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References

  • Adelman JP, Bond CT, Pessia M, Maylie J (1995). Episodic ataxia results from voltage-dependent potassium channels with altered functions. Neuron 15:14491454.
  • Arroyo EJ, Scherer SS (2000). On the molecular architecture of myelinated fibers. Histochem Cell Biol 113:118.
  • Arroyo EJ, Xu Y-T, Zhou L, Messing A, Peles E, Chiu SY, Scherer SS (1999). Myelinating Schwann cells determine the internodal localization of Kv1.1, Kv1.2, Kvβ2, and Caspr. J Neurocytol 28:333347.
  • Balice-Gordon RJ, Bone LJ, Scherer SS (1998). Functional gap junctions in the Schwann cell myelin sheath. J Cell Biol 142:10951104.
  • Bartsch U, Pesheva P, Raff M, Schachner M (1993). Expression of janusin (J1-160/180) in the retina and optic nerve of the developing and adult mouse. Glia 9:5769.
  • Bennett V, Lambert S, Davis JQ, Zhang X (1997). Molecular architecture of the specialized axonal membrane at the node of Ranvier. Soc Gen Physiol 52:107120.
  • Berghs S, Aggujaro D, Dirkx R, Maksimova E, Stabach P, Hermel JM, Zhang JP, Philbrick W, Slepnev V, Ort T, Solimena M (2000). Beta IV 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.
  • Bergoffen J, Scherer SS, Wang S, Oronzi-Scott M, Bone L, Paul DL, Chen K, Lensch MW, Chance P, Fischbeck K (1993). Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science 262:20392042.
  • Bhat MA, Rios JC, Lu Y, Garcia-Fresco GP, Ching W, St. Martin M, Li JJ, Einheber S, Chesler M, Rosenbluth J, Salzer JL, Bellen HJ (2001). Axon-glia interactions and the domain organization of myelinated axons requires Neurexin IV/Caspr/Paranodin. Neuron 30:369383.
  • Boerkoel CF, Takashima H, Stankiexicz P, Garcia CA, Leber SM, Rhee-Morris L, Lupski JR (2000). Periaxin mutations cause recessive Dejerine-Sottas neuropathy. Am J Hum Genet 68:325333.
  • Boiko T, Rasband MN, Levinson SR, Coldwell JH, Mandel G, Trimmer JS, Matthews G (2001). Compact myelin dictates the differential targeting of two sodium channel isoforms in the same axon. Neuron 30:91104.
  • Bosio A, Binczek E, Stoffel W (1996). Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system myelin by disrupted galactocerebroside synthesis. Proc Natl Acad Sci USA 93:1328013285.
  • Bosio A, Bussow H, Adam J, Stoffel W (1998). Galactosphingolipids and axon-glial interaction in myelin of the central nervous system. Cell Tissue Res 292:199210.
  • Boyle MET, Berglund EO, Murai KK, Weber L, Peles E, Ranscht B (2001). Contactin orchestrates assembly of the septate-like junctions at the paranode in myelinated peripheral nerve. Neuron 30:385397.
  • Browne DL, Gancher ST, Nutt JG, Brunt ERP, Smith EA, Kramer P, Litt M (1994). Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nature Genet 8:136140.
  • Brunt ERP, Van Weerden TW (1990). Familial paroxysmal kinesigenic ataxia and continuous myokymia. Brain 113:13611382.
  • Bunge MB (1993). Schwann Cell Regulation of Extracellular Matrix Biosynthesis and Assembly. In: Peripheral Neuropathy. DyckPJ, ThomasPK, LowPA, PodusloJF (Eds). W.B. Saunders, Philadelphia, Vol. 1, pp 229316.
  • Burgess DL, Kohrman DC, Galt J, Plummer NW, Jones JM, Spear B, Meisler MH (1995). Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’. Nature Genet 10:461465.
  • 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 Nat Acad Sci USA 97:56165620.
  • Chandross KJ, Kessler JA, Cohen RI, Simburger E, Spray DC, Bieri P, Dermietzel R (1996). Altered connexin expression after peripheral nerve injury. Mol Cell Neurosci 7:501518.DOI: 10.1006/mcne.1996.0036
  • Chiu SY, Ritchie JM (1980). Potassium channels in nodal and internodal axonal membrane of mammalian myelinated fibres. Nature 284:170171.
