-
1
-
-
0030979840
-
Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32
-
Anzini P, Neuberg DH-H, Schachner M, Nelles E, Willecke K, Zielasek J, Toyka K, Suter U, Martini R (1997): Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32. J Neurosci 17:4545-4551.
-
(1997)
J Neurosci
, vol.17
, pp. 4545-4551
-
-
Anzini, P.1
Neuberg, D.H.-H.2
Schachner, M.3
Nelles, E.4
Willecke, K.5
Zielasek, J.6
Toyka, K.7
Suter, U.8
Martini, R.9
-
2
-
-
0025963272
-
Gap junctions: New tools, new answers, new questions
-
Bennett MV, Barrio LC, Bargiello TA, Spray DC, Hertzberg E, Saez JC (1991): Gap junctions: New tools, new answers, new questions. Neuron 6:305-320.
-
(1991)
Neuron
, vol.6
, pp. 305-320
-
-
Bennett, M.V.1
Barrio, L.C.2
Bargiello, T.A.3
Spray, D.C.4
Hertzberg, E.5
Saez, J.C.6
-
3
-
-
0027772413
-
Connexin mutations in X-linked Charcot-Marie-Tooth disease
-
Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, Paul DL, Chen K, Lensch MW, Chance PF, Fischbeck KH (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
Scott, M.O.4
Bone, L.J.5
Paul, D.L.6
Chen, K.7
Lensch, M.W.8
Chance, P.F.9
Fischbeck, K.H.10
-
5
-
-
0031290336
-
Charcot-Marie-Tooth diseases and related peripheral neuropathies
-
De Jonghe E, Timmermann V, Neli E, Martin JJ, Van Broeckhoven CJ (1997): Charcot-Marie-Tooth diseases and related peripheral neuropathies. J Peripheral Nerv Syst 2:370-387.
-
(1997)
J Peripheral Nerv Syst
, vol.2
, pp. 370-387
-
-
De Jonghe, E.1
Timmermann, V.2
Neli, E.3
Martin, J.J.4
Van Broeckhoven, C.J.5
-
6
-
-
0028244197
-
The cytoplasmic domain of myelin glycoprotein P0 interacts with negatively charged phospholipid bilayers
-
Ding Y, Brunden KR (1994): The cytoplasmic domain of myelin glycoprotein P0 interacts with negatively charged phospholipid bilayers. J Biol Chem 269:10764-10770.
-
(1994)
J Biol Chem
, vol.269
, pp. 10764-10770
-
-
Ding, Y.1
Brunden, K.R.2
-
7
-
-
0027491911
-
Quantitation of changes in the expression of multiple genes by simultaneous polymerase chain reaction
-
Dukas K, Sarfati P, Vaysse N, Pradayrol L (1993): Quantitation of changes in the expression of multiple genes by simultaneous polymerase chain reaction. Anal Biochem 215:66-72.
-
(1993)
Anal Biochem
, vol.215
, pp. 66-72
-
-
Dukas, K.1
Sarfati, P.2
Vaysse, N.3
Pradayrol, L.4
-
8
-
-
0025253083
-
Protein zero of peripheral nerve myelin: Biosynthesis, membrane insertion, and evidence for homotypic interaction
-
D'Urso D, Brophy PJ, Staugaitis SM, Gillespie CS, Frey AB, Stempak JG, Colman DR (1990): Protein zero of peripheral nerve myelin: Biosynthesis, membrane insertion, and evidence for homotypic interaction. Neuron 4:449-460.
-
(1990)
Neuron
, vol.4
, pp. 449-460
-
-
D'Urso, D.1
Brophy, P.J.2
Staugaitis, S.M.3
Gillespie, C.S.4
Frey, A.B.5
Stempak, J.G.6
Colman, D.R.7
-
9
-
-
0025194356
-
Role of myelin P0 protein as a homophilic adhesion molecule
-
Filbin MT, Walsh FS, Trapp BD, Pizzey JA, Tennekoon GI (1990): Role of myelin P0 protein as a homophilic adhesion molecule. Nature 344:871-872.
