FAQ

POLR1C gene

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

Topic mentions per year

Topic mentions per year

1994-2017
01219942017

Related topics

Related topics

3 relations
DNA-Directed RNA PolymerasePOLR1B genePOLR1D gene

Related mentions per year

Related mentions per year

1961-2018
1960198020002020
POLR1C gene
DNA-Directed RNA Polymerase
POLR1B gene
POLR1D gene

Papers overview

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2016
2016
Pathogenesis of POLR1C-dependent Type 3 Treacher Collins Syndrome revealed by a zebrafish model.
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
Treacher Collins syndrome: a clinical and molecular study based on a large series of patients
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
[The research progress of Treacher Collins syndrome].
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
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III
A small proportion of 4H (Hypomyelination, Hypodontia and Hypogonadotropic Hypogonadism) or RNA polymerase III (POLR3)-related… (More)
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2014
2014
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome
Purpose:Treacher Collins syndrome is a mandibulofacial dysostosis caused by mutations in genes involved in ribosome biogenesis… (More)
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2007
2007
An advanced sheep (Ovis aries, 2n = 54) cytogenetic map and assignment of 88 new autosomal loci by fluorescence in situ hybridization and R-banding
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
Binomial Distribution Sample Confidence Interval Estimation for Positive and Negative Likelihood Ratio Medical Key Parameters
Likelihood Ratio medical key parameters calculated on categorical results from diagnostic tests are usually express accompanied… (More)
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2002
2002
WRN helicase accelerates the transcription of ribosomal RNA as a component of an RNA polymerase I-associated complex
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
Mouse RNA polymerase I 16-kDa subunit able to associate with 40-kDa subunit is a homolog of yeast AC19 subunit of RNA polymerases I and III.
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
High conservation of subunit composition of RNA polymerase I(A) between yeast and mouse and the molecular cloning of mouse RNA polymerase I 40-kDa subunit RPA40.
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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