Jacques Durand, Ph.D

Affiliations: 
CNRS, Paris, Île-de-France, France 
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"Jacques Durand"
Mean distance: 17.11 (cluster 11)
 
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Publications

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Durand J, Filipchuk A, Pambo-Pambo A, et al. (2015) Developing electrical properties of postnatal mouse lumbar motoneurons. Frontiers in Cellular Neuroscience. 9: 349
Filipchuk AA, Durand J. (2012) Postnatal dendritic development in lumbar motoneurons in mutant superoxide dismutase 1 mouse model of amyotrophic lateral sclerosis. Neuroscience. 209: 144-54
Durand JP. (2011) Family cultures and pediatric care | Cultures familiales et soins pédiatriques Archives De Pediatrie. 18: H7-H8
Kulagina IB, Durand J. (2011) Comparative analysis of geometry and electrical properties of simulated normal and genetically modified motoneurons Neurophysiology. 43: 217-222
Elbasiouny SM, Amendola J, Durand J, et al. (2010) Evidence from computer simulations for alterations in the membrane biophysical properties and dendritic processing of synaptic inputs in mutant superoxide dismutase-1 motoneurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 5544-58
Pambo-Pambo A, Durand J, Gueritaud JP. (2009) Early excitability changes in lumbar motoneurons of transgenic SOD1G85R and SOD1G(93A-Low) mice. Journal of Neurophysiology. 102: 3627-42
Amendola J, Durand J. (2008) Morphological differences between wild-type and transgenic superoxide dismutase 1 lumbar motoneurons in postnatal mice. The Journal of Comparative Neurology. 511: 329-41
Filipchuk AA, Durand J, Korogod SM. (2008) Charge transfer effectiveness as an electrotonic indicator of the structural differences between samples of dendritic morphology Neurophysiology. 40: 422-425
Amendola J, Gueritaud JP, Lamotte d'Incamps B, et al. (2007) Postnatal electrical and morphological abnormalities in lumbar motoneurons from transgenic mouse models of amyotrophic lateral sclerosis. Archives Italiennes De Biologie. 145: 311-23
Bories C, Amendola J, Lamotte d'Incamps B, et al. (2007) Early electrophysiological abnormalities in lumbar motoneurons in a transgenic mouse model of amyotrophic lateral sclerosis. The European Journal of Neuroscience. 25: 451-9
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