-
1
-
-
0034950760
-
Expression of connexin 43 and connexin 32 gap-junction proteins in epilepsy-associated brain tumors and in the perilesional epileptic cortex
-
Aronica E, Gorter JA, Jansen GH, Leenstra S, Yankaya B, Troost D (2001) Expression of connexin 43 and connexin 32 gap-junction proteins in epilepsy-associated brain tumors and in the perilesional epileptic cortex. Acta Neuropathol 101:449-459
-
(2001)
Acta Neuropathol
, vol.101
, pp. 449-459
-
-
Aronica, E.1
Gorter, J.A.2
Jansen, G.H.3
Leenstra, S.4
Yankaya, B.5
Troost, D.6
-
2
-
-
0027772413
-
Connexin mutations in X-linked Charcot-Marie-Tooth disease
-
Bergoffen J, Scherer SS, Wang S et al (1993) Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science 262:2039-2042
-
(1993)
Science
, vol.262
, pp. 2039-2042
-
-
Bergoffen, J.1
Scherer, S.S.2
Wang, S.3
-
3
-
-
34848834431
-
MLC1 is associated with the dystrophin-glycoprotein complex at astrocytic endfeet
-
Boor I, Nagtegaal M, Kamphorst W et al (2007) MLC1 is associated with the dystrophin-glycoprotein complex at astrocytic endfeet. Acta Neuropathol 114:403-410
-
(2007)
Acta Neuropathol
, vol.114
, pp. 403-410
-
-
Boor, I.1
Nagtegaal, M.2
Kamphorst, W.3
-
5
-
-
0024535322
-
Differential ultrastructural localization of myelin basic protein, myelin/oligodendroglial glycoprotein, and 2',3'-cyclic nucleotide 3'-phosphodiesterase in the CNS of adult rats
-
Brunner C, Lassmann H, Waehneldt TV, Matthieu JM, Linington C (1989) Differential ultrastructural localization of myelin basic protein, myelin/oligodendroglial glycoprotein, and 2',3'-cyclic nucleotide 3'-phosphodiesterase in the CNS of adult rats. J Neurochem 52:296-304
-
(1989)
J Neurochem
, vol.52
, pp. 296-304
-
-
Brunner, C.1
Lassmann, H.2
Waehneldt, T.V.3
Matthieu, J.M.4
Linington, C.5
-
6
-
-
79952978219
-
Expression of connexin 43 in the human epileptic and drug-resistant cerebral cortex
-
Garbelli R, Frassoni C, Condorelli DF et al (2011) Expression of connexin 43 in the human epileptic and drug-resistant cerebral cortex. Neurology 76:895-902
-
(2011)
Neurology
, vol.76
, pp. 895-902
-
-
Garbelli, R.1
Frassoni, C.2
Condorelli, D.F.3
-
7
-
-
0032953756
-
Connexin-43 hemichannels opened by metabolic inhibition
-
John SA, Kondo R, Wang SY, Goldhaber JI, Weiss JN (1999) Connexin-43 hemichannels opened by metabolic inhibition. J Biol Chem 274:236-240
-
(1999)
J Biol Chem
, vol.274
, pp. 236-240
-
-
John, S.A.1
Kondo, R.2
Wang, S.Y.3
Goldhaber, J.I.4
Weiss, J.N.5
-
8
-
-
26944484034
-
Connexin-47 and connexin-32 in gap junctions of oligodendrocyte somata, myelin sheaths, paranodal loops and Schmidt-Lanterman incisures: Implications for ionic homeostasis and potassium siphoning
-
Kamasawa N, Sik A, Morita M et al (2005) Connexin-47 and connexin-32 in gap junctions of oligodendrocyte somata, myelin sheaths, paranodal loops and Schmidt-Lanterman incisures: Implications for ionic homeostasis and potassium siphoning. Neuroscience 136:65-86
-
(2005)
Neuroscience
, vol.136
, pp. 65-86
-
-
Kamasawa, N.1
Sik, A.2
Morita, M.3
-
9
-
-
79959503871
-
Astrocytopathy in Baló's disease
-
Kira J (2011) Astrocytopathy in Baló's disease. Mult Scler 17:771-779
-
(2011)
Mult Scler
, vol.17
, pp. 771-779
-
-
Kira, J.1
