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Stockmann, Marianne, Meyer-Ohlendorf, Marie, Achberger, Kevin, Putz, Stefan, Demestre, Maria, Yin, Haishan, Hendrich, Corinna, Linta, Leonhard, Heinrich, Jutta, Brunner, Cornelia, Proepper, Christian, Kuh, Georges F., Baumann, Bernd, Langer, Torben, Schwalenstöcker, Birgit, Braunstein, Kerstin E., von Arnim, Christine, Schneuwly, Stephan, Meyer, Thomas, Wong, Philip C., Boeckers, Tobias M., Ludolph, Albert C., Liebau, Stefan
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Published in Journal of Neural Transmission (01.05.2013)
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A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons
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Published in Human molecular genetics (15.11.2010)
Published in Human molecular genetics (15.11.2010)
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The RNA of the glutamate transporter EAAT2 is variably spliced in amyotrophic lateral sclerosis and normal individuals
Meyer, Thomas, Fromm, Andrea, Münch, Christoph, Schwalenstöcker, Birgit, Fray, Anne E, Ince, Paul G, Stamm, Stefan, Grön, Georg, Ludolph, Albert C, Shaw, Pamela J
Published in Journal of the neurological sciences (15.11.1999)
Published in Journal of the neurological sciences (15.11.1999)
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Neuroprotective Function of Cellular Prion Protein in a Mouse Model of Amyotrophic Lateral Sclerosis
Steinacker, Petra, Hawlik, Andreas, Lehnert, Stefan, Jahn, Olaf, Meier, Stephen, Görz, Evamaria, Braunstein, Kerstin E, Krzovska, Marija, Schwalenstöcker, Birgit, Jesse, Sarah, Pröpper, Christian, Böckers, Tobias, Ludolph, Albert, Otto, Markus
Published in The American journal of pathology (01.03.2010)
Published in The American journal of pathology (01.03.2010)
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PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis
Eschbach, Judith, Schwalenstöcker, Birgit, Soyal, Selma M, Bayer, Hanna, Wiesner, Diana, Akimoto, Chizuru, Nilsson, Ann-Charloth, Birve, Anna, Meyer, Thomas, Dupuis, Luc, Danzer, Karin M, Andersen, Peter M, Witting, Anke, Ludolph, Albert C, Patsch, Wolfgang, Weydt, Patrick
Published in Human molecular genetics (01.09.2013)
Published in Human molecular genetics (01.09.2013)
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A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1
Fergani, Anissa, Eschbach, Judith, Oudart, Hugues, Larmet, Yves, Schwalenstocker, Birgit, Ludolph, Albert C, Loeffler, Jean-Philippe, Dupuis, Luc
Published in Molecular neurodegeneration (26.04.2011)
Published in Molecular neurodegeneration (26.04.2011)
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Guidelines for preclinical animal research in ALS/MND: A consensus meeting
Ludolph, Albert C., Bendotti, Caterina, Blaugrund, Eran, Chio, Adriano, Greensmith, Linda, Loeffler, Jean-Philippe, Mead, Richard, Niessen, Heiko G., Petri, Susanne, Pradat, Pierre-Francois, Robberecht, Wim, Ruegg, Markus, Schwalenstöcker, Birgit, Stiller, Detlev, van den Berg, Leonard, Vieira, Fernando, von Horsten, Stephan
Published in Amyotrophic lateral sclerosis (2010)
Published in Amyotrophic lateral sclerosis (2010)
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Conference Proceeding
Tau isoforms expression in transgenic mouse model of amyotrophic lateral sclerosis
Usarek, Ewa, Kuźma-Kozakiewicz, Magdalena, Schwalenstöcker, Birgit, Kaźmierczak, Beata, Münch, Christoph, Ludolph, Albert C, Barańczyk-Kuźma, Anna
Published in Neurochemical research (01.05.2006)
Published in Neurochemical research (01.05.2006)
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PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis
Eschbach, J., Schwalenstocker, B., Soyal, S. M., Bayer, H., Wiesner, D., Akimoto, C., Nilsson, A.-C., Birve, A., Meyer, T., Dupuis, L., Danzer, K. M., Andersen, P. M., Witting, A., Ludolph, A. C., Patsch, W., Weydt, P.