  • Coetzee T, Dupree JL, Popko B (1998). Demyelination and altered expression of myelin-associated glycoprotein isoforms in the central nervous system of galactolipid-deficient mice. J Neurosci Res 54:613622.
  • Coetzee T, Fujita N, Dupree J, Shi R, Blight A, Suzuki K, Suzuki K, Popko B (1996). Myelination in the absence of galactocerebroside and sulfatide: normal structure with abnormal function and regional instability. Cell 86:209219.
  • Comi G, Ciafaloni E, De Silva HAR, Prelle A, Bardoni A, Rigoletto C, Robotti M, Bresolin N, Moggio M, Fortunato F, Ciscato P, Turconi A, Roses AD, Scarlato G (1995). A G+1[RIGHTWARDS ARROW] A transversion at the 5′ splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient. Hum Mol Gen 4:21712174.
  • D'Urso D, Ehrhardt P, Muller HW (1999). Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin. J Neurosci 19:33963403.
  • D'Urso D, Prior R, Greiner-Petter R, Gabreels-Festen AAWM, Muller HW (1998). Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22. J Neurosci 18:731740.
  • Davis JQ, Bennett V (1994). Ankyrin binding activity shared by the neurofascin/L1/NrCAM family of nervous system cell adhesion molecules. J Biol Chem 269:2716327166.
  • 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.
  • Davis JQ, McLaughlin T, Bennett V (1993). Ankyrin-binding proteins related to nervous system cell adhesion molecules: candidates to provide transmembrane and intercellular connections in adult brain. J Cell Biol 121:121133.
  • Duchen LW, Stefani E (1971). Electrophysiological studies of neuromuscular transmission hereditary “motor end-plate disease” of the mouse. J Physiol 212:535548.
  • Dupree JL, Coetzee T, Blight A, Suzuki K, Popko B (1998). Myelin galactolipids are essential for proper node of Ranvier formation in the CNS. J Neurosci 18:16421649.
  • Dupree JL, Girault JA, Popko B (1999). Axo-glial interactions regulate the localization of axonal paranodal proteins. J Cell Biol 147:11451151.
  • Einheber S, Milner T, Giancotti F, Salzer J (1993). Axonal regulation of Schwann cell integrin expression suggests a role for α6β4 in myelination. J Cell Biol 123:625638.
  • Einheber S, Zanazzi G, Ching W, Scherer SS, Milner TA, Peles E, Salzer JL (1997). The axonal membrane protein Caspr/Neurexin IV is a component of the septate-like paranodal junctions that assemble during myelination. J Cell Biol 139:14951506.
  • Ellisman MH, Levinson SR (1982). Immunocytochemical localization of sodium channel distributions in the excitable membranes of Electrophorus electricus. Proc Natl Acad Sci USA 79:67076711.
  • Fannon AM, Sherman DL, Ilyina-Gragerova G, Brophy PJ, Friedrich VL, Colman DR (1995). Novel E-cadherin mediated adhesion in peripheral nerve: Schwann cell architecture is stabilized by autotypic adherens junctions. J Cell Biol 129:189202.
  • Feder N (1971). Microperoxidase—an ultrastructural tracer of low molecular weight. J Cell Biol 51:339343.
  • Feltri ML, Scherer SS, Nemni R, Kamholz J, Vogelbacker H, Oronzi-Scott M, Canal N, Quaranta V, Wrabetz L (1994). β4 integrin expression in myelinating Schwann cells is ab-axonally polarized, developmentally-regulated, and axonally-dependent. Development 120:12871301.
  • Ffrench-Constant C, Miller RH, Kruse J, Schachner M, Raff MC (1986). Molecular specialization of astrocyte processes at nodes of Ranvier in rat optic nerve. J Cell Biol 102:844852.
  • Fjell J, Hjelmstrom P, Hormuzdiar W, Milenkovic M, Aglieco F, Tyrrell L, Dib-Haji S, Waxman SG, Black JA (2000). Localization of the tetrodotoxin-resistant sodium channel NaN in nociceptors. Neuroreport 11:199202.
  • Frei R, Dowling J, Carenini S, Fuchs E, Martini R (1999). Myelin formation by Schwann cells in the absence of β4 integrin. Glia 27:269274.
  • Funch PG, Faber DS (1984). Measurement of myelin sheath resistances: implications for axonal conduction and pathophysiology. Science 225:538540.