-
10
-
-
4644307412
-
Unique distribution of gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes
-
Kleopa KA, Orthmann JL, Enriquez A, Paul DL, Scherer SS (2004) Unique distribution of gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes. Glia 47:346-357
-
(2004)
Glia
, vol.47
, pp. 346-357
-
-
Kleopa, K.A.1
Orthmann, J.L.2
Enriquez, A.3
Paul, D.L.4
Scherer, S.S.5
-
11
-
-
34247150637
-
Nogo - A is a reliable oligodendroglial marker in adult human and mouse CNS and in demyelinated lesions
-
Kuhlmann T, Remington L, Maruschak B, Owens T, Brück W (2007) Nogo-A is a reliable oligodendroglial marker in adult human and mouse CNS and in demyelinated lesions. J Neuropathol Exp Neurol 66:238-246
-
(2007)
J Neuropathol Exp Neurol
, vol.66
, pp. 238-246
-
-
Kuhlmann, T.1
Remington, L.2
Maruschak, B.3
Owens, T.4
Brück, W.5
-
12
-
-
0032526198
-
Immunopathology of multiple sclerosis: Report on an international meeting held at the institute of neurology of the University of Vienna
-
Lassmann H, Raine CS, Antel J, Prineas JW (1998) Immunopathology of multiple sclerosis: report on an international meeting held at the institute of neurology of the University of Vienna. J Neuroimmunol 86:213-217
-
(1998)
J Neuroimmunol
, vol.86
, pp. 213-217
-
-
Lassmann, H.1
Raine, C.S.2
Antel, J.3
Prineas, J.W.4
-
13
-
-
0037441439
-
Hypoxia-like tissue injury as a component of multiple sclerosis lesions
-
Lassmann H (2003) Hypoxia-like tissue injury as a component of multiple sclerosis lesions. J Neurol Sci 206:187-191
-
(2003)
J Neurol Sci
, vol.206
, pp. 187-191
-
-
Lassmann, H.1
-
14
-
-
0036255381
-
Neurological manifestations of the oculodentodigital dysplasia syndrome
-
Loddenkemper T, Grote K, Evers S, Oelerich M, Stögbauer F (2002) Neurological manifestations of the oculodentodigital dysplasia syndrome. J Neurol 249:584-595
-
(2002)
J Neurol
, vol.249
, pp. 584-595
-
-
Loddenkemper, T.1
Grote, K.2
Evers, S.3
Oelerich, M.4
Stögbauer, F.5
-
15
-
-
0342906187
-
Heterogeneity of multiple sclerosis lesions: Implications for the pathogenesis of demyelination
-
Lucchinetti C, Brück W, Parisi J, Scheithauer B, Rodriguez M, Lassmann H (2000) Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination. Ann Neurol 47:707-717
-
(2000)
Ann Neurol
, vol.47
, pp. 707-717
-
-
Lucchinetti, C.1
Brück, W.2
Parisi, J.3
Scheithauer, B.4
Rodriguez, M.5
Lassmann, H.6
-
16
-
-
78650178901
-
Multiple sclerosis pathology during early and late disease phases: Pathogenic and clinical relevance
-
Zhang J (ed) Springer, New York
-
Lucchinetti C (2007) Multiple sclerosis pathology during early and late disease phases: pathogenic and clinical relevance. In: Zhang J (ed) Immune regulation and immunotherapy in autoimmune disease. Springer, New York, pp 214-264
-
(2007)
Immune Regulation and Immunotherapy in Autoimmune Disease
, pp. 214-264
-
-
Lucchinetti, C.1
-
17
-
-
67449119205
-
Deletion of astrocyte connexins 43 and 30 leads to a dysmyelinating phenotype and hippocampal CA1 vacuolation
-
Lutz SE, Zhao Y, Gulinello M, Lee SC, Raine CS, Brosnan CF (2009) Deletion of astrocyte connexins 43 and 30 leads to a dysmyelinating phenotype and hippocampal CA1 vacuolation. J Neurosci 29:7743-7752
-
(2009)
