A perfect message: RNA surveillance and nonsense-mediated decay
about
Using microarrays to facilitate positional cloning: identification of tomosyn as an inhibitor of neurosecretion.Cloning of a novel phosphatidylinositol kinase-related kinase: characterization of the human SMG-1 RNA surveillance proteinHuman SMG-1, a novel phosphatidylinositol 3-kinase-related protein kinase, associates with components of the mRNA surveillance complex and is involved in the regulation of nonsense-mediated mRNA decayCharacterization of human Smg5/7a: a protein with similarities to Caenorhabditis elegans SMG5 and SMG7 that functions in the dephosphorylation of Upf1.Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex IThe DEAD-box RNA helicase DDX3 associates with export messenger ribonucleoproteins as well as tip-associated protein and participates in translational controlRecruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnessesThe apolipoprotein B mRNA editing complex performs a multifunctional cycle and suppresses nonsense-mediated decayInteractions between UPF1, eRFs, PABP and the exon junction complex suggest an integrated model for mammalian NMD pathwaysIdentification of a human decapping complex associated with hUpf proteins in nonsense-mediated decay.Exp5 exports eEF1A via tRNA from nuclei and synergizes with other transport pathways to confine translation to the cytoplasmFunctional proteomic analysis of human nucleolusRestoration of LDL receptor function in cells from patients with autosomal recessive hypercholesterolemia by retroviral expression of ARH1Complexes between the nonsense-mediated mRNA decay pathway factor human upf1 (up-frameshift protein 1) and essential nonsense-mediated mRNA decay factors in HeLa cellsMutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardationDigenic junctional epidermolysis bullosa: mutations in COL17A1 and LAMB3 genes.Magoh, a human homolog of Drosophila mago nashi protein, is a component of the splicing-dependent exon-exon junction complex.Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing proteinThe exon junction complex is detected on CBP80-bound but not eIF4E-bound mRNA in mammalian cells: dynamics of mRNP remodeling.Mutations in the AIRE gene: effects on subcellular location and transactivation function of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy proteinThe human LSm1-7 proteins colocalize with the mRNA-degrading enzymes Dcp1/2 and Xrnl in distinct cytoplasmic foci.Translational and structural requirements of the early nodulin gene enod40, a short-open reading frame-containing RNA, for elicitation of a cell-specific growth response in the alfalfa root cortexIdentification and characterization of human orthologues to Saccharomyces cerevisiae Upf2 protein and Upf3 protein (Caenorhabditis elegans SMG-4)SMG-2 is a phosphorylated protein required for mRNA surveillance in Caenorhabditis elegans and related to Upf1p of yeastSECIS-SBP2 interactions dictate selenocysteine incorporation efficiency and selenoprotein hierarchyThe spliceosome deposits multiple proteins 20-24 nucleotides upstream of mRNA exon-exon junctionsNMR solution structure and function of the C-terminal domain of eukaryotic class 1 polypeptide chain release factorPre-mRNA splicing alters mRNP composition: evidence for stable association of proteins at exon-exon junctionsSensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastomaNewfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomaliesA nuclear translation-like factor eIF4AIII is recruited to the mRNA during splicing and functions in nonsense-mediated decayAutosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A113' end mRNA processing: molecular mechanisms and implications for health and diseaseNuclear Pnn/DRS protein binds to spliced mRNPs and participates in mRNA processing and export via interaction with RNPS1Discs-large homolog 1 regulates smooth muscle orientation in the mouse ureter.The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporterSwitched alternative splicing of oncogene CoAA during embryonal carcinoma stem cell differentiationThe acute myeloid leukemia-associated protein, DEK, forms a splicing-dependent interaction with exon-product complexesUntranslated regions of mRNAs.
P2860
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P2860
A perfect message: RNA surveillance and nonsense-mediated decay
description
1999 nî lūn-bûn
@nan
1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
A perfect message: RNA surveillance and nonsense-mediated decay
@ast
A perfect message: RNA surveillance and nonsense-mediated decay
@en
type
label
A perfect message: RNA surveillance and nonsense-mediated decay
@ast
A perfect message: RNA surveillance and nonsense-mediated decay
@en
prefLabel
A perfect message: RNA surveillance and nonsense-mediated decay
@ast
A perfect message: RNA surveillance and nonsense-mediated decay
@en
P3181
P1433
P1476
A perfect message: RNA surveillance and nonsense-mediated decay
@en
P2093
A E Kulozik
P304
P3181
P356
10.1016/S0092-8674(00)80542-5
P407
P577
1999-02-01T00:00:00Z