  • Gabreels-Festen AAWM, Hoogendijk JE, Meijerink PHS, Gabreels FJM, Bolhuis PA, Vanbeersum S, Kulkens T, Nelis E, Jennekens FGI, Devisser M, Vanengelen BGM, Van Broeckhoven C, Mariman ECM (1996). Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease. Neurology 47:761765.
  • Giese KP, Martini R, Lemke G, Soriano P, Schachner M (1992). Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons. Cell 71:565576.
  • Gillespie CS, Sherman DL, Fleetwood-Walker SM, Cottrell DF, Tait S, Garry EM, Wallace VCJ, Ure J, Griffiths IR, Smith A, Brophy PJ (2000). Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice. Neuron 26:523531.
  • Guilbot A, Williams A, Ravise N, Verny C, Brice A, Sherman DL, Brophy PJ, LeGuern E, Delague V, Bareil C, Megarbane A, Claustres M (2001). A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease. Hum Mol Genet 10:415421.
  • Gulbis JM, Mann S, MacKinnon R (1999). Structure of a voltage-dependent K+ channel beta subunit. Cell 97:943952.
  • Haimovich B, Bonilla E, Casadei J, Barchi RL (1984). Immunocytochemical localization of the mammalian voltage-dependent sodium channel using polyclonal antibodies against the purified protein. J Neurosci 4:22592268.
  • Hall SM, Williams PL (1970). Studies on the ‘incisures’ of Schmidt and Lanterman. J Cell Sci 6:767791.
  • Hayashi K, Yonemura S, Matsui T, Tsukita S, Tsukita S (1999). Immunofluorescence detection of ezrin/radixin/moesin (ERM) proteins with their carboxyl-terminal threonine phosphorylated in cultured cells and tissues. Application of a novel fixation protocol using trichloroacetic acid (TCA) as a fixative. J Cell Sci 112:11491158.
  • Hildebrand C, Bowe CM, Remahl IN (1994). Myelination and myelin sheath remodelling in normal and pathological PNS nerve fibres. Prog Neurobiol 43:85141.
  • Hirano A, Becker NH, Zimmerman HM (1969). Isolation of the periaxonal space of the central myelinated nerve fiber with regard to the diffusion of peroxidase. J Histochem Cytochem 17:512516.
  • Hopkins WF, Allen ML, Mouamed KM, Tempel BL (1994). Properties of voltage-gated K+ currents expressed in Xenopus oocytes by mKv1.1, mKv1.2 and their heteromultimers as revealed by mutagenesis of the dendrotoxin-binding site in Kv1.1. Pflügers Arch 428:382390.
  • Ichimura T, Ellisman MH (1991). Three-dimensional fine structure of cytoskeletal-membrane interactions at nodes of Ranvier. J Neurocytol 20:667681.
  • Imumura M, Araishi K, Noguchi S, Ozawa E (2000). A sarcoglycan-dystrophin complex anchors DP116 and utrophin in the peripheral nervous system. Hum Mol Genet 9:30913100.
  • Kaplan MR, Cho M-H, Ullian EM, Isom LL, Levinson SR, Barres BA (2001). Differential control of clustering of the sodium channels Nav1.2 and Nav1.6 at developing CNS nodes of Ranvier. Neuron 40:105119.
  • Kocsis JD, Ruiz JA, Waxman SG (1983). Maturation of mammalian myelinated fibers: changes in action-potential characteristics following 4-aminopyridine application. J Neurophysiol 50:449463.
  • Koenig E, Repasky E (1985). A regional analysis of α-spectrin in the isolated Mauthner neuron and in isolated axons of the goldfish and rabbit. J Neurosci 5:705714.
  • Kordeli E, Davis J, Trapp B, Bennett V (1990). An isoform of ankyrin is localized at nodes of Ranvier in myelinated axons of central and peripheral nerves. J Cell Biol 110:13411352.
  • Kordeli E, Lambert S, Bennett V (1995). AnkyrinG: a new ankyrin gene with neural-specific isoforms localized at the axonal initial segment and node of Ranvier. J Biol Chem 270:23522359.
  • Kreusch A, Pfaffinger PJ, Stevens CF, Choe S (1998). Crystal structure of the tetramerization domain of the Shaker potassium channel. Nature 392:945948.
  • Lambert S, Davis JQ, Bennett V (1997). Morphogenesis of the node of Ranvier: co-clusters of ankyrin and ankyrin-binding integral proteins define early developmental intermediates. J Neurosci 17:70257036.
