Verbeek D - Search Results

1

ULK overexpression mitigates motor deficits and neuropathology in mouse models of Machado-Joseph disease.

Vasconcelos-Ferreira A, Martins IM, Lobo D, Pereira D, Lopes MM, Faro R, Lopes SM, Verbeek D, Schmidt T, Nóbrega C, Pereira de Almeida L. Vasconcelos-Ferreira A, et al. Among authors: verbeek d. Mol Ther. 2022 Jan 5;30(1):370-387. doi: 10.1016/j.ymthe.2021.07.012. Epub 2021 Jul 21. Mol Ther. 2022. PMID: 34298131 Free PMC article.

2

Conformation effects of CpG methylation on single-stranded DNA oligonucleotides: analysis of the opioid peptide dynorphin-coding sequences.

Taqi MM, Wärmländer SK, Yamskova O, Madani F, Bazov I, Luo J, Zubarev R, Verbeek D, Gräslund A, Bakalkin G. Taqi MM, et al. Among authors: verbeek d. PLoS One. 2012;7(6):e39605. doi: 10.1371/journal.pone.0039605. Epub 2012 Jun 29. PLoS One. 2012. PMID: 22768096 Free PMC article.

3

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

Leotti VB, de Vries JJ, Oliveira CM, de Mattos EP, Te Meerman GJ, Brunt ER, Kampinga HH, Jardim LB, Verbeek DS. Leotti VB, et al. Ann Neurol. 2021 Jan;89(1):66-73. doi: 10.1002/ana.25919. Epub 2020 Oct 7. Ann Neurol. 2021. PMID: 32978817

4

Genetics of the dominant ataxias.

Verbeek DS, van de Warrenburg BP. Verbeek DS, et al. Semin Neurol. 2011 Nov;31(5):461-9. doi: 10.1055/s-0031-1299785. Epub 2012 Jan 21. Semin Neurol. 2011. PMID: 22266884 Review.

5

WDR45, one gene associated with multiple neurodevelopmental disorders.

Cong Y, So V, Tijssen MAJ, Verbeek DS, Reggiori F, Mauthe M. Cong Y, et al. Autophagy. 2021 Dec;17(12):3908-3923. doi: 10.1080/15548627.2021.1899669. Epub 2021 Apr 12. Autophagy. 2021. PMID: 33843443 Free PMC article. Review.

6

Identification and Copy Number Variant Analysis of Enhancer Regions of Genes Causing Spinocerebellar Ataxia.

Ghorbani F, de Boer EN, Fokkens MR, de Boer-Bergsma J, Verschuuren-Bemelmans CC, Wierenga E, Kasaei H, Noordermeer D, Verbeek DS, Westers H, van Diemen CC. Ghorbani F, et al. Among authors: verbeek ds. Int J Mol Sci. 2024 Oct 18;25(20):11205. doi: 10.3390/ijms252011205. Int J Mol Sci. 2024. PMID: 39456985 Free PMC article.

7

Reply: PLD3 and spinocerebellar ataxia.

Ma KY, Verbeek DS. Ma KY, et al. Brain. 2018 Nov 1;141(11):e79. doi: 10.1093/brain/awy259. Brain. 2018. PMID: 30312384 No abstract available.

8

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

Duarri A, Lin MC, Fokkens MR, Meijer M, Smeets CJ, Nibbeling EA, Boddeke E, Sinke RJ, Kampinga HH, Papazian DM, Verbeek DS. Duarri A, et al. Cell Mol Life Sci. 2015 Sep;72(17):3387-99. doi: 10.1007/s00018-015-1894-2. Epub 2015 Apr 9. Cell Mol Life Sci. 2015. PMID: 25854634 Free PMC article.

9

Spinocerebellar ataxia type 23: a genetic update.

Verbeek DS. Verbeek DS. Cerebellum. 2009 Jun;8(2):104-7. doi: 10.1007/s12311-008-0085-1. Epub 2008 Dec 17. Cerebellum. 2009. PMID: 19089525 Free PMC article.

10

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.

Duarri A, Jezierska J, Fokkens M, Meijer M, Schelhaas HJ, den Dunnen WF, van Dijk F, Verschuuren-Bemelmans C, Hageman G, van de Vlies P, Küsters B, van de Warrenburg BP, Kremer B, Wijmenga C, Sinke RJ, Swertz MA, Kampinga HH, Boddeke E, Verbeek DS. Duarri A, et al. Ann Neurol. 2012 Dec;72(6):870-80. doi: 10.1002/ana.23700. Ann Neurol. 2012. PMID: 23280838

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