Publications by authors named "Dineke Verbeek"

41Publications

Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23.

Brain Pathol 2020 Oct 12:e12905. Epub 2020 Oct 12.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.

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http://dx.doi.org/10.1111/bpa.12905DOI Listing
October 2020

Cross-disease analysis of depression, ataxia and dystonia highlights a role for synaptic plasticity and the cerebellum in the pathophysiology of these comorbid diseases.

Biochim Biophys Acta Mol Basis Dis 2020 Oct 2;1867(1):165976. Epub 2020 Oct 2.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.bbadis.2020.165976DOI Listing
October 2020

CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3.

Ann Neurol 2020 Sep 25. Epub 2020 Sep 25.

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/ana.25919DOI Listing
September 2020

Cortical pencil lining on SWI MRI in NBIA and healthy aging.

BMC Neurol 2019 Oct 14;19(1):233. Epub 2019 Oct 14.

Department of Neurology, University Medical Center Groningen, Hanzeplein 1, 9700 RB, Groningen, The Netherlands.

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http://dx.doi.org/10.1186/s12883-019-1471-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790995PMC
October 2019

Reply: PLD3 and spinocerebellar ataxia.

Brain 2018 11;141(11):e79

Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.

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https://academic.oup.com/brain/article/141/11/e79/5127750
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http://dx.doi.org/10.1093/brain/awy259DOI Listing
November 2018

Why do so many genetic insults lead to Purkinje Cell degeneration and spinocerebellar ataxia?

Neurosci Lett 2019 01 5;688:49-57. Epub 2018 Feb 5.

University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.neulet.2018.02.004DOI Listing
January 2019

Corrigendum to "Spinocerebellar ataxia: miRNAs expose biological pathways underlying pervasive Purkinje cell degeneration" [Neurobiol. Dis. 2017 Dec 108 148-158].

Neurobiol Dis 2018 Aug 2;116:179. Epub 2017 Dec 2.

Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.nbd.2017.11.005DOI Listing
August 2018

Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function.

Cell Rep 2017 Aug;20(9):2100-2115

Department of Biomedical, Metabolic and Neuronal Sciences, University of Modena and Reggio Emilia, and Center for Neuroscience and Neurotechnology, 41125 Modena, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2017.08.018DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583511PMC
August 2017

Spinocerebellar ataxia: miRNAs expose biological pathways underlying pervasive Purkinje cell degeneration.

Neurobiol Dis 2017 Dec 18;108:148-158. Epub 2017 Aug 18.

Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.nbd.2017.08.003DOI Listing
December 2017

Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.

Neurosci Biobehav Rev 2017 Apr 28;75:22-39. Epub 2017 Jan 28.

University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.neubiorev.2017.01.033DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921080PMC
April 2017

Unmet Needs in Dystonia: Genetics and Molecular Biology-How Many Dystonias?

Front Neurol 2016 16;7:241. Epub 2017 Jan 16.

Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, and German Center for Neurodegenerative Diseases (DZNE) , Tübingen , Germany.

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http://journal.frontiersin.org/article/10.3389/fneur.2016.00
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http://dx.doi.org/10.3389/fneur.2016.00241DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237827PMC
January 2017

Altered secondary structure of Dynorphin A associates with loss of opioid signalling and NMDA-mediated excitotoxicity in SCA23.

Hum Mol Genet 2016 07 3;25(13):2728-2737. Epub 2016 Jun 3.

Department of Genetics, University of Groningen, University Medical Centre GroningenGroningen, the Netherlands

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http://dx.doi.org/10.1093/hmg/ddw130DOI Listing
July 2016

Reply: SCA23 and prodynorphin: is it time for gene retraction?

Brain 2016 08 1;139(Pt 8):e43. Epub 2016 May 1.

Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands

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http://dx.doi.org/10.1093/brain/aww094DOI Listing
August 2016

Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner.

Cell Mol Life Sci 2015 Sep 9;72(17):3387-99. Epub 2015 Apr 9.

Department of Genetics, University of Groningen, University Medical Center Groningen, PO Box 30 001, 9700 RB, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s00018-015-1894-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531139PMC
September 2015

Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystonia.

J Neurol 2015 May 1;262(5):1340-3. Epub 2015 Apr 1.

Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s00415-015-7718-3DOI Listing
May 2015

First patho-anatomical investigation of the brain of a SCA19 patient.

