Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects.
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Ribosomopathies: how a common root can cause a tree of pathologiesNotchless-dependent ribosome synthesis is required for the maintenance of adult hematopoietic stem cellsZebrafish models for dyskeratosis congenita reveal critical roles of p53 activation contributing to hematopoietic defects through RNA processingTranscriptome analysis of the zebrafish model of Diamond-Blackfan anemia from RPS19 deficiency via p53-dependent and -independent pathways.Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disordersp53 upregulation is a frequent response to deficiency of cell-essential genesThe role of the DNA damage response in zebrafish and cellular models of Diamond Blackfan anemia.Defects of protein production in erythroid cells revealed in a zebrafish Diamond-Blackfan anemia model for mutation in RPS19.Tbl3 regulates cell cycle length during zebrafish development.Nucleolar stress with and without p53.Systematic transcriptome analysis of the zebrafish model of diamond-blackfan anemia induced by RPS24 deficiency.Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implicationsAssessment 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.Studying synthetic lethal interactions in the zebrafish system: insight into disease genes and mechanisms.Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT PathwayThe Ribosome Biogenesis Protein Nol9 Is Essential for Definitive Hematopoiesis and Pancreas Morphogenesis in Zebrafish.Expression of ribosomopathy genes during Xenopus tropicalis embryogenesis.The p53 pathway in hematopoiesis: lessons from mouse models, implications for humans.Zebrafish Craniofacial Development: A Window into Early PatterningSelenoprotein H is an essential regulator of redox homeostasis that cooperates with p53 in development and tumorigenesisThe search for evolutionary developmental origins of aging in zebrafish: a novel intersection of developmental and senescence biology in the zebrafish model system.Molecular mechanisms of pathology and treatment in Diamond Blackfan Anaemia.Scission of the p53-MDM2 Loop by Ribosomal Proteins.Understanding the regulation of vertebrate hematopoiesis and blood disorders - big lessons from a small fish.Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia.Differential proteomic analysis in human cells subjected to ribosomal stress.Rpl22 Loss Selectively Impairs αβ T Cell Development by Dysregulating Endoplasmic Reticulum Stress Signaling.Why is an energy metabolic defect the common outcome in BMFS?Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy.The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome.Hematopoietic defects in rps29 mutant zebrafish depend upon p53 activation.How Ribosomes Translate Cancer.Ribosomal protein L11 is related to brain maturation during the adult phase in Apis cerana cerana (Hymenoptera, Apidae).Spliceosomal components protect embryonic neurons from R-loop-mediated DNA damage and apoptosis.Innate immune system activation in zebrafish and cellular models of Diamond Blackfan Anemia.Zebrafish Models of Rare Hereditary Pediatric Diseases.
P2860
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P2860
Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects.
description
2010 nî lūn-bûn
@nan
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
2010年论文
@zh
2010年论文
@zh-cn
name
Ribosomal protein L11 mutation ...... poietic and metabolic defects.
@en
type
label
Ribosomal protein L11 mutation ...... poietic and metabolic defects.
@en
prefLabel
Ribosomal protein L11 mutation ...... poietic and metabolic defects.
@en
P2093
P2860
P1476
Ribosomal protein L11 mutation ...... poietic and metabolic defects.
@en
P2093
Kathleen M Sakamoto
Nadia Danilova
P2860
P304
P356
10.1111/J.1365-2141.2010.08396.X
P407
P577
2010-11-29T00:00:00Z