-
1
-
-
0027772413
-
Connexin mutations in X-linked Charcot-Marie-Tooth disease
-
BERGOFFEN, J., S.S. SCHERER, S. WANG, M.O. SCOTT, L.J. BONE, D.L. PAUL, K. CHEN, M.W. LENSCH, P. CHANCE & K.H. FISCHBECK. 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.9
Fischbeck, K.H.10
-
3
-
-
0030660232
-
Connexin32 and X-linked Charcot-Marie-Tooth disease
-
BONE, L.J., S.M. DESCHENES, R.J. BALICE-GORDON, K.H. FISCHBECK & S.S. SCHERER, 1997. Connexin32 and X-linked Charcot-Marie-Tooth disease. Neurobiol. Dis. 4: 221-230.
-
(1997)
Neurobiol. Dis.
, vol.4
, pp. 221-230
-
-
Bone, L.J.1
Deschenes, S.M.2
Balice-Gordon, R.J.3
Fischbeck, K.H.4
Scherer, S.S.5
-
4
-
-
0027359513
-
Screening of dominantly inherited Charcot-Marie-Tooth neuropathies
-
IONASESCU, V.V., R. IONASESCU & C. SEARBY. 1993. Screening of dominantly inherited Charcot-Marie-Tooth neuropathies. Muscle Nerve 16: 1232-1238.
-
(1993)
Muscle Nerve
, vol.16
, pp. 1232-1238
-
-
Ionasescu, V.V.1
Ionasescu, R.2
Searby, C.3
-
5
-
-
0023254209
-
Hereditary motor and sensory neuropathy, X-linked
-
ROZEAR, M.P., M.A. PERICAK-VANCE, K.H. FISCHBECK, J.M. STAJICH, P.C. GASKELL, P. KRENDEL, D.G. GRAHAM, D.V. DAWSON & A.D. ROSES. 1987. Hereditary motor and sensory neuropathy, X-linked. Neurology 37: 1460-1465.
-
(1987)
Neurology
, vol.37
, pp. 1460-1465
-
-
Rozear, M.P.1
Pericak-Vance, M.A.2
Fischbeck, K.H.3
Stajich, J.M.4
Gaskell, P.C.5
Krendel, P.6
Graham, D.G.7
Dawson, D.V.8
Roses, A.D.9
-
6
-
-
0027723256
-
Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families
-
NICHOLSON, G. & J. NASH. 1993. Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families. Neurology 43: 2558-2564.
-
(1993)
Neurology
, vol.43
, pp. 2558-2564
-
-
Nicholson, G.1
Nash, J.2
-
7
-
-
0025085880
-
X-linked dominant hereditary motor and sensory neuropathy
-
HAHN, A.F., W.F. BROWN, W.J. KOOPMAN & T.E. FEASBY, 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
-
8
-
-
0032066457
-
X-linked dominant Charcot-Marie-Tooth disease: Nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln)
-
SENDEREK, J., C. BERGMANN, S. QUASTHOFF, V.T. RAMAEKERS & J.M. SCHRODER. 1998. X-linked dominant Charcot-Marie-Tooth disease: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln). Acta Neuropathol. (Berlin) 95: 443-449.
-
(1998)
Acta Neuropathol. (Berlin)
, vol.95
, pp. 443-449
-
-
Senderek, J.1
Bergmann, C.2
Quasthoff, S.3
Ramaekers, V.T.4
Schroder, J.M.5
-
10
-
-
0028014579
-
Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease
-
FAIRWEATHER, N., C. BELL, S. COCHRANE, J. CHELLY, S. WANG, M.L. MOSTACCIUOLO, A.P. MONACO & N.E. HAITES. 1994. Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease. Hum. Mol. Genet. 3: 29-34.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 29-34
-
-
Fairweather, N.1
Bell, C.2
Cochrane, S.3
Chelly, J.4
Wang, S.5
Mostacciuolo, M.L.6
Monaco, A.P.7
Haites, N.E.8
-
11
-
-
0028088839
-
Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathy
-
IONASESCU, V., C. SEARBY & R. IONASESCU. 1994. Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathy. Hum. Mol. Genet. 3: 355-358.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 355-358
-
-
Ionasescu, V.1
Searby, C.2
Ionasescu, R.3
-
12
-
-
0029431669
-
New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease
-
BONE, L.J., N. DAHL, M.W. LENSCH, P.F. CHANCE, T. KELLY, E. LE GUERN, S. MAGI, G. PARRY, H. SHAPIRO, S. WANG & K.H. FISCHBECK. 1995. New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease. Neurology 45: 1863-1866.