J Neurosci
, vol.29
, pp. 7743-7752
-
-
Lutz, S.E.1
Zhao, Y.2
Gulinello, M.3
Lee, S.C.4
Raine, C.S.5
Brosnan, C.F.6
-
18
-
-
79955819402
-
Deletion of oligodendrocyte Cx32 and astrocyte Cx43 causes white matter vacuolation, astrocyte loss and early mortality
-
Magnotti LM, Goodenough DA, Paul DL (2011) Deletion of oligodendrocyte Cx32 and astrocyte Cx43 causes white matter vacuolation, astrocyte loss and early mortality. Glia 59:1064-1074
-
(2011)
Glia
, vol.59
, pp. 1064-1074
-
-
Magnotti, L.M.1
Goodenough, D.A.2
Paul, D.L.3
-
19
-
-
34249687030
-
Heterogeneity of aquaporin-4 autoimmunity and spinal cord lesions in multiple sclerosis in Japanese
-
Matsuoka T, Matsushita T, Kawano Y et al (2007) Heterogeneity of aquaporin-4 autoimmunity and spinal cord lesions in multiple sclerosis in Japanese. Brain 130:1206-1223
-
(2007)
Brain
, vol.130
, pp. 1206-1223
-
-
Matsuoka, T.1
Matsushita, T.2
Kawano, Y.3
-
20
-
-
78149411856
-
Aquaporin-4 astrocytopathy in Baló's disease
-
Matsuoka T, Suzuki SO, Iwaki T, Tabira T, Ordinario AT, Kira J (2010) Aquaporin-4 astrocytopathy in Baló's disease. Acta Neuropathol 120:651-660
-
(2010)
Acta Neuropathol
, vol.120
, pp. 651-660
-
-
Matsuoka, T.1
Suzuki, S.O.2
Iwaki, T.3
Tabira, T.4
Ordinario, A.T.5
Kira, J.6
-
21
-
-
80051890726
-
Reappraisal of aquaporin-4 astrocytopathy in Asian neuromyelitis optica and multiple sclerosis patients
-
doi:10.1111/j.1750-3639.2011.00475.x
-
Matsuoka T, Suzuki SO, Suenaga T, Iwaki T, Kira J (2011) Reappraisal of aquaporin-4 astrocytopathy in Asian neuromyelitis optica and multiple sclerosis patients. Brain Pathol. doi: 10.1111/j.1750-3639.2011.00475.x
-
(2011)
Brain Pathol.
-
-
Matsuoka, T.1
Suzuki, S.O.2
Suenaga, T.3
Iwaki, T.4
Kira, J.5
-
22
-
-
67649383226
-
Aquaporin-4 autoimmune syndrome and anti-aquaporin-4 antibody-negative opticospinal multiple sclerosis in Japanese
-
Matsushita T, Isobe N, Matsuoka T et al (2009) Aquaporin-4 autoimmune syndrome and anti-aquaporin-4 antibody-negative opticospinal multiple sclerosis in Japanese. Mult Scler 15:834-847
-
(2009)
Mult Scler
, vol.15
, pp. 834-847
-
-
Matsushita, T.1
Isobe, N.2
Matsuoka, T.3
-
23
-
-
0038383619
-
Connexins are critical for normal myelination in the CNS
-
Menichella DM, Goodenough DA, Sirkowski E, Scherer SS, Paul DL (2003) Connexins are critical for normal myelination in the CNS. J Neurosci 23:5963-5973
-
(2003)
J Neurosci
, vol.23
, pp. 5963-5973
-
-
Menichella, D.M.1
Goodenough, D.A.2
Sirkowski, E.3
Scherer, S.S.4
Paul, D.L.5
-
24
-
-
34249711828
-
Loss of aquaporin 4 in lesions of neuromyelitis optica: Distinction from multiple sclerosis
-
Misu T, Fujihara K, Kakita A et al (2007) Loss of aquaporin 4 in lesions of neuromyelitis optica: distinction from multiple sclerosis. Brain 130:1224-1234
-
(2007)
Brain
, vol.130
, pp. 1224-1234
-
-
Misu, T.1
Fujihara, K.2
Kakita, A.3
-
25
-
-
0025169152
-
A case of demyelinating disease showing a peculiar honeycomblike and lamellar structure on magnetic resonance imaging
-
Miyata K, Itoyama Y, Kobayashi T, Yasumori K, Goto I (1990) A case of demyelinating disease showing a peculiar honeycomblike and lamellar structure on magnetic resonance imaging. Rinsho Shinkeigaku 30:402-406
-
(1990)
