Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Donato, Di Pierro"'
Autor:
Diego Sbardella, Grazia Raffaella Tundo, Luisa Campagnolo, Giuseppe Valacchi, Augusto Orlandi, Paolo Curatolo, Giovanna Borsellino, Maurizio D’Esposito, Chiara Ciaccio, Silvia Di Cesare, Donato Di Pierro, Cinzia Galasso, Marta Elena Santarone, Joussef Hayek, Massimiliano Coletta, Stefano Marini
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-1 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/ca4a5efff3834f5aae38c88c3d351b02
Publikováno v:
Sensors, Vol 6, Iss 11, Pp 1428-1439 (2006)
Over the last twenty years, newly developed chemical sensor systems (socalled“electronic noses") have odour analyses made possible. This paper describes theapplications of these systems for microbial detection in different fields such as
Externí odkaz:
https://doaj.org/article/d99128f142f84d7fa585092b9d6a4d9d
Autor:
Luisa Campagnolo, Cinzia Galasso, Marta Elena Santarone, Silvia Di Cesare, Joussef Hayek, Chiara Ciaccio, Augusto Orlandi, Grazia R. Tundo, Donato Di Pierro, Maurizio D'Esposito, Paolo Curatolo, Diego Sbardella, Massimiliano Coletta, Giuseppe Valacchi, Giovanna Borsellino, Stefano Marini
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-1 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-1 (2021)
Rett Syndrome (RTT), which affects approximately 1:10.000 live births, is a X-linked pervasive neuro-developmental disorder which is caused, in the vast majority of cases, by a sporadic mutation in the Methyl-CpG-binding protein-2 (MeCP2) gene. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6057f3ede6341321c69a9367537212e5
http://europepmc.org/articles/PMC8184957
http://europepmc.org/articles/PMC8184957
Autor:
Paolo Curatolo, Cinzia Galasso, Chiara Ciaccio, Grazia R. Tundo, Stefano Marini, Donato Di Pierro, Diego Sbardella, Massimiliano Coletta, Roberta Bernardini, Virginia Pironi
Publikováno v:
Molecular and Cellular Biochemistry. 463:101-113
Nutritional supplements are traditionally employed for overall health and for managing some health conditions, although controversies are found concerning the role of antioxidants-mediated benefits in vivo. Consistently with its critical role in syst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90781f204302f1227dc0e867ed624e46
https://doi.org/10.1007/s11010-019-03633-5
https://doi.org/10.1007/s11010-019-03633-5
Autor:
Diego Sbardella, Alessandra di Masi, Giovanna De Simone, Magda Gioia, Giovanni Francesco Fasciglione, Massimo Coletta, Alessio Bocedi, Grazia R. Tundo, Donato Di Pierro, Paolo Ascenzi, Paolo Calligari, Chiara Ciaccio
Publikováno v:
Biochemical Pharmacology
Graphical abstract
In the Fall of 2019 a sudden and dramatic outbreak of a pulmonary disease (Coronavirus Disease COVID-19), due to a new Coronavirus strain (i.e., SARS-CoV-2), emerged in the continental Chinese area of Wuhan and quickly diffuse
In the Fall of 2019 a sudden and dramatic outbreak of a pulmonary disease (Coronavirus Disease COVID-19), due to a new Coronavirus strain (i.e., SARS-CoV-2), emerged in the continental Chinese area of Wuhan and quickly diffuse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9389928342b4ecffed17d0e2b7b49a10
https://pubmed.ncbi.nlm.nih.gov/32956643
https://pubmed.ncbi.nlm.nih.gov/32956643
Autor:
Diego, Sbardella, Grazia, Raffaella, Tundo, Vincenzo, Cunsolo, Giuseppe, Grasso, Raffaella, Cascella, Valerio, Caputo, Anna Maria, Santoro, Danilo, Mailardi, Pecorelli, Alessandra, Chiara, Ciaccio, Donato, Di Pierro, Silvia, Leoncini, Luisa, Campagnolo, Virginia, Pironi, Francesco, Oddone, Priscilla, Manni, Salvatore, Foti, Emiliano, Giardina, Claudio, De Felice, Joussef, Hayekk, Paolo, Curatolo, Cinzia, Galasso, Valacchi, Giuseppe, Massimiliano, Coletta, Grazia, Graziani, Stefano, Marini
Publikováno v:
Biochimica et biophysica acta. Molecular basis of disease 1866 (2020). doi:10.1016/j.bbadis.2020.165793
info:cnr-pdr/source/autori:Sbardella, Diego; Tundo, Grazia Raffaella; Cunsolo, Vincenzo; Grasso, Giuseppe; Cascella, Raffaella; Caputo, Valerio; Santoro, Anna Maria; Milardi, Danilo; Pecorelli, Alessandra; Ciaccio, Chiara; Di Pierro, Donato; Leoncini, Silvia; Campagnolo, Luisa; Pironi, Virginia; Oddone, Francesco; Manni, Priscilla; Foti, Salvatore; Giardina, Emiliano; De Felice, Claudio; Hayek, Joussef; Curatolo, Paolo; Galasso, Cinzia; Valacchi, Giuseppe; Coletta, Massimiliano; Graziani, Grazia; Marini, Stefano/titolo:Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations/doi:10.1016%2Fj.bbadis.2020.165793/rivista:Biochimica et biophysica acta. Molecular basis of disease/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:1866
info:cnr-pdr/source/autori:Sbardella, Diego; Tundo, Grazia Raffaella; Cunsolo, Vincenzo; Grasso, Giuseppe; Cascella, Raffaella; Caputo, Valerio; Santoro, Anna Maria; Milardi, Danilo; Pecorelli, Alessandra; Ciaccio, Chiara; Di Pierro, Donato; Leoncini, Silvia; Campagnolo, Luisa; Pironi, Virginia; Oddone, Francesco; Manni, Priscilla; Foti, Salvatore; Giardina, Emiliano; De Felice, Claudio; Hayek, Joussef; Curatolo, Paolo; Galasso, Cinzia; Valacchi, Giuseppe; Coletta, Massimiliano; Graziani, Grazia; Marini, Stefano/titolo:Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations/doi:10.1016%2Fj.bbadis.2020.165793/rivista:Biochimica et biophysica acta. Molecular basis of disease/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:1866
Rett Syndrome (RTT) is a rare X-linked neurodevelopmental disorder which affects about 1: 10000 live births. In >95% of subjects RTT is caused by a mutation in Methyl-CpG binding protein-2 (MECP2) gene, which encodes for a transcription regulator wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::216b50fe174c2824e75e1324b6fc1b1a
http://hdl.handle.net/2108/245871
http://hdl.handle.net/2108/245871
Autor:
Anna Maria Caccuri, Eleonora Nicolai, Federica Sinibaldi, Giampiero Mei, Almerinda Di Venere, Donato Di Pierro
Publikováno v:
Biotechnology and Applied Biochemistry. 65:38-45
The ability of a C-terminal truncated form of TRAF2 to bind synthetic vesicles has been quantitatively studied by steady-state fluorescence energy transfer from the protein to large unilamellar vesicles (LUVs) prepared with different lipid mixtures.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70fe1c1cf821a565e08f658828e3db60
https://doi.org/10.1002/bab.1615
https://doi.org/10.1002/bab.1615
Autor:
Augusto Orlandi, Luisa Campagnolo, Grazia R. Tundo, Diego Sbardella, Giovanna Borsellino, Massimiliano Coletta, Maurizio D'Esposito, Joussef Hayek, Donato Di Pierro, Marta Elena Santarone, Chiara Ciaccio, Paolo Curatolo, Cinzia Galasso, Silvia Di Cesare, Stefano Marini, Giuseppe Valacchi
Publikováno v:
Scientific Reports
Scientific reports (Nature Publishing Group) 7 (2017): 12297. doi:10.1038/s41598-017-12069-0
info:cnr-pdr/source/autori:Sbardella, Diego; Tundo, Grazia Raffaella; Campagnolo, Luisa; Valacchi, Giuseppe; Orlandi, Augusto; Curatolo, Paolo; Borsellino, Giovanna; D'Esposito, Maurizio; Ciaccio, Chiara; Di Cesare, Silvia; Di Pierro, Donato; Galasso, Cinzia; Santarone, Marta Elena; Hayek, Joussef; Coletta, Massimiliano; Marini, Stefano/titolo:Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome/doi:10.1038%2Fs41598-017-12069-0/rivista:Scientific reports (Nature Publishing Group)/anno:2017/pagina_da:12297/pagina_a:/intervallo_pagine:12297/volume:7
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Scientific reports (Nature Publishing Group) 7 (2017): 12297. doi:10.1038/s41598-017-12069-0