-
(1995)
Neurology
, vol.45
, pp. 1863-1866
-
-
Bone, L.J.1
Dahl, N.2
Lensch, M.W.3
Chance, P.F.4
Kelly, T.5
Le Guern, E.6
Magi, S.7
Parry, G.8
Shapiro, H.9
Wang, S.10
Fischbeck, K.H.11
-
13
-
-
0029788204
-
Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy
-
IONASESCU, W., C. SEARBY, R. IONASESCU, I.M. NEUHAUS & R. WERNER. 1996. Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy. Neurology 47: 541-544.
-
(1996)
Neurology
, vol.47
, pp. 541-544
-
-
Ionasescu, W.1
Searby, C.2
Ionasescu, R.3
Neuhaus, I.M.4
Werner, R.5
-
14
-
-
16944366517
-
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 Cx32 mutations in 35 families
-
ROUGER, H., E. LEGUERN, N. BIKOUK, R. GOUIDER, S. TARDIEU, E. PLASSART, M. GUGENHEIM, J.M. VALLAT, J.P. LOUBOUTIN, P. BOUCHE, Y. AGID & A. BRICE. 1997. Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families. Hum. Mutat. 10: 443-452.
-
(1997)
Hum. Mutat.
, vol.10
, pp. 443-452
-
-
Rouger, H.1
Leguern, E.2
Bikouk, N.3
Gouider, R.4
Tardieu, S.5
Plassart, E.6
Gugenheim, M.7
Vallat, J.M.8
Louboutin, J.P.9
Bouche, P.10
Agid, Y.11
Brice, A.12
-
15
-
-
0030896412
-
Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)
-
JANSSEN, E.A., S. KEMP, G.W. HENSELS, O.G. SIE, C.E. DE DIE-SMULDERS, J.E. HOOGENDIJK , M. DE VISSER & P.A. BOLHUIS. 1997. Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1). Hum. Genet. 99: 501-505.
-
(1997)
Hum. Genet.
, vol.99
, pp. 501-505
-
-
Janssen, E.A.1
Kemp, S.2
Hensels, G.W.3
Sie, O.G.4
De Die-Smulders, C.E.5
Hoogendijk, J.E.6
De Visser, M.7
Bolhuis, P.A.8
-
16
-
-
0030930298
-
Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance
-
SILANDER, K., P. MERETOJA, H. PIHKO, V. JUVONEN, J. ISSAKAINEN, P. AULA & M.L. SAVONTAUS. 1997. Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance. Hum. Genet. 100: 391-397.
-
(1997)
Hum. Genet.
, vol.100
, pp. 391-397
-
-
Silander, K.1
Meretoja, P.2
Pihko, H.3
Juvonen, V.4
Issakainen, J.5
Aula, P.6
Savontaus, M.L.7
-
17
-
-
0031719065
-
Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene
-
AINSWORTH, P.J., C.F. BOLTON, B.C. MURPHY, J.A. STUART & A.F. HAHN. 1998. Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene. Hum. Genet. 103: 242-244.
-
(1998)
Hum. Genet.
, vol.103
, pp. 242-244
-
-
Ainsworth, P.J.1
Bolton, C.F.2
Murphy, B.C.3
Stuart, J.A.4
Hahn, A.F.5
-
18
-
-
0039900799
-
World survey of mutations in inherited peripheral neuropathies
-
NELIS, E., N. HAITES & C. VAN BROECKHOVEN. 1998. World survey of mutations in inherited peripheral neuropathies (abstract). J. Periph. Nerv. Syst. 3: 300.
-
(1998)
J. Periph. Nerv. Syst.
, vol.3
, pp. 300
-
-
Nelis, E.1
Haites, N.2
Van Broeckhoven, C.3
-
19
-
-
0028906886
-
The topogenic fate of the polytopic transmembrane proteins synaptophysin and connexin is determined by their membrane-spanning domains
-
LEUBE, R.E. 1995. The topogenic fate of the polytopic transmembrane proteins synaptophysin and connexin is determined by their membrane-spanning domains. J. Cell Sci. 108: 883-894.
