Renate K. Hukema

Rotterdam, ZH 3015GD, Netherlands

Last Updated: 09/26/2026

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Found 36 publications

Modelling fragile X-associated neuropsychiatric disorders in young inducible 90CGG premutation mice.

Modelling fragile X-associated neuropsychiatric disorders in young inducible 90CGG premutation mice.

Journal: Brain : a journal of neurology

Published: December 25, 2024

Implementing Advance Care Planning and Care Coordination in the Care for People With Parkinson Disease: A Feasibility Study.

Implementing Advance Care Planning and Care Coordination in the Care for People With Parkinson Disease: A Feasibility Study.

Journal: The Journal of neuroscience nursing : journal of the American Association of Neuroscience Nurses

Published: August 16, 2024

Editorial: Proceedings of the "Fourth International Conference of the FMR1 Premutation: Basic Mechanisms, Clinical Involvement and Therapy".

Editorial: Proceedings of the "Fourth International Conference of the FMR1 Premutation: Basic Mechanisms, Clinical Involvement and Therapy".

Journal: Frontiers in molecular biosciences

Published: February 24, 2021

Small molecule 1a reduces FMRpolyG-mediated toxicity in in vitro and in vivo models for FMR1 premutation.

Small molecule 1a reduces FMRpolyG-mediated toxicity in in vitro and in vivo models for FMR1 premutation.

Journal: Human molecular genetics

Published: September 10, 2020

Lack of a Clear Behavioral Phenotype in an Inducible FXTAS Mouse Model Despite the Presence of Neuronal FMRpolyG-Positive Aggregates.

Lack of a Clear Behavioral Phenotype in an Inducible FXTAS Mouse Model Despite the Presence of Neuronal FMRpolyG-Positive Aggregates.

Journal: Frontiers in molecular biosciences

Published: August 26, 2020

Neuropathology of FMR1-premutation carriers presenting with dementia and neuropsychiatric symptoms.

Neuropathology of FMR1-premutation carriers presenting with dementia and neuropsychiatric symptoms.

Journal: Brain communications

Published: June 26, 2020

Inducible expression of human C9ORF72 36x G4C2 hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice.

Inducible expression of human C9ORF72 36x G4C2 hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice.

Journal: Disease models & mechanisms

Published: March 09, 2020

Short antisense oligonucleotides alleviate the pleiotropic toxicity of RNA harboring expanded CGG repeats.

Short antisense oligonucleotides alleviate the pleiotropic toxicity of RNA harboring expanded CGG repeats.

Journal: Nature communications

Published: December 23, 2019

In silico, in vitro, and in vivo Approaches to Identify Molecular Players in Fragile X Tremor and Ataxia Syndrome.

In silico, in vitro, and in vivo Approaches to Identify Molecular Players in Fragile X Tremor and Ataxia Syndrome.

Journal: Frontiers in molecular biosciences

Published: November 22, 2019

Reduction of Fmr1 mRNA Levels Rescues Pathological Features in Cortical Neurons in a Model of FXTAS.

Reduction of Fmr1 mRNA Levels Rescues Pathological Features in Cortical Neurons in a Model of FXTAS.

Journal: Molecular therapy. Nucleic acids

Published: July 18, 2019

Refining the Spectrum of Neuronal Intranuclear Inclusion Disease: A Case Report.

Refining the Spectrum of Neuronal Intranuclear Inclusion Disease: A Case Report.

Journal: Journal of neuropathology and experimental neurology

Published: June 01, 2019

Astroglial-targeted expression of the fragile X CGG repeat premutation in mice yields RAN translation, motor deficits and possible evidence for cell-to-cell propagation of FXTAS pathology.

Astroglial-targeted expression of the fragile X CGG repeat premutation in mice yields RAN translation, motor deficits and possible evidence for cell-to-cell propagation of FXTAS pathology.

Journal: Acta neuropathologica communications

Published: February 08, 2019

Showing 1-12 of 36

Last Updated: 09/26/2026