-
(1990)
Nature
, vol.344
, pp. 871-872
-
-
Filbin, M.T.1
Walsh, F.S.2
Trapp, B.D.3
Pizzey, J.A.4
Tennekoon, G.I.5
-
10
-
-
0026615047
-
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons
-
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 71:565-576.
-
(1992)
Cell
, vol.71
, pp. 565-576
-
-
Giese, K.P.1
Martini, R.2
Lemke, G.3
Soriano, P.4
Schachner, M.5
-
11
-
-
0025085880
-
X-linked dominant hereditary motor and sensory neuropathy
-
Hahn AF, Brown WF, Koopman WJ, Feasby TE (1990): X-linked dominant hereditary motor and sensory neuropathy. Brain 113:1511-1525.
-
(1990)
Brain
, vol.113
, pp. 1511-1525
-
-
Hahn, A.F.1
Brown, W.F.2
Koopman, W.J.3
Feasby, T.E.4
-
12
-
-
0018835608
-
Compact myelin exists in the absence of myelin basic protein in the shiverer mutant mouse
-
Kirschner DA, Ganser AL (1980): Compact myelin exists in the absence of myelin basic protein in the shiverer mutant mouse. Nature 283:207-210.
-
(1980)
Nature
, vol.283
, pp. 207-210
-
-
Kirschner, D.A.1
Ganser, A.L.2
-
13
-
-
0030028301
-
The gap junction communication channel
-
Kumar NM, Gilula NB (1996): The gap junction communication channel. Cell 84:381-388.
-
(1996)
Cell
, vol.84
, pp. 381-388
-
-
Kumar, N.M.1
Gilula, N.B.2
-
14
-
-
0021849731
-
Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin
-
Lemke G, Axel R (1985): Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin. Cell 40:501-508.
-
(1985)
Cell
, vol.40
, pp. 501-508
-
-
Lemke, G.1
Axel, R.2
-
15
-
-
0030696172
-
Animal models for inherited peripheral neuropathies
-
Martini R (1997): Animal models for inherited peripheral neuropathies. J Anat 191:321-336.
-
(1997)
J Anat
, vol.191
, pp. 321-336
-
-
Martini, R.1
-
16
-
-
0029065654
-
Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin
-
Martini R, Mohajeri MH, Kasper S, Giese KP, Schachner M (1995a): Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin. J Neurosci 15:4488-4495.
-
(1995)
J Neurosci
, vol.15
, pp. 4488-4495
-
-
Martini, R.1
Mohajeri, M.H.2
Kasper, S.3
Giese, K.P.4
Schachner, M.5
-
17
-
-
0028824925
-
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies
-
Martini R, Zielasek J, Toyka KV, Giese KP, Schachner M (1995b): Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies. Nat Genet 11:281-286.
-
(1995)
Nat Genet
, vol.11
, pp. 281-286
-
-
Martini, R.1
Zielasek, J.2
Toyka, K.V.3
Giese, K.P.4
Schachner, M.5
-
18
-
-
0030769839
-
Altered gap junctional communication, intercellular signaling, and growth in cultured astrocytes deficient in connexin 43
-
Naus CC, Bechberger JF, Zhang Y, Venance L, Yamasaki H, Juneja SC, Kidder GM, Giaume C (1997): Altered gap junctional communication, intercellular signaling, and growth in cultured astrocytes deficient in connexin 43. J Neurosci Res 49:528-540.