-
(1995)
J. Cell Sci.
, vol.108
, pp. 883-894
-
-
Leube, R.E.1
-
20
-
-
0031007349
-
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
-
KELSELL, D.P., J. DUNLOP, H.P. STEVENS, N.J. LENCH , J.N. LIANG, G. PARRY, R.F. MUELLER & I.M. LEIGH. 1997. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 387: 80-83.
-
(1997)
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
Dunlop, J.2
Stevens, H.P.3
Lench, N.J.4
Liang, J.N.5
Parry, G.6
Mueller, R.F.7
Leigh, I.M.8
-
21
-
-
3643059295
-
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness
-
MORELL, R.J., H.J. KIM, L.J. HOOD, L. GOFORTH, K. FRIDERICI, R. FISHER, G. VAN CAMP, C.I. BERLIN, C. ODDOUX, H. OSTRER, B. KEATS & T.B. FRIEDMAN. 1998. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. N. Engl. J. Med. 339: 1500-1505.
-
(1998)
N. Engl. J. Med.
, vol.339
, pp. 1500-1505
-
-
Morell, R.J.1
Kim, H.J.2
Hood, L.J.3
Goforth, L.4
Friderici, K.5
Fisher, R.6
Van Camp, G.7
Berlin, C.I.8
Oddoux, C.9
Ostrer, H.10
Keats, B.11
Friedman, T.B.12
-
22
-
-
17344373747
-
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
-
XIA, J., C. LIU, B. TANG, Q. PAN, L. HUANG, H.P. DAI, B.R. ZHANG, W. XIE, D.X. HU, D. ZHENG, X.L. SHI, D.A. WANG, K. XIA, K.P. YU, X.D. LIAO, Y. FENG, Y.F. YANG, J.Y. XIAO, D.H. XIH & J.Z. HUANG. 1998. Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment. Nat. Genet. 20: 370-373.
-
(1998)
Nat. Genet.
, vol.20
, pp. 370-373
-
-
Xia, J.1
Liu, C.2
Tang, B.3
Pan, Q.4
Huang, L.5
Dai, H.P.6
Zhang, B.R.7
Xie, W.8
Hu, D.X.9
Zheng, D.10
Shi, X.L.11
Wang, D.A.12
Xia, K.13
Yu, K.P.14
Liao, X.D.15
Feng, Y.16
Yang, Y.F.17
Xiao, J.Y.18
Xih, D.H.19
Huang, J.Z.20
more..
-
23
-
-
0031796918
-
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
-
RICHARD, G., L.E. SMITH, R.A. BAILEY, P. ITIN, D. HOHL, E.H. EPSTEIN, JR., J.J. DIGIOVANNA, J.G. COMPTON & S.J. BALE. 1998. Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nat. Genet. 20: 366-369.
-
(1998)
Nat. Genet.
, vol.20
, pp. 366-369
-
-
Richard, G.1
Smith, L.E.2
Bailey, R.A.3
Itin, P.4
Hohl, D.5
Epstein, E.H.6
Digiovanna, J.J.7
Compton, J.G.8
Bale, S.J.9
-
24
-
-
0031959735
-
A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome Iq
-
SHIEZLS, A., D. MACKAY, A. IONIDES, V. BERRY, A. MOORE & S. BHATTACHARYA. 1998. A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome Iq. Am. J. Hum. Genet. 62: 526-532.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 526-532
-
-
Shiezls, A.1
Mackay, D.2
Ionides, A.3
Berry, V.4
Moore, A.5
Bhattacharya, S.6
-
25
-
-
0141498594
-
Connexin46 mutations in autosomal dominant congenital cataract
-
MACKAY, D., A. IONIDES, Z. KIBAR, G. ROULEAU, V. BERRY, A. MOORE, A. SHIELS & S. BHATTACHARYA. 1999. Connexin46 mutations in autosomal dominant congenital cataract. Am. J. Hum. Genet. 64: 1357-1364.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1357-1364
-
-
Mackay, D.1
Ionides, A.2
Kibar, Z.3
Rouleau, G.4
Berry, V.5
Moore, A.6
Shiels, A.7
Bhattacharya, S.8
-
26
-
-
0023033171
-
Cloning and characterization of human and rat liver cDNAs coding for a gap junction protein
-
KUMAR, N.M. & N.B. GILULA. 1986. Cloning and characterization of human and rat liver cDNAs coding for a gap junction protein. J. Cell Biol. 103: 767-776.
