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“Interaction of transactive response DNA binding protein 43 with nuclear factor κB in mild cognitive impairment with episodic memory deficits.”, Acta Neuropathol Commun, vol. 2, p. 37, 2014.
, “Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].”, PLoS One, vol. 7, no. 6, p. e39338, 2012.
, “Interaction between αCaMKII and GluN2B controls ERK-dependent plasticity.”, J Neurosci, vol. 32, no. 31, pp. 10767-79, 2012.
, “Deregulation of TDP-43 in amyotrophic lateral sclerosis triggers nuclear factor κB-mediated pathogenic pathways.”, J Exp Med, vol. 208, no. 12, pp. 2429-47, 2011.
, “Intracerebroventricular infusion of monoclonal antibody or its derived Fab fragment against misfolded forms of SOD1 mutant delays mortality in a mouse model of ALS.”, J Neurochem, vol. 113, no. 5, pp. 1188-99, 2010.
, “Neuronal over-expression of chromogranin A accelerates disease onset in a mouse model of ALS.”, J Neurochem, vol. 115, no. 5, pp. 1102-11, 2010.
, “On BC1 RNA and the fragile X mental retardation protein.”, Proc Natl Acad Sci U S A, vol. 105, no. 2, pp. 734-9, 2008.
, “Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation.”, J Neurochem, vol. 102, no. 1, pp. 170-8, 2007.
, “Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis.”, Nat Neurosci, vol. 9, no. 1, pp. 108-18, 2006.
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