externí odkaz:
https://doaj.org/article/5463f6a1c64c4a72ad3996a5fdafb402
Autor:
Ana Boavida, Luisa M. R. Napolitano, Diana Santos, Giuseppe Cortone, Silvia Onesti, Nanda K. Jegadesan, Dana Branzei, Francesca M. Pisani
FANCJ is a DNA helicase linked to Fanconi anemia and frequently mutated in breast and ovarian cancers. If and how FANCJ is recruited to the replisome is unknown. Here, we report that FANCJ directly binds to AND-1 (the vertebrate ortholog of budding y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98d9448808e10bbb953f4c03451904de
https://doi.org/10.1101/2022.10.21.513143
https://doi.org/10.1101/2022.10.21.513143
Autor:
Luisa M. R. Napolitano, Martina Moretti, Silvia Ravera, Viviana Chiappetta, Giuseppe Cortone, Nicoletta Zini, Barbara Crescenzi, Flavio Faletra, Roberta Bottega, Enrico Cappelli, Francesca M. Pisani, Michela Faleschini, Anna Savoia, Silvia Onesti, Silvia Arniani, Job de Lange, Cristina Mecucci, Fabio Sirchia, Barbara Medagli
Publikováno v:
Journal of cellular physiology
236 (2021): 5664–5675. doi:10.1002/jcp.30265
info:cnr-pdr/source/autori:Bottega, Roberta; Ravera, Silvia; Napolitano, Luisa M. R.; Chiappetta, Viviana; Zini, Nicoletta; Crescenzi, Barbara; Arniani, Silvia; Faleschini, Michela; Cortone, Giuseppe; Faletra, Flavio; Medagli, Barbara; Sirchia, Fabio; Moretti, Martina; de Lange, Job; Cappelli, Enrico; Mecucci, Cristina; Onesti, Silvia; Pisani, Francesca M.; Savoia, Anna/titolo:Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia./doi:10.1002%2Fjcp.30265/rivista:Journal of cellular physiology (Print)/anno:2021/pagina_da:5664/pagina_a:5675/intervallo_pagine:5664–5675/volume:236
Journal of Cellular Physiology, 236(8), 5664-5675. Wiley-Liss Inc.
Bottega, R, Ravera, S, Napolitano, L M R, Chiappetta, V, Zini, N, Crescenzi, B, Arniani, S, Faleschini, M, Cortone, G, Faletra, F, Medagli, B, Sirchia, F, Moretti, M, de Lange, J, Cappelli, E, Mecucci, C, Onesti, S, Pisani, F M & Savoia, A 2021, ' Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells : A comparison with Fanconi anemia ', Journal of Cellular Physiology, vol. 236, no. 8, pp. 5664-5675 . https://doi.org/10.1002/jcp.30265
236 (2021): 5664–5675. doi:10.1002/jcp.30265
info:cnr-pdr/source/autori:Bottega, Roberta; Ravera, Silvia; Napolitano, Luisa M. R.; Chiappetta, Viviana; Zini, Nicoletta; Crescenzi, Barbara; Arniani, Silvia; Faleschini, Michela; Cortone, Giuseppe; Faletra, Flavio; Medagli, Barbara; Sirchia, Fabio; Moretti, Martina; de Lange, Job; Cappelli, Enrico; Mecucci, Cristina; Onesti, Silvia; Pisani, Francesca M.; Savoia, Anna/titolo:Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia./doi:10.1002%2Fjcp.30265/rivista:Journal of cellular physiology (Print)/anno:2021/pagina_da:5664/pagina_a:5675/intervallo_pagine:5664–5675/volume:236
Journal of Cellular Physiology, 236(8), 5664-5675. Wiley-Liss Inc.
