Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Annie Glatigny"'
Autor:
Simon Gosset, Annie Glatigny, Mélina Gallopin, Zhou Yi, Marion Salé, Marie-Hélène Mucchielli-Giorgi
Publikováno v:
PeerJ, Vol 10, p e14204 (2022)
Background Protein–protein interactions (PPIs) are essential to almost every process in a cell. Analysis of PPI networks gives insights into the functional relationships among proteins and may reveal important hub proteins and sub-networks correspo
Externí odkaz:
https://doaj.org/article/5ab6c13515254043b10e23f757262ab1
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
Autor:
Laras Pitayu, Vincent Procaccio, Agnès Rötig, Jean-Paul Lasserre, Pascal Reynier, Annie Glatigny, Déborah Tribouillard-Tanvier, Natalia Skoczen, Joanna Rytka, Alain Dautant, Roza Kucharczyk, Lars M. Steinmetz, Jean-Paul di Rago, Raeka S. Aiyar, Marc Blondel, Geneviève Dujardin, Agnès Delahodde
Publikováno v:
Disease Models & Mechanisms, Vol 8, Iss 6, Pp 509-526 (2015)
Disease Models & Mechanisms
Disease Models & Mechanisms, Cambridge Company of Biologists, 2015, 8 (6), pp.509-26. ⟨10.1242/dmm.020438⟩
Disease Models & Mechanisms, Cambridge Company of Biologists, 2015, 8 (6), pp.509-26
Disease Models & Mechanisms, 2015, 8 (6), pp.509-26. ⟨10.1242/dmm.020438⟩
Disease Models & Mechanisms, 2015, 8 (6), pp.509-26
Disease Models & Mechanisms
Disease Models & Mechanisms, Cambridge Company of Biologists, 2015, 8 (6), pp.509-26. ⟨10.1242/dmm.020438⟩
Disease Models & Mechanisms, Cambridge Company of Biologists, 2015, 8 (6), pp.509-26
Disease Models & Mechanisms, 2015, 8 (6), pp.509-26. ⟨10.1242/dmm.020438⟩
Disease Models & Mechanisms, 2015, 8 (6), pp.509-26
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
Autor:
Annie Glatigny, Marie-HÊlène Mucchielli-Giorgi, Alexa Bourand-Plantefol, Geneviève Dujardin, Philippe Gambette
Publikováno v:
BMC Systems Biology
BMC Systems Biology, BioMed Central, 2017, 11 (67), pp.1-12. ⟨10.1186/s12918-017-0442-0⟩
BMC Systems Biology, Vol 11, Iss 1, Pp 1-12 (2017)
BMC Systems Biology, BioMed Central, 2017, 11 (67), pp.1-12. 〈10.1186/s12918-017-0442-0〉
BMC Systems Biology, 2017, 11 (67), pp.1-12. ⟨10.1186/s12918-017-0442-0⟩
BMC Systems Biology, BioMed Central, 2017, 11 (67), pp.1-12. ⟨10.1186/s12918-017-0442-0⟩
BMC Systems Biology, Vol 11, Iss 1, Pp 1-12 (2017)
BMC Systems Biology, BioMed Central, 2017, 11 (67), pp.1-12. 〈10.1186/s12918-017-0442-0〉
BMC Systems Biology, 2017, 11 (67), pp.1-12. ⟨10.1186/s12918-017-0442-0⟩
Background Large sets of protein-protein interaction data coming either from biological experiments or predictive methods are available and can be combined to construct networks from which information about various cell processes can be extracted. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c103b673f58238a6e9d53fd35a3817
https://hal-upec-upem.archives-ouvertes.fr/hal-01560671/file/Glatigny_et_al-2017-BMC_Systems_Biology.pdf
https://hal-upec-upem.archives-ouvertes.fr/hal-01560671/file/Glatigny_et_al-2017-BMC_Systems_Biology.pdf
Autor:
Marie-Hélène Mucchielli-Giorgi, Renaud Legouis, Zhou Yi, Virginie Redeker, Marion Manil-Ségalen, Laila Sago, Annie Glatigny
Publikováno v:
Journal of Proteome Research
Journal of Proteome Research, American Chemical Society, 2016, 15 (5), pp.1515-1523. ⟨10.1021/acs.jproteome.5b01158⟩
Journal of Proteome Research, 2016, 15 (5), pp.1515-1523. ⟨10.1021/acs.jproteome.5b01158⟩
Journal of Proteome Research, American Chemical Society, 2016, 15 (5), pp.1515-1523. 〈10.1021/acs.jproteome.5b01158〉
Journal of Proteome Research, American Chemical Society, 2016, 15 (5), pp.1515-1523. ⟨10.1021/acs.jproteome.5b01158⟩
Journal of Proteome Research, 2016, 15 (5), pp.1515-1523. ⟨10.1021/acs.jproteome.5b01158⟩
Journal of Proteome Research, American Chemical Society, 2016, 15 (5), pp.1515-1523. 〈10.1021/acs.jproteome.5b01158〉
International audience; Affinity purifications followed by mass spectrometric analysis are used to identify protein-protein interactions. Because quantitative proteomic data are noisy, it is necessary to develop statistical methods to eliminate false
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fee1a827972e742ae781d7b117c721b1
https://hal.archives-ouvertes.fr/hal-01405694
https://hal.archives-ouvertes.fr/hal-01405694
Autor:
Thomas Tang, Annie Glatigny, Hervé Delacroix, Marie-Hélène Mucchielli, Nicolas Francois, Nicolas Agier, Lawrence Aggerbeck
Publikováno v:
Bioinformatics. 23:2686-2691
Motivation: Two-colour microarrays are widely used to perform transcriptome analysis. In most cases, it appears that the ‘red’ and ‘green’ images resulting from the scan of a microarray slide are slightly shifted one with respect to the other
Autor:
Annie Glatigny, Céline Jenzer, Céline Largeau, Christophe Lefebvre, Marion Manil-Ségalen, Renaud Legouis
Publikováno v:
Autophagy. 10(10)
We recently described in C. elegans embryos, the acquisition of specialized functions for orthologs of yeast Atg8 (e.g., mammalian MAP1LC3/LC3) in allophagy, a selective and developmentally regulated autophagic process. During the formation of double
Autor:
Jann P. Primus, Victoria Finnerty, Annie Glatigny, Claudio Scazzocchio, Laila Amrani, Loretta Arcangeli
Publikováno v:
Molecular Microbiology. 38:114-125
The molybdopterin cofactor (MoCF) is required for the activity of a variety of oxidoreductases. The xanthine oxidase class of molybdoenzymes requires the MoCF to have a terminal, cyanolysable sulphur ligand. In the sulphite oxidase/nitrate reductase
Publikováno v:
Molecular Microbiology. 31:1065-1073
Molybdenum-containing enzymes of the hydroxylase class (such as xanthine dehydrogenase, aldehyde oxidase and nicotinate dehydrogenase) require a terminal sulphur atom attached to the molybdenum to hydroxylate their specific substrates. The transulphu
Publikováno v:
Journal of Molecular Biology. 278:431-438
We describe the sequence changes of a number of mutations of the Aspergillus nidulans xanthine dehydrogenase (XDH). We have located the amino acids affected by these changes in the three-dimensional (3D) structure of aldehyde oxido-reductase (MOP) fr