-
1
-
-
25544450006
-
Coexistence of missense mutation of HERG and mitochondrial DNA in Japanese long QT family
-
AKIMOTO, K., FURUTANI, M., KASANUKI, H., IMAMMURA, S.-I., FURUTANI, Y., TAKAO, A., MONMA, K. & MATSUOKA, R. (1996). Coexistence of missense mutation of HERG and mitochondrial DNA in Japanese long QT family. Circulation 94, I164.
-
(1996)
Circulation
, vol.94
-
-
Akimoto, K.1
Furutani, M.2
Kasanuki, H.3
Imammura, S.-I.4
Furutani, Y.5
Takao, A.6
Monma, K.7
Matsuoka, R.8
-
2
-
-
0030012835
-
Missense mutation in the pore region of HERG causes familial long QT syndrome
-
BENSON, D. W., MACRAE, C. A., VESELY, M. R., WALSH, E. P., SEIDMAN, J. G., SEIDMAN, C. E. & SATLER, C. A. (1996). Missense mutation in the pore region of HERG causes familial long QT syndrome. Circulation 93, 1791-1795.
-
(1996)
Circulation
, vol.93
, pp. 1791-1795
-
-
Benson, D.W.1
MacRae, C.A.2
Vesely, M.R.3
Walsh, E.P.4
Seidman, J.G.5
Seidman, C.E.6
Satler, C.A.7
-
4
-
-
0028914969
-
A molecular basis for cardiac arrhythmia. HERG mutations cause long QT syndrome
-
CURRAN, M. E., SPLAWSKI, I., TIMOTHY, K. W., VINCENT, G. M., GREEN, E. D. & KEATING, M. T. (1995). A molecular basis for cardiac arrhythmia. HERG mutations cause long QT syndrome. Cell 80, 795-803.
-
(1995)
Cell
, vol.80
, pp. 795-803
-
-
Curran, M.E.1
Splawski, I.2
Timothy, K.W.3
Vincent, G.M.4
Green, E.D.5
Keating, M.T.6
-
5
-
-
0030218890
-
A mutation in HERG associated with notched T waves in long QT syndrome
-
DAUSSE, E., BERTHET, M., DENJOY, I., ANDRE-FOUET, X., CRUAUD, C., BENNACEUR, M., FAURE, S., COUMEL, P., SCHWARTZ, K. & GUICHENEY, P. (1996). A mutation in HERG associated with notched T waves in long QT syndrome. Journal of Molecular and Cellular Cardiology 28, 1609-1615.
-
(1996)
Journal of Molecular and Cellular Cardiology
, vol.28
, pp. 1609-1615
-
-
Dausse, E.1
Berthet, M.2
Denjoy, I.3
Andre-Fouet, X.4
Cruaud, C.5
Bennaceur, M.6
Faure, S.7
Coumel, P.8
Schwartz, K.9
Guicheney, P.10
-
6
-
-
0028343497
-
The brain Kv1.1 potassium channel: In vitro and in vivo studies on subunit assembly and posttranslational processing
-
DEAL, K. K., LOVINGER, D. M. & TAMKUN, M. M. (1994). The brain Kv1.1 potassium channel: in vitro and in vivo studies on subunit assembly and posttranslational processing. Journal of Neuroscience 14, 1666-1676.
-
(1994)
Journal of Neuroscience
, vol.14
, pp. 1666-1676
-
-
Deal, K.K.1
Lovinger, D.M.2
Tamkun, M.M.3
-
7
-
-
0026601458
-
Site-directed mutagenesis of virtually any plasmid by eliminating a unique site
-
DENG, W. P. & NICKOLOFF, J. A. (1992). Site-directed mutagenesis of virtually any plasmid by eliminating a unique site. Analytical Biochemistry 200, 81-88.
-
(1992)
Analytical Biochemistry
, vol.200
, pp. 81-88
-
-
Deng, W.P.1
Nickoloff, J.A.2
-
8
-
-
0029053448
-
The role of N-glycans in the secretory pathway
-
FIEDLER, K. & SIMONS, K. (1995). The role of N-glycans in the secretory pathway. Cell 81, 309-312.
-
(1995)
Cell
, vol.81
, pp. 309-312
-
-
Fiedler, K.1
Simons, K.2
-
9
-
-
0032055472
-
Carbohydrate-mediated Golgi to cell surface transport and apical targetting of membrane proteins
-
GUT, A., KAPPELER, F., HYKA, N., BALDA, M. S., HAURI, H.-P. & MATTER, K. (1998). Carbohydrate-mediated Golgi to cell surface transport and apical targetting of membrane proteins. EMBO Journal 17, 1919-1929.
