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TRPM4 gene

Known as: TRPM4, FLJ20041, TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY M, MEMBER 4 
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Brugada syndrome (BrS) is a condition defined by ST-segment alteration in right precordial leads and a risk of sudden death… Expand
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Highly Cited
2012
Highly Cited
2012
Very recently, mutations in the TRPM4 gene have been identified in four pedigrees as the cause of an autosomal dominant form of… Expand
Highly Cited
2010
Highly Cited
2010
Background—Isolated cardiac conduction block is a relatively common condition in young and elderly populations. Genetic… Expand
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Highly Cited
2009
Highly Cited
2009
Progressive familial heart block type I (PFHBI) is a progressive cardiac bundle branch disease in the His-Purkinje system that… Expand
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Highly Cited
2006
Highly Cited
2006
Transient receptor potential (TRP) channel, melastatin subfamily (TRPM)4 is a Ca2+‐activated monovalent cation channel that… Expand
Highly Cited
2005
Highly Cited
2005
Non-selective cation (NSC) channels activated by intracellular Ca2+ ([Ca2+]i) play an important role in Ca2+ signaling and… Expand
Highly Cited
2004
Highly Cited
2004
Local control of cerebral blood flow is regulated in part through myogenic constriction of resistance arteries. Although this… Expand
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Highly Cited
2004
Highly Cited
2004
TRPM4 has recently been described as a calcium-activated nonselective (CAN) cation channel that mediates membrane depolarization… Expand
Highly Cited
2003
Highly Cited
2003
TRPM4 is a Ca2+-activated but Ca2+-impermeable cation channel. An increase of [Ca2+]i induces activation and subsequent reduction… Expand
Highly Cited
2002
Highly Cited
2002
Calcium-activated nonselective (CAN) cation channels are expressed in various excitable and nonexcitable cells supporting… Expand
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