NPTX2 gene

Known as: NARP, PENTRAXIN II, NEURONAL, NPTX2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1985-2018
0519852018

Papers overview

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2015
2015
Mitochondrial diseases include a group of maternally inherited genetic disorders caused by mutations in mtDNA. In most of these… (More)
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2010
2010
Mutations in the mitochondrial DNA (mtDNA) encoded subunit 6 of ATPase (ATP6) are associated with variable disease expression… (More)
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2010
2010
AIMS The prevalence and natural history of cardiovascular disease in adult patients with respiratory chain disease (RCD) is… (More)
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2006
2006
We used engineered zinc finger peptides (ZFPs) to bind selectively to predetermined sequences in human mtDNA. Surprisingly, we… (More)
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Narcolepsy with cataplexy is associated with a loss of orexin/hypocretin. It is speculated that an autoimmune process… (More)
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Highly Cited
2004
Highly Cited
2004
A T8993G point mutation in the mtDNA results in a Leu156Arg substitution in the MTATP6 subunit of the mitochondrial F1F0-ATPase… (More)
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Highly Cited
1999
Highly Cited
1999
In recent years, genetic defects of the mitochondrial genome (mtDNA) were shown to be associated with a heterogeneous group of… (More)
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1997
1997
AIM To contribute to the establishment of a rational clinical, neuroradiological, and molecular approach to neurogenic muscle… (More)
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1993
1993
Mitochondria were prepared from three lymphoblast cell lines from patients with high percentage copy numbers of the human mtDNA… (More)
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1985
1985
We have examined the specificity and the mechanism of acetylcholine receptor (AChR) accumulation at embryonic chick nerve-muscle… (More)
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