1014 related articles for article (PubMed ID: 17352383)
1. Gangliosides contribute to stability of paranodal junctions and ion channel clusters in myelinated nerve fibers.
Susuki K; Baba H; Tohyama K; Kanai K; Kuwabara S; Hirata K; Furukawa K; Furukawa K; Rasband MN; Yuki N
Glia; 2007 May; 55(7):746-57. PubMed ID: 17352383
[TBL] [Abstract][Full Text] [Related]
2. Nodal protrusions, increased Schmidt-Lanterman incisures, and paranodal disorganization are characteristic features of sulfatide-deficient peripheral nerves.
Hoshi T; Suzuki A; Hayashi S; Tohyama K; Hayashi A; Yamaguchi Y; Takeuchi K; Baba H
Glia; 2007 Apr; 55(6):584-94. PubMed ID: 17299768
[TBL] [Abstract][Full Text] [Related]
3. Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants.
Ulzheimer JC; Peles E; Levinson SR; Martini R
Mol Cell Neurosci; 2004 Jan; 25(1):83-94. PubMed ID: 14962742
[TBL] [Abstract][Full Text] [Related]
4. The raft-associated protein MAL is required for maintenance of proper axon--glia interactions in the central nervous system.
Schaeren-Wiemers N; Bonnet A; Erb M; Erne B; Bartsch U; Kern F; Mantei N; Sherman D; Suter U
J Cell Biol; 2004 Aug; 166(5):731-42. PubMed ID: 15337780
[TBL] [Abstract][Full Text] [Related]
5. Paranodal axoglial junction is required for the maintenance of the Nav1.6-type sodium channel in the node of Ranvier in the optic nerves but not in peripheral nerve fibers in the sulfatide-deficient mice.
Suzuki A; Hoshi T; Ishibashi T; Hayashi A; Yamaguchi Y; Baba H
Glia; 2004 May; 46(3):274-83. PubMed ID: 15048850
[TBL] [Abstract][Full Text] [Related]
6. Spatiotemporal ablation of myelinating glia-specific neurofascin (Nfasc NF155) in mice reveals gradual loss of paranodal axoglial junctions and concomitant disorganization of axonal domains.
Pillai AM; Thaxton C; Pribisko AL; Cheng JG; Dupree JL; Bhat MA
J Neurosci Res; 2009 Jun; 87(8):1773-93. PubMed ID: 19185024
[TBL] [Abstract][Full Text] [Related]
7. Disruption of neurofascin and gliomedin at nodes of Ranvier precedes demyelination in experimental allergic neuritis.
Lonigro A; Devaux JJ
Brain; 2009 Jan; 132(Pt 1):260-73. PubMed ID: 18953054
[TBL] [Abstract][Full Text] [Related]
8. Induction of paranodal myelin detachment and sodium channel loss in vivo by Campylobacter jejuni DNA-binding protein from starved cells (C-Dps) in myelinated nerve fibers.
Piao H; Minohara M; Kawamura N; Li W; Mizunoe Y; Umehara F; Goto Y; Kusunoki S; Matsushita T; Ikenaka K; Maejima T; Nabekura J; Yamasaki R; Kira J
J Neurol Sci; 2010 Jan; 288(1-2):54-62. PubMed ID: 19880143
[TBL] [Abstract][Full Text] [Related]
9. Differential expression of gangliosides on the surfaces of myelinated nerve fibers.
Ganser AL; Kirschner DA
J Neurosci Res; 1984; 12(2-3):245-55. PubMed ID: 6502752
[TBL] [Abstract][Full Text] [Related]
10. CNP is required for maintenance of axon-glia interactions at nodes of Ranvier in the CNS.
Rasband MN; Tayler J; Kaga Y; Yang Y; Lappe-Siefke C; Nave KA; Bansal R
Glia; 2005 Apr; 50(1):86-90. PubMed ID: 15657937
[TBL] [Abstract][Full Text] [Related]
11. Anti-GM1 antibodies cause complement-mediated disruption of sodium channel clusters in peripheral motor nerve fibers.
Susuki K; Rasband MN; Tohyama K; Koibuchi K; Okamoto S; Funakoshi K; Hirata K; Baba H; Yuki N
J Neurosci; 2007 Apr; 27(15):3956-67. PubMed ID: 17428969
[TBL] [Abstract][Full Text] [Related]
12. Neurofascin interactions play a critical role in clustering sodium channels, ankyrin G and beta IV spectrin at peripheral nodes of Ranvier.
Koticha D; Maurel P; Zanazzi G; Kane-Goldsmith N; Basak S; Babiarz J; Salzer J; Grumet M
Dev Biol; 2006 May; 293(1):1-12. PubMed ID: 16566914
[TBL] [Abstract][Full Text] [Related]
13. Paranodal transverse bands are required for maintenance but not initiation of Nav1.6 sodium channel clustering in CNS optic nerve axons.
Rasband MN; Taylor CM; Bansal R
Glia; 2003 Nov; 44(2):173-82. PubMed ID: 14515333
[TBL] [Abstract][Full Text] [Related]
14. Proteomic analysis of optic nerve lipid rafts reveals new paranodal proteins.
Ogawa Y; Rasband MN
J Neurosci Res; 2009 Nov; 87(15):3502-10. PubMed ID: 19156860
[TBL] [Abstract][Full Text] [Related]
15. Localization of Caspr2 in myelinated nerves depends on axon-glia interactions and the generation of barriers along the axon.
Poliak S; Gollan L; Salomon D; Berglund EO; Ohara R; Ranscht B; Peles E
J Neurosci; 2001 Oct; 21(19):7568-75. PubMed ID: 11567047
[TBL] [Abstract][Full Text] [Related]
16. Ion channel redistribution and function during development of the myelinated axon.
Vabnick I; Shrager P
J Neurobiol; 1998 Oct; 37(1):80-96. PubMed ID: 9777734
[TBL] [Abstract][Full Text] [Related]
17. Glial regulation of the axonal membrane at nodes of Ranvier.
Schafer DP; Rasband MN
Curr Opin Neurobiol; 2006 Oct; 16(5):508-14. PubMed ID: 16945520
[TBL] [Abstract][Full Text] [Related]
18. Human gangliosides and bacterial lipo-oligosaccharides in the development of autoimmune neuropathies.
Yuki N
Methods Mol Biol; 2010; 600():51-65. PubMed ID: 19882120
[TBL] [Abstract][Full Text] [Related]
19. Tight junctions in Schwann cells of peripheral myelinated axons: a lesson from claudin-19-deficient mice.
Miyamoto T; Morita K; Takemoto D; Takeuchi K; Kitano Y; Miyakawa T; Nakayama K; Okamura Y; Sasaki H; Miyachi Y; Furuse M; Tsukita S
J Cell Biol; 2005 May; 169(3):527-38. PubMed ID: 15883201
[TBL] [Abstract][Full Text] [Related]
20. Molecular specializations at nodes and paranodes in peripheral nerve.
Scherer SS
Microsc Res Tech; 1996 Aug; 34(5):452-61. PubMed ID: 8837021
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