-
(1997)
J Neurosci Res
, vol.49
, pp. 528-540
-
-
Naus, C.C.1
Bechberger, J.F.2
Zhang, Y.3
Venance, L.4
Yamasaki, H.5
Juneja, S.C.6
Kidder, G.M.7
Giaume, C.8
-
19
-
-
0343687249
-
Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin 32 deficient mice
-
Nelles E, Bützler C, Jung D, Temme A, Gabriel H-D, Dahl V, Traub O, Stümpel F, Jungermann K, Zielasek J, Toyka KV, Dermietzel R, Willecke K (1996): Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin 32 deficient mice. Proc Natl Acad Sci USA 93:9565-9570.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 9565-9570
-
-
Nelles, E.1
Bützler, C.2
Jung, D.3
Temme, A.4
Gabriel, H.-D.5
Dahl, V.6
Traub, O.7
Stümpel, F.8
Jungermann, K.9
Zielasek, J.10
Toyka, K.V.11
Dermietzel, R.12
Willecke, K.13
-
20
-
-
0022531305
-
Molecular cloning of cDNA for rat liver gap junction protein
-
Paul DL (1986): Molecular cloning of cDNA for rat liver gap junction protein. J Cell Biol 103:123-134.
-
(1986)
J Cell Biol
, vol.103
, pp. 123-134
-
-
Paul, D.L.1
-
21
-
-
0029143157
-
New functions for gap junctions
-
Paul DL (1995): New functions for gap junctions. Curr Opin Cell Biol 7:665-672.
-
(1995)
Curr Opin Cell Biol
, vol.7
, pp. 665-672
-
-
Paul, D.L.1
-
22
-
-
0029563471
-
Connexin 32 is a myelin-related protein in the PNS and CNS
-
Scherer SS, Deschenes SM, Xu Y-T, Grinspan JB, Fishbeck KH, Paul DL (1995): Connexin 32 is a myelin-related protein in the PNS and CNS. J Neurosci 15:8281-8294.
-
(1995)
J Neurosci
, vol.15
, pp. 8281-8294
-
-
Scherer, S.S.1
Deschenes, S.M.2
Xu, Y.-T.3
Grinspan, J.B.4
Fishbeck, K.H.5
Paul, D.L.6
-
23
-
-
0025601660
-
Recombinant peripheral myelin protein P0 confers both adhesion and neurite outgrowth-promoting properties
-
Schneider-Schaulies J, von Brunn A, Schachner M (1990): Recombinant peripheral myelin protein P0 confers both adhesion and neurite outgrowth-promoting properties. J Neurosci Res 27:286-297.
-
(1990)
J Neurosci Res
, vol.27
, pp. 286-297
-
-
Schneider-Schaulies, J.1
Von Brunn, A.2
Schachner, M.3
-
24
-
-
0030246987
-
Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin
-
Shapiro L, Doyle JP, Hensley P, Colman DR, Hendrickson WA (1996): Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin. Neuron 17:435-449.
-
(1996)
Neuron
, vol.17
, pp. 435-449
-
-
Shapiro, L.1
Doyle, J.P.2
Hensley, P.3
Colman, D.R.4
Hendrickson, W.A.5
-
25
-
-
0029060906
-
X-linked Charcot-Marie-Tooth disease and other potential gap-junction diseases of the nervous system
-
Spray DC, Dermietzel R (1995): X-linked Charcot-Marie-Tooth disease and other potential gap-junction diseases of the nervous system. Trends Neurosci 18:256-262.
-
(1995)
Trends Neurosci
, vol.18
, pp. 256-262
-
-
Spray, D.C.1
Dermietzel, R.2
-
26
-
-
16044362374
-
Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type IB, Déjérine-Sottas, and congenital hypomyelination
-
Warner LE, Hilz MJ, Appel SH, Killian JM, Kolodry EH, Karpati G, Carpenter S, Watters GV, Wheeler C, Witt D, Bodell A, Nelis E, Van Broeckhoven C, Lupski JR (1996): Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type IB, Déjérine-Sottas, and congenital hypomyelination. Neuron 17:451-460.
-
(1996)
Neuron
, vol.17
, pp. 451-460
-
-
Warner, L.E.1
Hilz, M.J.2
Appel, S.H.3
Killian, J.M.4
Kolodry, E.H.5
Karpati, G.6
Carpenter, S.7
Watters, G.V.8
Wheeler, C.9
Witt, D.10
Bodell, A.11
Nelis, E.12
Van Broeckhoven, C.13
Lupski, J.R.14
|