-
1
-
-
0026485739
-
Acetylcholine receptor channel structure probed in cysteine-substitution mutants
-
Akabas MH, Stauffer DA, Xu M, Karlin A (1992) Acetylcholine receptor channel structure probed in cysteine-substitution mutants. Science 258:307-310
-
(1992)
Science
, vol.258
, pp. 307-310
-
-
Akabas, M.H.1
Stauffer, D.A.2
Xu, M.3
Karlin, A.4
-
2
-
-
0028950604
-
Chloride currents across the membrane of mammalian skeletal muscle fibres
-
Lond
-
Fahlke C, Rüdel R (1995) Chloride currents across the membrane of mammalian skeletal muscle fibres. J Physiol (Lond) 484:355-368
-
(1995)
J Physiol
, vol.484
, pp. 355-368
-
-
Fahlke, C.1
Rüdel, R.2
-
3
-
-
0029162517
-
An aspartic acid residue important for voltage-dependent gating of human muscle chloride channels
-
Fahlke C, Rüdel R, Mitrovic N, Zhou M, George AL Jr (1995) An aspartic acid residue important for voltage-dependent gating of human muscle chloride channels. Neuron 15:1-20
-
(1995)
Neuron
, vol.15
, pp. 1-20
-
-
Fahlke, C.1
Rüdel, R.2
Mitrovic, N.3
Zhou, M.4
George Jr., A.L.5
-
4
-
-
0029738742
-
Mechanism of voltage-dependent gating in skeletal muscle chloride channels
-
Fahlke C, Rosenbohm A, Mitrovic N, George AL Jr, Rüdel R (1996) Mechanism of voltage-dependent gating in skeletal muscle chloride channels. Biophys J 71:695-706
-
(1996)
Biophys J
, vol.71
, pp. 695-706
-
-
Fahlke, C.1
Rosenbohm, A.2
Mitrovic, N.3
George Jr., A.L.4
Rüdel, R.5
-
5
-
-
0027481915
-
Molecular basis of Thomson's disease (autosomal dominant myotonia congenita)
-
George AL Jr, Crackover MA, Abdalla JA, Hudson AJ, Ebers GC (1993) Molecular basis of Thomson's disease (autosomal dominant myotonia congenita). Nature (Genet) 3:305-310
-
(1993)
Nature (Genet)
, vol.3
, pp. 305-310
-
-
George Jr., A.L.1
Crackover, M.A.2
Abdalla, J.A.3
Hudson, A.J.4
Ebers, G.C.5
-
6
-
-
0027997634
-
Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita
-
George AL Jr, Sloan-Brown K, Fenichel GM, Mitchell GA, Spiegel R, Pascuzzi RM (1994) Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita. Hum Mol Genet 3:2071-2072
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2071-2072
-
-
George Jr., A.L.1
Sloan-Brown, K.2
Fenichel, G.M.3
Mitchell, G.A.4
Spiegel, R.5
Pascuzzi, R.M.6
-
7
-
-
0015847039
-
A new technique for the assay of infectivity of human adenovirus 5 DNA
-
Graham RL, van der Eb AJ (1973) A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology 52: 456-467
-
(1973)
Virology
, vol.52
, pp. 456-467
-
-
Graham, R.L.1
Van Der Eb, A.J.2
-
8
-
-
0028170444
-
2+: An endogenous moculator of ligand- And voltage-gated ion channels
-
2+: an endogenous moculator of ligand- and voltage-gated ion channels. Neuropharmacology 33:935-952
-
(1994)
Neuropharmacology
, vol.33
, pp. 935-952
-
-
Harrison, N.L.1
Gibbons, S.J.2
-
9
-
-
0028287533
-
Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion
-
Heine R, George AL Jr, Pika U, Deymeer F, Rüdel R, Lehmann-Horn F (1994) Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion. Hum Mol Genet 3:1123-1128
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1123-1128
-
-
Heine, R.1
George Jr., A.L.2
Pika, U.3
Deymeer, F.4
Rüdel, R.5
Lehmann-Horn, F.6
-
10
-
-
0028913998
-
Overexcited or inactive: Ion channels in muscle disease
-
Hoffman EP, Lehmann-Horn F, Rüdel R (1995) Overexcited or inactive: ion channels in muscle disease. Cell 80:681-686
-
(1995)
Cell
, vol.80
, pp. 681-686
-
-
Hoffman, E.P.1
Lehmann-Horn, F.2
Rüdel, R.3
-
12
-
-
0029183476
-
Properties of voltage-gated chloride channels of the CIC gene family
-
Lond
-
Jentsch TJ, Günther W, Pusch M, Schwappach B (1995) Properties of voltage-gated chloride channels of the CIC gene family. J Physiol (Lond) 482:19S-25S
-
(1995)
J Physiol
, vol.482
-
-
Jentsch, T.J.1
Günther, W.2
Pusch, M.3
Schwappach, B.4
-
13
-
-
0026705098
-
The skeletal muscle chloride channel in dominant and recessive myotonia
-
Koch MC, Steinmeyer K, Lorenz C, Ricker K, Wolff, Otto M, Lehmann-Horn F, Grzeschik KH, Jentsch TJ (1992) The skeletal muscle chloride channel in dominant and recessive myotonia. Science 257:797-800
-
(1992)
Science
, vol.257
, pp. 797-800
-
-
Koch, M.C.1
Steinmeyer, K.2
Lorenz, C.3
Ricker, K.4
Wolff5
Otto, M.6
Lehmann-Horn, F.7
Grzeschik, K.H.8
Jentsch, T.J.9
-
14
-
-
0028941130
-
+ channel probed by sulfhydryl-specitlc reagents after cysteine substitution mutagenesis
-
+ channel probed by sulfhydryl-specitlc reagents after cysteine substitution mutagenesis. Biophys J 68:900-905
