Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons
Dupuis, Luc, Gonzalez de Aguilar, Jose-Luis, Echaniz-Laguna, Andoni, Eschbach, Judith, Rene, Frédérique, Oudart, Hugues, Halter, Benoit, Huze, Caroline, Schaeffer, Laurent, Bouillaud, Frédéric, Loeffler, Jean-Philippe
Published in PloS one (30.04.2009)
Published in PloS one (30.04.2009)
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Journal Article
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age
Eschbach, Judith, Sinniger, Jérôme, Bouitbir, Jamal, Fergani, Anissa, Schlagowski, Anna-Isabel, Zoll, Joffrey, Geny, Bernard, René, Frédérique, Larmet, Yves, Marion, Vincent, Baloh, Robert H, Harms, Matthew B, Shy, Michael E, Messadeq, Nadia, Weydt, Patrick, Loeffler, Jean-Philippe, Ludolph, Albert C, Dupuis, Luc
Published in Neurobiology of disease (01.10.2013)
Published in Neurobiology of disease (01.10.2013)
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Journal Article
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons
Braunstein, Kerstin E., Eschbach, Judith, Ròna-Vörös, Krisztina, Soylu, Rana, Mikrouli, Elli, Larmet, Yves, René, Frédérique, De Aguilar, Jose-Luis Gonzalez, Loeffler, Jean-Philippe, Müller, Hans-Peter, Bucher, Selina, Kaulisch, Thomas, Niessen, Heiko G., Tillmanns, Julia, Fischer, Kristina, Schwalenstöcker, Birgit, Kassubek, Jan, Pichler, Bernd, Stiller, Detlef, Petersen, Åsa, Ludolph, Albert C., Dupuis, Luc
Published in Human molecular genetics (15.11.2010)
Published in Human molecular genetics (15.11.2010)
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Journal Article
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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Journal Article
“OpenLAB”: A 2‐hour PCR‐based practical for high school students
Bouakaze, Caroline, Eschbach, Judith, Fouquerel, Elise, Gasser, Isabelle, Kieffer, Emmanuelle, Krieger, Sophie, Milosevic, Sara, Saandi, Thoueiba, Florentz, Catherine, Maréchal‐Drouard, Laurence, Labouesse, Michel
Published in Biochemistry and molecular biology education (01.09.2010)
Published in Biochemistry and molecular biology education (01.09.2010)
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Journal Article
Energy Metabolism in Residents in the Low- and Moderate Altitude Regions of Central Asia with MAFLD and Type 2 Diabetes Mellitus
Toktogulova, Nurgul, Breidert, Matthias, Eschbach, Judith, Kudaibergenova, Indira, Omurzakova, Uulkan, Uvaidillaeva, Feruzakhan, Tagaeva, Bermet, Sultanalieva, Roza, Eftekhari, Pierre
Published in Hormone and metabolic research (01.04.2024)
Published in Hormone and metabolic research (01.04.2024)
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Journal Article
Cover Image, Volume 85, Issue 1
Eschbach, Judith, Wagner, Alain, Beahr, Corinne, Bekel, Akkiz, Korganow, Anne‐Sophie, Quartier, Angelique, Peter, Jean‐Christophe, Eftekhari, Pierre
Published in Drug development research (01.02.2024)
Published in Drug development research (01.02.2024)
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Journal Article
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization
Eschbach, Judith, von Einem, Björn, Müller, Kathrin, Bayer, Hanna, Scheffold, Annika, Morrison, Bradley E., Rudolph, K. Lenhard, Thal, Dietmar R., Witting, Anke, Weydt, Patrick, Otto, Markus, Fauler, Michael, Liss, Birgit, McLean, Pamela J., Spada, Albert R. La, Ludolph, Albert C., Weishaupt, Jochen H., Danzer, Karin M.
Published in Annals of neurology (01.01.2015)
Published in Annals of neurology (01.01.2015)
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Journal Article
Drug upgrade: A complete methodology from old drug to new chemical entities using Nematic Protein Organization Technique
Eschbach, Judith, Wagner, Alain, Beahr, Corinne, Bekel, Akkiz, Korganow, Anne‐Sophie, Quartier, Angelique, Peter, Jean‐Christophe, Eftekhari, Pierre
Published in Drug development research (01.02.2024)
Published in Drug development research (01.02.2024)
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Journal Article
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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Journal Article
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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Journal Article
The Golgi-localized, gamma ear-containing, ARF-binding (GGA) protein family alters alpha synuclein (α-syn) oligomerization and secretion
von Einem, Bjoern, Eschbach, Judith, Kiechle, Martin, Wahler, Anke, Thal, Dietmar R, McLean, Pamela J, Weishaupt, Jochen H, Ludolph, Albert C, von Arnim, Christine A F, Danzer, Karin M
Published in Aging (Albany, NY.) (15.07.2017)
Published in Aging (Albany, NY.) (15.07.2017)
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Journal Article
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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Journal Article
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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Journal Article
Mutual exacerbation of peroxisome proliferator-activated receptor [gamma] coactivator 1[alpha] deregulation and [alpha]-synuclein oligomerization
Eschbach, Judith, von Einem, Björn, Muller, Kathrin, Bayer, Hanna, Scheffold, Annika, Morrison, Bradley E, Rudolph, K Lenhard, Thal, Dietmar R, Witting, Anke, Weydt, Patrick, Otto, Markus, Fauler, Michael, Liss, Birgit, McLean, Pamela J, Spada, Albert R La, Ludolph, Albert C, Weishaupt, Jochen H, Danzer, Karin M
Published in Annals of neurology (01.01.2015)
Published in Annals of neurology (01.01.2015)
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Journal Article
Mutual exacerbation of PGC-1α deregulation and α-synuclein oligomerization
Eschbach, Judith, von Einem, Björn, Müller, Kathrin, Bayer, Hanna, Scheffold, Annika, Morrison, Bradley E., Rudolph, K. Lenhard, Thal, Dietmar R., Witting, Anke, Weydt, Patrick, Otto, Markus, Fauler, Michael, Liss, Birgit, McLean, Pamela J., La Spada, Albert R., Ludolph, Albert C., Weishaupt, Jochen H., Danzer, Karin M.
Published in Annals of neurology (19.12.2014)
Published in Annals of neurology (19.12.2014)
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Journal Article
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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Journal Article