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  • Berghs S, Aggujaro D, Dirkx R, Maksimova E, Stabach P, Hermel JM, Zhang JP, Philbrick W, Slepnev V, Ort T & Solimena M (2000). βIV spectrin, a new spectrin localized at axon initial segments and nodes of Ranvier in the central and peripheral nervous system. J Cell Biol 151, 9851001.
  • Bouzidi M, Tricaud N, Giraud P, Kordeli E, Caillol G, Deleuze C, Couraud F & Alcaraz G (2002). Interaction of the Nav1.2a subunit of the voltage-dependent sodium channel with nodal ankyrinG. In vitro mapping of the interacting domains and association in synaptosomes. J Biol Chem 277, 2899629004.
  • Brechet A, Fache MP, Brachet A, Ferracci G, Baude A, Irondelle M, Pereira S, Leterrier C & Dargent B (2008). Protein kinase CK2 contributes to the organization of sodium channels in axonal membranes by regulating their interactions with ankyrin G. J Cell Biol 183, 11011114.
  • Caldwell JH, Schaller KL, Lasher RS, Peles E & Levinson SR (2000). Sodium channel NaV1.6 is localized at nodes of Ranvier, dendrites, and synapses. Proc Natl Acad Sci U S A 97, 56165620.
  • Chung HJ, Jan YN & Jan LY (2006). Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domains. Proc Natl Acad Sci U S A 103, 88708875.
  • Cooper EC, Aldape KD, Abosch A, Barbaro NM, Berger MS, Peacock WS, Jan YN & Jan LY (2000). Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy. Proc Natl Acad Sci U S A 97, 49144919.
  • Davis JQ, Lambert S & Bennett V (1996). Molecular composition of the node of Ranvier: identification of ankyrin-binding cell adhesion molecules neurofascin (mucin+ third FNIII domain-) and NrCAM at nodal axon segments. J Cell Biol 135, 13551367.
  • Dedek K, Kunath B, Kananura C, Reuner U, Jentsch TJ & Steinlein OK (2001). Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel. Proc Natl Acad Sci U S A 98, 1227212277.
  • Devaux J, Alcaraz G, Grinspan J, Bennett V, Joho R, Crest M & Scherer SS (2003). Kv3.1b is a novel component of CNS nodes. J Neurosci 23, 45094518.
  • Devaux J & Gow A (2008). Tight junctions potentiate the insulative properties of small CNS myelinated axons. J Cell Biol 183, 909921.
  • Devaux JJ, Kleopa KA, Cooper EC & Scherer SS (2004). KCNQ2 is a nodal K+ channel. J Neurosci 24, 12361244.
  • Drummond GB (2009). Reporting ethical matters in The Journal of Physiology: standards and advice. J Physiol 587, 713719.
  • Garrido JJ, Giraud P, Carlier E, Fernandes F, Moussif A, Fache MP, Debanne D & Dargent B (2003). A targeting motif involved in sodium channel clustering at the axonal initial segment. Science 300, 20912094.
  • Gutmann L & Gutmann L (2004). Myokymia and neuromyotonia 2004. J Neurol 251, 138142.
  • Hart IK, Waters C, Vincent A, Newland C, Beeson D, Pongs O, Morris C & Newsom-Davis J (1997). Autoantibodies detected to express K+ channels are implicated in neuromyotonia. Ann Neurol 41, 238246.
  • Holleran EA, Ligon LA, Tokito M, Stankewich MC, Morrow JS & Holzbaur EL (2001). βIII spectrin binds to the Arp1 subunit of dynactin. J Biol Chem 276, 3659836605.
  • Jenkins SM & Bennett V (2002). Developing nodes of Ranvier are defined by ankyrin-G clustering and are independent of paranodal axoglial adhesion. Proc Natl Acad Sci U S A 99, 23032308.
  • Kharkovets T, Hardelin JP, Safieddine S, Schweizer M, El-Amraoui A, Petit C & Jentsch TJ (2000). KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway. Proc Natl Acad Sci U S A 97, 43334338.
  • Kleopa KA & Barchi RL (2002). Genetic disorders of neuromuscular ion channels. Muscle Nerve 26, 299325.
  • Kleopa KA, Elman LB, Lang B, Vincent A & Scherer SS (2006). Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations. Brain 129, 15701584.
  • Komada M & Soriano P (2002). βIV-spectrin regulates sodium channel clustering through ankyrin-G at axon initial segments and nodes of Ranvier. J Cell Biol 156, 337348.
  • Kubisch C, Schroeder BC, Friedrich T, Lutjohann B, El-Amraoui A, Marlin S, Petit C & Jentsch TJ (1999). KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell 96, 437446.
  • Lacas-Gervais S, Guo J, Strenzke N, Scarfone E, Kolpe M, Jahkel M, De Camilli P, Moser T, Rasband MN & Solimena M (2004). βIVSigma1 spectrin stabilizes the nodes of Ranvier and axon initial segments. J Cell Biol 166, 983990.
