Diverse diseases from a ubiquitous process: the ribosomopathy paradox - Test2 - elhamkhani - TriplyDB

Diverse diseases from a ubiquitous process: the ribosomopathy paradox

Diverse diseases from a ubiquitous process: the ribosomopathy paradox

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Pathways to Specialized Ribosomes: The Brussels Lecture Ribosomopathies: how a common root can cause a tree of pathologies Hrr25/CK1δ-directed release of Ltv1 from pre-40S ribosomes is necessary for ribosome assembly and cell growth Ribosome biogenesis factor Tsr3 is the aminocarboxypropyl transferase responsible for 18S rRNA hypermodification in yeast and humans.Nucleolar stress with and without p53.Ribosomopathies and the paradox of cellular hypo- to hyperproliferation.Cellular differences in protein synthesis regulate tissue homeostasis.An overview of pre-ribosomal RNA processing in eukaryotes Reduced expression of the mouse ribosomal protein Rpl17 alters the diversity of mature ribosomes by enhancing production of shortened 5.8S rRNA.The Ribosome Biogenesis Protein Nol9 Is Essential for Definitive Hematopoiesis and Pancreas Morphogenesis in Zebrafish.Haploinsufficiency for Core Exon Junction Complex Components Disrupts Embryonic Neurogenesis and Causes p53-Mediated Microcephaly Expression of ribosomopathy genes during Xenopus tropicalis embryogenesis.Ribosome biogenesis dysfunction leads to p53-mediated apoptosis and goblet cell differentiation of mouse intestinal stem/progenitor cells Functions of ribosomal proteins in assembly of eukaryotic ribosomes in vivo.The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome.Activation of GCN2 kinase by ribosome stalling links translation elongation with translation initiation.Translation regulation by ribosomes: Increased complexity and expanded scope.Rps26 directs mRNA-specific translation by recognition of Kozak sequence elements.Structural Heterogeneity in Pre-40S Ribosomes.Osteosarcoma: Molecular Pathogenesis and iPSC Modeling.The Contributions of the Ribosome Biogenesis Protein Utp5/WDR43 to Craniofacial Development Principles of 60S ribosomal subunit assembly emerging from recent studies in yeast.Comparison of preribosomal RNA processing pathways in yeast, plant and human cells - focus on coordinated action of endo- and exoribonucleases.Placeholder factors in ribosome biogenesis: please, pave my way.Genetically regulated hepatic transcripts and pathways orchestrate haematological, biochemical and body composition traits.Ribosomopathy-like properties of murine and human cancers.Distinct 18S rRNA precursors are targets of the exosome complex, the exoribonuclease RRP6L2 and the terminal nucleotidyltransferase TRL in Arabidopsis thaliana.Inhibition of post-transcriptional steps in ribosome biogenesis confers cytoprotection against chemotherapeutic agents in a p53-dependent manner.Effects of the Bowen-Conradi syndrome mutation in EMG1 on its nuclear import, stability and nucleolar recruitment.The ubiquitin hybrid gene UBA52 regulates ubiquitination of ribosome and sustains embryonic development Proteotoxicity in cardiac amyloidosis: amyloidogenic light chains affect the levels of intracellular proteins in human heart cells.Reduced Expression of APUM24, Encoding a Novel rRNA Processing Factor, Induces Sugar-dependent Nucleolar Stress and Altered Sugar Responses in Arabidopsis thaliana.GRWD1, a new player among oncogenesis-related ribosomal/nucleolar proteins.EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome.mRNA Translation Gone Awry: Translation Fidelity and Neurological Disease.Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy., a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in

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Diverse diseases from a ubiquitous process: the ribosomopathy paradox

http://www.wikidata.org/entity/Q27694538

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2014 nî lūn-bûn

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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2014年の論文

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Diverse diseases from a ubiquitous process: the ribosomopathy paradox

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Diverse diseases from a ubiquitous process: the ribosomopathy paradox

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Diverse diseases from a ubiquitous process: the ribosomopathy paradox

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Diverse diseases from a ubiquitous process: the ribosomopathy paradox

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J.FEBSLET.2014.03.024

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Diverse diseases from a ubiquitous process: the ribosomopathy paradox

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Joy Armistead

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BMS1 is mutated in aplasia cutis congenita

NOL11, implicated in the pathogenesis of North American Indian childhood cirrhosis, is required for pre-rRNA transcription and processing

A telomerase component is defective in the human disease dyskeratosis congenita

The ribosome assembly factor Nep1 responsible for Bowen-Conradi syndrome is a pseudouridine-N1-specific methyltransferase

Ribosomal protein S7 as a novel modulator of p53-MDM2 interaction: binding to MDM2, stabilization of p53 protein, and activation of p53 function

The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor

Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome

The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA

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

Impaired ribosome biogenesis in Diamond-Blackfan anemia

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1491-1500

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Barbara Triggs-Raine

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2014-03-19T00:00:00Z

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