Zobrazeno 1 - 10
of 331
pro vyhledávání: '"Delahodde, A."'
Autor:
Nicola Facchinello, Claudio Laquatra, Lisa Locatello, Giorgia Beffagna, Raquel Brañas Casas, Chiara Fornetto, Alberto Dinarello, Laura Martorano, Andrea Vettori, Giovanni Risato, Rudy Celeghin, Giacomo Meneghetti, Massimo Mattia Santoro, Agnes Delahodde, Francesco Vanzi, Andrea Rasola, Luisa Dalla Valle, Maria Berica Rasotto, Tiziana Lodi, Enrico Baruffini, Francesco Argenton, Natascia Tiso
Publikováno v:
Cell Death and Disease, Vol 12, Iss 1, Pp 1-18 (2021)
Abstract The DNA polymerase gamma (Polg) is a nuclear-encoded enzyme involved in DNA replication in animal mitochondria. In humans, mutations in the POLG gene underlie a set of mitochondrial diseases characterized by mitochondrial DNA (mtDNA) depleti
Externí odkaz:
https://doaj.org/article/e5b4a8a5e87b4483a23748afb74ea087
Autor:
Kyle Thompson, Lucas Bianchi, Francesca Rastelli, Florence Piron-Prunier, Sophie Ayciriex, Claude Besmond, Laurence Hubert, Magalie Barth, Inês A. Barbosa, Charu Deshpande, Manali Chitre, Sarju G. Mehta, Eric J.M. Wever, Pascale Marcorelles, Sandra Donkervoort, Dimah Saade, Carsten G. Bönnemann, Katherine R. Chao, Chunyu Cai, Susan T. Iannaccone, Andrew F. Dean, Robert McFarland, Frédéric M. Vaz, Agnès Delahodde, Robert W. Taylor, Agnès Rötig
Publikováno v:
HGG Advances, Vol 3, Iss 2, Pp 100097- (2022)
Summary: Mitochondrial disorders are clinically and genetically heterogeneous, with variants in mitochondrial or nuclear genes leading to varied clinical phenotypes. TAMM41 encodes a mitochondrial protein with cytidine diphosphate-diacylglycerol synt
Externí odkaz:
https://doaj.org/article/3e06951a912a4d6080e971a99e6d10b0
The evolution of the luminosity of nova shells in the century following the nova outburst is studied for the lines H-alpha, H-beta, and [O III]. About 1200 flux measurements from 96 objects have been collected from the literature, from unpublished ob
Externí odkaz:
http://arxiv.org/abs/astro-ph/0112538
Autor:
Gillette, Thomas G., Gonzalez, Fernando, Delahodde, Agnes, Johnston, Stephen Albert, Kodadek, Thomas, Varshavsky, Alexander
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2004 Apr . 101(16), 5904-5909.
Externí odkaz:
https://www.jstor.org/stable/3371937
Autor:
Weaver, H. A., Sekanina, Z., Toth, I., Delahodde, C. E., Hainaut, O. R., Lamy, P. L., Bauer, J. M., Arpigny, C., Combi, M. R., Davies, J. K., Feldman, P. D., Festou, M. C., Hook, R., Jorda, L., Keesey, M. S. W., Lisse, C. M., Marsden, B. G., Meech, K. J., Tozzi, G. P., West, R.
Publikováno v:
Science, 2001 May . 292(5520), 1329-1333.
Externí odkaz:
https://www.jstor.org/stable/3083760
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0214287 (2019)
Eukaryotic organelles share different components and establish physical contacts to communicate throughout the cell. One of the best-recognized examples of such interplay is the metabolic cooperation and crosstalk between mitochondria and peroxisomes
Externí odkaz:
https://doaj.org/article/6dfe1d4f64b3420f905e9b5d7dc86501
Autor:
Giulia di Punzio, Maria Antonietta Di Noia, Agnès Delahodde, Carole Sellem, Claudia Donnini, Luigi Palmieri, Tiziana Lodi, Cristina Dallabona
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9, p 4461 (2021)
Mitochondrial diseases result from inherited or spontaneous mutations in mitochondrial or nuclear DNA, leading to an impairment of the oxidative phosphorylation responsible for the synthesis of ATP. To date, there are no effective pharmacological the
Externí odkaz:
https://doaj.org/article/f5a8e69591824453a9c3cf302a600029
Autor:
Jean-Paul Lasserre, Alain Dautant, Raeka S. Aiyar, Roza Kucharczyk, Annie Glatigny, Déborah Tribouillard-Tanvier, Joanna Rytka, Marc Blondel, Natalia Skoczen, Pascal Reynier, Laras Pitayu, Agnès Rötig, Agnès Delahodde, Lars M. Steinmetz, Geneviève Dujardin, Vincent Procaccio, Jean-Paul di Rago
Publikováno v:
Disease Models & Mechanisms, Vol 8, Iss 6, Pp 509-526 (2015)
Mitochondrial diseases are severe and largely untreatable. Owing to the many essential processes carried out by mitochondria and the complex cellular systems that support these processes, these diseases are diverse, pleiotropic, and challenging to st
Externí odkaz:
https://doaj.org/article/d739a034d8d041fb94f29fdbddc8e0fd
Publikováno v:
Science, 2002 Apr . 296(5567), 548-550.
Externí odkaz:
https://www.jstor.org/stable/3076462
Autor:
Kyle, Thompson, Lucas, Bianchi, Francesca, Rastelli, Florence, Piron-Prunier, Sophie, Ayciriex, Claude, Besmond, Laurence, Hubert, Magalie, Barth, Inês A, Barbosa, Charu, Deshpande, Manali, Chitre, Sarju G, Mehta, Eric J M, Wever, Pascale, Marcorelles, Sandra, Donkervoort, Dimah, Saade, Carsten G, Bönnemann, Katherine R, Chao, Chunyu, Cai, Susan T, Iannaccone, Andrew F, Dean, Robert, McFarland, Frédéric M, Vaz, Agnès, Delahodde, Robert W, Taylor, Agnès, Rötig
Publikováno v:
HGG advances. 3(2)
Mitochondrial disorders are clinically and genetically heterogeneous, with variants in mitochondrial or nuclear genes leading to varied clinical phenotypes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::77ca9e942951cc8b36754d4e542cb447
https://pubmed.ncbi.nlm.nih.gov/35321494
https://pubmed.ncbi.nlm.nih.gov/35321494