Ribosomal protein S19 binds to its own mRNA with reduced affinity in Diamond-Blackfan anemia.

[1]  Jason E. Farrar,et al.  Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia. , 2009, American journal of human genetics.

[2]  N. Dahl,et al.  Ribosomal protein S19 and S24 insufficiency cause distinct cell cycle defects in Diamond-Blackfan anemia. , 2009, Biochimica et biophysica acta.

[3]  E. Bongcam-Rudloff,et al.  Targeted Resequencing and Analysis of the Diamond-Blackfan Anemia Disease Locus RPS19 , 2009, PloS one.

[4]  H. R. Razzaghian,et al.  Posttranscriptional down‐regulation of small ribosomal subunit proteins correlates with reduction of 18S rRNA in RPS19 deficiency , 2009, FEBS letters.

[5]  Alan H Beggs,et al.  Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients. , 2008, American journal of human genetics.

[6]  J. Ladenson,et al.  The role of human ribosomal proteins in the maturation of rRNA and ribosome production. , 2008, RNA.

[7]  S. Karlsson,et al.  Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference , 2008, British journal of haematology.

[8]  C Conover Talbot,et al.  Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia. , 2008, Blood.

[9]  I. Dianzani,et al.  RPS19 mutations in patients with Diamond‐Blackfan anemia , 2008, Human mutation.

[10]  Daniel F Tardiff,et al.  L30 binds the nascent RPL30 transcript to repress U2 snRNP recruitment. , 2008, Molecular cell.

[11]  S. Karlsson,et al.  Ribosomal Protein S19 Deficiency Leads to Reduced Proliferation and Increased Apoptosis but Does Not Affect Terminal Erythroid Differentiation in a Cell Line Model of Diamond‐Blackfan Anemia , 2008, Stem cells.

[12]  Jiri Petrak,et al.  Ribosomal protein S17 gene (RPS17) is mutated in Diamond‐Blackfan anemia , 2007, Human mutation.

[13]  Robert P Perry,et al.  Balanced production of ribosomal proteins. , 2007, Gene.

[14]  I. Eperon,et al.  Human ribosomal protein S13 regulates expression of its own gene at the splicing step by a feedback mechanism , 2007, Nucleic acids research.

[15]  P. Gleizes,et al.  Molecular basis of Diamond–Blackfan anemia: structure and function analysis of RPS19 , 2007, Nucleic acids research.

[16]  I. Dianzani,et al.  Missense mutations associated with Diamond-Blackfan anemia affect the assembly of ribosomal protein S19 into the ribosome. , 2007, Human molecular genetics.

[17]  J. Ladenson,et al.  Cells depleted for RPS19, a protein associated with Diamond Blackfan Anemia, show defects in 18S ribosomal RNA synthesis and small ribosomal subunit production. , 2007, Blood cells, molecules & diseases.

[18]  D. Tollervey,et al.  Building Ribosomes: Even More Expensive Than Expected? , 2007, Current Biology.

[19]  S. Karlsson,et al.  Diamond-Blackfan anemia: erythropoiesis lost in translation. , 2007, Blood.

[20]  K. Sakamoto,et al.  The functions of RPS19 and their relationship to Diamond-Blackfan anemia: a review. , 2007, Molecular genetics and metabolism.

[21]  Jacqueline Noaillac-Depeyre,et al.  Impaired ribosome biogenesis in Diamond-Blackfan anemia. , 2007, Blood.

[22]  S. Karlsson,et al.  Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits. , 2007, Blood.

[23]  A. Beggs,et al.  Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia. , 2006, American journal of human genetics.

[24]  S. Ellis,et al.  Ribosomes and marrow failure: coincidental association or molecular paradigm? , 2006, Blood.

[25]  A. Ivanov,et al.  Human ribosomal protein S26 suppresses the splicing of its pre-mRNA. , 2005, Biochimica et biophysica acta.

[26]  Michael Zuker,et al.  Mfold web server for nucleic acid folding and hybridization prediction , 2003, Nucleic Acids Res..

[27]  A. Ivanov,et al.  Expression and purification of human ribosomal proteins S3, S5, S10, S19, and S26. , 2003, Protein expression and purification.

[28]  Hua Tang,et al.  Amino Acid-Induced Translation of TOP mRNAs Is Fully Dependent on Phosphatidylinositol 3-Kinase-Mediated Signaling, Is Partially Inhibited by Rapamycin, and Is Independent of S6K1 and rpS6 Phosphorylation , 2001, Molecular and Cellular Biology.

[29]  O. Meyuhas.  Synthesis of the translational apparatus is regulated at the translational level. , 2000, European journal of biochemistry.

[30]  J Stahl,et al.  Immunoelectron microscopic studies on the location of ribosomal proteins on the surface of the 40S ribosomal subunit from rat liver. , 1990, European journal of cell biology.

[31]  S. Ellis,et al.  Diamond Blackfan anemia: a disorder of red blood cell development. , 2008, Current topics in developmental biology.

[32]  S. Karlsson,et al.  Human RPS 19 , the gene mutated in Diamond-Blackfan anemia , encodes a ribosomal protein required for the maturation of 40 S ribosomal subunits , 2007 .

[33]  S. Ellis,et al.  Diamond Blackfan anemia: A paradigm for a ribosome-based disease. , 2006, Medical hypotheses.