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lysyl-isoleucyl-phenylalanyl-methionyl-lysine

Known as: KIFMK, Lys-Ile-Phe-Met-Lys 
 
National Institutes of Health

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2014
2014
A capillary electrophoresis method has been developed and validated to evaluate the stereospecific activity of recombinant human… Expand
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2008
2008
Ca(2+)-entry via L-type Ca(2+) channels (DHPR) is known to trigger ryanodine receptor (RyR)-mediated Ca(2+)-release from… Expand
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2004
2004
1. Acetyl-KIFMK-amide (KIFMK) restores fast inactivation to mutant sodium channels having a defective inactivation gate. Its… Expand
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2003
2003
Oligopeptide-mediated helix stabilization of peptides in hydrophobic solutions was previously found by NMR and CD spectroscopic… Expand
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1999
1999
Inactivation of sodium channels is thought to be mediated by an inactivation gate formed by the intracellular loop connecting… Expand
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1999
1999
1. Whole cell patch clamping of transfected HEK293 cells was used to examine the effects of a pentapeptide (KIFMK) containing the… Expand
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Highly Cited
1998
Highly Cited
1998
Na+ channel fast inactivation is thought to involve the closure of an intracellular inactivation gate over the channel pore… Expand
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1998
1998
We analyzed the kinetics of interaction between the peptide KIFMK, containing the isoleucine, phen-ylalanine, and methionine (IFM… Expand
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1997
1997
Abstract. Veratridine, an alkaloid isolated from the rhizome of V. album, binds and slows the inactivation of the brain sodium… Expand
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1996
1996
A pair of conserved methionine residues, located on the cytoplasmic linker between segments S4 and S5 in the fourth domain of… Expand
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