review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Carmichael GG | |
Maquat LE | |||
P2860 | cites work | Assembly of the Nuclear Transcription and Processing Machinery: Cajal Bodies (Coiled Bodies) and Transcriptosomes | Q22066088 |
Human Upf proteins target an mRNA for nonsense-mediated decay when bound downstream of a termination codon | Q24290775 | ||
Identification and characterization of human orthologues to Saccharomyces cerevisiae Upf2 protein and Upf3 protein (Caenorhabditis elegans SMG-4) | Q24550751 | ||
The spliceosome deposits multiple proteins 20-24 nucleotides upstream of mRNA exon-exon junctions | Q24595096 | ||
Identification of a regulated pathway for nuclear pre-mRNA turnover. | Q27931532 | ||
Transport of proteins and RNAs in and out of the nucleus | Q29619554 | ||
The protein Aly links pre-messenger-RNA splicing to nuclear export in metazoans | Q29620818 | ||
mRNA stability in eukaryotes | Q33885047 | ||
Double-stranded RNA as a template for gene silencing | Q33905186 | ||
Connecting transcription to messenger RNA processing | Q33934155 | ||
Tracking COL1A1 RNA in osteogenesis imperfecta. splice-defective transcripts initiate transport from the gene but are retained within the SC35 domain | Q36328426 | ||
Coupling of transcription with alternative splicing: RNA pol II promoters modulate SF2/ASF and 9G8 effects on an exonic splicing enhancer | Q38320513 | ||
A look at messenger RNP moving through the nuclear pore | Q41367422 | ||
RNA editing and hypermutation by adenosine deamination | Q41491657 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | quality control | Q827792 |
P304 | page(s) | 173-176 | |
P577 | publication date | 2001-01-01 | |
P1433 | published in | Cell | Q655814 |
P1476 | title | Quality control of mRNA function | |
P478 | volume | 104 |
Q34801779 | +1 Proteins and aging |
Q40042442 | 5'-triphosphate-dependent activation of PKR by RNAs with short stem-loops |
Q44447397 | A candidate-gene approach to clone the sorghum Brown midrib gene encoding caffeic acid O-methyltransferase |
Q45856096 | A case of coagulation factor V deficiency caused by compound heterozygous mutations in the factor V gene |
Q46959745 | A method to determine RNA and DNA oxidation simultaneously by HPLC-ECD: greater RNA than DNA oxidation in rat liver after doxorubicin administration |
Q35779276 | A nonsense mutation in the fibrillin-1 gene of a Marfan syndrome patient induces NMD and disrupts an exonic splicing enhancer |
Q36145979 | A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree |
Q37473942 | A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family |
Q34907703 | A nuclear variant of ErbB3 receptor tyrosine kinase regulates ezrin distribution and Schwann cell myelination |
Q35970662 | A plethora of virulence strategies hidden behind nuclear targeting of microbial effectors. |
Q34365128 | A quantitative analysis of intron effects on mammalian gene expression |
Q28185435 | A simple whole cell lysate system for in vitro splicing reveals a stepwise assembly of the exon-exon junction complex |
Q34889289 | A yeast homologue of Hsp70, Ssa1p, regulates turnover of the MFA2 transcript through its AU-rich 3' untranslated region |
Q29547735 | ATM and related protein kinases: safeguarding genome integrity |
Q24299834 | ATP is required for interactions between UAP56 and two conserved mRNA export proteins, Aly and CIP29, to assemble the TREX complex |
Q37182197 | Absence of spermatozoal CD46 protein expression and associated rapid acrosome reaction rate in striped field mice (Apodemus agrarius) |
Q33587424 | Allelic gene structure variations in Anopheles gambiae mosquitoes |
Q24811071 | Alternative splicing and nonsense-mediated mRNA decay regulate mammalian ribosomal gene expression |
Q37222930 | Alternative splicing and tumor progression |
Q38291477 | Alternative splicing of DNA damage response genes and gastrointestinal cancers. |
Q34586931 | Alternative splicing: multiple control mechanisms and involvement in human disease |
Q28258466 | An activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id) |
