Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Stefano Bonatti"'
Autor:
Simona Allocca, Michela Ciano, Maria Camilla Ciardulli, Chiara D’Ambrosio, Andrea Scaloni, Daniela Sarnataro, Maria Gabriella Caporaso, Massimo D’Agostino, Stefano Bonatti
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 7, p 1892 (2018)
The H1069Q substitution is the most frequent mutation of the Cu transporter ATP7B that causes Wilson disease in the Caucasian population. ATP7B localizes to the Golgi complex in hepatocytes, but, in the presence of excessive Cu, it relocates to the e
Externí odkaz:
https://doaj.org/article/b07666ef65e04605903d202d1cca61c4
Autor:
Michela Ciano, Lucia Perone, Stefano Bonatti, Raffaele Iorio, Silvia Parisi, Roman S. Polishchuk, Elena V. Polishchuk, Maria Gallo, Simona Allocca, Anna Musto, Giusy Ranucci
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-2 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-2 (2020)
H1069Q substitution represents the most frequent mutation of the copper transporter ATP7B causing Wilson disease in Caucasian population. ATP7B localizes to the Golgi complex in hepatocytes but moves in response to copper overload to the endo-lysosom
Autor:
Maurizio Renna, Massimo D'Agostino, M. Cannata Serio, Stefano Bonatti, Gianluca Scerra, Maria Gabriella Caporaso
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports
Scientific Reports
α-Crystallin B (CRYAB or HspB5) is a chaperone member of the small heat-shock protein family that prevents aggregation of many cytosolic client proteins by means of its ATP-independent holdase activity. Surprisingly, several reports show that CRYAB
Autor:
Simona Allocca, Michela Ciano, Lucrezia della Volpe, Maria Camilla Ciardulli, Stefano Bonatti, Massimo D'Agostino
Publikováno v:
Biochemical and Biophysical Research Communications
We have previously shown that αB-crystallin (CRYAB), a small heat shock protein (sHsp) that prevents irreversible aggregation of unfolded protein by an ATP-independent chaperone activity, plays a pivotal role in the biogenesis of multipass transmemb
Autor:
Stefano Bonatti, Massimo D'Agostino
All eukaryotic cells contain numerous membrane-enclosed compartments, such as nucleus, endoplasmic reticulum (ER), Golgi complex, mitochondria, endosomes, lysosomes, and peroxisomes. The function of each compartment is assured by a specific set of pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fd755d43d6faa058d14e2c00e3b3c14
https://doi.org/10.1016/b978-0-12-809633-8.12017-5
https://doi.org/10.1016/b978-0-12-809633-8.12017-5
Autor:
Michela Ciano, Maria Gabriella Caporaso, Maria Camilla Ciardulli, Daniela Sarnataro, Stefano Bonatti, Simona Allocca, Andrea Scaloni, Massimo D'Agostino, Chiara D'Ambrosio
Publikováno v:
International Journal of Molecular Sciences
Volume 19
Issue 7
International journal of molecular sciences (Online) 19 (2018). doi:10.3390/ijms19071892
info:cnr-pdr/source/autori:Allocca S, Ciano M, Ciardulli MC, D'Ambrosio C, Scaloni A, Sarnataro D, Caporaso MG, D'Agostino M, Bonatti S./titolo:An ?B-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population./doi:10.3390%2Fijms19071892/rivista:International journal of molecular sciences (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:19
International Journal of Molecular Sciences, Vol 19, Iss 7, p 1892 (2018)
Volume 19
Issue 7
International journal of molecular sciences (Online) 19 (2018). doi:10.3390/ijms19071892
info:cnr-pdr/source/autori:Allocca S, Ciano M, Ciardulli MC, D'Ambrosio C, Scaloni A, Sarnataro D, Caporaso MG, D'Agostino M, Bonatti S./titolo:An ?B-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population./doi:10.3390%2Fijms19071892/rivista:International journal of molecular sciences (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:19
International Journal of Molecular Sciences, Vol 19, Iss 7, p 1892 (2018)
The H1069Q substitution is the most frequent mutation of the Cu transporter ATP7B that causes Wilson disease in the Caucasian population. ATP7B localizes to the Golgi complex in hepatocytes, but, in the presence of excessive Cu, it relocates to the e
Autor:
Simona Allocca, Anna Musto, Giusy Ranucci, Michela Ciano, Stefano Bonatti, Silvia Parisi, Raffaele Iorio, Roman S. Polishchuk, Lucia Perone, Maria Gallo, Elena V. Polishchuk
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
Scientific Reports
Scientific Reports
H1069Q substitution represents the most frequent mutation of the copper transporter ATP7B causing Wilson disease in Caucasian population. ATP7B localizes to the Golgi complex in hepatocytes but moves in response to copper overload to the endo-lysosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f91041dec19cba98314d5eb6354c9998
http://hdl.handle.net/11588/717595
http://hdl.handle.net/11588/717595
Autor:
Agostino Bruno, Salvatore Di Maro, Serena F Generoso, Mariano Stornaiuolo, Mariateresa Giustiniano, Massimo Mallardo, Ettore Novellino, Daniela Sarnataro, Luciana Marinelli, Giuseppe La Regina, Sara Passacantilli, Sara Bottone, Romano Silvestri, Stefano Bonatti, Monica Dentice, Hilde Cassese
Publikováno v:
Nature Chemical Biology. 11:280-286
Upon binding, ligands can chaperone their protein targets by preventing them from misfolding and aggregating. Thus, an organic molecule that works as folding chaperone for a protein might be its specific ligand, and, similarly, the chaperone potentia
Autor:
Sara Francesca Colombo, Serena F Generoso, Gianluca Martire, Stefano Bonatti, Elena V. Polishchuk, Massimo D'Agostino, Arianna Crespi
Publikováno v:
The Journal of Membrane Biology. 247:1149-1159
The newly synthesized mutant L501fsX533 Frizzled-4 form and the alpha3beta4 nicotinic acetylcholine receptor expressed in the absence of nicotine accumulate in the endoplasmic reticulum of COS-7 cells and induce the formation of large areas of smooth
Autor:
Jean Ruf, Thomas Cuisset, Julien Fromonot, Jacques Quilici, Emmanuel Fenouillet, Laurie Bruzzese, Stefano Bonatti, Giovanna Mottola, Régis Guieu, Pierre Deharo
Publikováno v:
Canadian Journal of Physiology and Pharmacology
Canadian Journal of Physiology and Pharmacology, NRC Research Press, 2017, pp.272-7
Canadian Journal of Physiology and Pharmacology, 2017, pp.272-7
Canadian Journal of Physiology and Pharmacology, NRC Research Press, 2017, pp.272-7
Canadian Journal of Physiology and Pharmacology, 2017, pp.272-7
The role of hyperhomocysteinemia in coronary artery disease (CAD) patients remains unclear. The present study evaluated the relationship between homocysteine (HCys), adenosine plasma concentration (APC), plasma uric acid, and CAD severity evaluated u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08bb4cc5ccc0c6b91e86c11fa53e6d3c
https://hal.archives-ouvertes.fr/hal-01478198
https://hal.archives-ouvertes.fr/hal-01478198