Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Alba Signes"'
Autor:
Sara Vidoni, Michael E. Harbour, Sergio Guerrero-Castillo, Alba Signes, Shujing Ding, Ian M. Fearnley, Robert W. Taylor, Valeria Tiranti, Susanne Arnold, Erika Fernandez-Vizarra, Massimo Zeviani
Publikováno v:
Cell Reports, Vol 18, Iss 7, Pp 1727-1738 (2017)
The biogenesis of human cytochrome c oxidase (COX) is an intricate process in which three mitochondrial DNA (mtDNA)-encoded core subunits are assembled in a coordinated way with at least 11 nucleus-encoded subunits. Many chaperones shared between yea
Externí odkaz:
https://doaj.org/article/d2f36c1008504deab7320891faca21e8
Autor:
Alba Signes, Raffaele Cerutti, Anna S Dickson, Cristiane Benincá, Elizabeth C Hinchy, Daniele Ghezzi, Rosalba Carrozzo, Enrico Bertini, Michael P Murphy, James A Nathan, Carlo Viscomi, Erika Fernandez‐Vizarra, Massimo Zeviani
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 1, Pp n/a-n/a (2019)
Abstract Loss‐of‐function mutations in APOPT1, a gene exclusively found in higher eukaryotes, cause a characteristic type of cavitating leukoencephalopathy associated with mitochondrial cytochrome c oxidase (COX) deficiency. Although the genetic
Externí odkaz:
https://doaj.org/article/215a8a7301c4477ba2ac4a4276753ce7
Autor:
Alba Signes, Erika Fernandez-Vizarra
Publikováno v:
Essays in Biochemistry
The assembly of the five oxidative phosphorylation system (OXPHOS) complexes in the inner mitochondrial membrane is an intricate process. The human enzymes comprise core proteins, performing the catalytic activities, and a large number of ‘supernum
Autor:
Elizabeth C. Hinchy, Raffaele Cerutti, Rosalba Carrozzo, James A. Nathan, Erika Fernandez-Vizarra, Michael P. Murphy, Carlo Viscomi, Alba Signes, Daniele Ghezzi, Cristiane Benincá, Massimo Zeviani, Anna S Dickson, Enrico Bertini
Publikováno v:
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 11, Iss 1, Pp n/a-n/a (2019)
EMBO Molecular Medicine, Vol 11, Iss 1, Pp n/a-n/a (2019)
Loss‐of‐function mutations in APOPT1, a gene exclusively found in higher eukaryotes, cause a characteristic type of cavitating leukoencephalopathy associated with mitochondrial cytochrome c oxidase (COX) deficiency. Although the genetic associati
Autor:
Sergio Guerrero-Castillo, Shujing Ding, Susanne Arnold, Valeria Tiranti, Michael E. Harbour, Massimo Zeviani, Erika Fernandez-Vizarra, Ian M. Fearnley, Alba Signes, Robert W. Taylor, Sara Vidoni
Publikováno v:
Cell Reports, 18, 1727-1738
Cell Reports, Vol 18, Iss 7, Pp 1727-1738 (2017)
Cell Reports, 18, 7, pp. 1727-1738
Cell Reports, Vol 18, Iss 7, Pp 1727-1738 (2017)
Cell Reports, 18, 7, pp. 1727-1738
The biogenesis of human cytochrome c oxidase (COX) is an intricate process in which three mitochondrial DNA (mtDNA)-encoded core subunits are assembled in a coordinated way with at least 11 nucleus-encoded subunits. Many chaperones shared between yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::464331a554d72c7210ceb81e18dba6ed
http://hdl.handle.net/11577/3354178
http://hdl.handle.net/11577/3354178
Publikováno v:
European Journal of Pharmaceutics and Biopharmaceutics
We investigated the influence of pH and sodium chloride concentration on aggregation kinetics of a monoclonal antibody. Aggregation was induced by sodium chloride addition at low pH. Protein conformation before and after salt addition was determined