Perturbation of rRNA synthesis in the bap28 mutation leads to apoptosis mediated by p53 in the zebrafish central nervous system
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Impaired ribosome biogenesis in Diamond-Blackfan anemiaNucleolar responses to DNA double-strand breaksGuarding the 'translation apparatus': defective ribosome biogenesis and the p53 signaling pathwayMutation in utp15 disrupts vascular patterning in a p53-dependent manner in zebrafish embryosDiverse diseases from a ubiquitous process: the ribosomopathy paradoxThe Warsaw breakage syndrome-related protein DDX11 is required for ribosomal RNA synthesis and embryonic developmentAutophagy induction is a Tor- and Tp53-independent cell survival response in a zebrafish model of disrupted ribosome biogenesisRecruitment of factors linking transcription and processing of pre-rRNA to NOR chromatin is UBF-dependent and occurs independent of transcription in human cellsLoss of ribosomal protein L11 affects zebrafish embryonic development through a p53-dependent apoptotic response.Zebrafish models for dyskeratosis congenita reveal critical roles of p53 activation contributing to hematopoietic defects through RNA processingEwing sarcoma protein ewsr1 maintains mitotic integrity and proneural cell survival in the zebrafish embryo.p53 upregulation is a frequent response to deficiency of cell-essential genesThe pre-rRNA processing factor DEF is rate limiting for the pathogenesis of MYCN-driven neuroblastoma.Glioma-associated antigen HEATR1 induces functional cytotoxic T lymphocytes in patients with glioma.Zebrafish models of p53 functions.Tbl3 regulates cell cycle length during zebrafish development.Ubiquitin and ubiquitin-like proteins in the nucleolus: multitasking tools for a ribosome factory.Def functions as a cell autonomous factor in organogenesis of digestive organs in zebrafishTranscriptome analysis of newt lens regeneration reveals distinct gradients in gene expression patterns.p53-mediated biliary defects caused by knockdown of cirh1a, the zebrafish homolog of the gene responsible for North American Indian Childhood CirrhosisThe Ribosomal Protein-Mdm2-p53 Pathway and Energy Metabolism: Bridging the Gap between Feast and Famine.Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeEwing sarcoma ewsa protein regulates chondrogenesis of Meckel's cartilage through modulation of Sox9 in zebrafish.Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT PathwayAcrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction.Expression of ribosomopathy genes during Xenopus tropicalis embryogenesis.HEATR1 Negatively Regulates Akt to Help Sensitize Pancreatic Cancer Cells to Chemotherapy.Brachypodium distachyon T-DNA insertion lines: a model pathosystem to study nonhost resistance to wheat stripe rustA collection of Ds insertional mutants associated with defects in male gametophyte development and function in Arabidopsis thaliana.Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndromeThe primary open-angle glaucoma gene WDR36 functions in ribosomal RNA processing and interacts with the p53 stress-response pathway.Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genesA rapid and efficient method of genotyping zebrafish mutants.Tissue specific roles for the ribosome biogenesis factor Wdr43 in zebrafish development.Genomic characterization of the mouse ribosomal DNA locusThe nuclear pore complex function of Sec13 protein is required for cell survival during retinal development.Diamond Blackfan Anemia at the Crossroad between Ribosome Biogenesis and Heme MetabolismA new PICTure of nucleolar stress.The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome.Perturbation of RNA Polymerase I transcription machinery by ablation of HEATR1 triggers the RPL5/RPL11-MDM2-p53 ribosome biogenesis stress checkpoint pathway in human cells.
P2860
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P2860
Perturbation of rRNA synthesis in the bap28 mutation leads to apoptosis mediated by p53 in the zebrafish central nervous system
description
2006 nî lūn-bûn
@nan
2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Perturbation of rRNA synthesis ...... brafish central nervous system
@ast
Perturbation of rRNA synthesis ...... brafish central nervous system
@en
Perturbation of rRNA synthesis ...... brafish central nervous system
@nl
type
label
Perturbation of rRNA synthesis ...... brafish central nervous system
@ast
Perturbation of rRNA synthesis ...... brafish central nervous system
@en
Perturbation of rRNA synthesis ...... brafish central nervous system
@nl
prefLabel
Perturbation of rRNA synthesis ...... brafish central nervous system
@ast
Perturbation of rRNA synthesis ...... brafish central nervous system
@en
Perturbation of rRNA synthesis ...... brafish central nervous system
@nl
P2093
P2860
P3181
P356
P1476
Perturbation of rRNA synthesis ...... brafish central nervous system
@en
P2093
Elizabeth Laver
Mizuki Azuma
Reiko Toyama
P2860
P304
P3181
P356
10.1074/JBC.M601892200
P407
P577
2006-05-12T00:00:00Z