Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Valentina Grampa"'
Autor:
Valentina Grampa, Marion Delous, Mohamad Zaidan, Gweltas Odye, Sophie Thomas, Nadia Elkhartoufi, Emilie Filhol, Olivier Niel, Flora Silbermann, Corinne Lebreton, Sophie Collardeau-Frachon, Isabelle Rouvet, Jean-Luc Alessandri, Louise Devisme, Anne Dieux-Coeslier, Marie-Pierre Cordier, Yline Capri, Suonavy Khung-Savatovsky, Sabine Sigaudy, Rémi Salomon, Corinne Antignac, Marie-Claire Gubler, Alexandre Benmerah, Fabiola Terzi, Tania Attié-Bitach, Cécile Jeanpierre, Sophie Saunier
Publikováno v:
PLoS Genetics, Vol 12, Iss 3, p e1005894 (2016)
Ciliopathies are a group of genetic multi-systemic disorders related to dysfunction of the primary cilium, a sensory organelle present at the cell surface that regulates key signaling pathways during development and tissue homeostasis. In order to id
Externí odkaz:
https://doaj.org/article/80b9228e4b7a4d9cafbccaa2a58ded5c
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
Scientific Reports
Scientific Reports
Efforts to improve existing anti-HIV-1 therapies or develop preventatives have identified CCR5 as an important target and CCL5 as an ideal scaffold to sculpt potent HIV-1 entry inhibitors. We created novel human CCL5 variants that exhibit exceptional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eb300f7e4291aac2e548c58fda5ab4c
https://doi.org/10.1038/s41598-018-20300-9
https://doi.org/10.1038/s41598-018-20300-9
Autor:
Olivier Niel, Suonavy Khung-Savatovsky, Tania Attié-Bitach, Sabine Sigaudy, Emilie Filhol, Sophie Saunier, Yline Capri, Corinne Antignac, Sophie Collardeau-Frachon, Gweltas Odye, Mohamad Zaidan, Marion Delous, Sophie Thomas, Corinne Lebreton, Isabelle Rouvet, Valentina Grampa, Flora Silbermann, Rémi Salomon, Nadia Elkhartoufi, Alexandre Benmerah, Jean-Luc Alessandri, Marie-Pierre Cordier, Marie-Claire Gubler, Fabiola Terzi, Louise Devisme, Anne Dieux-Coeslier, Cécile Jeanpierre
Publikováno v:
PLoS Genetics, Vol 12, Iss 3, p e1005894 (2016)
PLoS Genetics
PLoS Genetics, 2016, 12 (3), pp.e1005894. ⟨10.1371/journal.pgen.1005894⟩
PLoS Genetics
PLoS Genetics, 2016, 12 (3), pp.e1005894. ⟨10.1371/journal.pgen.1005894⟩
Ciliopathies are a group of genetic multi-systemic disorders related to dysfunction of the primary cilium, a sensory organelle present at the cell surface that regulates key signaling pathways during development and tissue homeostasis. In order to id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e8f897b2f8a3956a98c7056a85084e7
http://europepmc.org/articles/PMC4788435?pdf=render
http://europepmc.org/articles/PMC4788435?pdf=render
Autor:
Isabelle Anselme, Mireille Montcouquiol, Sophie Saunier, Alexia Mahuzier, Christine Vesque, Sylvie Schneider-Maunoury, Helori-Mael Gaudé, Jerome Ezan, Flora Silbermann, Valentina Grampa, Delphine Delacour, Margot Leroux-Berger
Publikováno v:
Journal of Cell Biology
Journal of Cell Biology, Rockefeller University Press, 2012, 198 (5), pp.927-40. ⟨10.1083/jcb.201111009⟩
The Journal of Cell Biology
Journal of Cell Biology, 2012, 198 (5), pp.927-40. ⟨10.1083/jcb.201111009⟩
Journal of Cell Biology, Rockefeller University Press, 2012, 198 (5), pp.927-40. ⟨10.1083/jcb.201111009⟩
The Journal of Cell Biology
Journal of Cell Biology, 2012, 198 (5), pp.927-40. ⟨10.1083/jcb.201111009⟩
Rpgrip1l is required for planar localization of the basal body and acts within a ciliopathy protein complex by stabilizing dishevelled.
Cilia are at the core of planar polarity cellular events in many systems. However, the molecular mechanisms b
Cilia are at the core of planar polarity cellular events in many systems. However, the molecular mechanisms b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa9e8fd3aa118adef3c114b92d2d28cb
https://hal.archives-ouvertes.fr/hal-00762184
https://hal.archives-ouvertes.fr/hal-00762184
Autor:
Marion Delous, Cécile Burcklé, Helori-Mael Gaudé, Valentina Grampa, Christine Vesque, Fabiola Terzi, Sophie Saunier, E Montenont, Cécile Jeanpierre, Sylvie Schneider-Maunoury, Flora Silbermann, Corinne Antignac, Rodrick Montjean
Publikováno v:
CIÊNCIAVITAE
Cilia
Proceedings of the First International Cilia in Development and Disease Scientific Conference (2012)
First International Cilia in Development and Disease Scientific Conference
First International Cilia in Development and Disease Scientific Conference, pp.P100
Europe PubMed Central
First International Cilia in Development and Disease Scientific Conference, 1 (Suppl 1), pp.P100, 2012
Cilia
Proceedings of the First International Cilia in Development and Disease Scientific Conference (2012)
First International Cilia in Development and Disease Scientific Conference
First International Cilia in Development and Disease Scientific Conference, pp.P100
Europe PubMed Central
First International Cilia in Development and Disease Scientific Conference, 1 (Suppl 1), pp.P100, 2012
Nephronophthisis, a hereditary nephropathy characterized by interstitial fibrosis and cyst formation, is caused by mutations in NPHP genes encoding the ciliary proteins called nephrocystins. We investigate the function of nephrocystin-1, -4 and -8, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58154e130ba007ec7d91715efdb0d771
http://europepmc.org/abstract/PMC/PMC3555745
http://europepmc.org/abstract/PMC/PMC3555745