Q24530023 | An alternatively spliced isoform of transcriptional repressor ATF3 and its induction by stress stimuli |
Q34365317 | An endonuclease activity similar to Xenopus PMR1 catalyzes the degradation of normal and nonsense-containing human beta-globin mRNA in erythroid cells. |
Q29547273 | An extensive network of coupling among gene expression machines |
Q34364600 | Analysis of the products of mRNA decapping and 3'-to-5' decay by denaturing gel electrophoresis |
Q44734157 | Autoregulation of polypyrimidine tract binding protein by alternative splicing leading to nonsense-mediated decay |
Q42206362 | Bacterial RNA induces myocyte cellular dysfunction through the activation of PKR. |
Q34996254 | Beta-thalassaemia prototype of a single gene disorder with multiple phenotypes |
Q46049216 | Cardiac troponin T is essential in sarcomere assembly and cardiac contractility |
Q34122123 | Cauliflower mosaic virus: still in the news |
Q24293459 | Characterization of human Smg5/7a: a protein with similarities to Caenorhabditis elegans SMG5 and SMG7 that functions in the dephosphorylation of Upf1. |
Q24811082 | Cleavage of dsRNAs hyper-edited by ADARs occurs at preferred editing sites |
Q24291181 | Cloning of a novel phosphatidylinositol kinase-related kinase: characterization of the human SMG-1 RNA surveillance protein |
Q34402084 | Co-transcriptional splicing of pre-messenger RNAs: considerations for the mechanism of alternative splicing |
Q35290709 | ColVI myopathies: where do we stand, where do we go? |
Q42060855 | Commitment of apolipoprotein B RNA to the splicing pathway regulates cytidine-to-uridine editing-site utilization |
Q73128265 | Complex formation among the RNA export proteins Nup98, Rae1/Gle2, and TAP |
Q34738413 | Control of eukaryotic protein synthesis by upstream open reading frames in the 5'-untranslated region of an mRNA |
Q37847790 | Control of human beta-globin mRNA stability and its impact on beta-thalassemia phenotype. |
Q27641014 | Crystal structure of theDrosophilaMago nashi–Y14 complex |
Q24677437 | Cytoplasmic foci are sites of mRNA decay in human cells |
Q37071684 | Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome |
Q37259559 | Dilated cardiomyopathy caused by tissue-specific ablation of SC35 in the heart |
Q44407006 | Disease-associated mutations in conserved residues of ALK-1 kinase domain |
Q42511112 | Distinct tumor protein p53 mutants in breast cancer subgroups |
Q46592463 | Dominant optic atrophy caused by a novel OPA1 splice site mutation (IVS20+1G-->A) associated with intron retention |
Q35880915 | Effects of length and location on the cellular response to double-stranded RNA. |
Q35249273 | Efficient production of Fah-null heterozygote pigs by chimeric adeno-associated virus-mediated gene knockout and somatic cell nuclear transfer. |
Q59303864 | Error prevention and mitigation as forces in the evolution of genes and genomes |
Q27938653 | Evidence against a direct role for the Upf proteins in frameshifting or nonsense codon readthrough. |
Q24291673 | Evidence for a pioneer round of mRNA translation: mRNAs subject to nonsense-mediated decay in mammalian cells are bound by CBP80 and CBP20 |
Q44826313 | Ex vivo analysis of aberrant splicing induced by two donor site mutations in PKLR of a patient with severe pyruvate kinase deficiency |
Q24317462 | Exp5 exports eEF1A via tRNA from nuclei and synergizes with other transport pathways to confine translation to the cytoplasm |
Q34142078 | Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy |
Q37864582 | Extremes in rapid cellular morphogenesis: post-transcriptional regulation of spermatogenesis in Marsilea vestita |
Q39455987 | Factors affecting splicing strength of yeast genes |
Q34048030 | From General Aberrant Alternative Splicing in Cancers and Its Therapeutic Application to the Discovery of an Oncogenic DMTF1 Isoform. |
Q34365653 | Functional dissection of hnRNP D suggests that nuclear import is required before hnRNP D can modulate mRNA turnover in the cytoplasm |
Q42156950 | Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codons |
