POLR1D gene

Known as: polymerase (RNA) I subunit D, MGC9850, RPO1-3 
 

Topic mentions per year

Topic mentions per year

1996-2017
012319962017

Papers overview

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2016
2016
Purpose:Treacher Collins/Franceschetti syndrome (TCS; OMIM 154500) is a disorder of craniofacial development belonging to the… (More)
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2016
2016
Treacher Collins Syndrome (TCS) is a rare congenital birth disorder (1 in 50,000 live births) characterized by severe… (More)
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Review
2016
Review
2016
Treacher Collins syndrome (TCS, OMIM 154500), also known as Franceschetti-Klein syndrome, is a rare disorder that affects the… (More)
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2016
2016
Ribosome biogenesis is a global process required for growth and proliferation of all cells, yet perturbation of ribosome… (More)
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2014
2014
Purpose:Treacher Collins syndrome is a mandibulofacial dysostosis caused by mutations in genes involved in ribosome biogenesis… (More)
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Highly Cited
2011
Highly Cited
2011
We identified a deletion of a gene encoding a subunit of RNA polymerases I and III, POLR1D, in an individual with Treacher… (More)
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2005
2005
Likelihood Ratio medical key parameters calculated on categorical results from diagnostic tests are usually express accompanied… (More)
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2005
2005
Yeast Gtr1p and its human homolog RRAG A belong to the Ras-like small G-protein superfamily and genetically interact with RCC1, a… (More)
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1996
1996
We have previously isolated a mouse RPA40 (mRPA40) cDNA encoding the 40-kDa subunit of mouse RNA polymerase I and demonstrated… (More)
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