Publications by authors named "Rose Goodchild"

Claim this Profile
T
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders.
Afshin Saffari, Tracy Lau, Homa Tajsharghi, Ehsan Ghayoor Karimiani, Ariana Kariminejad, Rose Goodchild

Brain· August 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Preservation of Fluorescence Signal and Imaging Optimization for Integrated Light and Electron Microscopy.
Pieter Baatsen, Sergio Gabarre, Katlijn Vints, Rosanne Wouters, Dorien Vandael, Rose Goodchild

Front Cell Dev Biol· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Torsin and NEP1R1-CTDNEP1 phosphatase affect interphase nuclear pore complex insertion by lipid-dependent and lipid-independent mechanisms.
Julie Jacquemyn, Joyce Foroozandeh, Katlijn Vints, Jef Swerts, Patrik Verstreken, Rose Goodchild

EMBO J· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Excess Lipin enzyme activity contributes to TOR1A recessive disease and DYT-TOR1A dystonia.
Ana Cascalho, Joyce Foroozandeh, Lise Hennebel, Jef Swerts, Christine Klein, Rose E Goodchild

Brain· June 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impaired dopamine- and adenosine-mediated signaling and plasticity in a novel rodent model for DYT25 dystonia.
Libo Yu-Taeger, Thomas Ott, Paola Bonsi, Celina Tomczak, Zinah Wassouf, Rose Goodchild

Neurobiol Dis· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mice Deficient in Nucleoporin Nup210 Develop Peripheral T Cell Alterations.
Annemarie van Nieuwenhuijze, Oliver Burton, Pierre Lemaitre, Alice E Denton, Ana Cascalho, Rose E Goodchild

Front Immunol· October 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RGS9-2 rescues dopamine D2 receptor levels and signaling in dystonia mouse models.
Paola Bonsi, Giulia Ponterio, Valentina Vanni, Annalisa Tassone, Giuseppe Sciamanna, Rose E Goodchild

EMBO Mol Med· January 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Excess LINC complexes impair brain morphogenesis in a mouse model of recessive TOR1A disease.
Beatriz Dominguez Gonzalez, Karolien Billion, Stef Rous, Benjamin Pavie, Christian Lange, Rose Goodchild

Hum Mol Genet· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
New twist defines a spectrum of TOR1A neurological disease.
Ana Cascalho, Rose E Goodchild

Mov Disord· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Abnormal striatal plasticity in a DYT11/SGCE myoclonus dystonia mouse model is reversed by adenosine A2A receptor inhibition.
M Maltese, G Martella, P Imbriani, Jeroen Schuermans, Karolien Billion, Rose E Goodchild

Neurobiol Dis· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The ins and outs of endoplasmic reticulum-controlled lipid biosynthesis.
Julie Jacquemyn, Ana Cascalho, Rose E Goodchild

EMBO Rep· November 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Integrity of the Linker of Nucleoskeleton and Cytoskeleton Is Required for Efficient Herpesvirus Nuclear Egress.
Barbara G Klupp, Teresa Hellberg, Harald Granzow, Kati Franzke, Beatriz Dominguez Gonzalez, Rose E Goodchild

J Virol· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia?
Ana Cascalho, Julie Jacquemyn, Rose E Goodchild

Mov Disord· March 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Torsins Are Essential Regulators of Cellular Lipid Metabolism.
Micheline Grillet, Beatriz Dominguez Gonzalez, Adria Sicart, Maria Pöttler, Ana Cascalho, Rose E Goodchild

Dev Cell· August 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Membrane Lipids in Presynaptic Function and Disease.
Elsa Lauwers, Rose Goodchild, Patrik Verstreken

Neuron· April 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Access of torsinA to the inner nuclear membrane is activity dependent and regulated in the endoplasmic reticulum.
Rose E Goodchild, Abigail L Buchwalter, Teresa V Naismith, Kristen Holbrook, Karolien Billion

J Cell Sci· August 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
New genetic insights highlight 'old' ideas on motor dysfunction in dystonia.
Rose E Goodchild, Kathrin Grundmann, Antonio Pisani

Trends Neurosci· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The nuclear envelope localization of DYT1 dystonia torsinA-ΔE requires the SUN1 LINC complex component.
Michael T Jungwirth, Dhivya Kumar, Danielle Y Jeong, Rose E Goodchild

BMC Cell Biol· May 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Relative tissue expression of homologous torsinB correlates with the neuronal specific importance of DYT1 dystonia-associated torsinA.
Michael Jungwirth, Mary Lynn Dear, Patricia Brown, Kristen Holbrook, Rose Goodchild

Hum Mol Genet· March 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Type III neuregulin-1 is required for normal sensorimotor gating, memory-related behaviors, and corticostriatal circuit components.
Ying-Jiun J Chen, Madeleine A Johnson, Michael D Lieberman, Rose E Goodchild, Scott Schobel

J Neurosci· July 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope.
Rose E Goodchild, Connie Eunji Kim, William T Dauer

Neuron· December 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein.
Rose E Goodchild, William T Dauer

J Cell Biol· March 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation.
Rose E Goodchild, William T Dauer

Proc Natl Acad Sci U S A· January 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mouse models of torsinA dysfunction.
William Dauer, Rose Goodchild

Adv Neurol· October 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Resistance of alpha -synuclein null mice to the parkinsonian neurotoxin MPTP.
William Dauer, Nikolai Kholodilov, Miquel Vila, Anne-Cecile Trillat, Rose Goodchild

Proc Natl Acad Sci U S A· October 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis