Published in Blood on May 02, 2007
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Regulation of HDM2 activity by the ribosomal protein L11. Cancer Cell (2003) 5.44
Nucleophosmin and cancer. Nat Rev Cancer (2006) 4.82
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Mutations in SBDS are associated with Shwachman-Diamond syndrome. Nat Genet (2002) 4.62
Regulation of p53 translation and induction after DNA damage by ribosomal protein L26 and nucleolin. Cell (2005) 4.16
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Impaired control of IRES-mediated translation in X-linked dyskeratosis congenita. Science (2006) 3.37
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CONGENITAL HYPOPLASIA OF THE EXOCRINE PANCREAS. Acta Paediatr (1964) 2.61
The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast. Nat Genet (2007) 2.58
Mitotic occupancy and lineage-specific transcriptional control of rRNA genes by Runx2. Nature (2007) 2.28
Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits. Blood (2006) 2.22
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Interaction of FANCD2 and NBS1 in the DNA damage response. Nat Cell Biol (2002) 1.96
The Shwachman-Diamond SBDS protein localizes to the nucleolus. Blood (2005) 1.95
The Saccharomyces cerevisiae TIF6 gene encoding translation initiation factor 6 is required for 60S ribosomal subunit biogenesis. Mol Cell Biol (2001) 1.84
Specific Role for Yeast Homologs of the Diamond Blackfan Anemia-associated Rps19 Protein in Ribosome Synthesis. J Biol Chem (2005) 1.79
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Nucleophosmin is essential for ribosomal protein L5 nuclear export. Mol Cell Biol (2006) 1.72
Mutations of the SBDS gene are present in most patients with Shwachman-Diamond syndrome. Blood (2004) 1.58
The Shwachman-Bodian-Diamond syndrome protein family is involved in RNA metabolism. J Biol Chem (2005) 1.52
Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman-Diamond Syndrome. J Biol Chem (2005) 1.51
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A surfeit of factors: why is ribosome assembly so much more complicated in eukaryotes than bacteria? RNA Biol (2004) 1.43
Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulator. Am J Hum Genet (2005) 1.40
Translocation of nucleolar phosphoprotein B23 (37 kDa/pI 5.1) induced by selective inhibitors of ribosome synthesis. Biochim Biophys Acta (1985) 1.39
The social life of ribosomal proteins. FEBS J (2005) 1.38
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Effect of protein synthesis inhibitors and low concentrations of actinomycin D on ribosomal RNA synthesis. FEBS Lett (1979) 1.30
Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality. Mol Cell Biol (2006) 1.29
Translational efficiency in patients with Diamond-Blackfan anemia. Haematologica (2006) 1.25
Human histone chaperone nucleophosmin enhances acetylation-dependent chromatin transcription. Mol Cell Biol (2005) 1.22
Protein NPM3 interacts with the multifunctional nucleolar protein B23/nucleophosmin and inhibits ribosome biogenesis. J Biol Chem (2004) 1.08
Proteins C23 and B23 are the major nucleolar silver staining proteins. Life Sci (1979) 1.04
Nucleophosmin interacts with and inhibits the catalytic function of eukaryotic initiation factor 2 kinase PKR. J Biol Chem (2003) 0.96
Phylogeny, sequence conservation, and functional complementation of the SBDS protein family. Genomics (2006) 0.96
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NPM mutations in acute myelogenous leukemia. N Engl J Med (2005) 0.94
Quantitative proteomic analysis using a MALDI quadrupole time-of-flight mass spectrometer. Anal Chem (2001) 0.89
Agonist and antagonist dual effect of the cross-linked S19 ribosomal protein dimer in the C5a receptor-mediated respiratory burst reaction of phagocytic leukocytes. Inflamm Res (2005) 0.86
Disease-specific induced pluripotent stem cells. Cell (2008) 16.95
An extensive network of coupling among gene expression machines. Nature (2002) 11.84
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TREX is a conserved complex coupling transcription with messenger RNA export. Nature (2002) 6.53
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Human mRNA export machinery recruited to the 5' end of mRNA. Cell (2006) 3.32
Sus1, a functional component of the SAGA histone acetylase complex and the nuclear pore-associated mRNA export machinery. Cell (2004) 3.16
Recruitment of the human TREX complex to mRNA during splicing. Genes Dev (2005) 3.13
SR proteins function in coupling RNAP II transcription to pre-mRNA splicing. Mol Cell (2007) 3.04
The signal sequence coding region promotes nuclear export of mRNA. PLoS Biol (2007) 2.09
TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements. Blood (2008) 1.99
Splicing promotes rapid and efficient mRNA export in mammalian cells. Proc Natl Acad Sci U S A (2008) 1.98
Functional coupling of RNAP II transcription to spliceosome assembly. Genes Dev (2006) 1.98
A nuclear translation-like factor eIF4AIII is recruited to the mRNA during splicing and functions in nonsense-mediated decay. Proc Natl Acad Sci U S A (2004) 1.97
The Shwachman-Diamond SBDS protein localizes to the nucleolus. Blood (2005) 1.95
Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage. Blood (2010) 1.88
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Fanconi anemia pathway-deficient tumor cells are hypersensitive to inhibition of ataxia telangiectasia mutated. J Clin Invest (2007) 1.80
Cotranscriptional recruitment of the serine-arginine-rich (SR)-like proteins Gbp2 and Hrb1 to nascent mRNA via the TREX complex. Proc Natl Acad Sci U S A (2004) 1.70
The anti-tumor drug E7107 reveals an essential role for SF3b in remodeling U2 snRNP to expose the branch point-binding region. Genes Dev (2011) 1.64
Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1. Stem Cells (2010) 1.60
Human DDX3 functions in translation and interacts with the translation initiation factor eIF3. Nucleic Acids Res (2008) 1.57
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FUS-SMN protein interactions link the motor neuron diseases ALS and SMA. Cell Rep (2012) 1.50
Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood. Blood (2003) 1.49
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Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway. Blood (2004) 1.18
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Mental illness recognition and referral by Catholic priests in North Carolina. Psychiatr Serv (2012) 0.75
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