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ribosomal protein S19

Known as: 40S Ribosomal Protein S19, RPS19, S19 ribosomal protein 
Encoded by human RPS19 Gene (S19E Family), 144-aa 16-kDa cytoplasmic Ribosomal Protein S19 is a component of the 40S ribosomal subunit. S19 lacks… Expand
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Diamond-Blackfan anemia (DBA) is associated with developmental defects and profound anemia. Mutations in genes encoding a… Expand
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Highly Cited
2012
Highly Cited
2012
Haploinsufficiency of ribosomal proteins (RPs) has been proposed to be the common basis for the anemia observed in Diamond… Expand
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Highly Cited
2011
Highly Cited
2011
Diamond-Blackfan anemia (DBA) is a congenital erythroid hypoplasia caused by a functional haploinsufficiency of genes encoding… Expand
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Review
2010
Review
2010
Ribosomopathies compose a collection of disorders in which genetic abnormalities cause impaired ribosome biogenesis and function… Expand
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Review
2010
Review
2010
The identification as cooperating targets of Proviral Integrations of Moloney virus in murine lymphomas suggested early on that… Expand
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Highly Cited
2010
Highly Cited
2010
Diamond-Blackfan anemia (DBA), an inherited bone marrow failure syndrome characterized by anemia that usually presents before the… Expand
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Highly Cited
2008
Highly Cited
2008
Mutations in several ribosomal proteins (RPs) lead to Diamond-Blackfan anemia (DBA), a syndrome characterized by defective… Expand
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Highly Cited
2008
Highly Cited
2008
Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, congenital abnormalities, and… Expand
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Highly Cited
2005
Highly Cited
2005
Diamond-Blackfan anemia (DBA) is a congenital red cell aplasia in which 25% of the patients have a mutation in the ribosomal… Expand
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Highly Cited
1999
Highly Cited
1999
Diamond–Blackfan anaemia (DBA) is a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors… Expand
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