-
(1998)
EMBO Journal
, vol.17
, pp. 1919-1929
-
-
Gut, A.1
Kappeler, F.2
Hyka, N.3
Balda, M.S.4
Hauri, H.-P.5
Matter, K.6
-
11
-
-
0030667061
-
The number and location of glycans on influenza hemagglutinin determine folding and association with calnexin and calreticulin
-
HEBERT, D. N., ZHANG, J.-X., CHEN, W., FOELLMER, B. & HELENIUS, A. (1997). The number and location of glycans on influenza hemagglutinin determine folding and association with calnexin and calreticulin. Journal of Cell Biology 139, 613-623.
-
(1997)
Journal of Cell Biology
, vol.139
, pp. 613-623
-
-
Hebert, D.N.1
Zhang, J.-X.2
Chen, W.3
Foellmer, B.4
Helenius, A.5
-
12
-
-
0020027832
-
Inhibition of glycosylation with tunicamycin blocks assembly of newly synthesized acetylcholine receptor subunits in muscle cells
-
MERLIE, J. P., SEBBANE, R., TZARTOS, S. & LINDSTROM, J. (1982). Inhibition of glycosylation with tunicamycin blocks assembly of newly synthesized acetylcholine receptor subunits in muscle cells. Journal of Biological Chemistry 257, 2694-2701.
-
(1982)
Journal of Biological Chemistry
, vol.257
, pp. 2694-2701
-
-
Merlie, J.P.1
Sebbane, R.2
Tzartos, S.3
Lindstrom, J.4
-
13
-
-
0021929401
-
Location of functional region of acetylcholine receptor alpha-subunits by site-directed mutagenesis
-
MISHINA, M., TOBIMATSU, T., IMOTO, K., TANAKA, K., FUJITA, Y., FUKUDA, K., KURASAKI, M., TAKAHASHI, H., MORIMOTO, Y., HIROSE, T., INAYAMA, S., TAKAHASHI, T., KUNO, M. & NUMA, S. (1985). Location of functional region of acetylcholine receptor alpha-subunits by site-directed mutagenesis. Nature 313, 364-369.
-
(1985)
Nature
, vol.313
, pp. 364-369
-
-
Mishina, M.1
Tobimatsu, T.2
Imoto, K.3
Tanaka, K.4
Fujita, Y.5
Fukuda, K.6
Kurasaki, M.7
Takahashi, H.8
Morimoto, Y.9
Hirose, T.10
Inayama, S.11
Takahashi, T.12
Kuno, M.13
Numa, S.14
-
14
-
-
0028930710
-
The role of N-glycosylation in the targeting and activity of the GLYT1 glycine transporter
-
OLIVARES, L., ARAGON, C., GIMENEZ, C. & ZAFRA F. (1995). The role of N-glycosylation in the targeting and activity of the GLYT1 glycine transporter. Journal of Biological Chemistry 270, 9437-9442.
-
(1995)
Journal of Biological Chemistry
, vol.270
, pp. 9437-9442
-
-
Olivares, L.1
Aragon, C.2
Gimenez, C.3
Zafra, F.4
-
15
-
-
0342300768
-
A truncated form of HERG identified in human heart
-
POND, A. & NERBONNE, J. M. (1996). A truncated form of HERG identified in human heart. Circulation 94, I641.
-
(1996)
Circulation
, vol.94
-
-
Pond, A.1
Nerbonne, J.M.2
-
16
-
-
0029847602
-
Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS
-
RODEN, D. M., LAZZARA, R., ROSEN, M., SCHWARTZ, P. J., TOWBIN, J. & VINCENT, G. M. (1996). Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS. Circulation 94, 1996-2012.
-
(1996)
Circulation
, vol.94
, pp. 1996-2012
-
-
Roden, D.M.1
Lazzara, R.2
Rosen, M.3
Schwartz, P.J.4
Towbin, J.5
Vincent, G.M.6
-
17
-
-
0029002969
-
A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel
-
SANGUINETTI, M. C., JIANG, C., CURRAN, M. E. & KEATING, M. T. (1995). A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel. Cell 81, 299-307.
