Ribosomopathies: human disorders of ribosome dysfunction.
about
Genome-wide interrogation of Mammalian stem cell fate determinants by nested chromosome deletionsNPM1/B23: A Multifunctional Chaperone in Ribosome Biogenesis and Chromatin RemodelingDiamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28The nucleolus under stressThe importance of ribosome production, and the 5S RNP-MDM2 pathway, in health and diseaseDevelopment, Maintenance, and Reversal of Multiple Drug Resistance: At the Crossroads of TFPI1, ABC Transporters, and HIF1Why is start codon selection so precise in eukaryotes?Human diseases of the SSU processomeRibosomal proteins as unrevealed caretakers for cellular stress and genomic instabilityBasic mechanisms in RNA polymerase I transcription of the ribosomal RNA genesEvolutionary conservation and expression of human RNA-binding proteins and their role in human genetic diseaseThe inherited bone marrow failure syndromesCohesinopathies of a feather flock togetherPerturbations at the ribosomal genes loci are at the centre of cellular dysfunction and human diseaseGuarding the 'translation apparatus': defective ribosome biogenesis and the p53 signaling pathwayA kinome-wide RNAi screen in Drosophila Glia reveals that the RIO kinases mediate cell proliferation and survival through TORC2-Akt signaling in glioblastomaThe conserved Bud20 zinc finger protein is a new component of the ribosomal 60S subunit export machineryHrr25/CK1δ-directed release of Ltv1 from pre-40S ribosomes is necessary for ribosome assembly and cell growthRibosome biogenesis factor Tsr3 is the aminocarboxypropyl transferase responsible for 18S rRNA hypermodification in yeast and humans.Role of ribosomal protein mutations in tumor development (Review)What Is the Impact of mRNA 5' TL Heterogeneity on Translational Start Site Selection and the Mammalian Cellular Phenotype?Regulatory Roles of Rpl22 in Hematopoiesis: An Old Dog with New TricksGradual processing of the ITS1 from the nucleolus to the cytoplasm during synthesis of the human 18S rRNAThe Warsaw breakage syndrome-related protein DDX11 is required for ribosomal RNA synthesis and embryonic developmentBoth endonucleolytic and exonucleolytic cleavage mediate ITS1 removal during human ribosomal RNA processingYeast Kre33 and human NAT10 are conserved 18S rRNA cytosine acetyltransferases that modify tRNAs assisted by the adaptor Tan1/THUMPD1The human 18S rRNA base methyltransferases DIMT1L and WBSCR22-TRMT112 but not rRNA modification are required for ribosome biogenesisAutophagy induction is a Tor- and Tp53-independent cell survival response in a zebrafish model of disrupted ribosome biogenesisAn extraribosomal function of ribosomal protein L13a in macrophages resolves inflammationEukaryotic translation initiation factor 6 is a novel regulator of reactive oxygen species-dependent megakaryocyte maturationNotchless-dependent ribosome synthesis is required for the maintenance of adult hematopoietic stem cellsThe 5S RNP couples p53 homeostasis to ribosome biogenesis and nucleolar stressLoss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.PICT-1 is a key nucleolar sensor in DNA damage response signaling that regulates apoptosis through the RPL11-MDM2-p53 pathwayCohesion promotes nucleolar structure and functionA protein inventory of human ribosome biogenesis reveals an essential function of exportin 5 in 60S subunit exportThe ribosomal protein Rpl22 controls ribosome composition by directly repressing expression of its own paralog, Rpl22l1GATA factor mutations in hematologic disease.Haematopoietic stem cells require a highly regulated protein synthesis rate.Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders
P2860
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P2860
Ribosomopathies: human disorders of ribosome dysfunction.
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Ribosomopathies: human disorders of ribosome dysfunction.
@ast
Ribosomopathies: human disorders of ribosome dysfunction.
@en
type
label
Ribosomopathies: human disorders of ribosome dysfunction.
@ast
Ribosomopathies: human disorders of ribosome dysfunction.
@en
prefLabel
Ribosomopathies: human disorders of ribosome dysfunction.
@ast
Ribosomopathies: human disorders of ribosome dysfunction.
@en
P2860
P1433
P1476
Ribosomopathies: human disorders of ribosome dysfunction.
@en
P2093
Anupama Narla
Benjamin L Ebert
P2860
P304
P356
10.1182/BLOOD-2009-10-178129
P407
P577
2010-03-01T00:00:00Z