Julien Amendola
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Explore the profile of Julien Amendola including associated specialties, affiliations and a list of published articles.
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10
Citations
297
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Recent Articles
1.
Amendola J, Boumedine N, Sangiardi M, El Far O
Sci Rep
. 2015 Sep;
5:14455.
PMID: 26399440
Superior cervical ganglion neurons (SCGN) are often used to investigate neurotransmitter release mechanisms. In this study, we optimized the dissociation and culture conditions of rat SCGN cultures for dual patch...
2.
Durand J, Filipchuk A, Pambo-Pambo A, Amendola J, Borisovna Kulagina I, Gueritaud J
Front Cell Neurosci
. 2015 Sep;
9:349.
PMID: 26388736
We studied the rapid changes in electrical properties of lumbar motoneurons between postnatal days 3 and 9 just before mice weight-bear and walk. The input conductance and rheobase significantly increased...
3.
Dufour M, Woodhouse A, Amendola J, Goaillard J
Elife
. 2014 Oct;
3.
PMID: 25329344
Neurons have complex electrophysiological properties, however, it is often difficult to determine which properties are the most relevant to neuronal function. By combining current-clamp measurements of electrophysiological properties with multi-variate...
4.
Pertici V, Amendola J, Laurin J, Gigmes D, Madaschi L, Carelli S, et al.
ASN Neuro
. 2013 Apr;
5(2):149-66.
PMID: 23614684
There have been considerable interests in attempting to reverse the deficit because of an SCI (spinal cord injury) by restoring neural pathways through the lesion and by rebuilding the tissue...
5.
Amendola J, Woodhouse A, Martin-Eauclaire M, Goaillard J
J Neurosci
. 2012 Feb;
32(6):2166-81.
PMID: 22323729
The level of expression of ion channels has been demonstrated to vary over a threefold to fourfold range from neuron to neuron, although the expression of distinct channels may be...
6.
Elbasiouny S, Amendola J, Durand J, Heckman C
J Neurosci
. 2010 Apr;
30(16):5544-58.
PMID: 20410108
A critical step in improving our understanding of the development of amyotrophic lateral sclerosis (ALS) is to identify the factors contributing to the alterations in the excitability of motoneurons and...
7.
Amendola J, Durand J
J Comp Neurol
. 2008 Sep;
511(3):329-41.
PMID: 18803237
Quantitative analysis of the dendritic arborizations of wild-type (WT) and superoxide dismutase 1 (SOD1) postnatal mouse motoneurons was performed following intracellular staining and 3D reconstructions with Neurolucida system. The population...
8.
Bories C, Amendola J, Lamotte dIncamps B, Durand J
Eur J Neurosci
. 2007 Feb;
25(2):451-9.
PMID: 17284186
Amyotrophic lateral sclerosis is a lethal, adult-onset disease characterized by progressive degeneration of motoneurons. Recent data have suggested that the disease could be linked to abnormal development of the motor...
9.
Durand J, Amendola J, Bories C, Lamotte dIncamps B
J Physiol Paris
. 2006 Feb;
99(2-3):211-20.
PMID: 16448809
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative and fatal human disorder characterized by progressive loss of motor neurons. Transgenic mouse models of ALS are very useful to study the initial...
10.
Amendola J, Verrier B, Roubertoux P, Durand J
Eur J Neurosci
. 2004 Nov;
20(10):2822-6.
PMID: 15548226
Most neurodegenerative diseases become manifest at an adult age but abnormalities or pathological symptoms appear earlier. It is important to identify the initial mechanisms underlying such progressive neurodegenerative disease in...