Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Anais Bouissou"'
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-19 (2018)
The actomyosin cytoskeleton plays an important role in polarised cell migration. Here the authors identify lymphocyte-specific protein (LSP)-1 as a regulator of actomyosin contractility in macrophages, by competing with supervillin for myosin IIA act
Externí odkaz:
https://doaj.org/article/f3f5c58257864c0498c0aecf08fa9c52
Autor:
Nicolas Lecland, Alain Debec, Audrey Delmas, Sara Moutinho-Pereira, Nicolas Malmanche, Anais Bouissou, Clémence Dupré, Aimie Jourdan, Brigitte Raynaud-Messina, Helder Maiato, Antoine Guichet
Publikováno v:
Biology Open, Vol 2, Iss 3, Pp 314-323 (2013)
Summary In animal cells the centrosome is commonly viewed as the main cellular structure driving microtubule (MT) assembly into the mitotic spindle apparatus. However, additional pathways, such as those mediated by chromatin and augmin, are involved
Externí odkaz:
https://doaj.org/article/3056278dc2014bdeb3b17f5d11a92c70
Autor:
Marion Jasnin, Jordan Hervy, Stéphanie Balor, Anaïs Bouissou, Amsha Proag, Raphaël Voituriez, Jonathan Schneider, Thomas Mangeat, Isabelle Maridonneau-Parini, Wolfgang Baumeister, Serge Dmitrieff, Renaud Poincloux
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
Actin filaments generate force in diverse contexts, although how they can produce nanonewtons of force is unclear. Here, the authors apply cryo-electron tomography, quantitative analysis, and modelling to reveal the podosome core is a dense, spring-l
Externí odkaz:
https://doaj.org/article/6a755f77948444fda10cc78808a00945
Autor:
Thomas Mangeat, Simon Labouesse, Marc Allain, Awoke Negash, Emmanuel Martin, Aude Guénolé, Renaud Poincloux, Claire Estibal, Anaïs Bouissou, Sylvain Cantaloube, Elodie Vega, Tong Li, Christian Rouvière, Sophie Allart, Debora Keller, Valentin Debarnot, Xia Bo Wang, Grégoire Michaux, Mathieu Pinot, Roland Le Borgne, Sylvie Tournier, Magali Suzanne, Jérome Idier, Anne Sentenac
Publikováno v:
Cell Reports: Methods, Vol 1, Iss 1, Pp 100009- (2021)
Summary: Current super-resolution microscopy (SRM) methods suffer from an intrinsic complexity that might curtail their routine use in cell biology. We describe here random illumination microscopy (RIM) for live-cell imaging at super-resolutions matc
Externí odkaz:
https://doaj.org/article/b7ddc3df410e4b26b598a7b09dc81564