Ribosome defects in disorders of erythropoiesis
暂无分享,去创建一个
[1] J. Kutok,et al. Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells. , 2011, Blood.
[2] S. Karlsson,et al. Chronic RPS19 Deficiency Leads to Bone Marrow Failure In a Mouse Model for Diamond Blackfan Anemia , 2010 .
[3] I. Weissman,et al. Haploinsufficiency of Ribosomal Protein S6 In Mice Mimics Bone Marrow Failure Syndromes In Humans , 2010 .
[4] D. Bodine,et al. A transgenic mouse model demonstrates a dominant negative effect of a point mutation in the RPS19 gene associated with Diamond-Blackfan anemia. , 2010, Blood.
[5] B. Ebert,et al. Ribosomopathies: human disorders of ribosome dysfunction. , 2010, Blood.
[6] Jason E. Farrar,et al. Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia. , 2009, American journal of human genetics.
[7] A. Warren,et al. A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q− syndrome , 2009, Nature Medicine.
[8] Yanping Zhang,et al. Signaling to p53: ribosomal proteins find their way. , 2009, Cancer cell.
[9] B. Ebert. Deletion 5q in myelodysplastic syndrome: a paradigm for the study of hemizygous deletions in cancer , 2009, Leukemia.
[10] D. Sakai,et al. Treacher Collins syndrome: unmasking the role of Tcof1/treacle. , 2009, The international journal of biochemistry & cell biology.
[11] K. B. McIntosh,et al. How common are extraribosomal functions of ribosomal proteins? , 2009, Molecular cell.
[12] S. Ellis,et al. Diamond-Blackfan anemia: diagnosis, treatment, and molecular pathogenesis. , 2009, Hematology/oncology clinics of North America.
[13] P. Pandolfi,et al. Absence of nucleolar disruption after impairment of 40S ribosome biogenesis reveals an rpL11-translation-dependent mechanism of p53 induction , 2009, Nature Cell Biology.
[14] Jiri Petrak,et al. Identification of mutations in the ribosomal protein L5 (RPL5) and ribosomal protein L11 (RPL11) genes in Czech patients with Diamond‐Blackfan anemia , 2009, Human mutation.
[15] Shuo Lin,et al. Ribosomal protein S19 deficiency in zebrafish leads to developmental abnormalities and defective erythropoiesis through activation of p53 protein family. , 2008, Blood.
[16] 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.
[17] Moshe Oren,et al. Mdm2 regulates p53 mRNA translation through inhibitory interactions with ribosomal protein L26. , 2008, Molecular cell.
[18] A. Chakraborty,et al. Deficiency of ribosomal protein S19 during early embryogenesis leads to reduction of erythrocytes in a zebrafish model of Diamond-Blackfan anemia. , 2008, Human molecular genetics.
[19] C Conover Talbot,et al. Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia. , 2008, Blood.
[20] J. Ladenson,et al. The role of human ribosomal proteins in the maturation of rRNA and ribosome production. , 2008, RNA.
[21] Christopher Y. Park,et al. Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects , 2008, Nature Genetics.
[22] M. Cazzola,et al. Haploinsufficiency of RPS14 in 5q− syndrome is associated with deregulation of ribosomal- and translation-related genes , 2008, British journal of haematology.
[23] M. Clemens,et al. Activation of p53 stimulates proteasome‐dependent truncation of eIF4E‐binding protein 1 (4E‐BP1) , 2008, Biology of the cell.
[24] P. Gleizes,et al. Mutation of ribosomal protein RPS24 in Diamond-Blackfan anemia results in a ribosome biogenesis disorder. , 2008, Human molecular genetics.
[25] J. Soudet,et al. The post-transcriptional steps of eukaryotic ribosome biogenesis , 2008, Cellular and Molecular Life Sciences.
[26] Jiri Petrak,et al. Ribosomal protein S17 gene (RPS17) is mutated in Diamond‐Blackfan anemia , 2007, Human mutation.
