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Filtres: Author is Yves De Koninck [Enlever les filtres]
Postnatal changes in the Rexed lamination and markers of nociceptive afferents in the superficial dorsal horn of the rat. J Comp Neurol. 2008;508(4):592-604.
Pyramidal neurons switch from integrators in vitro to resonators under in vivo-like conditions. J Neurophysiol. 2008;100(6):3030-42.
Expression of CCR2 in both resident and bone marrow-derived microglia plays a critical role in neuropathic pain. J Neurosci. 2007;27(45):12396-406.
Transformation of the output of spinal lamina I neurons after nerve injury and microglia stimulation underlying neuropathic pain. Mol Pain. 2007;3:27.
Dendritic spine viscoelasticity and soft-glassy nature: balancing dynamic remodeling with structural stability. Biophys J. 2007;92(4):1419-30.
Altered chloride homeostasis in neurological disorders: a new target. Curr Opin Pharmacol. 2007;7(1):93-9.
Two-photon excitation fluorescence microscopy with a high depth of field using an axicon. Appl Opt. 2006;45(36):9246-52.
Reduction of anion reversal potential subverts the inhibitory control of firing rate in spinal lamina I neurons: towards a biophysical basis for neuropathic pain. Mol Pain. 2006;2:32.
[Two-photon laser scanning fluorescence microscopy for functional cellular imaging: Advantages and challenges or One photon is good... but two is better!]. Med Sci (Paris). 2006;22(10):837-44.
Nonlinear interaction between shunting and adaptation controls a switch between integration and coincidence detection in pyramidal neurons. J Neurosci. 2006;26(36):9084-97.
Spatial and temporal relationship between monocyte chemoattractant protein-1 expression and spinal glial activation following peripheral nerve injury. J Neurochem. 2006;97(3):772-83.
Imbalance towards inhibition as a substrate of aging-associated cognitive impairment. Neurosci Lett. 2006;397(1-2):64-8.
BDNF from microglia causes the shift in neuronal anion gradient underlying neuropathic pain. Nature. 2005;438(7070):1017-21.
Destruction of polymer growth substrates for cell cultures in two-photon microscopy. J Microsc. 2005;220(Pt 2):120-7.
Differential maturation of GABA action and anion reversal potential in spinal lamina I neurons: impact of chloride extrusion capacity. J Neurosci. 2005;25(42):9613-23.
Morphology and neurokinin 1 receptor expression of spinothalamic lamina I neurons in the rat spinal cord. J Comp Neurol. 2005;491(1):56-68.
Integration time in a subset of spinal lamina I neurons is lengthened by sodium and calcium currents acting synergistically to prolong subthreshold depolarization. J Neurosci. 2005;25(19):4743-54.
Role of cation-chloride-cotransporters (CCC) in pain and hyperalgesia. Curr Top Med Chem. 2005;5(6):547-55.
Trans-synaptic shift in anion gradient in spinal lamina I neurons as a mechanism of neuropathic pain. Nature. 2003;424(6951):938-42.
Gain control of firing rate by shunting inhibition: roles of synaptic noise and dendritic saturation. Proc Natl Acad Sci USA. 2003;100(4):2076-81.
Four cell types with distinctive membrane properties and morphologies in lamina I of the spinal dorsal horn of the adult rat. J Physiol (Lond). 2002;539(Pt 3):817-36.
Aging causes a preferential loss of cholinergic innervation of characterized neocortical pyramidal neurons. Cereb Cortex. 2002;12(3):329-37.
Region-specific developmental specialization of GABA-glycine cosynapses in laminas I-II of the rat spinal dorsal horn. J Neurosci. 2001;21(20):7871-80.
Cholinergic nerve terminals establish classical synapses in the rat cerebral cortex: synaptic pattern and age-related atrophy. Neuroscience. 2001;105(2):277-85.