Christine Fagotto‐Kaufmann

发表

Early fibrillin-1 assembly monitored through a modifiable recombinant cell approach.

D. Reinhardt, L. Sakai, É. Bergeron, 2014, Biomacromolecules.

Complex contributions of fibronectin to initiation and maturation of microfibrils.

D. Mosher, D. Reinhardt, J. Djokić, 2013, The Biochemical journal.

The UBL domain of PLIC‐1 regulates aggresome formation

F. Bedford, Émilie Dumontier, Christine Fagotto‐Kaufmann, 2006, EMBO reports.

Pathogenic TRIO variants associated with neurodevelopmental disorders perturb the molecular regulation of TRIO and axon pathfinding in vivo

D. Baralle, A. Debant, S. Schmidt, 2023, Molecular Psychiatry.

Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders

J. Hehir-Kwa, B. D. de Vries, D. Baralle, 2020, American journal of human genetics.

Mutations specific to the Rac-GEF domain of TRIO cause intellectual disability and microcephaly

D. Baralle, C. Mercer, S. Mehta, 2016, Journal of Medical Genetics.

The +TIP Navigator-1 is an actin–microtubule crosslinker that regulates axonal growth cone motility

N. Galjart, A. Debant, J. Boudeau, 2020, The Journal of cell biology.

Classical and Neonatal Marfan Syndrome Mutations in Fibrillin-1 Cause Differential Protease Susceptibilities and Protein Function*

G. Iyengar, D. Reinhardt, D. Brömme, 2011, The Journal of Biological Chemistry.

Fibrillin assembly requires fibronectin.

M. McKee, D. Mosher, D. Reinhardt, 2008, Molecular biology of the cell.

Fibulin-3, -4, and -5 Are Highly Susceptible to Proteolysis, Interact with Cells and Heparin, and Form Multimers*

V. Nelea, D. Reinhardt, J. Djokić, 2013, The Journal of Biological Chemistry.

Fibrillin assembly requires fibronectin.

M. McKee, D. Mosher, D. Reinhardt, 2008, Molecular biology of the cell.

Mutations specific to the Rac-GEF domain of TRIO cause intellectual disability and microcephaly

S. Mehta, A. Debant, E. Seaby, 2016, Journal of Medical Genetics.