  • MacKenzie ML, Ghabriel MN, Allt G (1984). Nodes of Ranvier and Schmidt-Lanterman incisures: an in vivo lanthanum tracer study. J Neurocytol 13:10431055.
  • Matsumura K, Yamada H, Saito F, Sunada Y, Shimizu T (1997). Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse. Neuromuscular Disord 7:712.
  • Melendez-Vasquez CV, Rios JC, Zanazzi G, Lambert S, Bretscher A, Salzer JL (2001). Nodes of Ranvier form in association with ezrin-radixin-moesin (ERM)-positive Schwann cell processes. Proc Nat Acad Sci USA 98:12351240.
  • 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.
  • Mi HY, Deerinck TJ, Ellisman MH, Schwarz TL (1995). Differential distribution of closely related potassium channels in rat Schwann cells. J Neurosci 15:37613774.
  • Mikol DD, Hong HL, Cheng HL, Feldman EL (1999). Caveolin-1 expression in Schwann cells. Glia 27:3952.
  • Miller RG, Da Silva PP (1977). Particle rosettes in the periaxonal Schwann cell membrane and particle clusters in the axolemma of rat sciatic nerve. Brain Res 130:135141.
  • Mirsky R, Jessen KR (1999). The neurobiology of Schwann cells. Brain Pathol 9:293311.
  • Murakami T, Garcia CA, Reiter LT, Lupski JR (1996). Charcot-Marie-Tooth disease and related inherited neuropathies. Medicine 75:233250.DOI: 10.1097/00005792-199609000-00001
  • Naef R, Adlkofer K, Lescher B, Suter U (1997). Aberrant protein trafficking in Trembler suggests a disease mechanism for hereditary human peripheral neuropathies. Mol Cell Neurosci 9:1325.
  • Naef R, Suter U (1999). Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies. Neurobiol Disease 6:114.
  • Notterpek L, Shooter EM, Snipes GJ (1997). Upregulation of the endosomal-lysosomal pathway in the Trembler-J neuropathy. J Neurosci 17:41904200.
  • Ohara R, Yamakawa H, Nakayama M, Ohara O (2000). Type II brain 4.1 (4.1B/KIAA0987), a member of the protein 4.1 family, is localized to neuronal paranodes. Mol Brain Res 85:4152.
  • Ozawa E, Noguchi S, Mizuno Y, Hagiwara Y, Yoshida M (1998). From dystrophinopathy to sarcoglycanopathy: evolution of the concept of muscular dystrophy. Muscle Nerve 21:421438.DOI: 10.1002/(sici)1097-4598(199804)21:4<421::aid-mus1>3.0.co;2-b
  • Parkinson NJ, Olsson CL, Hallows JL, McKee-Johnson J, Keogh BP, Noben-Trauth K, Kujawa SG, Tempel BL (2001). Mutant beta-spectrin 4 causes auditory and motor neuropathies in quivering mice. Nat Genet 29:6165.
  • Parra M, Gascard P, Walensky LD, Gimm JA, Blackshaw S, Chan N, Takakuwa Y, Berger T, Lee G, Chasis JA, Snyder SH, Mohandas N, Conboy JG (2000). Molecular and functional characterization of protein 4.1B, a novel member of the protein 4.1 family with high level, focal expression in brain. J Biol Chem 275:32473255.
  • Peles E, Salzer JL (2000). Molecular domains of myelinated fibers. Curr Opin Neurobiol 10:558565.
  • Podratz JL, Rodriguez EH, DiNonno ES, Windebank AJ (1998). Myelination by Schwann cells in the absence of extracellular matrix assembly. Glia 23:383388.DOI: 10.1002/(sici)1098-1136(199808)23:4<383::aid-glia10>3.0.co;2-o
  • Poliak S, Gollan L, Martinez R, Custer A, Einheber S, Salzer JL, Trimmer J, Shrager P, Peles E (1999). Caspr2, a new member of the neurexin superfamily is localized at the juxtaparanodes of myelinated axons and associates with K+ channels. Neuron 24:10371047.
  • Poliak S, Gollan L, Salomon D, Berglund EO, Ranscht B, Peles E (2001). Localization of Caspr2 in myelinated nerves depends on axon-glia interactions and the generation of barriers along the axon. J Neurosci 21:75687575.
  • Popko B (2000). Myelin galactolipids: Mediators of axon-glial interactions? Glia 29:149153.
  • Raine CS (1982). Differences between the nodes of Ranvier of large and small diameter fibres in the P.N.S. J Neurocytol 11:935947.