Neuropathol Appl Neurobiol 2014 Aug;40(5):640-4

Dr. Senckenbergisches Chronomedizinisches Institut, J.W. Goethe University, Frankfurt/Main, Germany.

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http://dx.doi.org/10.1111/nan.12128DOI Listing
August 2014

SCA14 mutation V138E leads to partly unfolded PKCγ associated with an exposed C-terminus, altered kinetics, phosphorylation and enhanced insolubilization.

J Neurochem 2014 Mar 13;128(5):741-51. Epub 2013 Nov 13.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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http://doi.wiley.com/10.1111/jnc.12491
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http://dx.doi.org/10.1111/jnc.12491DOI Listing
March 2014

The L450F [Corrected] mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together.

Neurogenetics 2013 Nov 21;14(3-4):257-8. Epub 2013 Aug 21.

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s10048-013-0370-0DOI Listing
November 2013

Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases.

J Neurol 2013 Jul 8;260(7):1807-12. Epub 2013 Mar 8.

Department of Genetics, University of Groningen, University Medical Center Groningen, Oostersingel Entrance 47, P.O. Box 30 001, 9700 RB Groningen, The Netherlands.

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http://link.springer.com/10.1007/s00415-013-6882-6
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http://dx.doi.org/10.1007/s00415-013-6882-6DOI Listing
July 2013

Non-opioid nociceptive activity of human dynorphin mutants that cause neurodegenerative disorder spinocerebellar ataxia type 23.

Peptides 2012 Jun 17;35(2):306-10. Epub 2012 Apr 17.

Department of Pharmaceutical Biosciences, Division of Biological Research on Drug Dependence, Uppsala University, Uppsala, Sweden.

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http://dx.doi.org/10.1016/j.peptides.2012.04.006DOI Listing
June 2012

Genetics of the dominant ataxias.

Semin Neurol 2011 Nov 21;31(5):461-9. Epub 2012 Jan 21.

Department of Medical Genetics, University Medical Centre Groningen, Groningen.

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http://dx.doi.org/10.1055/s-0031-1299785DOI Listing
November 2011

Perturbations of model membranes induced by pathogenic dynorphin A mutants causing neurodegeneration in human brain.

Biochem Biophys Res Commun 2011 Jul 25;411(1):111-4. Epub 2011 Jun 25.

Department of Biochemistry and Biophysics, Arrhenius Laboratories for Natural Sciences, Stockholm University, 10691 Stockholm, Sweden.

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http://dx.doi.org/10.1016/j.bbrc.2011.06.105DOI Listing
July 2011

Spinocerebellar ataxia type 23: a genetic update.

Authors:
Dineke S Verbeek

Cerebellum 2009 Jun 17;8(2):104-7. Epub 2008 Dec 17.

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s12311-008-0085-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694919PMC
June 2009

PKC gamma mutations in spinocerebellar ataxia type 14 affect C1 domain accessibility and kinase activity leading to aberrant MAPK signaling.

J Cell Sci 2008 Jul 24;121(Pt 14):2339-49. Epub 2008 Jun 24.

Department of Cell Biology and Histology, Academic Medical Center, University of Amsterdam, AZ Amsterdam, The Netherlands.

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http://dx.doi.org/10.1242/jcs.027698DOI Listing
July 2008

Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.

Hum Genet 2005 Jun 20;117(1):88-91. Epub 2005 Apr 20.

Department of Biomedical Genetics, University Medical Center Utrecht, Stratenum, The Netherlands.

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http://link.springer.com/10.1007/s00439-005-1278-z
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http://dx.doi.org/10.1007/s00439-005-1278-zDOI Listing
June 2005

Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations.

Eur J Hum Genet 2004 Jun;12(6):441-6

Department of Medical Genetics, University Medical Center, Stratenum, Universiteitsweg 100, 3584 CG Utrecht, The Netherlands.

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http://dx.doi.org/10.1038/sj.ejhg.5201167DOI Listing
June 2004

Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.

Hum Genet 2002 Oct 30;111(4-5):388-93. Epub 2002 Aug 30.

Department of Medical Genetics, University Medical Center Utrecht, Lundlaan 6, 3584 EA Utrecht, The Netherlands.

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http://dx.doi.org/10.1007/s00439-002-0782-7DOI Listing
October 2002