Q40472961 | Functional significance of a deep intronic mutation in the ATM gene and evidence for an alternative exon 28a. |
Q35256585 | G protein-coupled receptors involved in GnRH regulation: molecular insights from human disease |
Q35112564 | Gene Regulation at the RNA Layer: RNA Binding Proteins in Intercellular Signaling Networks |
Q37200666 | Gene regulation by sense-antisense overlap of polyadenylation signals. |
Q34774548 | Glutaredoxin 2 (Grx2) gene deletion induces early onset of age-dependent cataracts in mice |
Q33668518 | GroEL dependency affects codon usage--support for a critical role of misfolding in gene evolution |
Q34113108 | Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV. |
Q33188510 | Heat sensitivity in a bentgrass variant. Failure to accumulate a chloroplast heat shock protein isoform implicated in heat tolerance |
Q44649321 | Homodirectional changes in transcriptome composition and mRNA translation induced by rapamycin and heat shock |
Q36768143 | How a small DNA virus uses dsRNA but not RNAi to regulate its life cycle |
Q35114297 | How introns influence and enhance eukaryotic gene expression |
Q24291647 | Human 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 decay |
Q24683257 | Impaired FGF signaling contributes to cleft lip and palate |
Q37417487 | Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism |
Q39940501 | In Vivo Evidence that Defects in the Transcriptional Elongation Factors RPB2, TFIIS, and SPT5 Enhance Upstream Poly(A) Site Utilization |
Q24537459 | In vivo identification of ribonucleoprotein-RNA interactions |
Q40017495 | Inosine-containing dsRNA binds a stress-granule-like complex and downregulates gene expression in trans |
Q42868567 | Interaction of yeast eIF4G with spliceosome components: implications in pre-mRNA processing events. |
Q34326750 | Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia |
Q52672265 | Intron retention in viruses and cellular genes: Detention, border controls and passports. |
Q41974443 | JAK kinases are required for the bacterial RNA and poly I:C induced tyrosine phosphorylation of PKR. |
Q37587854 | Kisspeptin and clinical disorders. |
Q52871123 | Loss of Hep Par 1 immunoreactivity in the livers of patients with carbamoyl phosphate synthetase 1 deficiency. |
Q51766228 | Loss of mRNA surveillance pathways results in widespread protein aggregation. |
Q30442563 | Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism |
Q57412259 | Macromolecular mobility inside the cell nucleus |
Q47868972 | Making structural sense of nonsense-mediated decay. |
Q28189675 | Messenger RNA editing in mammals: new members of the APOBEC family seeking roles in the family business |
Q24534359 | MicroRNA maturation: stepwise processing and subcellular localization |
Q40649754 | Missense, nonsense, and neutral mutations define juxtaposed regulatory elements of splicing in cystic fibrosis transmembrane regulator exon 9. |
Q39624824 | Molecular analysis of the first intron in the bovine myostatin gene |
Q48083893 | Molecular characterization of Portuguese patients with mucopolysaccharidosis type II shows evidence that the IDS gene is prone to splicing mutations |
Q34984140 | Mutant LYS2 mRNAs retained and degraded in the nucleus of Saccharomyces cerevisiae |
Q34597433 | Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism |
Q36938312 | Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum. |
Q59123119 | NF1mutation rather than individual genetic variability is the main determinant of theNF1-transcriptional profile of mutations affecting splicing |
Q27931019 | Nab2p is required for poly(A) RNA export in Saccharomyces cerevisiae and is regulated by arginine methylation via Hmt1p |
Q77808552 | Nonsense-mediated mRNA decay |
Q34417077 | Nonsense-mediated mRNA decay in Saccharomyces cerevisiae |
Q35133708 | Nonsense-mediated mRNA decay: insights into mechanism from the cellular abundance of human Upf1, Upf2, Upf3, and Upf3X proteins |
Q29616134 | Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics |
Q34325368 | Novel SLC7A7 large rearrangements in lysinuric protein intolerance patients involving the same AluY repeat. |
