Do all voltage-gated potassium channels use MiRPs?

No abstract is available for this paper.

• Publication year

  2001

• Venue

  Circulation Research

• Publication date

  2001-05-25

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1161/HH1001.091869PMID 11375265
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Distinct gene-specific mechanisms of arrhythmia revealed by cardiac gene transfer of two long QT disease genes, HERG and KCNE1

  2001cited by this paper
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  2001cited by this paper
• MinK-Related Peptide 1 Associates With Kv4.2 and Modulates Its Gating Function: Potential Role as &bgr; Subunit of Cardiac Transient Outward Channel?

  2001cited by this paper
• Analysis of the Cyclic Nucleotide Binding Domain of the HERG Potassium Channel and Interactions with KCNE2*

  2001cited by this paper
• MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis.

  2001cited by this paper
• A constitutively open potassium channel formed by KCNQ1 and KCNE3

  2000cited by this paper
• Mink Subdomains That Mediate Modulation of and Association with Kvlqt1

  2000cited by this paper
• Cyclic AMP regulates the HERG K(+) channel by dual pathways.

  2000cited by this paper
• A common polymorphism associated with antibiotic-induced cardiac arrhythmia.

  2000cited by this paper
• MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia.

  1999cited by this paper
• Long QT Syndrome-associated Mutations in the S4-S5 Linker of KvLQT1 Potassium Channels Modify Gating and Interaction with minK Subunits*

  1999cited by this paper
• A superfamily of small potassium channel subunits: form and function of the MinK-related peptides (MiRPs)

  1998cited by this paper
• Single-Channel Characteristics of Wild-Type IKs Channels and Channels formed with Two MinK Mutants that Cause Long QT Syndrome

  1998cited by this paper
• MinK-KvLQT1 Fusion Proteins, Evidence for Multiple Stoichiometries of the Assembled I sK Channel*

  1998cited by this paper
• The structure of the potassium channel: molecular basis of K+ conduction and selectivity.

  1998cited by this paper
• KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current

  1996cited by this paper
• Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel

  1996cited by this paper
• Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.

  1996cited by this paper
• Viral and cellular small integral membrane proteins can modify ion channels endogenous to Xenopus oocytes.

  1995cited by this paper
• Induction of endogenous channels by high levels of heterologous membrane proteins in Xenopus oocytes.

  1995cited by this paper
• Subunit composition of minK potassium channels.

  1995cited by this paper
• Are Xenopus oocytes unique in displaying functional IsK channel heterologous expression?

  1993cited by this paper
• The protein IsK is a dual activator of K+ and CI− channels

  1993cited by this paper
• Cloning of a membrane protein that induces a slow voltage-gated potassium current.

  1988cited by this paper

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  2023cites this paper
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  2009cites this paper
• [The role of genetic factors in development of atrial fibrillation].

  2007cites this paper
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  2007cites this paper
• Voltage-gated ion channels and gating modifier toxins.

  2007cites this paper
• Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome.

  2007cites this paper
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  2006cites this paper
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  2006cites this paper
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  2005cites this paper
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  2005cites this paper
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  2003cites this paper
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