-
1
-
-
0036678409
-
Mammalian mediator subunit mMED8 is an Elongin BC-interacting protein that can assemble with Cul2 and Rbx1 to reconstitute a ubiquitin ligase
-
DOI 10.1073/pnas.162424199
-
Brower, C.S., Sato, S., Tomomori-Sato, C., Kamura, T., Pause, A., Stearman, R., Klausner, R.D., Malik, S., Lane, W.S., Sorokina, I., Roeder, R.G., Conaway, J.W. & Conaway, R.C. (2002) Mammalian mediator subunit mMED8 is an Elongin BC-interacting protein that can assemble with Cul2 and Rbx1 to reconstitute a ubiquitin ligase. Proc Natl Acad Sci U S A99, 10353-10358. (Pubitemid 34906980)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.16
, pp. 10353-10358
-
-
Brower, C.S.1
Sato, S.2
Tomomori-Sato, C.3
Kamura, T.4
Pause, A.5
Stearman, R.6
Klausner, R.D.7
Malik, S.8
Lane, W.S.9
Sorokina, I.10
Roeder, R.G.11
Conaway, J.W.12
Conaway, R.C.13
-
2
-
-
0035874914
-
Electroconvulsive thresholds of inbred mouse strains
-
DOI 10.1006/geno.2001.6564
-
Frankel, W.N., Taylor, L., Beyer, B., Tempel, B.L. & White, H.S. (2001) Electroconvulsive thresholds of inbred mouse strains. Genomics74, 306-312. (Pubitemid 32675354)
-
(2001)
Genomics
, vol.74
, Issue.3
, pp. 306-312
-
-
Frankel, W.N.1
Taylor, L.2
Beyer, B.3
Tempel, B.L.4
White H.Steve5
-
3
-
-
33644773647
-
Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2
-
DOI 10.1093/hmg/ddl019
-
Kearney, J.A., Yang, Y., Beyer, B., Bergren, S.K., Claes, L., Dejonghe, P. & Frankel, W.N. (2006) Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2. Hum Mol Genet 15, 1043-1048. (Pubitemid 43338243)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.6
, pp. 1043-1048
-
-
Kearney, J.A.1
Yang, Y.2
Beyer, B.3
Bergren, S.K.4
Claes, L.5
DeJonghe, P.6
Frankel, W.N.7
-
4
-
-
4344710223
-
Genetic and phenotypic analysis of seizure susceptibility in PL/J mice
-
DOI 10.1007/s00335-004-3007-7
-
Kitami, T., Ernest, S., Gallaugher, L., Friedman, L., Frankel, W.N. & Nadeau, J.H. (2004) Genetic and phenotypic analysis of seizure susceptibility in PL/J mice. Mamm Genome15, 698-703. (Pubitemid 39159194)
-
(2004)
Mammalian Genome
, vol.15
, Issue.9
, pp. 698-703
-
-
Kitami, T.1
Ernest, S.2
Gallaugher, L.3
Friedman, L.4
Frankel, W.N.5
Nadeau, J.H.6
-
5
-
-
0031800709
-
Validation of corneally kindled mice: A sensitive screening model for partial epilepsy in man
-
DOI 10.1016/S0920-1211(98)00016-3, PII S0920121198000163
-
Matagne, A. & Klitgaard, H. (1998) Validation of corneally kindled mice: a sensitive screening model for partial epilepsy in man. Epilepsy Res31, 59-71. (Pubitemid 28305405)
-
(1998)
Epilepsy Research
, vol.31
, Issue.1
, pp. 59-71
-
-
Matagne, A.1
Klitgaard, H.2
-
6
-
-
0345035384
-
Corneal kindling in mice: Behavioral and pharmacological differences to conventional kindling
-
DOI 10.1016/S0920-1211(99)00062-5, PII S0920121199000625
-
Potschka, H. & Loscher, W. (1999) Corneal kindling in mice: behavioral and pharmacological differences to conventional kindling. Epilepsy Res37, 109-120. (Pubitemid 29457792)
-
(1999)
Epilepsy Research
, vol.37
, Issue.2
, pp. 109-120
-
-
Potschka, H.1
Loscher, W.2
-
8
-
-
17344372328
-
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
-
DOI 10.1038/ng0198-25
-
Singh, N.A., Charlier, C., Stauffer, D., DuPont, B.R., Leach, R.J., Melis, R., Ronen, G.M., Bjerre, I., Quattlebaum, T., Murphy, J.V., McHarg, M.L., Gagnon, D., Rosales, T.O., Peiffer, A., V.E., A. & Leppert, M. (1998) A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns. Nature Genet 18, 25-29. (Pubitemid 28027874)
-
(1998)
Nature Genetics
, vol.18
, Issue.1
, pp. 25-29
-
-
Singh, N.A.1
Charlier, C.2
Stauffer, D.3
DuPont, B.R.4
Leach, R.J.5
Melis, R.6
Ronen, G.M.7
Bjerre, I.8
Quattlebaum, T.9
Murphy, J.V.10
McHarg, M.L.11
Gagnon, D.12
Rosales, T.O.13
Peiffer, A.14
Elving Anderson, V.15
Leppert, M.16
-
9
-
-
65449188232
-
Jalview Version 2 - Amultiple sequence alignment editor and analysis workbench
-
Waterhouse, A.M., Procter, J.B., Martin, D.M., Clamp, M. & Barton, G.J. (2009) Jalview Version 2 - amultiple sequence alignment editor and analysis workbench. Bioinformatics25, 1189-1191.
-
(2009)
Bioinformatic
, vol.25
, pp. 1189-1191
-
-
Waterhouse, A.M.1
Procter, J.B.2
Martin, D.M.3
Clamp, M.4
Barton, G.J.5
-
10
-
-
0038702369
-
Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low eletroconvulsive threshold
-
DOI 10.1093/hmg/ddg118
-
Yang, Y., Beyer, B.J., Otto, J.F., O'Brien, T.P., Letts, V.A., White, H.S. & Frankel, W.N. (2003) Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive threshold. Hum Mol Genet 12, 975-984. (Pubitemid 36553517)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.9
, pp. 975-984
-
-
Yang, Y.1
Beyer, B.J.2
Otto, J.F.3
O'Brien, T.P.4
Letts, V.A.5
White, H.S.6
Frankel, W.N.7
-
11
-
-
34547629265
-
Complex seizure disorder caused by Brunol4 deficiency in mice
-
Yang, Y., Mahaffey, C.L., Berube, N., Maddatu, T.P., Cox, G.A. & Frankel, W.N. (2007) Complex seizure disorder caused by Brunol4 deficiency in mice. PLoS Genet 3, e124.
-
(2007)
PLoS Genet
, vol.3
-
-
Yang, Y.1
Mahaffey, C.L.2
Berube, N.3
Maddatu, T.P.4
Cox, G.A.5
Frankel, W.N.6
|