RPGRIP1L gene

Known as: MKS5, JBTS7, NEPHROCYSTIN 8 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1979-2017
05101519792017

Papers overview

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2014
2014
Common polymorphisms in the first intron of FTO are associated with increased body weight in adults. Previous studies have… (More)
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2011
2011
Recent studies have established ciliary dysfunction as the underlying cause of a broad range of multi-organ phenotypes, known as… (More)
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2010
2010
OBJECTIVE To identify genetic causes of COACH syndrome BACKGROUND COACH syndrome is a rare autosomal recessive disorder… (More)
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Highly Cited
2009
Highly Cited
2009
Despite rapid advances in the identification of genes involved in disease, the predictive power of the genotype remains limited… (More)
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2009
2009
The mechanical properties of tissues, tissue analogs, and biomaterials are dependent on their underlying microstructure. As such… (More)
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2008
Highly Cited
2008
Two recent, large whole-genome association studies (GWAS) in European populations have associated a approximately 47-kb region… (More)
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Highly Cited
2008
Highly Cited
2008
Recent studies have shown that SNPs in the FTO gene predispose to childhood and adult obesity. In this study, we examined the… (More)
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Highly Cited
2007
Highly Cited
2007
Cerebello-oculo-renal syndrome (CORS), also called Joubert syndrome type B, and Meckel (MKS) syndrome belong to the group of… (More)
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2007
2007
The purpose of this study was to evaluate safety and efficacy of Procarbazine (PCB) and fotemustine (FTM) combination in the… (More)
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2005
2005
BACKGROUND Although flutamide (FTM), an androgen-receptor antagonist, normalizes the depressed immune and cardiac function in… (More)
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