Delphine Bouhy
Antwerpen, VLG 2610, Belgium
Last Updated: 09/26/2026
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Found 8 publications
A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8.
Journal: Acta neuropathologica
Published: May 19, 2017
Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 Locus.
Journal: Journal of neuromuscular diseases
Published: November 18, 2016
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease.
Journal: Acta neuropathologica communications
Published: November 04, 2016
The hnRNP family: insights into their role in health and disease.
Journal: Human genetics
Published: March 23, 2016
Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
Journal: Annals of neurology
Published: May 03, 2013
Animal models of Charcot-Marie-Tooth disease and their relevance for understanding the disease in humans
Journal: Revue neurologique
Published: February 20, 2013
Charcot-Marie-Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments.
Journal: Acta neuropathologica
Published: January 07, 2013
Neurofilament phosphorylation and their proline-directed kinases in health and disease.
Journal: Journal of the peripheral nervous system : JPNS
Published: January 03, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026