TPM1 gene

Known as: TROPOMYOSIN, SKELETAL MUSCLE ALPHA, TPM1, TROPOMYOSIN 1 
This gene plays a role in muscle contraction.
National Institutes of Health

Papers overview

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2011
2011
BACKGROUND Left ventricular noncompaction of the myocardium (LVNC) has been recognized as a cardiomyopathy with a genetic… (More)
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Highly Cited
2010
Highly Cited
2010
BACKGROUND Rare variants in >30 genes have been shown to cause idiopathic or familial dilated cardiomyopathy (DCM), but the… (More)
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Highly Cited
2009
Highly Cited
2009
PURPOSE We aim to examine miR-21 expression in tongue squamous cell carcinomas (TSCC) and correlate it with patient clinical… (More)
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2009
2009
INTRODUCTION AND OBJECTIVES Mutation of a sarcomeric gene is the most frequent cause of hypertrophic cardiomyopathy. For each… (More)
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Highly Cited
2008
Highly Cited
2008
MicroRNAs (miRNAs) are a class of naturally occurring small non-coding RNAs that target protein-coding mRNAs at the post… (More)
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2003
2003
OBJECTIVES This study was initiated to identify the disease-causing genetic defect in a family with hypertrophic cardiomyopathy… (More)
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2002
2002
We sought to define the pathogenic mutation in a family with hypertrophic cardiomyopathy (HC) and a markedly arrhythmogenic… (More)
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Highly Cited
1997
Highly Cited
1997
In Saccharomyces cerevisiae, the growing bud inherits a portion of the mitochondrial network from the mother cell soon after it… (More)
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Highly Cited
1995
Highly Cited
1995
Sequence analysis of chromosome IX of Saccharomyces cerevisiae revealed an open reading frame of 166 residues, designated TPM2… (More)
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Highly Cited
1992
Highly Cited
1992
Disruption of the yeast tropomyosin gene TPM1 results in the apparent loss of actin cables from the cytoskeleton (Liu, H., and A… (More)
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