Peroxisome Biogenesis Disorder, Complementation Group 1

Known as: CG1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1988-2017
012319882017

Papers overview

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2017
2017
The rules of k-mer non-random usage and the biological functions are worthy of special attention. Firstly, the article studied… (More)
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2017
2017
OBJECTIVE To investigate the histopathological nature of myofascial trigger points (MTrPs) or spots (MTrSs) at different stages… (More)
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2016
2016
The aim of this study was to enhance the dissolution and bioavailability of telmisartan (TLM), a poorly water soluble drug by co… (More)
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2015
2015
Several experimental and animal studies have demonstrated that substances rich in antioxidants can reduce the physicochemical and… (More)
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2010
2010
Genetically identical inbred mouse strains are one of the most useful tools in dissecting the genetic basis of complex disorders… (More)
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2009
2009
Prior experience with the elevated plus maze (EPM) increases the avoidance of rodents to the open arms and impairs the anxiolytic… (More)
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2001
2001
1. The injection of acetylcholine (ACh) into the medial prefrontal cortex (MPFC) caused marked hypotensive response in either… (More)
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Highly Cited
1997
Highly Cited
1997
The peroxisome biogenesis disorders (PBDs) are a group of lethal autosomal-recessive diseases caused by defects in peroxisomal… (More)
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1988
1988
A monoclonal antibody (CG1) which recognizes tropomyosin isoforms 1 and 3 of chicken embryo fibroblasts was used to detect what… (More)
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