  • Rambukkana A (2001). Molecular basis for the peripheral nerve predilection of Mycobacterium leprae. Curr Opin Microbiol 4:2127.
  • Ramón y Cajal S (1928). Degeneration and Regeneration of the Nervous System. May RM (Ed). Oxford University Press, Oxfordp 769.
  • Rasband M, Trimmer JS, Schwarz TL, Levinson SR, Ellisman MH, Schachner M, Shrager P (1998). Potassium channel distribution, clustering, and function in remyelinating rat axons. J Neurosci 18:3647.
  • Rieger F, Daniloff JK, Pincon-Raymond M, Crossin KC, Grumet M, Edelman GM (1986). Neuronal cell adhesion molecules and cytotactin are colocalized at the node of Ranvier. J Cell Biol 103:379391.
  • Rieger F, Pincon-Raymond M, Lombet A, Ponzio G, Lazdunski M, Sidman RL (1984). Paranodal dysmyelination and increase in tetrodotoxin binding sites in the sciatic nerve of the motor end-plate disease (med/med) mouse during postnatal development. Dev Biol 101:401409.
  • Rios JC, Melandez-Vasquez CV, Einheber S, Lustig M, Grumet M, Hemperly J, Peles E, Salzer JL (2000). Contactin-associated protein (Caspr) and contactin form a complex that is targeted to the paranodal junctions during myelination. J Neurosci 20:83548364.
  • Rosenbluth J (1976). Intramembranous particle distribution at the node of Ranvier and adjacent axolemma in myelinated axons of the frog brain. J Neurocytol 5:731745.
  • Samsam M, Frei R, Marziniak M, Martini R, Sommer C (2002). Impaired sensory function in heterozygous P0 knockout mice is associated with nodal changes in sensory nerves. J Neurosci Res 67:167173.DOI: 10.1002/jnr.10115
  • Sandri C, Van Buren JM, Akert K (1982). Membrane morphology of the vertebrate nervous system. Prog Brain Res 46:201265.
  • Scherer SS, Deschênes SM, Xu Y-T, Grinspan JB, Fischbeck KH, Paul DL (1995). Connexin32 is a myelin-related protein in the PNS and CNS. J Neurosci 15:82818294.
  • Scherer SS, Salzer JL (1996). Axon-Schwann Cell Interactions in Peripheral Nerve Regeneration. In: Glial Cell Development. JessenKR, RichardsonWD (Eds). Oxford University Press, Oxford, pp 299330.
  • Scherer SS, Xu T, Crino P, Arroyo EJ, Gutmann DH (2001). Ezrin, radixin, and moesin are components of Schwann cell microvilli. J Neurosci Res 65:150164.
  • Shapiro L, Doyle JP, Hensley P, Colman DR, Hendrickson WA (1996). Crystal stucture of the extracellular domain from P0, the major structural protein of peripheral nerve myelin. Neuron 17:435449.
  • Sherman DL, Fabrizi C, Gillespie CS, Brophy PJ (2001). Specific disruption of a Schwann cell dystrophin-related protein complex in a demyelinating neuropathy. Neuron 30:677687.DOI: 10.1016/s0896-6273(01)00327-0
  • Shorer Z, Philpot J, Muntoni F, Sewry C, Dubowitz V (1995). Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy. J Child Neurol 10:472475.
  • Smart SL, Lopantsev V, Zhang CL, Robbins CA, Wang H, Chiu SY, Schwartzkroin PA, Messing A, Tempel BL (1998). Deletion of the Kv1.1 potassium channel causes epilepsy in mice. Neuron 20:809819.
  • Srinivasan Y, Elmer L, Davis H, Bennett V, Angelides K (1988). Ankyrin and spectrin associate with voltage-dependent sodium channels in brain. Nature 333:177180.
  • Stolinski C, Breathnach AS (1982). Freeze-fracture replication of mammalian peripheral nerve—a review. J Neurol Sci 57:128.
  • Stolinski C, Breathnach AS, Martin B, Thomas PK, King RMH, Gabriel G (1981). Associated particle aggregates in juxtaparanodal axolemma and adaxonal Schwann cell membrane of rat peripheral nerve. J Neurocytol 10:679691.
  • Stolinski C, Breathnach AS, Thomas PK, Gabriel G, King RMH (1985). Distribution of particle aggregates in the internodal axolemma and adaxonal Schwann cell membrane of rodent peripheral nerve. J Neurol Sci 67:213222.