-
(1995)
Cell
, vol.81
, pp. 299-307
-
-
Sanguinetti, M.C.1
Jiang, C.2
Curran, M.E.3
Keating, M.T.4
-
18
-
-
0028175781
-
Glycosylation of shaker potassium channel protein in insect cell culture and in Xenopus oocytes
-
SANTACRUZ-TOLOZA, L., HUANG, Y., JOHN, S. A. & PAPAZIAN, D. M. (1994). Glycosylation of shaker potassium channel protein in insect cell culture and in Xenopus oocytes. Biochemistry 33, 5607-5613.
-
(1994)
Biochemistry
, vol.33
, pp. 5607-5613
-
-
Santacruz-Toloza, L.1
Huang, Y.2
John, S.A.3
Papazian, D.M.4
-
19
-
-
0031948555
-
Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome
-
SATLER, C. A., VESELY, M. R., DUGGAL, P., GINSBURG, G. S. & BEGGS, A. H. (1998). Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome. Human Genetics 102, 265-272.
-
(1998)
Human Genetics
, vol.102
, pp. 265-272
-
-
Satler, C.A.1
Vesely, M.R.2
Duggal, P.3
Ginsburg, G.S.4
Beggs, A.H.5
-
20
-
-
0029793031
-
Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome
-
SATLER, C. A., WALSH, E. P., VESELY, M. R., PLUMMER, M. H., GINSBURG, G. S. & JACOB, H. J. (1996). Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome. American Journal of Medical Genetics 66, 27-35.
-
(1996)
American Journal of Medical Genetics
, vol.66
, pp. 27-35
-
-
Satler, C.A.1
Walsh, E.P.2
Vesely, M.R.3
Plummer, M.H.4
Ginsburg, G.S.5
Jacob, H.J.6
-
21
-
-
16944362512
-
Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome
-
TANAKA, T., NAGAI, R., TOMOIKE, H., TAKATA, S., YANO, K., YABUTA, K., HANEDA, N., NAKANO, O., SHIBATA, A., SAWAYAMA, T., KASAI, H., YAZAKI, Y. & NAKAMURA, Y. (1997). Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome. Circulation 95, 565-567.
-
(1997)
Circulation
, vol.95
, pp. 565-567
-
-
Tanaka, T.1
Nagai, R.2
Tomoike, H.3
Takata, S.4
Yano, K.5
Yabuta, K.6
Haneda, N.7
Nakano, O.8
Shibata, A.9
Sawayama, T.10
Kasai, H.11
Yazaki, Y.12
Nakamura, Y.13
-
22
-
-
0020582852
-
Glycosylation is required for maintenance of functional sodium channels in neuroblastoma cells
-
WAECHTER, C. J., SCHMIDT, J. W. & CATTERALL, W. A. (1983) Glycosylation is required for maintenance of functional sodium channels in neuroblastoma cells. Journal of Biological Chemistry 258, 5117-5123.
-
(1983)
Journal of Biological Chemistry
, vol.258
, pp. 5117-5123
-
-
Waechter, C.J.1
Schmidt, J.W.2
Catterall, W.A.3
-
23
-
-
0028840915
-
Degradation of CFTR by the ubiquitin-proteasome pathway
-
WARD, C. L. & KOPITO, R. R. (1995). Degradation of CFTR by the ubiquitin-proteasome pathway. Cell 83, 121-127.
-
(1995)
Cell
, vol.83
, pp. 121-127
-
-
Ward, C.L.1
Kopito, R.R.2
-
25
-
-
0344401419
-
Multiple mechansims of HERG channel dysfunction in human long QT associated mutation
-
ZHOU, Z., GONG, Q., EPSTEIN, M. & JANUARY, C. T. (1998a). Multiple mechansims of HERG channel dysfunction in human long QT associated mutation. Biophysical Journal 74, A26.
-
(1998)
Biophysical Journal
, vol.74
-
-
Zhou, Z.1
Gong, Q.2
Epstein, M.3
January, C.T.4
-
26
-
-
0031982513
-
Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature
-
ZHOU, Z., GONG, Q., YE, B., FAN, Z., MAKIELSKI, J. C., ROBERTSON, G. A. & JANUARY, C. T. (1998b). Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature. Biophysical Journal 74, 230-241.
-
(1998)
Biophysical Journal
, vol.74
, pp. 230-241
-
-
Zhou, Z.1
Gong, Q.2
Ye, B.3
Fan, Z.4
Makielski, J.C.5
Robertson, G.A.6
January, C.T.7
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