Language
English
German
^M
Dutch
Spanish
Title:
HERG sequence correction
Source:
Science [0036-8075] Trudeau, M C yr:1996
Basic
Sorry, no full text available...
Please use the document delivery service (see below)
Holding information
Holdings in library search engine
ALBERT
Document delivery
Request document via
Library/Bibliothek
Users interested in this article also expressed an interest in the following:
description
1.
Warmke, J.W. W.
"A family of potassium channel genes related to eag in Drosophila and mammals."
Proceedings of the National Academy of Sciences of the United States of America
91.8 (1994): 3438-3442.
description
2.
Kamarck, Michael E.
"Somatic cell hybrid mapping panels."
Experimental cell research
152.1 (1984): 1-14.
description
3.
Krishnan, Y.
"Mechanisms underlying the protein-kinase mediated regulation of the HERG potassium channel synthesis."
Biochimica et biophysica acta. Molecular cell research
1823.8 (2012): 1273-1284.
description
4.
Itoh, T.
"Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome."
Human genetics
102.4 (1998): 435-439.
description
5.
Gutman, G A A.
"Molecular evolution of voltage-sensitive ion channel genes: on the origins of electrical excitability."
Molecular Biology and Evolution
10.1 (1992): 221-42.
description
6.
Smith, Jennifer L.
Circulation. Arrhythmia and Electrophysiology
(2018).
description
7.
Li, Min T.
"Crystal Structure and Functional Analysis of the HERG Potassium Channel N Terminus."
Cell
95.5 (1998): 649-655.
description
8.
Thibault, K.
"Cortical effect of oxaliplatin associated with sustained neuropathic pain : Exacerbation of cortical activity and down-regulation of potassium channel expression in somatosensory cortex."
Pain
153.8 (2012): 1636-1647.
description
9.
Jan, L Y N.
"Tracing the roots of ion channels."
Cell
69.5 (1992): 715-718.
description
10.
Julius, D.
"New structural motif for ligand-gated ion channels defined by an ionotropic ATP receptor."
Nature
371.6497: 519-523.
description
11.
Curran, M E E.
"A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome."
Cell
80.5 (1995): 795-803.
description
12.
Kontula, K.
"Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland."
Annals of medicine
36.1 (2004): 53-63.
View More...
View Less...
Select All
Clear All
Save Citations
Select Format
Reference Manager
ProCite
EndNote
RefWorks
Submit citation export
Advanced
Author
Other articles by this author? -- in
GeoRef
author:
Trudeau, M C
Warmke, J W
Ganetzky, B
Robertson, G A
last name
initials
Other articles by this author? -- in
Online Contents Geosciences
author:
Trudeau, M C
Warmke, J W
Ganetzky, B
Robertson, G A
last name
initials
Other articles by this author? -- using
Web of Science
author:
Trudeau, M C
Warmke, J W
Ganetzky, B
Robertson, G A
last name
initials
Web Search
Find related information in
a Web Search Engine
Excite
Google
HotBot
Ixquick
ZOO
Ask
Yahoo!
Bing
Naver
Search Terms:
Search for related information in
Google Scholar
Article Title
Author Name
Journal Title
Other Search
Search Terms:
A service provided by the
Library of the Wissenschaftspark Albert Einstein
, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.