Maria-victoria Hinckelmann
Grenoble, France
Last Updated: 09/26/2026
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Found 11 publications
The Arp1/11 minifilament of dynactin primes the endosomal Arp2/3 complex.
Journal: Science advances
Published: June 30, 2020
Increasing brain palmitoylation rescues behavior and neuropathology in Huntington disease mice.
Journal: Science advances
Published: January 28, 2020
De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder.
Journal: American journal of human genetics
Published: December 30, 2019
Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogeny.
Journal: Human molecular genetics
Published: August 12, 2019
TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis.
Journal: Nature communications
Published: May 15, 2018
Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development.
Journal: Human molecular genetics
Published: July 31, 2017
Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development.
Journal: American journal of human genetics
Published: April 05, 2017
Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport.
Journal: Nature communications
Published: April 21, 2016
Releasing the brake: restoring fast axonal transport in neurodegenerative disorders.
Journal: Trends in cell biology
Published: July 10, 2013
Huntingtin's function in axonal transport is conserved in Drosophila melanogaster.
Journal: PloS one
Published: January 29, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026