Calmodulin inhibitors improve erythropoiesis in Diamond-Blackfan anemia

De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome

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The Genetic Landscape of Diamond-Blackfan Anemia

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Perspective on Diamond–Blackfan anemia: lessons from a rare congenital bone marrow failure syndrome

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Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors

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RAP-011 improves erythropoiesis in zebrafish model of Diamond-Blackfan anemia through antagonizing lefty1

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Glucocorticoids improve erythroid progenitor maintenance and dampenTrp53response in a mouse model of Diamond-Blackfan anaemia

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Dysregulation of the Transforming Growth Factor β Pathway in Induced Pluripotent Stem Cells Generated from Patients with Diamond Blackfan Anemia

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Partial Loss of Rpl11 in Adult Mice Recapitulates Diamond-Blackfan Anemia and Promotes Lymphomagenesis

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Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genesTSR2andRPS28

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Altered translation of GATA1 in Diamond-Blackfan anemia

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Defects of protein production in erythroid cells revealed in a zebrafish Diamond–Blackfan anemia model for mutation in RPS19

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The emerging importance of ribosomal dysfunction in the pathogenesis of hematologic disorders

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Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

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Calcium-Dependent Interaction of Calmodulin with Human 80S Ribosomes and Polyribosomes

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Dietary L-leucine improves the anemia in a mouse model for Diamond-Blackfan anemia

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Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry

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L-leucine improves the anemia and developmental defects associated with Diamond-Blackfan anemia and del(5q) MDS by activating the mTOR pathway

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Bone Marrow Failure in Fanconi Anemia Is Triggered by an Exacerbated p53/p21 DNA Damage Response that Impairs Hematopoietic Stem and Progenitor Cells

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Frameshift mutation in p53 regulatorRPL26is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia

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Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia

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Annexin A2 and PSF proteins interact with p53 IRES and regulate translation of p53 mRNA

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Chromatin Isolation by RNA Purification (ChIRP)

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A zebrafish model of dyskeratosis congenita reveals hematopoietic stem cell formation failure resulting from ribosomal protein-mediated p53 stabilization

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Dexamethasone and lenalidomide have distinct functional effects on erythropoiesis

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Induction of human fetal hemoglobin via the NRF2 antioxidant response signaling pathway

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Mice with ribosomal protein S19 deficiency develop bone marrow failure and symptoms like patients with Diamond-Blackfan anemia

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Defective ribosome assembly in Shwachman-Diamond syndrome

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Hematopoietic defects in rps29 mutant zebrafish depend upon p53 activation

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Establishing Rps6 hemizygous mice as a model for studying how ribosomal protein haploinsufficiency impairs erythropoiesis

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Rpl27a mutation in the sooty foot ataxia mouse phenocopies high p53 mouse models

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Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells

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Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects

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5'-3'-UTR interactions regulate p53 mRNA translation and provide a target for modulating p53 induction after DNA damage

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A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q– syndrome

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Many ribosomal protein mutations are associated with growth impairment and tumor predisposition in zebrafish

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Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

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Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

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Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function

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Loss of p53 synthesis in zebrafish tumors with ribosomal protein gene mutations

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