Bottega, R, Ravera, S, Napolitano, L M R, Chiappetta, V, Zini, N, Crescenzi, B, Arniani, S, Faleschini, M, Cortone, G, Faletra, F, Medagli, B, Sirchia, F, Moretti, M, de Lange, J, Cappelli, E, Mecucci, C, Onesti, S, Pisani, F M & Savoia, A 2021, ' Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells : A comparison with Fanconi anemia ', Journal of Cellular Physiology, vol. 236, no. 8, pp. 5664-5675 . https://doi.org/10.1002/jcp.30265
Warsaw breakage syndrome (WABS), is caused by biallelic mutations of DDX11, a gene coding a DNA helicase. We have recently reported two affected sisters, compound heterozygous for a missense (p.Leu836Pro) and a frameshift (p.Lys303Glufs*22) variant.
Publikováno v:
Pflugers Archiv : European journal of physiology. 473(9)
Cyclic nucleotide-gated (CNG) channels are key to the signal transduction machinery of certain sensory modalities both in vertebrate and invertebrate organisms. They translate a chemical change in cyclic nucleotide concentration into an electrical si
Autor:
Paolo Gasparini, Roberta Bottega, Silvia Onesti, Enrico Cappelli, Anna Carbone, Flavio Faletra, Anna Savoia, Fabio Corsolini, Luisa M. R. Napolitano
Background: Warsaw Breakage Syndrome (WABS) is an ultra rare cohesinopathy caused by biallelic mutation of DDX11 gene. It is clinically characterized by pre and postnatal growth delay, microcephaly, hearing loss with cochlear hypoplasia, skin color a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9430448597687df70dc5999543c5b37e
http://hdl.handle.net/11368/2957690
http://hdl.handle.net/11368/2957690
Publikováno v:
Genes (Basel) 9 (2018). doi:10.3390/genes9110564
info:cnr-pdr/source/autori:Pisani F. M., Napolitano E., Napolitano L. M. R., Onesti S./titolo:Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11/doi:10.3390%2Fgenes9110564/rivista:Genes (Basel)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:9
Genes
Genes, Vol 9, Iss 11, p 564 (2018)
info:cnr-pdr/source/autori:Pisani F. M., Napolitano E., Napolitano L. M. R., Onesti S./titolo:Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11/doi:10.3390%2Fgenes9110564/rivista:Genes (Basel)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:9
Genes
Genes, Vol 9, Iss 11, p 564 (2018)
DDX11/ChlR1 (Chl1 in yeast) is a DNA helicase involved in sister chromatid cohesion and in DNA repair pathways. The protein belongs to the family of the iron–sulphur cluster containing DNA helicases, whose deficiencies have been linked to a number
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e6fd91430ba6227832792b6a07a2a8b
Autor:
Luisa M. R. Napolitano, Dan Cojoc, Vincent Torre, Simone Mortal, Elisa D’Este, Federico Iseppon, Andrea Perissinotto
Publikováno v:
Frontiers in Cellular Neuroscience
Frontiers in cellular neuroscience 11 (2017). doi:10.3389/fncel.2017.00402
info:cnr-pdr/source/autori:Mortal S.; Iseppon F.; Perissinotto A.; D'Este E.; Cojoc D.; Napolitano L.M.R.; Torre V./titolo:Actin waves do not boost neurite outgrowth in the early stages of neuron maturation/doi:10.3389%2Ffncel.2017.00402/rivista:Frontiers in cellular neuroscience/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:11
Frontiers in Cellular Neuroscience, Vol 11 (2017)
Frontiers in cellular neuroscience 11 (2017). doi:10.3389/fncel.2017.00402
info:cnr-pdr/source/autori:Mortal S.; Iseppon F.; Perissinotto A.; D'Este E.; Cojoc D.; Napolitano L.M.R.; Torre V./titolo:Actin waves do not boost neurite outgrowth in the early stages of neuron maturation/doi:10.3389%2Ffncel.2017.00402/rivista:Frontiers in cellular neuroscience/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:11
Frontiers in Cellular Neuroscience, Vol 11 (2017)
During neurite development, Actin Waves (AWs) emerge at the neurite base and move up to its tip, causing a transient retraction of the Growth Cone (GC). Many studies have shown that AWs are linked to outbursts of neurite growth and, therefore, contri