NOP10 gene

Known as: NOP10P, NOP10 ribonucleoprotein, NOP10 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2018
012319992018

Papers overview

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2015
2015
H/ACA ribonucleoproteins (RNPs) are comprised of four conserved proteins, dyskerin, NHP2, NOP10, and GAR1, and a function… (More)
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2013
2013
Dyskeratosis congenita is a rare inherited bone marrow failure characterized by excessively short telomeres in highly… (More)
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2012
2012
Dyskeratosis congenita (DC) is a rare inherited bone-marrow failure syndrome with high clinical heterogeneity. Cells derived from… (More)
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2011
2011
BACKGROUND Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome characterised by dystrophic nails, abnormal… (More)
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2010
2010
Dyskeratosis congenita (DC) is a rare genetic syndrome that gives rise to a variety of disorders in affected individuals… (More)
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Highly Cited
2008
Highly Cited
2008
Patients with dyskeratosis congenita (DC), a heterogeneous inherited bone marrow failure syndrome, have abnormalities in telomere… (More)
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Highly Cited
2008
Highly Cited
2008
Dyskeratosis congenita is a premature aging syndrome characterized by muco-cutaneous features and a range of other abnormalities… (More)
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Highly Cited
2007
Highly Cited
2007
Dyskeratosis congenita (DC) is characterized by multiple features including mucocutaneous abnormalities, bone marrow failure and… (More)
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Review
2006
Review
2006
The non-protein-coding transcriptional output of the cell is far greater than previously thought. Although the functions, if any… (More)
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