Publications
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Filters: Keyword is DNA-Binding Proteins [Clear All Filters]
, “Long-Term Effects of Repetitive Mild Traumatic Injury on the Visual System in Wild-Type and TDP-43 Transgenic Mice.”, Int J Mol Sci, vol. 22, no. 12, 2021.
, “Repetitive Traumatic Brain Injury Is Associated With TDP-43 Alterations, Neurodegeneration, and Glial Activation in Mice.”, J Neuropathol Exp Neurol, vol. 80, no. 1, pp. 2-14, 2021.
, “TDP-43 triggers immune response via mitochondrial DNA release.”, Cell Res, vol. 31, no. 4, pp. 379-380, 2021.
, “Co-occurrence of mixed proteinopathies in late-stage Huntington's disease.”, Acta Neuropathol, vol. 135, no. 2, pp. 249-265, 2018.
, “Early retinal neurodegeneration and impaired Ran-mediated nuclear import of TDP-43 in progranulin-deficient FTLD.”, J Exp Med, vol. 211, no. 10, pp. 1937-45, 2014.
, “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.
, “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, pp. 18186-95, 2012.
, “Methylene blue administration fails to confer neuroprotection in two amyotrophic lateral sclerosis mouse models.”, Neuroscience, vol. 209, pp. 136-43, 2012.
, “TDP-43 aggregation in neurodegeneration: are stress granules the key?”, Brain Res, vol. 1462, pp. 16-25, 2012.
, “TDP-43 in central nervous system development and function: clues to TDP-43-associated neurodegeneration.”, Biol Chem, vol. 393, no. 7, pp. 589-94, 2012.
, “Accumulation of transactive response DNA binding protein 43 in mild cognitive impairment and Alzheimer disease.”, J Neuropathol Exp Neurol, vol. 70, no. 9, pp. 788-98, 2011.
, “ALS pathogenesis: recent insights from genetics and mouse models.”, Prog Neuropsychopharmacol Biol Psychiatry, vol. 35, no. 2, pp. 363-9, 2011.
, “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.
, “Identification of neuronal RNA targets of TDP-43-containing ribonucleoprotein complexes.”, J Biol Chem, vol. 286, no. 2, pp. 1204-15, 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, pp. 2610-26, 2011.
, “TDP-43 is directed to stress granules by sorbitol, a novel physiological osmotic and oxidative stressor.”, Mol Cell Biol, vol. 31, no. 5, pp. 1098-108, 2011.
, “TDP-43 is a developmentally regulated protein essential for early embryonic development.”, J Biol Chem, vol. 285, no. 9, pp. 6826-34, 2010.
, “Manipulation of protein kinases reveals different mechanisms for upregulation of heat shock proteins in motor neurons and non-neuronal cells.”, Mol Cell Neurosci, vol. 34, no. 1, pp. 20-33, 2007.
, “Neurochemical characterization of dopaminergic neurons in human striatum.”, Parkinsonism Relat Disord, vol. 11, no. 5, pp. 277-86, 2005.
, “Tyrosine hydroxylase-positive neurons intrinsic to the human striatum express the transcription factor Nurr1.”, Eur J Neurosci, vol. 20, no. 8, pp. 2089-95, 2004.
, “A novel syndrome of congenital lid and punctal anomalies, corneal and chorioretinal dystrophy.”, Ophthalmic Genet, vol. 24, no. 2, pp. 111-6, 2003.
, “The distinct HERG missense mutation L564P causes long QT syndrome in one French Canadian family.”, Can J Cardiol, vol. 16, no. 3, pp. 307-12, 2000.
, “Modulation of HERG potassium channel properties by external pH.”, Pflugers Arch, vol. 438, no. 3, pp. 419-22, 1999.
