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SLMAP gene

Known as: SLMAP, sarcolemma associated protein, SLAP 
National Institutes of Health

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SLMAP protein, human

Papers overview

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Highly Cited
2007
Highly Cited
2007
Sex-specific and exercise-acquired cardioprotection is abolished by sarcolemmal KATP channel blockade in the rat heart.
The present study was conducted to determine whether the infarct sparing effect of short-term exercise is dependent on the… 
Highly Cited
2006
Highly Cited
2006
Sex differences in myocardial infarct size are abolished by sarcolemmal KATP channel blockade in rat.
This study was conducted to examine the relationship between myocardial ATP-sensitive potassium (K(ATP)) channels and sex… 
Highly Cited
2005
Highly Cited
2005
Sarcolemmal KATP channel triggers delayed ischemic preconditioning in rats.
Previous work from our laboratory has shown that the sarcolemmal K(ATP) channel (sK(ATP)) is required as a trigger for delayed… 
Highly Cited
2002
Highly Cited
2002
Sarcolemmal KATP Channel Triggers Opioid-Induced Delayed Cardioprotection in the Rat
Recently, the involvement of sarcolemmal KATP (sarcKATP) channels in ischemic and pharmacological preconditioning (IPC and PPC… 
Highly Cited
2002
Highly Cited
2002
Delayed cardioprotection by isoflurane: role of K(ATP) channels.
Isoflurane mimics the cardioprotective effect of acute ischemic preconditioning with an acute memory phase. We determined whether… 
1999
1999
Free oxygen radicals contribute to high incidence of reperfusion-induced arrhythmias in isolated rat heart.
Highly Cited
1995
Highly Cited
1995
Reciprocal changes in the postnatal expression of the sarcolemmal Na+-Ca(2+)-exchanger and SERCA2 in rat heart.
Highly Cited
1994
Highly Cited
1994
Steady-state mRNA levels of the sarcolemmal Na(+)-Ca2+ exchanger peak near birth in developing rabbit and rat hearts.
To functionally compensate for an underdeveloped sarcoplasmic reticulum in immature cardiomyocytes, it has been proposed that the… 
Highly Cited
1992
Highly Cited
1992
Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy
X-LINKED recessive Duchenne muscular dystrophy (DMD) is caused by the absence of dystrophin, a membrane cytoskeletal protein1,2… 
1975
1975
Fine structure of the myotendinous junction and “terminal coupling” in the skeletal muscle of the lamprey, Lampetra japonica
The myotendinous junction in the skeletal muscle of adult lamprey Lampetra japonica was studied with an electron microscope… 
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