-
(1995)
Biophys J
, vol.68
, pp. 900-905
-
-
Kürz, L.L.1
Zühlke, R.D.2
Zhang, H.J.3
Joho, R.H.4
-
15
-
-
1842290578
-
Inhibition of human muscle chloride channels by histidine- and cysteine-reactive compounds
-
Kürz LL, Wagner S, George AL Jr, Rüdel R (1996) Inhibition of human muscle chloride channels by histidine- and cysteine-reactive compounds (abstract). Pflügers Arch 431:R86
-
(1996)
Pflügers Arch
, vol.431
-
-
Kürz, L.L.1
Wagner, S.2
George Jr., A.L.3
Rüdel, R.4
-
16
-
-
0028307668
-
Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia
-
Lorenz C, Meyer-Kleine Ch, Steinmeyer K, Koch MC, Jentsch TJ (1994) Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia. Hum Mol Genet 3:941-946
-
(1994)
Hum Mol Genet
, vol.3
, pp. 941-946
-
-
Lorenz, C.1
Meyer-Kleine, Ch.2
Steinmeyer, K.3
Koch, M.C.4
Jentsch, T.J.5
-
17
-
-
0030032336
-
Novel muscle chloride channel mutations and their effects on heterozygous carriers
-
Mailänder V, Heine R, Deymeer F, Lehmann-Horn F (1996) Novel muscle chloride channel mutations and their effects on heterozygous carriers. Am J Hum Genet 58:317-324
-
(1996)
Am J Hum Genet
, vol.58
, pp. 317-324
-
-
Mailänder, V.1
Heine, R.2
Deymeer, F.3
Lehmann-Horn, F.4
-
18
-
-
0028820679
-
Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia
-
Meyer-Klcine C, Steinmeyer K, Ricker K, Jentsch TJ, Koch MC (1995) Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia. Am J Hum Genet 57:1325-1334
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1325-1334
-
-
Meyer-Klcine, C.1
Steinmeyer, K.2
Ricker, K.3
Jentsch, T.J.4
Koch, M.C.5
-
19
-
-
0028102941
-
Purification, reconstitution, and subunit composition of a voltage-gated chloride channel from Torpedo electroplax
-
Middleton RE, Pheasant DJ, Miller C (1994) Purification, reconstitution, and subunit composition of a voltage-gated chloride channel from Torpedo electroplax. Biochemistry 33: 13189-13198
-
(1994)
Biochemistry
, vol.33
, pp. 13189-13198
-
-
Middleton, R.E.1
Pheasant, D.J.2
Miller, C.3
-
20
-
-
0017632673
-
Modification of histidyl residues in proteins by diethylpyrocarbonate
-
Miles EW (1977) Modification of histidyl residues in proteins by diethylpyrocarbonate. Methods Enzymol 47:431-142
-
(1977)
Methods Enzymol
, vol.47
, pp. 431-1142
-
-
Miles, E.W.1
-
21
-
-
0028040145
-
Low single channel conductance of the major skeletal muscle chloride channel. CIC-1
-
Pusch M, Steinmeyer K, Jentsch TJ (1994) Low single channel conductance of the major skeletal muscle chloride channel. CIC-1. Biophys J 66:149-152
-
(1994)
Biophys J
, vol.66
, pp. 149-152
-
-
Pusch, M.1
Steinmeyer, K.2
Jentsch, T.J.3
-
22
-
-
0029559938
-
Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel
-
Pusch M, Steinmeyer K, Koch MC, Jentsch TJ (1995) Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel. Neuron 15:1455-1463
-
(1995)
Neuron
, vol.15
, pp. 1455-1463
-
-
Pusch, M.1
Steinmeyer, K.2
Koch, M.C.3
Jentsch, T.J.4
-
23
-
-
0025932612
-
Inactivation of muscle chloride channel by transposon insertion in myotonic mice
-
Steinmeyer K, Klocke R, Ortland C, Gronemeier M, Jockusch H, Gründer S, Jentsch TJ (1991) Inactivation of muscle chloride channel by transposon insertion in myotonic mice. Nature 354:304-308
-
(1991)
Nature
, vol.354
, pp. 304-308
-
-
Steinmeyer, K.1
Klocke, R.2
Ortland, C.3
Gronemeier, M.4
Jockusch, H.5
Gründer, S.6
Jentsch, T.J.7
-
24
-
-
0026039594
-
Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel
-
Steinmeyer K, Ortland C, Jentsch TJ (1991) Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel. Nature 354:301-304
-
(1991)
Nature
, vol.354
, pp. 301-304
-
-
Steinmeyer, K.1
Ortland, C.2
Jentsch, T.J.3
-
25
-
-
0028032140
-
Multimeric structure of CIC-1 chloride channel revealed by mutations in dominant myotonia congenita
-
Steinmeyer K, Lorenz C, Pusch M, Koch MC, Jentsch TJ (1994) Multimeric structure of CIC-1 chloride channel revealed by mutations in dominant myotonia congenita. EMBO J 13:737-743
-
(1994)
EMBO J
, vol.13
, pp. 737-743
-
-
Steinmeyer, K.1
Lorenz, C.2
Pusch, M.3
Koch, M.C.4
Jentsch, T.J.5
-
27
-
-
8244223953
-
Action of protein-modifying reagents on the human muscle chloride channel hClC-1
-
Wagner S, George AL Jr, Rüdel R, Kürz LL (1996) Action of protein-modifying reagents on the human muscle chloride channel hClC-1 (abstract). Pflügers Arch 431:R85
-
(1996)
Pflügers Arch
, vol.431
-
-
Wagner, S.1
George Jr., A.L.2
Rüdel, R.3
Kürz, L.L.4
|