When the message goes awry: disease-producing mutations that influence mRNA content and performance.
about
Selective translational repression of truncated proteins from frameshift mutation-derived mRNAs in tumorsUsing microarrays to facilitate positional cloning: identification of tomosyn as an inhibitor of neurosecretion.New microRNAs from mouse and humanTranscript-selective translational silencing by gamma interferon is directed by a novel structural element in the ceruloplasmin mRNA 3' untranslated regionHuman SP-A1 (SFTPA1) variant-specific 3' UTRs and poly(A) tail differentially affect the in vitro translation of a reporter geneThe roles of TTP and BRF proteins in regulated mRNA decayIRAK-M is involved in the pathogenesis of early-onset persistent asthmaX chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation.The Icelandic founder mutation BRCA2 999del5: analysis of expressionA GFP-based reporter system to monitor nonsense-mediated mRNA decayNew and emerging targeted therapies for cystic fibrosisMutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathyMolecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutationsRapid deadenylation triggered by a nonsense codon precedes decay of the RNA body in a mammalian cytoplasmic nonsense-mediated decay pathwayCurrent themes in molecular pediatrics: molecular medicine and its applications.Predicting the impact of deleterious mutations in the protein kinase domain of FGFR2 in the context of function, structure, and pathogenesis--a bioinformatics approach.Polymorphic variation in cytochrome oxidase subunit genes.Membrane blebbing as an assessment of functional rescue of dysferlin-deficient human myotubes via nonsense suppression.Gene variants in noncoding regions and their possible consequences.Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia.A flexible Bayesian method for detecting allelic imbalance in RNA-seq dataImpact of nonsense-mediated mRNA decay on the global expression profile of budding yeast.The uORF-containing thrombopoietin mRNA escapes nonsense-mediated decay (NMD).Mutation analysis in primary immunodeficiency diseases: case studies.Next-generation sequencing: from understanding biology to personalized medicine.The unfolded protein response affects readthrough of premature termination codonsThe mRNA decay factor tristetraprolin (TTP) induces senescence in human papillomavirus-transformed cervical cancer cells by targeting E6-AP ubiquitin ligase.Genome-wide double-stranded RNA sequencing reveals the functional significance of base-paired RNAs in ArabidopsisOsteonectin/SPARC polymorphisms in Caucasian men with idiopathic osteoporosisDistinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome.Targets for cystic fibrosis therapy: proteomic analysis and correction of mutant cystic fibrosis transmembrane conductance regulatorCurcumin treatment abrogates endoplasmic reticulum retention and aggregation-induced apoptosis associated with neuropathy-causing myelin protein zero-truncating mutants.The ribosome filter hypothesis.SVA retrotransposons: Evolution and genetic instabilityPosttranscriptional and posttranslational regulation of C/EBP delta in G0 growth-arrested mammary epithelial cells.Nuclear translation: what is the evidence?Toward a rationale for the PTC124 (Ataluren) promoted readthrough of premature stop codons: a computational approach and GFP-reporter cell-based assayCCDC22: a novel candidate gene for syndromic X-linked intellectual disabilityPremature termination codons do not affect the rate of splicing of neighboring introns.Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cells.
P2860
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P2860
When the message goes awry: disease-producing mutations that influence mRNA content and performance.
description
2001 nî lūn-bûn
@nan
2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
When the message goes awry: di ...... mRNA content and performance.
@ast
When the message goes awry: di ...... mRNA content and performance.
@en
type
label
When the message goes awry: di ...... mRNA content and performance.
@ast
When the message goes awry: di ...... mRNA content and performance.
@en
prefLabel
When the message goes awry: di ...... mRNA content and performance.
@ast
When the message goes awry: di ...... mRNA content and performance.
@en
P1433
P1476
When the message goes awry: di ...... mRNA content and performance.
@en
P2093
P304
P356
10.1016/S0092-8674(01)00583-9
P407
P577
2001-11-01T00:00:00Z