Selective mitochondrial Ca2+uptake deficit in disease endstage vulnerable motoneurons of the SOD1G93Amouse model of amyotrophic lateral sclerosis

Author:

Fuchs Andrea,Kutterer Sylvie,Mühling Tobias,Duda Johanna,Schütz Burkhard,Liss Birgit,Keller Bernhard U.,Roeper Jochen

Publisher

Wiley

Subject

Physiology

Reference72 articles.

1. The role of calcium-binding proteins in selective motoneuron vulnerability in amyotrophic lateral sclerosis;Alexianu;Ann Neurol,1994

2. Postnatal electrical and morphological abnormalities in lumbar motoneurons from transgenic mouse models of amyotrophic lateral sclerosis;Amendola;Arch Ital Biol,2007

3. Development of hypoglossal motoneurons;Berger;J Appl Physiol,1996

4. Excitability properties of mouse motor axons in the mutant SOD1G93A model of amyotrophic lateral sclerosis;Boërio;Muscle Nerve,2010

5. Early electrophysiological abnormalities in lumbar motoneurons in a transgenic mouse model of amyotrophic lateral sclerosis;Bories;Eur J Neurosci,2007

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