PLS3 gene

Known as: PLASTIN 3, PLS3, T-PLASTIN 
 

Topic mentions per year

Topic mentions per year

2003-2018
024620032018

Papers overview

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2017
2017
Homozygous SMN1 loss causes spinal muscular atrophy (SMA), the most common lethal genetic childhood motor neuron disease. SMN1… (More)
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2016
2016
Homozygous loss of SMN1 causes spinal muscular atrophy (SMA), the most common and devastating childhood genetic motor-neuron… (More)
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2015
2015
Genetic factors play an important role in the development of osteoporosis. Several monogenic forms of osteoporosis have been… (More)
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2014
2014
Mutations in PLS3 have been identified as a cause of bone fragility in children, but the bone phenotype associated with PLS3… (More)
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2014
2014
Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disease in children caused by homozygous deletion of… (More)
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2013
2013
Plastin 3 (PLS3), a protein involved in the formation of filamentous actin (F-actin) bundles, appears to be important in human… (More)
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Highly Cited
2013
Highly Cited
2013
Circulating tumor cells (CTC) in blood have attracted attention both as potential seeds for metastasis and as biomarkers. However… (More)
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2013
2013
Recent evidence suggests that PLS3 (T-Plastin), an important member of the actin filamentous network, significantly influences… (More)
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Highly Cited
2008
Highly Cited
2008
Homozygous deletion of the survival motor neuron 1 gene (SMN1) causes spinal muscular atrophy (SMA), the most frequent genetic… (More)
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2003
2003
Protein kinase C (PKC) delta translocates to mitochondria during apo-ptosis,but its mitochondrial target remains unclear. We… (More)
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