POLR1C gene

Known as: RPA39, POLR1C, POLYMERASE I, RNA, SUBUNIT C 
 

Topic mentions per year

Topic mentions per year

1994-2017
01219942017

Papers overview

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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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2016
2016
Purpose:Treacher Collins/Franceschetti syndrome (TCS; OMIM 154500) is a disorder of craniofacial development belonging to the… (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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2015
2015
A small proportion of 4H (Hypomyelination, Hypodontia and Hypogonadotropic Hypogonadism) or RNA polymerase III (POLR3)-related… (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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2007
2007
Presented herein is an updated sheep cytogenetic map that contains 452 loci (291 type I and 161 type II) assigned to specific… (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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2002
2002
Werner syndrome (WS) is a rare autosmomal recessive genetic disorder causing premature aging. The gene (WRN) responsible for WS… (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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1994
1994
Mouse RNA polymerase I (or A) was purified from an ascites cell line MH134 to virtual homogeneity using a novel purification… (More)
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