Publications
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, “Neurofilament depletion improves microtubule dynamics via modulation of Stat3/stathmin signaling.”, Acta Neuropathol, vol. 132, no. 1, pp. 93-110, 2016.
, “Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis.”, Hum Mol Genet, 2016.
, “Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis.”, Hum Mol Genet, vol. 25, no. 21, pp. 4771-4786, 2016.
, “CD11b+Ly6G- myeloid cells mediate mechanical inflammatory pain hypersensitivity.”, Proc Natl Acad Sci U S A, vol. 112, no. 49, pp. E6808-17, 2015.
, “Dissociation of Axonal Neurofilament Content from Its Transport Rate.”, PLoS One, vol. 10, no. 7, p. e0133848, 2015.
, “Early and persistent abnormal decoding by glial cells at the neuromuscular junction in an ALS model.”, J Neurosci, vol. 35, no. 2, pp. 688-706, 2015.
, “Early-stage treatment with Withaferin A reduces levels of misfolded superoxide dismutase 1 and extends lifespan in a mouse model of amyotrophic lateral sclerosis.”, Neurotherapeutics, vol. 12, no. 1, pp. 217-33, 2015.
, “Functions of neurofilaments in synapses.”, Mol Psychiatry, vol. 20, no. 8, p. 915, 2015.
, “Inflammation Induces TDP-43 Mislocalization and Aggregation.”, PLoS One, vol. 10, no. 10, p. e0140248, 2015.
, “Neurofilament subunits are integral components of synapses and modulate neurotransmission and behavior in vivo.”, Mol Psychiatry, vol. 20, no. 8, pp. 986-94, 2015.
, “Type II spiral ganglion afferent neurons drive medial olivocochlear reflex suppression of the cochlear amplifier.”, Nat Commun, vol. 6, p. 7115, 2015.
, “Ubiquilin-2 drives NF-κB activity and cytosolic TDP-43 aggregation in neuronal cells.”, Mol Brain, vol. 8, no. 1, p. 71, 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, pp. 498-510, 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.
, “Loss of glial neurofascin155 delays developmental synapse elimination at the neuromuscular junction.”, J Neurosci, vol. 34, no. 38, pp. 12904-18, 2014.
, “Axonal transport deficits and neurodegenerative diseases.”, Nat Rev Neurosci, vol. 14, no. 3, pp. 161-76, 2013.
, “Giant axonal neuropathy-associated gigaxonin mutations impair intermediate filament protein degradation.”, J Clin Invest, vol. 123, no. 5, pp. 1964-75, 2013.
, “Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1.”, Hum Mol Genet, vol. 22, no. 19, pp. 3947-59, 2013.
, “Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival.”, Neuron, vol. 80, no. 1, pp. 80-96, 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, pp. 18186-95, 2012.
, “Local electronic structure and Fano interference in tunneling into a Kondo hole system.”, Phys Rev Lett, vol. 108, no. 18, p. 186401, 2012.
, “Localization of a toxic form of superoxide dismutase 1 protein to pathologically affected tissues in familial ALS.”, Proc Natl Acad Sci U S A, vol. 109, no. 14, pp. 5505-10, 2012.
, “Methylene blue administration fails to confer neuroprotection in two amyotrophic lateral sclerosis mouse models.”, Neuroscience, vol. 209, pp. 136-43, 2012.
, “Normal role of the low-molecular-weight neurofilament protein in mitochondrial dynamics and disruption in Charcot-Marie-Tooth disease.”, FASEB J, vol. 26, no. 3, pp. 1194-203, 2012.
