Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Marie Seveno"'
Autor:
Aditya S. Paul, Alexandra Miliu, Joao A. Paulo, Jonathan M. Goldberg, Arianna M. Bonilla, Laurence Berry, Marie Seveno, Catherine Braun-Breton, Aziz L. Kosber, Brendan Elsworth, Jose S. N. Arriola, Maryse Lebrun, Steven P. Gygi, Mauld H. Lamarque, Manoj T. Duraisingh
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-13 (2020)
Plasmodium protein phosphatase PP1 is essential for the asexual proliferation of malaria parasites. Here the authors show that PP1 regulates egress of parasites from host red blood cells, integrating parasite intrinsic pathways with environmental sig
Externí odkaz:
https://doaj.org/article/7d2715bdc7484f8c88c035dcb70a2f3f
Autor:
Nora Scarcelli, Adeline Barnaud, Wolf Eiserhardt, Urs A Treier, Marie Seveno, Amélie d'Anfray, Yves Vigouroux, Jean-Christophe Pintaud
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19954 (2011)
Chloroplast DNA sequences are of great interest for population genetics and phylogenetic studies. However, only a small set of markers are commonly used. Most of them have been designed for amplification in a large range of Angiosperms and are locate
Externí odkaz:
https://doaj.org/article/3133165a77c1437f941362a3db1f0dce
Autor:
Laurence Berry, Alexandra Miliu, Joao A. Paulo, Steven P. Gygi, Catherine Braun-Breton, Marie Seveno, Jonathan M. Goldberg, Maryse Lebrun, Brendan Elsworth, Manoj T. Duraisingh, Jose S. N. Arriola, Aziz L. Kosber, Arianna M. Bonilla, Aditya S. Paul, Mauld H. Lamarque
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-13 (2020)
Nature Communications, Vol 11, Iss 1, Pp 1-13 (2020)
Asexual proliferation of the Plasmodium parasites that cause malaria follows a developmental program that alternates non-canonical intraerythrocytic replication with dissemination to new host cells. We carried out a functional analysis of the Plasmod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c790f7ab0759696e4be1e3e94e979a4e
https://doi.org/10.1101/2020.01.05.890483
https://doi.org/10.1101/2020.01.05.890483
Autor:
Marie-Odile, Baudement, Axel, Cournac, Franck, Court, Marie, Seveno, Hugues, Parrinello, Christelle, Reynes, Robert, Sabatier, Tristan, Bouschet, Zhou, Yi, Sephora, Sallis, Mathilde, Tancelin, Cosette, Rebouissou, Guy, Cathala, Annick, Lesne, Julien, Mozziconacci, Laurent, Journot, Thierry, Forné
Publikováno v:
Genome research. 28(11)
The mammalian cell nucleus contains numerous discrete suborganelles named nuclear bodies. While recruitment of specific genomic regions into these large ribonucleoprotein (RNP) complexes critically contributes to higher-order functional chromatin org
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::282a386633c0fdf3bc46f547952562b6
https://pubmed.ncbi.nlm.nih.gov/30287550
https://pubmed.ncbi.nlm.nih.gov/30287550
Autor:
Marie Seveno, Mélanie Cavalier, Cécile Delettre, Marie O. Pequignot, Volker Baecker, Emmanuelle Sarzi, Christian P. Hamel, Jolanta Malgorzata Jagodzinska
Publikováno v:
Journal of Visualized Experiments.
