Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.
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Mice with a Mutation in the Mdm2 Gene That Interferes with MDM2/Ribosomal Protein Binding Develop a Defect in ErythropoiesisLoss of Forkhead box M1 promotes erythropoiesis through increased proliferation of erythroid progenitors.Altered translation of GATA1 in Diamond-Blackfan anemia.Systematic transcriptome analysis of the zebrafish model of diamond-blackfan anemia induced by RPS24 deficiency.The emerging importance of ribosomal dysfunction in the pathogenesis of hematologic disorders.Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implicationsRibosomopathies: mechanisms of disease.Dysregulation of RNA polymerase I transcription during disease.Lipopolysaccharide preconditioning protects hepatocytes from ischemia/reperfusion injury (IRI) through inhibiting ATF4-CHOP pathway in miceAssessment of hematopoietic failure due to Rpl11 deficiency in a zebrafish model of Diamond-Blackfan anemia by deep sequencing.Ribosomal protein mutations induce autophagy through S6 kinase inhibition of the insulin pathway.Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT PathwayTranscriptome analysis reveals a ribosome constituents disorder involved in the RPL5 downregulated zebrafish model of Diamond-Blackfan anemia.Ribosomal and hematopoietic defects in induced pluripotent stem cells derived from Diamond Blackfan anemia patients.Dysferlin and other non-red cell proteins accumulate in the red cell membrane of Diamond-Blackfan Anemia patients.Molecular convergence in ex vivo models of Diamond-Blackfan anemia.Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia.Loss of tumor suppressor RPL5/RPL11 does not induce cell cycle arrest but impedes proliferation due to reduced ribosome content and translation capacity.Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitorsAdult-onset Diamond-Blackfan anemia with a novel mutation in the exon 5 of RPL11: too late and too rare.Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy.Confounding in ex vivo models of Diamond-Blackfan anemia.The Evolution of the Ribosomal Protein-MDM2-p53 Pathway.Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia.An update on the pathogenesis and diagnosis of Diamond-Blackfan anemia
P2860
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P2860
Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Primary hematopoietic cells fr ...... erythroid phenotype in vitro.
@ast
Primary hematopoietic cells fr ...... erythroid phenotype in vitro.
@en
type
label
Primary hematopoietic cells fr ...... erythroid phenotype in vitro.
@ast
Primary hematopoietic cells fr ...... erythroid phenotype in vitro.
@en
prefLabel
Primary hematopoietic cells fr ...... erythroid phenotype in vitro.
@ast
Primary hematopoietic cells fr ...... erythroid phenotype in vitro.
@en
P2093
P2860
P50
P356
P1476
Primary hematopoietic cells fr ...... t erythroid phenotype in vitro
@en
P2093
DBA Group of Société d'Hématologie et d'Immunologie Pédiatrique-SHIP
G Tchernia
J Larghero
L Croisille
L Da Costa
M Faubladier
P2860
P356
10.1038/CDDIS.2012.88
P577
2012-07-26T00:00:00Z