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, “Cytoskeletal defects in amyotrophic lateral sclerosis (motor neuron disease).”, Novartis Found Symp, vol. 264, pp. 183-92; discussion 192-6, 227-30, 2005.
, “Disordered RNA chaperone proteins: from functions to disease.”, Cell Mol Life Sci, vol. 62, no. 13, pp. 1409-17, 2005.
, “FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.”, Hum Mol Genet, vol. 14, no. 6, pp. 835-44, 2005.
, “Morphology and distribution of dopaminergic neurons intrinsic to the human striatum.”, J Chem Neuroanat, vol. 29, no. 1, pp. 1-11, 2005.
, “Neurochemical characterization of dopaminergic neurons in human striatum.”, Parkinsonism Relat Disord, vol. 11, no. 5, pp. 277-86, 2005.
, “Neuronal fate determinants of adult olfactory bulb neurogenesis.”, Nat Neurosci, vol. 8, no. 7, pp. 865-72, 2005.
, “Up-regulation of peripherin is associated with alterations in synaptic plasticity in CA1 and CA3 regions of hippocampus.”, Neurobiol Dis, vol. 18, no. 2, pp. 409-20, 2005.
, “[35S]Methionine metabolic labeling to study axonal transport of neuronal intermediate filament proteins in vivo.”, Methods Cell Biol, vol. 78, pp. 555-71, 2004.
, “Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles.”, Proc Natl Acad Sci U S A, vol. 101, no. 36, pp. 13357-62, 2004.
, “The C-terminal region as a modulator of rNa(v)1.7 and rNa(v)1.8 expression levels.”, FEBS Lett, vol. 559, no. 1-3, pp. 39-44, 2004.
, “Differential modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by the local anesthetic lidocaine.”, Br J Pharmacol, vol. 142, no. 3, pp. 576-84, 2004.
, “Evidence of newly generated neurons in the human olfactory bulb.”, Brain Res Dev Brain Res, vol. 151, no. 1-2, pp. 159-68, 2004.
, “The fragile X mental retardation protein has nucleic acid chaperone properties.”, Nucleic Acids Res, vol. 32, no. 7, pp. 2129-37, 2004.
, “A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis.”, J Biol Chem, vol. 279, no. 44, pp. 45951-6, 2004.
, “Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome.”, J Med Genet, vol. 41, no. 4, p. e43, 2004.
, “Modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by protein kinase A and protein kinase C.”, J Neurophysiol, vol. 91, no. 4, pp. 1556-69, 2004.
, “Role of auxiliary beta1-, beta2-, and beta3-subunits and their interaction with Na(v)1.8 voltage-gated sodium channel.”, Biochem Biophys Res Commun, vol. 319, no. 2, pp. 531-40, 2004.
, “82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization.”, Hum Mol Genet, vol. 12, no. 14, pp. 1689-98, 2003.
, “Autosomal dominant macular dystrophy in a large Canadian family.”, Can J Ophthalmol, vol. 38, no. 1, pp. 33-40, 2003.
, “Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs.”, Hum Mol Genet, vol. 12, no. 23, pp. 3087-96, 2003.
, “A neurotoxic peripherin splice variant in a mouse model of ALS.”, J Cell Biol, vol. 160, no. 6, pp. 939-49, 2003.
, “Peripherin is not a contributing factor to motor neuron disease in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase.”, Neurobiol Dis, vol. 13, no. 2, pp. 158-66, 2003.
, “Peripherin-mediated death of motor neurons rescued by overexpression of neurofilament NF-H proteins.”, J Neurochem, vol. 85, no. 1, pp. 248-56, 2003.
, “Induction of peripherin expression in subsets of brain neurons after lesion injury or cerebral ischemia.”, Brain Res, vol. 946, no. 2, pp. 153-61, 2002.
, “Pathways to motor neuron degeneration in transgenic mouse models.”, Biochimie, vol. 84, no. 11, pp. 1151-60, 2002.