-
(1986)
J. Cell Biol.
, vol.103
, pp. 767-776
-
-
Kumar, N.M.1
Gilula, N.B.2
-
27
-
-
0029563471
-
Connexin32 is a myelin-related protein in the PNS and CNS
-
SCHERER, S.S., S.M. DESCHE̊NES, Y. XU, J.B. GRINSPAN, K.H. FISCHBECK & D.L. PAUL. 1995. Connexin32 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
Desche̊nes, S.M.2
Xu, Y.3
Grinspan, J.B.4
Fischbeck, K.H.5
Paul, D.L.6
-
28
-
-
0032563605
-
Functional gap junctions in the schwann cell myelin sheath
-
BALICE-GORDON, R.J., L.J. BONE & S.S. SCHERER. 1998. Functional gap junctions in the Schwann cell myelin sheath. J. Cell Biol. 142: 1095-1104.
-
(1998)
J. Cell Biol.
, vol.142
, pp. 1095-1104
-
-
Balice-Gordon, R.J.1
Bone, L.J.2
Scherer, S.S.3
-
29
-
-
0028018967
-
Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease
-
BRUZZONE, R., T.W. WHITE, S.S. SCHERER, K.H. FISCHBECK & D.L. PAUL. 1994. Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease. Neuron 13: 1253-1260.
-
(1994)
Neuron
, vol.13
, pp. 1253-1260
-
-
Bruzzone, R.1
White, T.W.2
Scherer, S.S.3
Fischbeck, K.H.4
Paul, D.L.5
-
30
-
-
0030723591
-
Altered trafficking of mutant connexin32
-
DESCHE̊NES, S.M., J.L. WALCOTT, T.L. WEXLER, S.S. SCHERER & K.H. FISCHBECK. 1997. Altered trafficking of mutant connexin32. J. Neurosci. 17: 9077-9084.
-
(1997)
J. Neurosci.
, vol.17
, pp. 9077-9084
-
-
Desche̊nes, S.M.1
Walcott, J.L.2
Wexler, T.L.3
Scherer, S.S.4
Fischbeck, K.H.5
-
31
-
-
0029977355
-
Connexin32 mutations from X-linked Charcot-Marie-Tooth disease patients; functional defects and dominant negative effects
-
OMORI, Y., M. MESNIL & H. YAMASAKI. 1996. Connexin32 mutations from X-linked Charcot-Marie-Tooth disease patients; functional defects and dominant negative effects. Mol. Biol. Cell 7: 907-916.
-
(1996)
Mol. Biol. Cell
, vol.7
, pp. 907-916
-
-
Omori, Y.1
Mesnil, M.2
Yamasaki, H.3
-
32
-
-
0032518241
-
Mutations of connexin32 in Charcot-Marie-Tooth disease type X interfere with cell-to-cell communication but not cell proliferation and myelin-specific gene expression
-
YOSHIMURA, T., M. SATAKE, A. OHNISHI, Y. TSUTSUMI & Y. FUJIKURA. 1998. Mutations of connexin32 in Charcot-Marie-Tooth disease type X interfere with cell-to-cell communication but not cell proliferation and myelin-specific gene expression. J. Neurosci. Res. 51: 154-161.
-
(1998)
J. Neurosci. Res.
, vol.51
, pp. 154-161
-
-
Yoshimura, T.1
Satake, M.2
Ohnishi, A.3
Tsutsumi, Y.4
Fujikura, Y.5
-
33
-
-
0030777706
-
Changes in permeability caused by connexin32 mutations underlie X-linked Charcot-Marie-Tooth disease
-
OH, S., Y. RI, M.V.L. BENNETT, E.B. TREXLER, V.K. VERSELIS & T.A. BARGIELLO. 1997. Changes in permeability caused by connexin32 mutations underlie X-linked Charcot-Marie-Tooth disease. Neuron 19: 927-938.
-
(1997)
Neuron
, vol.19
, pp. 927-938
-
-
Oh, S.1
Ri, Y.2
Bennett, M.V.L.3
Trexler, E.B.4
Verselis, V.K.5
Bargiello, T.A.6
-
34
-
-
0033554359
-
A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female
-
This volume
-
LIN, G.S., J.D. GLASS, S. SHUMAS, S.S. SCHERER & K.H. FISCHBECK. 1999. A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female. Ann. N.Y. Acad. Sci. 883: 481-484. (This volume.)
