-
2
-
-
0032536030
-
A potassium channel mutation in neonatal human epilepsy
-
Biervert, C. et al. A potassium channel mutation in neonatal human epilepsy. Science 279, 403-406 (1998).
-
(1998)
Science
, vol.279
, pp. 403-406
-
-
Biervert, C.1
-
3
-
-
0031974209
-
A pore mutation in a novel KQT-Iike potassium channel in an idiopathic epilepsy family
-
Charlier, C. et al. A pore mutation in a novel KQT-Iike potassium channel in an idiopathic epilepsy family. Nature Genet. 18, 53-55 (1998).
-
(1998)
Nature Genet.
, vol.18
, pp. 53-55
-
-
Charlier, C.1
-
4
-
-
17344372328
-
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
-
Singh, N. A. et al. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns. Nature Genet. 18, 25-29 (1993).
-
(1993)
Nature Genet.
, vol.18
, pp. 25-29
-
-
Singh, N.A.1
-
5
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
Wang, Q. et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genet. 12, 17-23 (1996).
-
(1996)
Nature Genet.
, vol.12
, pp. 17-23
-
-
Wang, Q.1
-
6
-
-
0024502803
-
Benign familial neonatal convulsions linked to genetic markers on chromosome 20
-
Leppert, M. et al. Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Nature 337, 647-648 (1989).
-
(1989)
Nature
, vol.337
, pp. 647-648
-
-
Leppert, M.1
-
7
-
-
0027359350
-
Genetic heterogeneity in benign familial neonatal convulsions: Identification of a new locus on chromosome 8q
-
Lewis, T. B., Leach, R. J., Ward, K., O'Connell, P. & Ryan, S. G. Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q. Am. J. Hum. Genet. 53, 670-675 (1993).
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 670-675
-
-
Lewis, T.B.1
Leach, R.J.2
Ward, K.3
O'Connell, P.4
Ryan, S.G.5
-
8
-
-
0025252308
-
Heteropolymeric potassium channels expressed in Xenopus oocytes from cloned subunits
-
Christie, M. J., North, R. A., Osborne, P. B., Douglass, J. & Adelman, J. P. Heteropolymeric potassium channels expressed in Xenopus oocytes from cloned subunits. Neuron 2, 405-411 (1990).
-
(1990)
Neuron
, vol.2
, pp. 405-411
-
-
Christie, M.J.1
North, R.A.2
Osborne, P.B.3
Douglass, J.4
Adelman, J.P.5
-
9
-
-
0025362581
-
Evidence for the formation of heteromuhimeric potassium channels in Xenopus oocytes
-
Isacoff, E. Y., Jan, Y. N. & Jan, L. Y. Evidence for the formation of heteromuhimeric potassium channels in Xenopus oocytes. Nature 345, 530-534 (1990).
-
(1990)
Nature
, vol.345
, pp. 530-534
-
-
Isacoff, E.Y.1
Jan, Y.N.2
Jan, L.Y.3
-
10
-
-
0025287606
-
Heteromuhimeric channels formed by rat brain potassium-channel proteins
-
Ruppersberg, J. P. et al. Heteromuhimeric channels formed by rat brain potassium-channel proteins. Nature 345, 535-537 (1990).
-
(1990)
Nature
, vol.345
, pp. 535-537
-
-
Ruppersberg, J.P.1
-
11
-
-
0029952101
-
Ks, cardiac potassium current
-
Ks, cardiac potassium current. Nature 384, 78-80 (1996).
-
(1996)
Nature
, vol.384
, pp. 78-80
-
-
Barhanin, J.1
-
12
-
-
0029854263
-
Ks potassium channel
-
Ks potassium channel Nature 384, 80-83 (1996).
-
(1996)
Nature
, vol.384
, pp. 80-83
-
-
Sanguinetti, M.C.1
-
13
-
-
0030799943
-
+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias
-
+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias. EMBQ J. 16, 5472-5479 (1997).
-
(1997)
EMBQ J.
, vol.16
, pp. 5472-5479
-
-
Chouabe, C.1
-
14
-
-
0029840732
-
KVtQT1 mutations in three families with familial or sporadic long QT syndrome
-
Russell, M. W., Macdonald, D., Collins, F. S. & Brody, L. C KVtQT1 mutations in three families with familial or sporadic long QT syndrome. Hum. Mol. Genet. 5, 1319-1324 (1996).
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1319-1324
-
-
Russell, M.W.1
Macdonald, D.2
Collins, F.S.3
Brody, L.C.4
-
15
-
-
0030782276
-
+ channel mutations found in inherited cardiac arrhythmias
-
+ channel mutations found in inherited cardiac arrhythmias. Hum. Mol. Genet. 6, 1943-1949 (1997).
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1943-1949
-
-
Wollnik, B.1
-
16
-
-
0030005755
-
The I.MA.G.E. Consortium: An integrated molecular analysis of genomes and their expression
-
Lennon, G., Auffray, C., Polymeropoulos, M. & Soares, M. B. The I.MA.G.E. Consortium: an integrated molecular analysis of genomes and their expression. Genomics 33, 151-152 (1996).
-
(1996)
Genomics
, vol.33
, pp. 151-152
-
-
Lennon, G.1
Auffray, C.2
Polymeropoulos, M.3
Soares, M.B.4
-
17
-
-
0029843417
-
Heteromultimeric CLC chloride channels with novel properties
-
Lorenz, C., Pusch, M. & Jentsch, T. J. Heteromultimeric CLC chloride channels with novel properties. Proc. Natl Acad. Sci USA 93, 13362-13366 (1996).
-
(1996)
Proc. Natl Acad. Sci USA
, vol.93
, pp. 13362-13366
-
-
Lorenz, C.1
Pusch, M.2
Jentsch, T.J.3
-
18
-
-
0028793540
-
Distribution of somatostatin receptor subtype I mRNA in the developing cerebral hemispheres of the rat
-
Hartmann, D., Fehr, S., Meyerhof, W. & Richter, D. Distribution of somatostatin receptor subtype I mRNA in the developing cerebral hemispheres of the rat. Dev. Neurosci. 17, 246-255 (1995).
-
(1995)
Dev. Neurosci.
, vol.17
, pp. 246-255
-
-
Hartmann, D.1
Fehr, S.2
Meyerhof, W.3
Richter, D.4
-
19
-
-
0030934771
-
Molecular dissection of gating in the ClC-2 chloride channel
-
Jordt, S.-E. & Jentsch, T. J. Molecular dissection of gating in the ClC-2 chloride channel. EMBO J. 16, 1582-1592 (1997).
-
(1997)
EMBO J.
, vol.16
, pp. 1582-1592
-
-
Jordt, S.-E.1
Jentsch, T.J.2
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