Reply to Valenza and Cattaneo: SIRT2-mediated neuroprotection and cholesterol dyshomeostasis in Huntington’s disease

Por Luthi-Carter, Ruth, Kazantsev, Aleksey G.
Publicado em 2010

Cross-species and cross-platform gene expression studies with the Bioconductor-compliant R package 'annotationTools'

Por Luthi-Carter Ruth, Kuhn Alexandre, Delorenzi Mauro
Publicado em 2008-01-01

Cross-species and cross-platform gene expression studies with the Bioconductor-compliant R package 'annotationTools'

Por Kuhn, Alexandre, Luthi-Carter, Ruth, Delorenzi, Mauro
Publicado em 2008

Decreased Striatal RGS2 Expression Is Neuroprotective in Huntington's Disease (HD) and Exemplifies a Compensatory Aspect of HD-Induced Gene Regulation

Por Seredenina, Tamara, Gokce, Ozgun, Luthi-Carter, Ruth
Publicado em 2011

Short-Term Striatal Gene Expression Responses to Brain-Derived Neurotrophic Factor Are Dependent on MEK and ERK Activation

Por Gokce, Ozgun, Runne, Heike, Kuhn, Alexandre, Luthi-Carter, Ruth
Publicado em 2009

The Ratio of Monomeric to Aggregated Forms of Aβ40 and Aβ42 Is an Important Determinant of Amyloid-β Aggregation, Fibrillogenesis, and Toxicity

Por Jan, Asad, Gokce, Ozgun, Luthi-Carter, Ruth, Lashuel, Hilal A.
Publicado em 2008

Isolation and expression of a rat brain cDNA encoding glutamate carboxypeptidase II

Por Luthi-Carter, Ruth, Berger, Urs V., Barczak, Amy K., Enna, Matthew, Coyle, Joseph T.
Publicado em 1998

Computational deconvolution of genome wide expression data from Parkinson's and Huntington's disease brain tissues using population-specific expression analysis

Por Capurro, Alberto, Bodea, Liviu-Gabriel, Schaefer, Patrick, Luthi-Carter, Ruth, Perreau, Victoria M.
Publicado no Front Neurosci (2015)

Comprehensive Expression Analyses of Neural Cell-Type-Specific miRNAs Identify New Determinants of the Specification and Maintenance of Neuronal Phenotypes

Por Jovičić, Ana, Roshan, Reema, Moisoi, Nicoleta, Pradervand, Sylvain, Moser, Roger, Pillai, Beena, Luthi-Carter, Ruth
Publicado no J Neurosci (2013)

Expression analysis of novel striatal-enriched genes in Huntington disease

Por Mazarei, Gelareh, Neal, Scott J., Becanovic, Kristina, Luthi-Carter, Ruth, Simpson, Elizabeth M., Leavitt, Blair R.
Publicado em 2010

MicroRNA-22 (miR-22) Overexpression Is Neuroprotective via General Anti-Apoptotic Effects and May also Target Specific Huntington’s Disease-Related Mechanisms

Por Jovicic, Ana, Zaldivar Jolissaint, Julien Francisco, Moser, Roger, Silva Santos, Mariana de Fatima, Luthi-Carter, Ruth
Publicado em 2013

Gene expression profiling of R6/2 transgenic mice with different CAG repeat lengths reveals genes associated with disease onset and progression in Huntington's disease

Por Tang, Bin, Seredenina, Tamara, Coppola, Giovanni, Kuhn, Alexandre, Geschwind, Daniel H., Luthi-Carter, Ruth, Thomas, Elizabeth A.
Publicado em 2011

Connectivity mapping uncovers small molecules that modulate neurodegeneration in Huntington’s disease models

Por Smalley, Joshua L., Breda, Carlo, Mason, Robert P., Kooner, Gurdeep, Luthi-Carter, Ruth, Gant, Timothy W., Giorgini, Flaviano
Publicado no J Mol Med (Berl) (2015)

Calpain Hydrolysis of α- and β2-Adaptins Decreases Clathrin-dependent Endocytosis and May Promote Neurodegeneration

Por Rudinskiy, Nikita, Grishchuk, Yulia, Vaslin, Anne, Puyal, Julien, Delacourte, André, Hirling, Harald, Clarke, Peter G. H., Luthi-Carter, Ruth
Publicado em 2009

Transcriptional changes in Huntington disease identified using genome-wide expression profiling and cross-platform analysis

Por Becanovic, Kristina, Pouladi, Mahmoud A., Lim, Raymond S., Kuhn, Alexandre, Pavlidis, Paul, Luthi-Carter, Ruth, Hayden, Michael R., Leavitt, Blair R.
Publicado em 2010

Synchrotron infrared micro-spectroscopy detects the evolution of Huntington’s disease neuropathology and suggests unique correlates of dysfunction in white versus grey brain matter...

Por Bonda, Markus, Perrin, Valérie, Vileno, Bertrand, Runne, Heike, Kretlow, Ariane, Forró, László, Luthi-Carter, Ruth, Miller, Lisa M., Jeney, Sylvia
Publicado em 2011

Involvement of autophagy in hypoxic-excitotoxic neuronal death

Por Ginet, Vanessa, Spiehlmann, Amélie, Rummel, Coralie, Rudinskiy, Nikita, Grishchuk, Yulia, Luthi-Carter, Ruth, Clarke, Peter GH, Truttmann, Anita C, Puyal, Julien
Publicado no Autophagy (2014)

Dysregulation of Gene Expression in Primary Neuron Models of Huntington's Disease Shows That Polyglutamine-Related Effects on the Striatal Transcriptome May Not Be Dependent on Bra...

Por Runne, Heike, Régulier, Etienne, Kuhn, Alexandre, Zala, Diana, Gokce, Ozgun, Perrin, Valérie, Sick, Beate, Aebischer, Patrick, Déglon, Nicole, Luthi-Carter, Ruth
Publicado no J Neurosci (2008)

Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral blood

Por Runne, Heike, Kuhn, Alexandre, Wild, Edward J., Pratyaksha, Wirahpati, Kristiansen, Mark, Isaacs, Jeremy D., Régulier, Etienne, Delorenzi, Mauro, Tabrizi, Sarah J., Luthi-Carter, Ruth
Publicado em 2007

In vivo cell-autonomous transcriptional abnormalities revealed in mice expressing mutant huntingtin in striatal but not cortical neurons

Por Thomas, Elizabeth A., Coppola, Giovanni, Tang, Bin, Kuhn, Alexandre, Kim, SoongHo, Geschwind, Daniel H., Brown, Timothy B., Luthi-Carter, Ruth, Ehrlich, Michelle E.
Publicado em 2011