Anne-Marie Tassin

Affiliations: 
Sciences de la vie CNRS, Paris, Île-de-France, France 
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"Anne-Marie Tassin"

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Michel Bornens research scientist CNRS

Children

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Thibaut 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
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