-
(1999)
Ann. N.Y. Acad. Sci.
, vol.883
, pp. 481-484
-
-
Lin, G.S.1
Glass, J.D.2
Shumas, S.3
Scherer, S.S.4
Fischbeck, K.H.5
-
35
-
-
0343687249
-
Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice
-
NELLES, E., C. BUTZLER, D. JUNG, A. TEMME, H.D. GABRIEL, U. DAHL, O. TRAUB, F. STUMPEL, K. JUNGERMANN, J. ZIELASEK, K.V. TOYKA, R. DERMIETZEL & K. WILLECKE. 1996. Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice. Proc. Natl. Acad. Sci. USA 93: 9565-9570.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 9565-9570
-
-
Nelles, E.1
Butzler, C.2
Jung, D.3
Temme, A.4
Gabriel, H.D.5
Dahl, U.6
Traub, O.7
Stumpel, F.8
Jungermann, K.9
Zielasek, J.10
Toyka, K.V.11
Dermietzel, R.12
Willecke, K.13
-
36
-
-
0030979840
-
Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein conncxin32
-
ANZINI, P., D.H.H. NEUBERG, M. SCHACHNER, E. NELLES, K. WILLECKE, J. ZIELASEK , K.V. TOYKA U. SUTER & R. MARTINI. 1997. Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein conncxin32. J. Neurosci. 17: 4545-4561.
-
(1997)
J. Neurosci.
, vol.17
, pp. 4545-4561
-
-
Anzini, P.1
Neuberg, D.H.H.2
Schachner, M.3
Nelles, E.4
Willecke, K.5
Zielasek, J.6
Toyka, K.V.7
Suter, U.8
Martini, R.9
-
37
-
-
0032171653
-
Connexin32-null mice develop a demyelinating peripheral neuropathy
-
SCHERER, S.S., Y.T. XU, E. NELLES, K. FISCHBECK, K. WILLECKE & L.J. BONE. 1998. Connexin32-null mice develop a demyelinating peripheral neuropathy. Glia 24: 8-20.
-
(1998)
Glia
, vol.24
, pp. 8-20
-
-
Scherer, S.S.1
Xu, Y.T.2
Nelles, E.3
Fischbeck, K.4
Willecke, K.5
Bone, L.J.6
-
38
-
-
0032807346
-
Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease
-
ABEL, A., L.J. BONE, A. MESSING, S.S. SCHERER & K.H. FISCHBECK. 1999. Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease. J. Neuropathol. Exp. Neurol. 58: 702-710.
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 702-710
-
-
Abel, A.1
Bone, L.J.2
Messing, A.3
Scherer, S.S.4
Fischbeck, K.H.5
-
39
-
-
0039900798
-
Transgenic mice expressing a connexin32 mutation develop demyelinating peripheral neuropathy
-
BONE, L.J., R.J. BALICE-GORDON, A. ABEL, A. MESSING, K. FISCHBECK & S.S. SCHERER. 1997. Transgenic mice expressing a connexin32 mutation develop demyelinating peripheral neuropathy (abstract). Soc. Neurosci. Abstr. 23: 586.
-
(1997)
Soc. Neurosci. Abstr.
, vol.23
, pp. 586
-
-
Bone, L.J.1
Balice-Gordon, R.J.2
Abel, A.3
Messing, A.4
Fischbeck, K.5
Scherer, S.S.6
-
40
-
-
0040493845
-
Expression of a connexin-32 transgene in myelinating schwann cells prevents demyelination in connexin-32-null mice
-
XU, Y.T., L.J. BONE, K. WILLECKE, A. MESSING, K. FISCHBECK & S.S. SCHERER. 1998. Expression of a connexin-32 transgene in myelinating Schwann cells prevents demyelination in connexin-32-null mice (abstract). Ann. Neurol. 44: 989.
-
(1998)
Ann. Neurol.
, vol.44
, pp. 989
-
-
Xu, Y.T.1
Bone, L.J.2
Willecke, K.3
Messing, A.4
Fischbeck, K.5
Scherer, S.S.6
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