Rinsho Shinkeigaku
, vol.30
, pp. 402-406
-
-
Miyata, K.1
Itoyama, Y.2
Kobayashi, T.3
Yasumori, K.4
Goto, I.5
-
26
-
-
0033519348
-
Claudin-11/OSP-based tight junctions of myelin sheaths in brain and Sertoli cells in testis
-
Morita K, Sasaki H, Fujimoto K, Furuse M, Tsukita S (1999) Claudin-11/OSP-based tight junctions of myelin sheaths in brain and Sertoli cells in testis. J Cell Biol 145:579-588
-
(1999)
J Cell Biol
, vol.145
, pp. 579-588
-
-
Morita, K.1
Sasaki, H.2
Fujimoto, K.3
Furuse, M.4
Tsukita, S.5
-
27
-
-
0032889958
-
Connexin30 in rodent, cat and human brain: Selective expression in gray matter astrocytes, co-localization with connexin43 at gap junctions and late developmental appearance
-
Nagy JI, Patel D, Ochalski PA, Stelmack GL (1999) Connexin30 in rodent, cat and human brain: selective expression in gray matter astrocytes, co-localization with connexin43 at gap junctions and late developmental appearance. Neuroscience 88:447-468
-
(1999)
Neuroscience
, vol.88
, pp. 447-468
-
-
Nagy, J.I.1
Patel, D.2
Ochalski, P.A.3
Stelmack, G.L.4
-
28
-
-
79957603294
-
Asparagine 175 of connexin32 is a critical residue for docking and forming functional heterotypic gap junction channels with connexin26
-
Nakagawa S, Gong XQ, Maeda S et al (2011) Asparagine 175 of connexin32 is a critical residue for docking and forming functional heterotypic gap junction channels with connexin26. J Biol Chem 286:19672-19681
-
(2011)
J Biol Chem
, vol.286
, pp. 19672-19681
-
-
Nakagawa, S.1
Gong, X.Q.2
Maeda, S.3
-
29
-
-
33748864085
-
Enhanced connexin 43 immunoreactivity in penumbral areas in the human brain following ischemia
-
Nakase T, Yoshida Y, Nagata K (2006) Enhanced connexin 43 immunoreactivity in penumbral areas in the human brain following ischemia. Glia 54:369-375
-
(2006)
Glia
, vol.54
, pp. 369-375
-
-
Nakase, T.1
Yoshida, Y.2
Nagata, K.3
-
31
-
-
60149110304
-
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations
-
Orthmann-Murphy JL, Salsano E, Abrams CK et al (2009) Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. Brain 132:426-438
-
(2009)
Brain
, vol.132
, pp. 426-438
-
-
Orthmann-Murphy, J.L.1
Salsano, E.2
Abrams, C.K.3
-
32
-
-
77957601341
-
Neuromyelitis optica: A demyelinating disease characterized by acute destruction and regeneration of perivascular astrocytes
-
Parratt JD, Prineas JW (2010) Neuromyelitis optica: a demyelinating disease characterized by acute destruction and regeneration of perivascular astrocytes. Mult Scler 16:1156-1172
-
(2010)
Mult Scler
, vol.16
, pp. 1156-1172
-
-
Parratt, J.D.1
Prineas, J.W.2
-
33
-
-
0037320927
-
Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia
-
Paznekas WA, Boyadjiev SA, Shapiro R et al (2003) Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia. Am J Hum Genet 72:408-418
-
(2003)
Am J Hum Genet
, vol.72
, pp. 408-418
-
-
Paznekas, W.A.1
Boyadjiev, S.A.2
Shapiro, R.3
-
34
-
-
34249650146
-
Pattern-specific loss of aquaporin-4 immunoreactivity distinguishes neuromyelitis optica from multiple sclerosis
-
Roemer SF, Parisi JE, Lennon VA et al (2007) Pattern-specific loss of aquaporin-4 immunoreactivity distinguishes neuromyelitis optica from multiple sclerosis. Brain 130:1194-1205
-
(2007)