Published in Human molecular genetics (01.09.2013)
Published in Human molecular genetics (01.09.2013)
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Differential regulation of 5′ splice variants of the glutamate transporter EAAT2 in an in vivo model of chemical hypoxia induced by 3-nitropropionic acid
Münch, Christoph, Zhu, Bing-gen, Leven, Annette, Stamm, Stefan, Einkörn, Hermann, Schwalenstöcker, Birgit, Ludolph, Albert C., Riepe, Matthias W., Meyer, Thomas
Published in Journal of neuroscience research (15.03.2003)
Published in Journal of neuroscience research (15.03.2003)
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Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease
Dupuis, Luc, Fergani, Anissa, Braunstein, Kerstin E., Eschbach, Judith, Holl, Nathalie, Rene, Frédérique, Gonzalez De Aguilar, Jose-Luis, Zoerner, Björn, Schwalenstocker, Birgit, Ludolph, Albert C., Loeffler, Jean-Philippe
Published in Experimental neurology (2009)
Published in Experimental neurology (2009)
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Full-length PGC-1[alpha] salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation
Rona-Voros, Krisztina, Eschbach, Judith, Vernay, Aurelia, Wiesner, Diana, Schwalenstocker, Birgit, Geniquet, Pauline, Mousson De Camaret, Benedicte, Echaniz-Laguna, Andoni, Loeffler, Jean-Philippe, Ludolph, Albert C, Weydt, Patrick, Dupuis, Luc
Published in Human molecular genetics (20.12.2013)
Published in Human molecular genetics (20.12.2013)
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Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation
Rona-Voros, Krisztina, Eschbach, Judith, Vernay, Aurélia, Wiesner, Diana, Schwalenstocker, Birgit, Geniquet, Pauline, Mousson De Camaret, Bénédicte, Echaniz-Laguna, Andoni, Loeffler, Jean-Philippe, Ludolph, Albert C, Weydt, Patrick, Dupuis, Luc
Published in Human molecular genetics (20.12.2013)
Published in Human molecular genetics (20.12.2013)
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Splicing of the glutamate transporter EAAT2: a candidate gene of amyotrophic lateral sclerosis
MEYER, THOMAS, MÜNCH, CHRISTOPH, LIEBAU, STEFAN, FROMM, ANDREA, SCHWALENSTÖCKER, BIRGIT, VÖLKEL, HELGE, LUDOLPH, ALBERT C
Published in Journal of neurology, neurosurgery and psychiatry (01.12.1998)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.1998)
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5'-heterogeneity of the human excitatory amino acid transporter cDNA EAAT2 (GLT-1)
Münch, C, Schwalenstöcker, B, Knappenberger, B, Liebau, S, Völkel, H, Ludolph, A C, Meyer, T
Published in Neuroreport (11.05.1998)
Published in Neuroreport (11.05.1998)
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Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues
Eschbach, Judith, Fergani, Anissa, Oudart, Hugues, Robin, Jean-Patrice, Rene, Frédérique, Gonzalez de Aguilar, Jose-Luis, Larmet, Yves, Zoll, Joffrey, Hafezparast, Majid, Schwalenstocker, Birgit, Loeffler, Jean-Philippe, Ludolph, Albert C., Dupuis, Luc
Published in Biochimica et biophysica acta (2011)
Published in Biochimica et biophysica acta (2011)
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Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues
Eschbach, Judith, Fergani, Anissa, Oudart, Hugues, Robin, Jean-Patrice, Rene, Frédérique, de Aguilar, Jose-Luis Gonzalez, Larmet, Yves, Zoll, Joffrey, Hafezparast, Majid, Schwalenstocker, Birgit, Loeffler, Jean-Philippe, Ludolph, Albert C., Dupuis, Luc
Published in Biochimica et biophysica acta. Molecular basis of disease (18.11.2010)
Published in Biochimica et biophysica acta. Molecular basis of disease (18.11.2010)
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Differential RNA cleavage and polyadenylation of the glutamate transporter EAAT2 in the human brain
Münch, Christoph, Schwalenstöcker, Birgit, Hermann, Christine, Cirovic, Stanko, Stamm, Stefan, Ludolph, Albert, Meyer, Thomas
Published in Brain research. Molecular brain research. (15.09.2000)
Published in Brain research. Molecular brain research. (15.09.2000)
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Age-related changes in tau expression in transgenic mouse model of amyotrophic lateral sclerosis
Barańczyk-Kuźma, Anna, Usarek, Ewa, Kuźma-Kozakiewcz, Magdalena, Kaźmierczak, Beata, Gajewska, Beata, Schwalenstocker, Birgit, Ludolph, Albert C
Published in Neurochemical research (01.03.2007)
Published in Neurochemical research (01.03.2007)
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