Proteomic analysis of human Nop56p-associated pre-ribosomal ribonucleoprotein complexes. Possible link between Nop56p and the nucleolar protein treacle responsible for Treacher Collins syndrome.
about
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factorSplicing factor 2-associated protein p32 participates in ribosome biogenesis by regulating the binding of Nop52 and fibrillarin to preribosome particlesNOP132 is required for proper nucleolus localization of DEAD-box RNA helicase DDX47Parvulin (Par14), a peptidyl-prolyl cis-trans isomerase, is a novel rRNA processing factor that evolved in the metazoan lineageEBP1 is a nucleolar growth-regulating protein that is part of pre-ribosomal ribonucleoprotein complexesDwarfism and impaired gut development in insulin-like growth factor II mRNA-binding protein 1-deficient miceTreacher Collins syndrome: etiology, pathogenesis and preventionTreacher Collins syndrome: unmasking the role of Tcof1/treacleThe novel ATP-binding cassette protein ARB1 is a shuttling factor that stimulates 40S and 60S ribosome biogenesis.ISG20L2, a novel vertebrate nucleolar exoribonuclease involved in ribosome biogenesisHuman fibrillarin forms a sub-complex with splicing factor 2-associated p32, protein arginine methyltransferases, and tubulins alpha 3 and beta 1 that is independent of its association with preribosomal ribonucleoprotein complexesThe Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylationDistinct cytoplasmic maturation steps of 40S ribosomal subunit precursors require hRio2Recruitment of factors linking transcription and processing of pre-rRNA to NOR chromatin is UBF-dependent and occurs independent of transcription in human cellsProteomic analysis of the Arabidopsis nucleolus suggests novel nucleolar functionsRibosome biogenesis in skeletal development and the pathogenesis of skeletal disordersMDM2 mediates nonproteolytic polyubiquitylation of the DEAD-Box RNA helicase DDX24Fishing the molecular bases of Treacher Collins syndromeSilencing of RNA helicase II/Gualpha inhibits mammalian ribosomal RNA production.Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.Whole-genome screening identifies proteins localized to distinct nuclear bodiesTandem affinity purification combined with inducible shRNA expression as a tool to study the maturation of macromolecular assembliesA genomic strategy for the functional validation of colorectal cancer genes identifies potential therapeutic targets.Potential roles for ubiquitin and the proteasome during ribosome biogenesis.Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.Animal models of Diamond Blackfan anemia.Proteome Analysis of Poplar Seed Vigor.RNAi knockdown of Nopp140 induces Minute-like phenotypes in Drosophila.The nucleolus: reviewing oldies to have new understandings.Burkitt's lymphoma-associated c-Myc mutations converge on a dramatically altered target gene response and implicate Nol5a/Nop56 in oncogenesisCnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genesTissue specific roles for the ribosome biogenesis factor Wdr43 in zebrafish development.The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability.Rare syndromes of the head and face: mandibulofacial and acrofacial dysostoses.Regulation of the mouse Treacher Collins syndrome homolog (Tcof1) promoter through differential repression of constitutive expression.Identifying host factors associated with DNA replicated during virus infection.An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes.Early and selective reduction of NOP56 (Asidan) and RNA processing proteins in the motor neuron of ALS model mice.Human cell growth regulator Ly-1 antibody reactive homologue accelerates processing of preribosomal RNA.Defective replication initiation results in locus specific chromosome breakage and a ribosomal RNA deficiency in yeast.
P2860
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P2860
Proteomic analysis of human Nop56p-associated pre-ribosomal ribonucleoprotein complexes. Possible link between Nop56p and the nucleolar protein treacle responsible for Treacher Collins syndrome.
description
2003 nî lūn-bûn
@nan
2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Proteomic analysis of human No ...... for Treacher Collins syndrome.
@ast
Proteomic analysis of human No ...... for Treacher Collins syndrome.
@en
type
label
Proteomic analysis of human No ...... for Treacher Collins syndrome.
@ast
Proteomic analysis of human No ...... for Treacher Collins syndrome.
@en
prefLabel
Proteomic analysis of human No ...... for Treacher Collins syndrome.
@ast
Proteomic analysis of human No ...... for Treacher Collins syndrome.
@en
P2093
P2860
P356
P1476
Proteomic analysis of human No ...... for Treacher Collins syndrome.
@en
P2093
Mitsuaki Yanagida
Nobuhiro Takahashi
Takashi Shinkawa
Toshiaki Isobe
Toshiya Hayano
Yoshio Yamauchi
P2860
P304
34309-34319
P356
10.1074/JBC.M304304200
P407
P577
2003-05-30T00:00:00Z