[27] T. Golub,et al. Identification of RPS14 as a 5q- syndrome gene by RNA interference screen , 2007, Nature.
[28] W. Wang,et al. Ribosomal protein S7 as a novel modulator of p53–MDM2 interaction: binding to MDM2, stabilization of p53 protein, and activation of p53 function , 2007, Oncogene.
[29] 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.
[30] 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.
[31] Jacqueline Noaillac-Depeyre,et al. Impaired ribosome biogenesis in Diamond-Blackfan anemia. , 2007, Blood.
[32] A. Beggs,et al. Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia. , 2006, American journal of human genetics.
[33] P. Greenberg,et al. Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion. , 2006, The New England journal of medicine.
[34] M. Dixon,et al. Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities , 2006, Proceedings of the National Academy of Sciences.
[35] S. Karlsson,et al. Erythropoiesis in the Rps19 disrupted mouse: Analysis of erythropoietin response and biochemical markers for Diamond-Blackfan anemia. , 2006, Blood cells, molecules & diseases.
[36] Sanda Šulić,et al. Inactivation of S6 ribosomal protein gene in T lymphocytes activates a p53-dependent checkpoint response. , 2005, Genes & development.
[37] Koichi Miyake,et al. Deficiency of ribosomal protein S19 in CD34+ cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemia. , 2005, Blood.
[38] Aravind Subramanian,et al. An RNA interference model of RPS19 deficiency in Diamond-Blackfan anemia recapitulates defective hematopoiesis and rescue by dexamethasone: identification of dexamethasone-responsive genes by microarray. , 2004, Blood.
[39] M. Dai,et al. Inhibition of MDM2-mediated p53 Ubiquitination and Degradation by Ribosomal Protein L5* , 2004, Journal of Biological Chemistry.
[40] M. Dai,et al. Ribosomal Protein L23 Activates p53 by Inhibiting MDM2 Function in Response to Ribosomal Perturbation but Not to Translation Inhibition , 2004, Molecular and Cellular Biology.
[41] K. Itahana,et al. Inhibition of HDM2 and Activation of p53 by Ribosomal Protein L23 , 2004, Molecular and Cellular Biology.
[42] T. Allio,et al. Ribosomal Protein L11 Negatively Regulates Oncoprotein MDM2 and Mediates a p53-Dependent Ribosomal-Stress Checkpoint Pathway , 2003, Molecular and Cellular Biology.
[43] M. Kubbutat,et al. Regulation of HDM2 activity by the ribosomal protein L11. , 2003, Cancer cell.
[44] Johan Richter,et al. Gene transfer improves erythroid development in ribosomal protein S19-deficient Diamond-Blackfan anemia. , 2002, Blood.
[45] N. Harris,et al. The World Health Organization (WHO) classification of the myeloid neoplasms. , 2002, Blood.
[46] Shengyun Fang,et al. Mdm2 Is a RING Finger-dependent Ubiquitin Protein Ligase for Itself and p53* , 2000, The Journal of Biological Chemistry.
[47] Peter Gustavsson,et al. The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia , 1999, Nature Genetics.
[48] I. Wool. Extraribosomal functions of ribosomal proteins. , 1996, Trends in biochemical sciences.
[49] J. Wasmuth,et al. Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome , 1996, Nature Genetics.
[50] J. Fryns,et al. Distinct haematological disorder with deletion of long arm of No. 5 chromosome , 1974, Nature.
[51] L. Lajtha,et al. A kinetic model of the erythron. , 1961, Proceedings of the Royal Society of Medicine.
[52] H. Josephs. Anaemia of infancy and early childhood. , 1936 .
[53] J. Stockman. Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function , 2009 .
[54] T. Leblanc,et al. Impaired ribosome biogenesis in Diamond-Blackfan anemia. Commentary , 2007 .
[55] 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 .
[56] K. Starling,et al. Hypoplastic anemia. , 1973, The Journal of pediatrics.