Q34574303 | Nuclear RNA turnover |
Q34286048 | Nuclear export of mRNA. |
Q30453281 | Nuclear interactions are necessary for translational enhancement by spleen necrosis virus RU5. |
Q34173493 | Nuclear translation: what is the evidence? |
Q24793210 | Odorant receptor expressed sequence tags demonstrate olfactory expression of over 400 genes, extensive alternate splicing and unequal expression levels |
Q35920650 | PSF acts through the human immunodeficiency virus type 1 mRNA instability elements to regulate virus expression |
Q24301026 | PYM binds the cytoplasmic exon-junction complex and ribosomes to enhance translation of spliced mRNAs |
Q35751728 | Post-Transcriptional Regulation of Endothelial Nitric Oxide Synthase Expression by Polypyrimidine Tract-Binding Protein 1. |
Q43652210 | Post-transcriptional inactivation of p53 in immortalized murine embryo fibroblast cells |
Q38114053 | Pre-mRNA processing factors meet the DNA damage response |
Q30940012 | Proteomic analysis of human Nop56p-associated pre-ribosomal ribonucleoprotein complexes. Possible link between Nop56p and the nucleolar protein treacle responsible for Treacher Collins syndrome |
Q34687780 | Quality control of gene expression in the nucleus |
Q27932977 | Quality control of mRNA 3'-end processing is linked to the nuclear exosome |
Q58381259 | RNA Processing and Human Disorders |
Q45072261 | RNA and protein evidence for haplo-insufficiency in Diamond-Blackfan anaemia patients with RPS19 mutations |
Q40712353 | RNA interference in human cells is restricted to the cytoplasm |
Q33909884 | Rare autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway. |
Q24813203 | Recognition of unknown conserved alternatively spliced exons |
Q47350856 | Regulated tissue-specific alternative splicing of enhanced green fluorescent protein transgenes conferred by alpha-tropomyosin regulatory elements in transgenic mice |
Q34546893 | Regulation of alternative RNA splicing by exon definition and exon sequences in viral and mammalian gene expression |
Q40476200 | Regulation of alternative splicing of Bcl-x by IL-6, GM-CSF and TPA. |
Q34806626 | Regulation of pathways of mRNA destabilization and stabilization |
Q34025462 | Regulatory effects of SKAR in interferon α signaling and its role in the generation of type I IFN responses |
Q34324350 | Requirements of the RNA polymerase II C-terminal domain for reconstituting pre-mRNA 3' cleavage. |
Q34396661 | Retroposition of processed pseudogenes: the impact of RNA stability and translational control |
Q52598134 | Ribosome components are associated with sites of transcription. |
Q38848112 | Role of frameshift ubiquitin B protein in Alzheimer's disease |
Q35548597 | Role of ubiquitin-mediated proteolysis in the pathogenesis of neurodegenerative disorders. |
Q58556295 | Roles of Smads Family and Alternative Splicing Variants of Smad4 in Different Cancers |
Q39895219 | Roles of polypyrimidine tract binding proteins in major immediate-early gene expression and viral replication of human cytomegalovirus |
Q43652357 | Rumpshaker-like proteolipid protein (PLP) ratio in a mouse model with unperturbed structural and functional integrity of the myelin sheath and axons in the central nervous system |
Q90360119 | SMG1 heterozygosity exacerbates haematopoietic cancer development in Atm null mice by increasing persistent DNA damage and oxidative stress |
Q24540541 | Sam68 enhances the cytoplasmic utilization of intron-containing RNA and is functionally regulated by the nuclear kinase Sik/BRK. |
Q73121121 | Screening for PAX6 gene mutations is consistent with haploinsufficiency as the main mechanism leading to various ocular defects |
Q35806763 | Selecting for functional alternative splices in ESTs |
Q28345098 | Specific cleavage of hyper-edited dsRNAs |
Q24623819 | Splicing enhances translation in mammalian cells: an additional function of the exon junction complex |
Q28572768 | Staufen recruitment into stress granules does not affect early mRNA transport in oligodendrocytes |
Q34324879 | Structural insight into poly(A) binding and catalytic mechanism of human PARN. |
