Sort by
Items per page

Send to

Choose Destination

Search results

Items: 16


RGS9-2 rescues dopamine D2 receptor levels and signaling in DYT1 dystonia mouse models.

Bonsi P, Ponterio G, Vanni V, Tassone A, Sciamanna G, Migliarini S, Martella G, Meringolo M, Dehay B, Doudnikoff E, Zachariou V, Goodchild RE, Mercuri NB, D'Amelio M, Pasqualetti M, Bezard E, Pisani A.

EMBO Mol Med. 2019 Jan;11(1). pii: e9283. doi: 10.15252/emmm.201809283.


Mice Deficient in Nucleoporin Nup210 Develop Peripheral T Cell Alterations.

van Nieuwenhuijze A, Burton O, Lemaitre P, Denton AE, Cascalho A, Goodchild RE, Malengier-Devlies B, Cauwe B, Linterman MA, Humblet-Baron S, Liston A.

Front Immunol. 2018 Sep 28;9:2234. doi: 10.3389/fimmu.2018.02234. eCollection 2018.


New twist defines a spectrum of TOR1A neurological disease.

Cascalho A, Goodchild RE.

Mov Disord. 2018 Jan;33(1):73. doi: 10.1002/mds.27269. Epub 2017 Dec 21. No abstract available.


The ins and outs of endoplasmic reticulum-controlled lipid biosynthesis.

Jacquemyn J, Cascalho A, Goodchild RE.

EMBO Rep. 2017 Nov;18(11):1905-1921. doi: 10.15252/embr.201643426. Epub 2017 Oct 26. Review.


Abnormal striatal plasticity in a DYT11/SGCE myoclonus dystonia mouse model is reversed by adenosine A2A receptor inhibition.

Maltese M, Martella G, Imbriani P, Schuermans J, Billion K, Sciamanna G, Farook F, Ponterio G, Tassone A, Santoro M, Bonsi P, Pisani A, Goodchild RE.

Neurobiol Dis. 2017 Dec;108:128-139. doi: 10.1016/j.nbd.2017.08.007. Epub 2017 Aug 18.


Integrity of the Linker of Nucleoskeleton and Cytoskeleton Is Required for Efficient Herpesvirus Nuclear Egress.

Klupp BG, Hellberg T, Granzow H, Franzke K, Dominguez Gonzalez B, Goodchild RE, Mettenleiter TC.

J Virol. 2017 Sep 12;91(19). pii: e00330-17. doi: 10.1128/JVI.00330-17. Print 2017 Oct 1.


Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia?

Cascalho A, Jacquemyn J, Goodchild RE.

Mov Disord. 2017 Mar;32(3):371-381. doi: 10.1002/mds.26880. Epub 2016 Dec 2. Review.


Torsins Are Essential Regulators of Cellular Lipid Metabolism.

Grillet M, Dominguez Gonzalez B, Sicart A, Pöttler M, Cascalho A, Billion K, Hernandez Diaz S, Swerts J, Naismith TV, Gounko NV, Verstreken P, Hanson PI, Goodchild RE.

Dev Cell. 2016 Aug 8;38(3):235-47. doi: 10.1016/j.devcel.2016.06.017. Epub 2016 Jul 21.


Access of torsinA to the inner nuclear membrane is activity dependent and regulated in the endoplasmic reticulum.

Goodchild RE, Buchwalter AL, Naismith TV, Holbrook K, Billion K, Dauer WT, Liang CC, Dear ML, Hanson PI.

J Cell Sci. 2015 Aug 1;128(15):2854-65. doi: 10.1242/jcs.167452. Epub 2015 Jun 19.


New genetic insights highlight 'old' ideas on motor dysfunction in dystonia.

Goodchild RE, Grundmann K, Pisani A.

Trends Neurosci. 2013 Dec;36(12):717-25. doi: 10.1016/j.tins.2013.09.003. Epub 2013 Oct 18. Review.


The nuclear envelope localization of DYT1 dystonia torsinA-ΔE requires the SUN1 LINC complex component.

Jungwirth MT, Kumar D, Jeong DY, Goodchild RE.

BMC Cell Biol. 2011 May 31;12:24. doi: 10.1186/1471-2121-12-24.


Type III neuregulin-1 is required for normal sensorimotor gating, memory-related behaviors, and corticostriatal circuit components.

Chen YJ, Johnson MA, Lieberman MD, Goodchild RE, Schobel S, Lewandowski N, Rosoklija G, Liu RC, Gingrich JA, Small S, Moore H, Dwork AJ, Talmage DA, Role LW.

J Neurosci. 2008 Jul 2;28(27):6872-83. doi: 10.1523/JNEUROSCI.1815-08.2008.


Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation.

Goodchild RE, Dauer WT.

Proc Natl Acad Sci U S A. 2004 Jan 20;101(3):847-52. Epub 2004 Jan 7.


Distribution of histamine H3-receptor binding in the normal human basal ganglia: comparison with Huntington's and Parkinson's disease cases.

Goodchild RE, Court JA, Hobson I, Piggott MA, Perry RH, Ince P, Jaros E, Perry EK.

Eur J Neurosci. 1999 Feb;11(2):449-56.


Supplemental Content

Loading ...
Support Center