Structural changes in the retina are common manifestations of ophthalmic diseases. Optical coherence tomography (OCT) enables their identification in vivo-rapidly, repetitively, and at a high resolution. This protocol describes OCT imaging in the mou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe8f962eac628606b040275a21b823b
https://doi.org/10.3791/55865
https://doi.org/10.3791/55865
Autor:
Sulev Kõks, Marie Seveno, Jolanta Malgorzata Jagodzinska, Cécile Delettre, Christian P. Hamel, D. Bonner-Wersinger
Publikováno v:
Acta Ophthalmologica. 95
Summary The Wolfram Syndrome (WS) is an early onset genetic disease (1/200 000) featuring diabetes mellitus and progressive optic neuropathy ensuing mutations in the WFS1 gene. To date, there is no treatment to stop the progression of the disease. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf6a1a2aee7b1dd3822d630b1ced36c3
https://doi.org/10.1111/j.1755-3768.2017.03174
https://doi.org/10.1111/j.1755-3768.2017.03174
Autor:
Jing Wang, Valérie Rigau, Guy Bielicki, Chantal Cazevieille, Marie Seveno, Jean-Luc Puel, Pascal Reynier, Naïg Gueguen, Christian P. Hamel, Anne-Laure Mausset-Bonnefont, Jean-Pierre Renou, Philippe Brabet, Benjamin Chaix, Cécile Delettre, Guy Lenaers, Nathalie Boddaert, Claire Angebault, Emmanuelle Sarzi
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2012, 135, pp.3599-3613. ⟨10.1093/brain/aws303⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2012, 135, pp.3599-3613. ⟨10.1093/brain/aws303⟩
International audience; Dominant optic atrophy is a rare inherited optic nerve degeneration caused by mutations in the mitochondrial fusion gene OPA1. Recently, the clinical spectrum of dominant optic atrophy has been extended to frequent syndromic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4827c6f21162fdcb704b576ac7fced4
https://doi.org/10.1093/brain/aws303
https://doi.org/10.1093/brain/aws303
Autor:
Cécile Delettre, Marie Seveno, Cecilia Rönnbäck, Dan Milea, Agnès Muller, Pascal Reynier, Joanna Grenier, Christian P. Hamel, Mathias Adrian, Mélanie Quiles, Angélique Caignard, Claire Angebault, Annie Lacroux, Emmanuelle Sarzi, Guy Lenaers, Christian Lavergne, Michael Larsen
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (12), pp.2539-2551. ⟨10.1093/hmg/ddw117⟩
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (12), pp.2539-2551. ⟨10.1093/hmg/ddw117⟩
International audience; OPA1 mutations are responsible for autosomal dominant optic atrophy (ADOA), a progressive blinding disease characterized by retinal ganglion cell (RGC) degeneration and large phenotypic variations, the underlying mechanisms of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71a344f72999fadd694667688291a2b8
https://hal.archives-ouvertes.fr/hal-01867305
https://hal.archives-ouvertes.fr/hal-01867305
Autor:
Jean-Christophe Pintaud, Wolf L. Eiserhardt, Yves Vigouroux, Marie Seveno, Nora Scarcelli, Urs A. Treier, Adeline Barnaud, Amélie d'Anfray
Publikováno v:
Scarcelli, N, Bernaud, A, Eiserhardt, W L, Treier, U, Seveno, M, d'Anfray, A, Vigouroux, Y & Pintaud, J-C 2011, ' A set of 100 chloroplast DNA primer pairs to study population genetics and phylogeny in monocotylenons ', P L o S One, vol. 6, no. 5 . https://doi.org/10.1371/journal.pone.0019954
PLoS ONE
PLoS ONE, Vol 6, Iss 5, p e19954 (2011)
PLoS ONE
PLoS ONE, Vol 6, Iss 5, p e19954 (2011)
Chloroplast DNA sequences are of great interest for population genetics and phylogenetic studies. However, only a small set of markers are commonly used. Most of them have been designed for amplification in a large range of Angiosperms and are locate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b6f0ce11200a545a0399b24052c13c5
http://www.documentation.ird.fr/hor/fdi:010053574
http://www.documentation.ird.fr/hor/fdi:010053574
Autor:
Deborah Garcia, Denis Sereno, Ali Ouaissi, Bruno Oury, Elodie Gazanion, Khatima Ait-Oudhia, Baptiste Vergnes, Marie Seveno
Publikováno v:
Parasitology international. 60(1)
To improve the management of leishmaniasis, new drugs and/or alternative therapeutic strategies are required. Combination therapy of antileishmanial drugs is currently considered as one of the most rational approaches to lower treatment failure rate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5f3d8326eb0e30caaa70f8a2a5f4bf1
https://pubmed.ncbi.nlm.nih.gov/20884376
https://pubmed.ncbi.nlm.nih.gov/20884376