  • Lemaillet G, Walker B & Lambert S (2003). Identification of a conserved ankyrin-binding motif in the family of sodium channel α subunits. J Biol Chem 278, 2733327339.
  • Lonigro A & Devaux JJ (2009). Disruption of neurofascin and gliomedin at nodes of Ranvier precedes demyelination in experimental allergic neuritis. Brain 132, 260273.
  • Main MJ, Cryan JE, Dupere JR, Cox B, Clare JJ & Burbidge SA (2000). Modulation of KCNQ2/3 potassium channels by the novel anticonvulsant retigabine. Mol Pharmacol 58, 253262.
  • Martin PM, Carnaud M, delCano GG, Irondelle M, Irinopoulou T, Girault JA, Dargent B & Goutebroze L (2008). Schwannomin-interacting protein-1 isoform IQCJ-SCHIP-1 is a late component of nodes of Ranvier and axon initial segments. J Neurosci 28, 61116117.
  • Menegoz M, Gaspar P, Le Bert M, Galvez T, Burgaya F, Palfrey C, Ezan P, Arnos F & Girault J-A (1997). Paranodin, a glycoprotein of neuronal paranodal membranes. Neuron 19, 319331.
  • Morris JA, Kandpal G, Ma L & Austin CP (2003). DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation. Hum Mol Genet 12, 15911608.
  • Ogawa Y, Schafer DP, Horresh I, Bar V, Hales K, Yang Y, Susuki K, Peles E, Stankewich MC & Rasband MN (2006). Spectrins and ankyrinB constitute a specialized paranodal cytoskeleton. J Neurosci 26, 52305239.
  • Pan ZM, Kao TC, Horvath Z, Lemos J, Sul JY, Cranstoun SD, Bennett V, Scherer SS & Cooper EC (2006). A common ankyrin-G-based mechanism retains KCNQ and Na-V channels at electrically active domains of the axon. J Neurosci 26, 25992613.
  • Parkinson NJ, Olsson CL, Hallows JL, McKee-Johnson J, Keogh BP, NobenTrauth K, Kujawa SG & Tempel BL (2001). Mutant β-spectrin 4 causes auditory and motor neuropathies in quivering mice. Nat Genet 29, 6165.
  • Poliak S, Salomon D, Elhanany H, Sabanay H, Kiernan B, Pevny L, Stewart CL, Xu XR, Chiu SY, Shrager P, Furley AJW & Peles E (2003). Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1. J Cell Biol 162, 11491160.
  • Rasmussen HB, FrokjaerJensen C, Jensen CS, Jensen HS, Jorgensen NK, Misonou H, Trimmer JS, Olesen SP & Schmitt N (2007). Requirement of subunit co-assembly and ankyrin-G for M-channel localization at the axon initial segment. J Cell Sci 120, 953963.
  • Stankewich MC, Gwynn B, Ardito T, Ji L, Kim J, Robledo RF, Lux SE, Peters LL & Morrow JS (2010). Targeted deletion of βIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes. Proc Natl Acad Sci U S A 107, 60226027.
  • Susuki K & Rasband MN (2008). Molecular mechanisms of node of Ranvier formation. Curr Opin Cell Biol 20, 616623.
  • Traka M, Goutebroze L, Denisenko N, Bessa M, Nifli A, Havaki S, Iwakura Y, Fukamauchi F, Watanabe K, Soliven B, Girault JA & Karagogeos D (2003). Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers. J Cell Biol 162, 11611172.
  • Trudeau MM, Dalton JC, Day JW, Ranum LP & Meisler MH (2006). Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation. J Med Genet 43, 527530.
  • Vabnick I, Trimmer JS, Schwarz TL, Levinson SR, Risal D & Shrager P (1999). Dynamic potassium channel distributions during axonal development prevent aberrant firing patterns. J Neurosci 19, 747758.
  • Vincent A, Lang B & Kleopa KA (2006). Autoimmune channelopathies and related neurological disorders. Neuron 52, 123138.
  • Winkels R, Jedlicka P, Weise FK, Schultz C, Deller T & Schwarzacher SW (2009). Reduced excitability in the dentate gyrus network of βIV-spectrin mutant mice in vivo. Hippocampus 19, 677686.
  • Wuttke TV, Jurkat-Rott K, Paulus W, Garncarek M, Lehmann-Horn F & Lerche H (2007). Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations. Neurology 69, 20452053.
  • Yang Y, Lacas-Gervais S, Morest DK, Solimena M & Rasband MN (2004). βIV spectrins are essential for membrane stability and the molecular organization of nodes of Ranvier. J Neurosci 24, 72307240.
  • Yang Y, Ogawa Y, Hedstrom KL & Rasband MN (2007). βIV spectrin is recruited to axon initial segments and nodes of Ranvier by ankyrinG. J Cell Biol 176, 509519.
  • Zhou L, Messing A & Chiu SY (1999). Determinants of excitability at transition zones in Kv1.1-deficient myelinated nerves. J Neurosci 19, 57685781.