Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Cristina Cerqua"'
Autor:
Lisa Gambarotto, Samuele Metti, Martina Chrisam, Cristina Cerqua, Patrizia Sabatelli, Andrea Armani, Carlo Zanon, Marianna Spizzotin, Silvia Castagnaro, Flavie Strappazzon, Paolo Grumati, Matilde Cescon, Paola Braghetta, Eva Trevisson, Francesco Cecconi, Paolo Bonaldo
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 13, Iss 4, Pp 2211-2224 (2022)
Abstract Background Maintaining healthy mitochondria is mandatory for muscle viability and function. An essential surveillance mechanism targeting defective and harmful mitochondria to degradation is the selective form of autophagy called mitophagy.
Externí odkaz:
https://doaj.org/article/20e28c3148de45fc84c282fe3f3670ae
Autor:
Denis Vecellio Reane, Cristina Cerqua, Sabrina Sacconi, Leonardo Salviati, Eva Trevisson, Anna Raffaello
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 5; Pages: 2517
Alternative splicing, the process by which exons within a pre-mRNA transcript are differentially joined or skipped, is crucial in skeletal muscle since it is required both during myogenesis and in post-natal life to reprogram the transcripts of contr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c3b3431a91ae0907d53cb417880cdd
Publikováno v:
Mitochondrial Diseases ISBN: 9783030701468
The mitochondrial respiratory chain, which provides to the cells most of their ATP requirement, is composed of five multisubunit complexes. Its biogenesis is a multi-step process characterized by the sequential formation of intermediate assemblies co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55fad10fb35840e743ee0c38c47fdf08
https://hdl.handle.net/11577/3473783
https://hdl.handle.net/11577/3473783
Autor:
Giampiero Viola, Luis Vazquez Fonseca, Eva Trevisson, Fabien Pierrel, Alberto Casarin, Cristina Cerqua, Leonardo Salviati
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9 (1), ⟨10.1038/s41598-019-43014-y⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-7 (2019)
Scientific Reports, Nature Publishing Group, 2019, 9 (1), ⟨10.1038/s41598-019-43014-y⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-7 (2019)
Coenzyme Q10 (CoQ10) deficiencies are a group of heterogeneous conditions that respond to ubiquinone administration if treated soon after the onset of symptoms. However, this treatment is only partially effective due to its poor bioavailability. We t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e813743d842acbf104bd8389e05b484b
http://hdl.handle.net/11577/3303578
http://hdl.handle.net/11577/3303578
Autor:
Eva Trevisson, Plácido Navas, Friedhelm Hildebrandt, Manuel Jesús Acosta, Maria Andrea Desbats, Cristina Calderan, Cristina Cerqua, Leonardo Salviati, Geppo Sartori, Shazia Ashraf, Matteo Cassina, Luis Vazquez Fonseca, Mara Doimo
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Human Mutation
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Human Mutation
© 2017 The Authors.
Mutations in COQ8B cause steroid-resistant nephrotic syndrome with variable neurological involvement. In yeast, COQ8 encodes a protein required for coenzyme Q (CoQ) biosynthesis, whose precise role is not clear. Humans harbo
Mutations in COQ8B cause steroid-resistant nephrotic syndrome with variable neurological involvement. In yeast, COQ8 encodes a protein required for coenzyme Q (CoQ) biosynthesis, whose precise role is not clear. Humans harbo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db2e6da796a18f326186d32ccf60ada6
http://hdl.handle.net/10261/242405
http://hdl.handle.net/10261/242405
Autor:
Eva Trevisson, Sabrina Sacconi, Leonardo Salviati, Geppo Sartori, Maria Cristina Baldoin, Giuseppe Basso, Cristina Cerqua, Maria Andrea Desbats, Valeria Morbidoni, Mara Doimo, Chiara Frasson
Cytochrome c oxidase (COX), complex IV of the mitochondrial respiratory chain, is comprised of 14 structural subunits, several prosthetic groups and metal cofactors, among which copper. Its biosynthesis involves a number of ancillary proteins, encode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdfec2cabe47bf45545c1f044a7a1068
http://hdl.handle.net/11577/3258100
http://hdl.handle.net/11577/3258100
Autor:
Annalisa Vetro, Cristina Cerqua, Geppo Sartori, Lucia Anna Stivala, Salvatore Savasta, Ivan Limongelli, Antonella Forlino, Giuliano Mazzini, Annalisa Russo Raucci, Leonardo Salviati, Orsetta Zuffardi, Andrea Mattevi, Paola Perucca, Debora Vergani, Silvia Maruelli
Meier-Gorlin syndrome (MGORS) is a rare disorder characterized by primordial dwarfism, microtia, and patellar aplasia/hypoplasia. Recessive mutations in ORC1, ORC4, ORC6, CDT1, CDC6, and CDC45, encoding members of the pre-replication (pre-RC) and pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11349519be6fff56220b922760d6e6ba
http://hdl.handle.net/11577/3280841
http://hdl.handle.net/11577/3280841
Autor:
Alessandro Martini, Eva Trevisson, Silvia Rossi, Maurizio Clementi, Leonardo Salviati, Cristina Cerqua, Matteo Cassina
Nager syndrome is a rare preaxial acrofacial dysostosis that is caused by heterozygous loss-of-function variants in SF3B4. This gene encodes for a protein required for the assembly of spliceosomal complexes, being a master gene for splicing regulatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b487655aa7c84a47d857f9ae81e987e5
https://europepmc.org/articles/PMC5315512/
https://europepmc.org/articles/PMC5315512/
Autor:
Eva Trevisson, Manuel Jesús Acosta, Cristina Cerqua, Leonardo Salviati, Maria Andrea Desbats, Luis Vazquez Fonseca, Roberta Zordan
Coenzyme Q (CoQ, or ubiquinone) is a remarkable lipid that plays an essential role in mitochondria as an electron shuttle between complexes I and II of the respiratory chain, and complex III. It is also a cofactor of other dehydrogenases, a modulator
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3e3326af49ad8e45a42f57ca39dd679
http://hdl.handle.net/11577/3188518
http://hdl.handle.net/11577/3188518
Autor:
Raffaele Baffa, Gerhard Wiche, Kai Stefan Dimmer, Luca Scorrano, Vassiliki Anesti, Dan Liu, Aswin Pyakurel, Deborah Naon, Cristina Cerqua
Publikováno v:
EMBO reports
EMBO Reports, Vol. 11, No 11 (2010) pp. 854-860
EMBO Reports, Vol. 11, No 11 (2010) pp. 854-860
Trichoplein/mitostatin (TpMs) is a keratin-binding protein that partly colocalizes with mitochondria and is often downregulated in epithelial cancers, but its function remains unclear. In this study, we report that TpMs regulates the tethering betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a5c6251ef17ba0a14ead9a2ebc27208