UTRN gene

Known as: UTROPHIN, UTRN, DMDL 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1972-2017
0204019722017

Papers overview

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Highly Cited
2007
Highly Cited
2007
Actin filaments (F-actin) are protein polymers that undergo rapid assembly and disassembly and control an enormous variety of… (More)
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Highly Cited
2001
Highly Cited
2001
Muscle fibers attach to laminin in the basal lamina using two distinct mechanisms: the dystrophin glycoprotein complex and the… (More)
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Highly Cited
2000
Highly Cited
2000
We describe a novel protein, Syne-1, that is associated with nuclear envelopes in skeletal, cardiac, and smooth muscle cells… (More)
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Highly Cited
2000
Highly Cited
2000
The absence of dystrophin complex leads to disorganization of the force-transmitting costameric cytoskeleton and disruption of… (More)
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Highly Cited
1998
Highly Cited
1998
Duchenne muscular dystrophy (DMD) is a lethal, progressive muscle wasting disease caused by a loss of sarcolemmal bound… (More)
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Highly Cited
1997
Highly Cited
1997
The syntrophins are a multigene family of intracellular dystrophin-associated proteins comprising three isoforms, alpha1, beta1… (More)
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Highly Cited
1997
Highly Cited
1997
Dystrophin-deficient mice (mdx) expressing a truncated (trc) utrophin transgene show amelioration of the dystrophic phenotype… (More)
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Highly Cited
1996
Highly Cited
1996
DUCHENNE muscular dystrophy (DMD) is a severe, progressive muscle-wasting disease that causes cardiac or respiratory failure1,2… (More)
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Highly Cited
1994
Highly Cited
1994
Synapse formation is characterized by the accumulation of molecules at the site of contact between pre- and postsynaptic cells… (More)
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Highly Cited
1992
Highly Cited
1992
DYSTROPHIN is associated with a complex of muscle membrane (sarcolemmal) glycoproteins that provide a linkage to the… (More)
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