info:cnr-pdr/source/autori:Sbardella, Diego; Tundo, Grazia Raffaella; Campagnolo, Luisa; Valacchi, Giuseppe; Orlandi, Augusto; Curatolo, Paolo; Borsellino, Giovanna; D'Esposito, Maurizio; Ciaccio, Chiara; Di Cesare, Silvia; Di Pierro, Donato; Galasso, Cinzia; Santarone, Marta Elena; Hayek, Joussef; Coletta, Massimiliano; Marini, Stefano/titolo:Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome/doi:10.1038%2Fs41598-017-12069-0/rivista:Scientific reports (Nature Publishing Group)/anno:2017/pagina_da:12297/pagina_a:/intervallo_pagine:12297/volume:7
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Rett Syndrome (RTT), which affects approximately 1:10.000 live births, is a X-linked pervasive neuro-developmental disorder which is caused, in the vast majority of cases, by a sporadic mutation in the Methyl-CpG-binding protein-2 (MeCP2) gene. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc74ba9f17b10d5ee4b84a29af02459a
http://hdl.handle.net/2108/192090
http://hdl.handle.net/2108/192090
Autor:
Diego Sbardella, Andrea Coletta, Stefano Marini, Magda Gioia, Peter van Endert, Grazia R. Tundo, Danilo Milardi, Fabio Polticelli, Giuseppe Grasso, Donato Di Pierro, Chiara Ciaccio, Massimo Coletta
Publikováno v:
Tundo, G R, Sbardella, D, Ciaccio, C, Grasso, G, Gioia, M, Coletta, A, Polticelli, F, Di Pierro, D, Milardi, D, van Endert, P, Marini, S & Coletta, M 2017, ' Multiple functions of insulin-degrading enzyme : a metabolic crosslight? ', Critical Reviews in Biochemistry and Molecular Biology, vol. 52, no. 5, pp. 554-582 . https://doi.org/10.1080/10409238.2017.1337707
Critical reviews in biochemistry and molecular biology 52 (2017): 554–582. doi:10.1080/10409238.2017.1337707
info:cnr-pdr/source/autori:Tundo, Grazia R.; Sbardella, Diego; Ciaccio, Chiara; Grasso, Giuseppe; Gioia, Magda; Coletta, Andrea; Polticelli, Fabio; Di Pierro, Donato; Milardi, Danilo; Van Endert, Peter; Marini, Stefano; Coletta, Massimo/titolo:Multiple functions of insulin-degrading enzyme: a metabolic crosslight?/doi:10.1080%2F10409238.2017.1337707/rivista:Critical reviews in biochemistry and molecular biology/anno:2017/pagina_da:554/pagina_a:582/intervallo_pagine:554–582/volume:52
Critical reviews in biochemistry and molecular biology 52 (2017): 554–582. doi:10.1080/10409238.2017.1337707
info:cnr-pdr/source/autori:Tundo, Grazia R.; Sbardella, Diego; Ciaccio, Chiara; Grasso, Giuseppe; Gioia, Magda; Coletta, Andrea; Polticelli, Fabio; Di Pierro, Donato; Milardi, Danilo; Van Endert, Peter; Marini, Stefano; Coletta, Massimo/titolo:Multiple functions of insulin-degrading enzyme: a metabolic crosslight?/doi:10.1080%2F10409238.2017.1337707/rivista:Critical reviews in biochemistry and molecular biology/anno:2017/pagina_da:554/pagina_a:582/intervallo_pagine:554–582/volume:52
Insulin-degrading enzyme (IDE) is a ubiquitous zinc peptidase of the inverzincin family, which has been initially discovered as the enzyme responsible for insulin catabolism; therefore, its involvement in the onset of diabetes has been largely invest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f06fac3cec088a1de604b460e7627cd
http://hdl.handle.net/20.500.11769/51760
http://hdl.handle.net/20.500.11769/51760
Autor:
Paola Cozza, Marta Elena Santarone, Grazia R. Tundo, Paolo Curatolo, Maurizio Casasco, Diego Sbardella, Chiara Ciaccio, Claudio De Felice, Cinzia Galasso, Marcello Rossi, Donato Di Pierro, Joussef Hayek, Massimo Coletta, Stefano Marini, Alessio Cortelazzo
Publikováno v:
Molecular and cellular biochemistry. 426(1-2)
Rett syndrome (RTT) is a neurodevelopmental disorder, mainly affecting females, which is associated to a mutation on the methyl-CpG-binding protein 2 gene. In the pathogenesis and progression of classic RTT, red blood cell (RBC) morphology has been s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1cb018e622e6ec948da5fb77d614372
https://pubmed.ncbi.nlm.nih.gov/28063007
https://pubmed.ncbi.nlm.nih.gov/28063007