Q30312038 | Tap and NXT promote translation of unspliced mRNA. |
Q27932831 | The C-terminal domain of myosin-like protein 1 (Mlp1p) is a docking site for heterogeneous nuclear ribonucleoproteins that are required for mRNA export |
Q27932088 | The DEAD box protein Dhh1 stimulates the decapping enzyme Dcp1 |
Q46491561 | The RISC subunit Tudor-SN binds to hyper-edited double-stranded RNA and promotes its cleavage |
Q27651271 | The RRM domain of poly(A)-specific ribonuclease has a noncanonical binding site for mRNA cap analog recognition |
Q35787562 | The Ro 60 kDa autoantigen: insights into cellular function and role in autoimmunity |
Q24310868 | The apolipoprotein B mRNA editing complex performs a multifunctional cycle and suppresses nonsense-mediated decay |
Q74353662 | The cleavage/polyadenylation activity triggered by a U-rich motif sequence is differently required depending on the poly(A) site location at either the first or last 3'-terminal exon of the 2'-5' oligo(A) synthetase gene |
Q24537105 | The exon junction complex is detected on CBP80-bound but not eIF4E-bound mRNA in mammalian cells: dynamics of mRNP remodeling |
Q28214585 | The fate of dsRNA in the nucleus: a p54(nrb)-containing complex mediates the nuclear retention of promiscuously A-to-I edited RNAs |
Q35618934 | The four Rs of RNA-directed evolution |
Q38354474 | The interaction of the cap-binding complex (CBC) with eIF4G is dispensable for translation in yeast |
Q41764853 | The intranuclear mobility of messenger RNA binding proteins is ATP dependent and temperature sensitive |
Q40632496 | The intronic prothrombin 19911A>G polymorphism influences splicing efficiency and modulates effects of the 20210G>A polymorphism on mRNA amount and expression in a stable reporter gene assay system |
Q24294881 | The mRNA surveillance protein hSMG-1 functions in genotoxic stress response pathways in mammalian cells |
Q34443571 | The many roles of an RNA editor. |
Q36494102 | The multiassembly problem: reconstructing multiple transcript isoforms from EST fragment mixtures |
Q43603839 | The open reading frame VI product of Cauliflower mosaic virus is a nucleocytoplasmic protein: its N terminus mediates its nuclear export and formation of electron-dense viroplasms |
Q34363968 | The rest is silence. |
Q40863011 | The role of immunostimulatory nucleic acids in septic shock |
Q42798672 | The transformation suppressor protein Pdcd4 shuttles between nucleus and cytoplasm and binds RNA. |
Q33371119 | The uORF-containing thrombopoietin mRNA escapes nonsense-mediated decay (NMD). |
Q27935190 | The yeast RNA-binding protein Rbp1p modifies the stability of mitochondrial porin mRNA. |
Q33285545 | Three novel ABCC5 splice variants in human retina and their role as regulators of ABCC5 gene expression |
Q42610027 | Transcriptional control of the arginine/lysine transporter, cat-1, by physiological stress. |
Q33775675 | Translation repression by GLD-1 protects its mRNA targets from nonsense-mediated mRNA decay in C. elegans |
Q74477661 | Transposable elements encoding functional proteins: pitfalls in unprocessed genomic data? |
Q24339199 | Tudor-SN interacts with and co-localizes with G3BP in stress granules under stress conditions |
Q33758082 | Turnover of primary transcripts is a major step in the regulation of mouse H19 gene expression |
Q28216838 | Two proteins essential for apolipoprotein B mRNA editing are expressed from a single gene through alternative splicing |
Q40815123 | Unspliced Rous sarcoma virus genomic RNAs are translated and subjected to nonsense-mediated mRNA decay before packaging |
Q50485414 | Variable clinical presentation of lysosomal beta-mannosidosis in patients with null mutations. |
Q24300691 | Y14 and hUpf3b form an NMD-activating complex |
Q33865334 | m6A mRNA modifications are deposited in nascent pre-mRNA and are not required for splicing but do specify cytoplasmic turnover. |
Q108225232 | Explaining Fertility Variation in Rural Communities: The Role of Electricity in Ghana | main subject | P921 |
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