  • Straub V, Campbell KP (1997). Muscular dystrophies and the dystrophin-glycoprotein complex. Curr Opin Neurol 10:168175.
  • Sunada Y, Bernier SM, Kozak CA, Yamada Y, Campbell KP (1994). Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. J Biol Chem 269:1372913732.
  • Suter U, Snipes GJ (1995). Biology and genetics of hereditary motor and sensory neuropathies. Annu Rev Neurosci 18:4575.
  • Tait S, Gunn-Moore F, Collinson JM, Huang J, Lubetzki C, Pedraza L, Sherman DL, Colman DR, Brophy PJ (2000). An oligodendrocyte cell adhesion molecule at the site of assembly of the paranodal axo-glial junction. J Cell Biol 150:657666.
  • Tao-Cheng J-H, Rosenbluth J (1984). Extranodal particle accumulations in the axolemma of myelinated frog optic axons. Brain Res 308:289300.
  • Thomas PK, Olsson Y (1993). Microscopic Anatomy and Function of the Connective Tissue Components of Peripheral Nerve. In: Peripheral Neuropathy. DyckPJ, ThomasPK, GriffinJW, LowPA, PodusloJF (Eds). W.B. Saunders, Philadelphia, pp 97120.
  • Tobler AR, Notterpek L, Naef R, Taylor V, Suter U, Shooter EM (1999). Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction. J Neurosci 19:20272036.
  • Trapp BD, Andrews SB, Wong A, O'Connell M, Griffin JW (1989). Co-localization of the myelin-associated glycoprotein and the microfilament components, F-actin and spectrin, in Schwann cells of myelinated nerve fibers. J Neurocytol 18:4760.
  • Vabnick I, Shrager P (1998). Ion channel redistribution and function during development of the myelinated axon. J Neurobiol 37:8096.DOI: 10.1002/(sici)1097-4695(199810)37:1<80::aid-neu7>3.3.co;2-u
  • 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.
  • Vallat JM, Sindou P, Preux PM, Tabaraud F, Milor AM, Couratier P, Leguern E, Brice A (1996). Ultrastructural PMP22 expression in inherited demyelinating neuropathies. Ann Neurol 39:813817.
  • Van Dyke DH, Griggs RC, Murphy MJ, Goldstein MN (1975). Hereditary myokymia and periodic ataxia. J Neurol Sci 25:109118.
  • Vonasek E, Mateu L, Luzzati V, Marquez G, Vargas R, Cespedes G, Cotua M, Borges J (2001). A reversible abnormal form of myelin: an X-ray scattering study of human sural and rat sciatic nerves. Eur Biophys J Biophys Lett 30:1116.
  • Wang H, Kunkel DD, Martin TM, Schwartkroin PA, Tempel BL (1993). Heteromultimeric K+ channels in terminal and juxtaparanodal regions of neurons. Nature 365:7579.
  • Xiao ZC, Ragsdale DS, Malhotra JD, Mattei LN, Braun PE, Schachner M, Isom LL (1999). Tenascin-R is a functional modulator of sodium channel beta subunits. J Biol Chem 274:2651126517.
  • Xu H, Wu X-R, Wewer UM, Engvall E (1994). Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene. Nature Genet 8:297302.
  • Yamada H, Denzer AJ, Hori H, Tanaka T, Anderson LVB, Fujita S, Fukutaohi H, Shimizu T, Ruegg MA, Matsumura K (1996). Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membrane. J Biol Chem 271:2341823423.
  • Zerr P, Adelman JP, Maylie J (1998). Episodic ataxia mutations in Kv1.1 alter potassium channel function by dominant negative effects or haploinsufficiency. J Neurosci 18:28422848.
  • Zhang X, Bennett V (1996). Identification of O-linked N-acetylglucosamine modification of ankyrinG isoforms targeted to nodes of Ranvier. J Biol Chem 271:3139131398.
  • Zhou DX, Lambert S, Malen PL, Carpenter S, Boland LM, Bennett V (1998a). AnkyrinG is required for clustering of voltage-gated Na channels at axon initial segments and for normal action potential firing. J Cell Biol 143:12951304.
  • Zhou L, Zhang CL, Messing A, Chiu SY (1998b). Temperature-sensitive neuromuscular transmission in Kv1.1 null mice: Role of potassium channels under the myelin sheath in young nerves. J Neurosci 18:72007215.