Marion Failler

发表

Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome.

A. Munnich, A. Mégarbané, F. Clerget-Darpoux, 2015, American journal of human genetics.

A distal centriolar protein network controls organelle maturation and asymmetry

B. Dynlacht, Marion Failler, Wenxiang Fu, 2018, Nature Communications.

Mutations of CEP83 cause infantile nephronophthisis and intellectual disability.

H. Kayserili, R. Salomon, C. Antignac, 2014, American journal of human genetics.

Loss‐of‐function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish

S. Saunier, J. Roume, C. Jeanpierre, 2018, Human molecular genetics.

Septins 2, 7 and 9 and MAP4 colocalize along the axoneme in the primary cilium and control ciliary length

U. Wolfrum, P. Cossart, S. Saunier, 2013, Journal of Cell Science.

Whole-genome screen identifies diverse pathways that negatively regulate ciliogenesis

F. Esteva, B. Dynlacht, D. Unutmaz, 2020, Molecular biology of the cell.

Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathies

S. Saunier, C. Bole-Feysot, P. Nitschké, 2018, Human molecular genetics.

Synaptoproteomic Analysis of a Rat Gene-Environment Model of Depression Reveals Involvement of Energy Metabolism and Cellular Remodeling Pathways

M. Popoli, A. Mathé, G. Racagni, 2015, The international journal of neuropsychopharmacology.

A distal centriolar protein network controls organelle maturation and asymmetry

B. Dynlacht, Marion Failler, Wenxiang Fu, 2018, Nature Communications.

The Mouseion at the JAXlibrary The Mouseion at the JAXlibrary

B. Dynlacht, D. Unutmaz, Mikito Owa, 2021 .