Brain
, vol.130
, pp. 1194-1205
-
-
Roemer, S.F.1
Parisi, J.E.2
Lennon, V.A.3
-
35
-
-
42649116417
-
Human oligodendrocytes express Cx31.3: Function and interactions with Cx32 mutants
-
Sargiannidou I, Ahn M, Enriquez A et al (2008) Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants. Neurobiol Dis 30:221-233
-
(2008)
Neurobiol Dis
, vol.30
, pp. 221-233
-
-
Sargiannidou, I.1
Ahn, M.2
Enriquez, A.3
-
36
-
-
77957275551
-
Inflammation induced by innate immunity in the central nervous system leads to primary astrocyte dysfunction followed by demyelination
-
Sharma R, Fischer MT, Bauer J et al (2010) Inflammation induced by innate immunity in the central nervous system leads to primary astrocyte dysfunction followed by demyelination. Acta Neuropathol 120:223-236
-
(2010)
Acta Neuropathol
, vol.120
, pp. 223-236
-
-
Sharma, R.1
Fischer, M.T.2
Bauer, J.3
-
37
-
-
40749110254
-
Central nervous system signs in X-Linked Charcot-Marie-Tooth disease after hyperventilation
-
Srinivasan J, Leventer RJ, Kornberg AJ, Dahl HH, Ryan MM (2008) Central nervous system signs in X-Linked Charcot-Marie-Tooth disease after hyperventilation. Pediatr Neurol 38:293-295
-
(2008)
Pediatr Neurol
, vol.38
, pp. 293-295
-
-
Srinivasan, J.1
Leventer, R.J.2
Kornberg, A.J.3
Dahl, H.H.4
Ryan, M.M.5
-
38
-
-
18744394057
-
Tissue preconditioning may explain concentric lesions in Baló's type of multiple sclerosis
-
Stadelmann C, Ludwin S, Tabira T et al (2005) Tissue preconditioning may explain concentric lesions in Baló's type of multiple sclerosis. Brain 128:979-987
-
(2005)
Brain
, vol.128
, pp. 979-987
-
-
Stadelmann, C.1
Ludwin, S.2
Tabira, T.3
-
39
-
-
0345600908
-
The CNS phenotype of X-linked Charcot-Marie-Tooth disease: More than a peripheral problem
-
Taylor RA, Simon EM, Marks HG, Scherer SS (2003) The CNS phenotype of X-linked Charcot-Marie-Tooth disease: More than a peripheral problem. Neurology 61:1475-1478
-
(2003)
Neurology
, vol.61
, pp. 1475-1478
-
-
Taylor, R.A.1
Simon, E.M.2
Marks, H.G.3
Scherer, S.S.4
-
40
-
-
3242693178
-
Mutations in the gene encoding gap junction protein alpha 12 (Connexin 46.6) cause PelizaeusMerzbacher-like disease
-
Uhlenberg B, Schuelke M, Ruschendorf F et al (2004) Mutations in the gene encoding gap junction protein alpha 12 (Connexin 46.6) cause PelizaeusMerzbacher-like disease. Am J Hum Genet 75:251-260
-
(2004)
Am J Hum Genet
, vol.75
, pp. 251-260
-
-
Uhlenberg, B.1
Schuelke, M.2
Ruschendorf, F.3
-
41
-
-
43549087861
-
Baló's disease showing benign clinical course and co-existence with multiple sclerosislike lesions in Chinese
-
Wang C, Zhang KN, Wu XM et al (2008) Baló's disease showing benign clinical course and co-existence with multiple sclerosislike lesions in Chinese. Mult Scler 14:418-424
-
(2008)
Mult Scler
, vol.14
, pp. 418-424
-
-
Wang, C.1
Zhang, K.N.2
Wu, X.M.3
-
42
-
-
0028078675
-
Concentric sclerosis (Baló): Morphometric and in situ hybridization study of lesions in six patients
-
Yao DL, Webster HD, Hudson LD et al (1994) Concentric sclerosis (Baló): morphometric and in situ hybridization study of lesions in six patients. Ann Neurol 35:18-30
-
(1994)
Ann Neurol
, vol.35
, pp. 18-30
-
-
Yao, D.L.1
Webster, H.D.2
Hudson, L.D.3
|