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Filtres: Keyword is Disease Models, Animal [Enlever les filtres]
« Repetitive Traumatic Brain Injury Is Associated With TDP-43 Alterations, Neurodegeneration, and Glial Activation in Mice. », J Neuropathol Exp Neurol, vol. 80, nᵒ 1, p. 2-14, 2021.
, « Cell-type-specific role for nucleus accumbens neuroligin-2 in depression and stress susceptibility. », Proc Natl Acad Sci U S A, vol. 115, nᵒ 5, p. 1111-1116, 2018.
, « Establishment of a repeated social defeat stress model in female mice. », Sci Rep, vol. 7, nᵒ 1, p. 12838, 2017.
, « Cystamine/cysteamine rescues the dopaminergic system and shows neurorestorative properties in an animal model of Parkinson's disease. », Neurobiol Dis, vol. 82, p. 430-444, 2015.
, « Pathogenesis of the Novel Autoimmune-Associated Long-QT Syndrome. », Circulation, vol. 132, nᵒ 4, p. 230-40, 2015.
, « Adeno-associated virus-mediated delivery of a recombinant single-chain antibody against misfolded superoxide dismutase for treatment of amyotrophic lateral sclerosis. », Mol Ther, vol. 22, nᵒ 3, p. 498-510, 2014.
, « Overlap of food addiction and substance use disorders definitions: analysis of animal and human studies. », Neuropharmacology, vol. 85, p. 81-90, 2014.
, « Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1. », Hum Mol Genet, vol. 22, nᵒ 19, p. 3947-59, 2013.
, « Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival. », Neuron, vol. 80, nᵒ 1, p. 80-96, 2013.
, « Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog. [corrected]. », Cell Stem Cell, vol. 12, nᵒ 4, p. 426-39, 2013.
, « Ablation of proliferating cells in the CNS exacerbates motor neuron disease caused by mutant superoxide dismutase. », PLoS One, vol. 7, nᵒ 4, p. e34932, 2012.
, « Abnormal regenerative responses and impaired axonal outgrowth after nerve crush in TDP-43 transgenic mouse models of amyotrophic lateral sclerosis. », J Neurosci, vol. 32, nᵒ 50, p. 18186-95, 2012.
, « Methylene blue administration fails to confer neuroprotection in two amyotrophic lateral sclerosis mouse models. », Neuroscience, vol. 209, p. 136-43, 2012.
, « Mouse model of intraluminal MCAO: cerebral infarct evaluation by cresyl violet staining. », J Vis Exp, nᵒ 69, 2012.
, « Real-time imaging after cerebral ischemia: model systems for visualization of inflammation and neuronal repair. », Methods Enzymol, vol. 506, p. 117-33, 2012.
, « ALS pathogenesis: recent insights from genetics and mouse models. », Prog Neuropsychopharmacol Biol Psychiatry, vol. 35, nᵒ 2, p. 363-9, 2011.
, « Animal models of human anxiety disorders: reappraisal from a developmental psychopathology vantage point. », Pediatr Res, vol. 69, nᵒ 5 Pt 2, p. 77R-84R, 2011.
, « Gigaxonin mutation analysis in patients with NIFID. », Neurobiol Aging, vol. 32, nᵒ 8, p. 1528-9, 2011.
, « Model system for live imaging of neuronal responses to injury and repair. », Mol Imaging, vol. 10, nᵒ 6, p. 434-45, 2011.
, « Pathological hallmarks of amyotrophic lateral sclerosis/frontotemporal lobar degeneration in transgenic mice produced with TDP-43 genomic fragments. », Brain, vol. 134, nᵒ Pt 9, p. 2610-26, 2011.
, « Distinct biochemical signatures characterize peripherin isoform expression in both traumatic neuronal injury and motor neuron disease. », J Neurochem, vol. 114, nᵒ 4, p. 1177-92, 2010.
, « Induction of protective immunity by vaccination with wild-type apo superoxide dismutase 1 in mutant SOD1 transgenic mice. », J Neuropathol Exp Neurol, vol. 69, nᵒ 10, p. 1044-56, 2010.
, « Maladaptive plasticity of serotonin axon terminals in levodopa-induced dyskinesia. », Ann Neurol, vol. 68, nᵒ 5, p. 619-28, 2010.
, « Neuronal over-expression of chromogranin A accelerates disease onset in a mouse model of ALS. », J Neurochem, vol. 115, nᵒ 5, p. 1102-11, 2010.
, « Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E. », Hum Mol Genet, vol. 19, nᵒ 13, p. 2616-29, 2010.
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