Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Guy Keryer"'
Publikováno v:
Biology of the Cell. 97:425-434
Background information. Centrosome movements at the onset of mitosis result from a balance between the pulling and pushing forces mediated by microtubules. The structural stability of the centrosome core structure, the centriole pair, is correlated w
Autor:
Karl-Ferdinand Lechtreck, Mette M. Mogensen, Guy Keryer, Annie Delouvée, Barbara Di Fiore, Anne-Marie Tassin, Claude Celati, Patrizia Lavia, Michel Bornens
Publikováno v:
Molecular Biology of the Cell. 14:4260-4271
The small Ran GTPase, a key regulator of nucleocytoplasmic transport, is also involved in microtubule assembly and nuclear membrane formation. Herein, we show by immunofluorescence, immunoelectron microscopy, and biochemical analysis that a fraction
Autor:
Philippe Collas, Friedrich W. Herberg, Cathrine R. Carlson, Lutz Vossebein, Kjetil Taskén, Bjørn Steen Skålhegg, Jean-Claude Labbé, Guy Keryer, Oliwia Witczak
Publikováno v:
Journal of Cell Science. 114:3243-3254
Protein kinase A regulatory subunit RIIalpha is tightly bound to centrosomal structures during interphase through interaction with the A-kinase anchoring protein AKAP450, but dissociates and redistributes from centrosomes at mitosis. The cyclin B-p34
Publikováno v:
Placenta. 19:295-314
Summary Human trophoblast cells offer a unique in vitro model to study aspects of the dynamic processes occuring during cell fusion and syncytium formation. In the human placenta, mononuclear cytotrophoblasts aggregate and fuse to form a multinucleat
Autor:
Michèle Rossignol, Nicole Stelly, André Adoutte, Janine Beisson, Jean Cohen, Stephen F. Ng, Nicole Garreau de Loubresse, Guy Keryer
Publikováno v:
European journal of protistology. 25(3)
Summary In ciliates, the major morphogenetic events take place in the cortex, a complex of membranes and closely associated filamentous networks. To analyze the problems of assembly and morphogenesis at the molecular level in Paramecium , we have dev
Autor:
Nathalie Spassky, Karen M. Smith, Robert J. Ferrante, Ioannis Dragatsis, Frédéric Saudou, Jose R. Pineda, Jinho Kim, Paula Dietrich, Guy Keryer, Géraldine Liot, Caroline Benstaali, Fabrice P. Cordelières
Huntington disease (HD) is a devastating autosomal-dominant neurodegenerative disorder. It is caused by expansion of a CAG repeat in the first exon of the huntingtin (HTT) gene that encodes a mutant HTT protein with a polyglutamine (polyQ) expansion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5aa360f6c849aabfc3e62aa9f536a62
https://europepmc.org/articles/PMC3223861/
https://europepmc.org/articles/PMC3223861/
Autor:
Sandrine Humbert, Béé Edicte C. Charrin, Yohanns Bellaïche, Juliette D. Godin, Maria Molina-Calavita, Laurent Nguyen, Guy Keryer, Kelly Colombo, Diana Zala, Marie Laure Volvert, François Guillemot, Paula Dietrich, Ioannis Dragatsis, Frédéric Saudou
Publikováno v:
Neuron
Neuron, Elsevier, 2010, 67 (3), pp.392-406. ⟨10.1016/j.neuron.2010.06.027⟩
Neuron, Elsevier, 2010, 67 (3), pp.392-406. ⟨10.1016/j.neuron.2010.06.027⟩
SummaryHuntingtin is the protein mutated in Huntington's disease, a devastating neurodegenerative disorder. We demonstrate here that huntingtin is essential to control mitosis. Huntingtin is localized at spindle poles during mitosis. RNAi-mediated si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81551f9cbb819874411cf2f658c1f3e3
https://hal.archives-ouvertes.fr/hal-03373901
https://hal.archives-ouvertes.fr/hal-03373901
Autor:
Raul Pardo, Frédéric Saudou, Ghislaine Poizat, Sandrine Humbert, Maria Molina-Calavita, Guy Keryer
Publikováno v:
Molecular Brain
Molecular Brain, 2010, 3 (1), pp.17. ⟨10.1186/1756-6606-3-17⟩
Molecular Brain, BioMed Central, 2010, 3 (1), pp.17. ⟨10.1186/1756-6606-3-17⟩
Molecular Brain, Vol 3, Iss 1, p 17 (2010)
Molecular Brain, 2010, 3 (1), pp.17. ⟨10.1186/1756-6606-3-17⟩
Molecular Brain, BioMed Central, 2010, 3 (1), pp.17. ⟨10.1186/1756-6606-3-17⟩
Molecular Brain, Vol 3, Iss 1, p 17 (2010)
Background Huntingtin (htt) is a multi-domain protein of 350 kDa that is mutated in Huntington's disease (HD) but whose function is yet to be fully understood. This absence of information is due in part to the difficulty of manipulating large DNA fra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::565bdc8d62cf18938f1210b2d829bea7
https://hal.science/hal-03297486
https://hal.science/hal-03297486
Publikováno v:
The EMBO Journal. 11:1723-1731
Immunocytochemical evidence of an association between the regulatory subunit RII of the cAMP-dependent protein kinase (cAMP-PK) and the Golgi apparatus in several cell types has been reported. In order to identify endogenous Golgi proteins binding RI
Publikováno v:
Developmental Biology. 148:205-218
In Paramecium, the morphogenesis of the cortex at cell division, which assures reconstruction of shape and surface pattern, has been shown to involve transcellular signals which spread across the cortex like a wave, originating principally from the o