Anne-Marie Tassin
Affiliations: | Sciences de la vie | CNRS, Paris, Île-de-France, France |
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"Anne-Marie Tassin"Children
Sign in to add traineeThibaut Eguether | grad student | CNRS | |
Paul Guichard | grad student | 2007-2010 | CURIE INSTITUT |
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Publications
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Bodin A, Greibill L, Gouju J, et al. (2023) Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells. Brain : a Journal of Neurology |
Le Borgne P, Greibill L, Laporte MH, et al. (2022) The evolutionary conserved proteins CEP90, FOPNL, and OFD1 recruit centriolar distal appendage proteins to initiate their assembly. Plos Biology. 20: e3001782 |
Bouhouche K, Le Borgne P, Lemullois M, et al. (2021) [Paramecium, a model organism to study ciliogenesis and ciliopathies]. Medecine Sciences : M/S. 37: 632-638 |
Klena N, Le Guennec M, Tassin AM, et al. (2020) Architecture of the centriole cartwheel-containing region revealed by cryo-electron tomography. The Embo Journal. e106246 |
Steib E, Laporte MH, Gambarotto D, et al. (2020) WDR90 is a centriolar microtubule wall protein important for centriole architecture integrity. Elife. 9 |
Gogendeau D, Lemullois M, Le Borgne P, et al. (2020) MKS-NPHP module proteins control ciliary shedding at the transition zone. Plos Biology. 18: e3000640 |
Le Guennec M, Klena N, Gambarotto D, et al. (2020) A helical inner scaffold provides a structural basis for centriole cohesion. Science Advances. 6: eaaz4137 |
Thomas L, Bouhouche K, Whitfield M, et al. (2020) TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella. American Journal of Human Genetics |
Fassad MR, Shoemark A, Legendre M, et al. (2018) Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus. American Journal of Human Genetics |
Fassad MR, Shoemark A, le Borgne P, et al. (2018) C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia. American Journal of Human Genetics. 102: 956-972 |