mRNA quality control: Marking the message for life or death.
about
Using microarrays to facilitate positional cloning: identification of tomosyn as an inhibitor of neurosecretion.Identification 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 cytoplasmIdentification of delta helicase as the bovine homolog of HUPF1: demonstration of an interaction with the third subunit of DNA polymerase delta.Complexes between the nonsense-mediated mRNA decay pathway factor human upf1 (up-frameshift protein 1) and essential nonsense-mediated mRNA decay factors in HeLa cellsIntron evolution as a population-genetic processNewfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1Aberrant RNA splicing and its functional consequences in cancer cellsAlternative splicing and nonsense-mediated mRNA decay regulate mammalian ribosomal gene expression.Stable mRNP formation and export require cotranscriptional recruitment of the mRNA export factors Yra1p and Sub2p by Hpr1pThe post-apoptotic fate of RNAs identified through high-throughput sequencing of human hairControl of VP16 translation by the herpes simplex virus type 1 immediate-early protein ICP27.Retinal TrkB receptors regulate neural development in the inner, but not outer, retinaA spontaneous point mutation produces monoamine oxidase A/B knock-out mice with greatly elevated monoamines and anxiety-like behavior.Activation of pre-mRNA splicing by human RNPS1 is regulated by CK2 phosphorylation.WIG1 is crucial for AGO2-mediated ACOT7 mRNA silencing via miRNA-dependent and -independent mechanismsMultifunctionality of the linker histones: an emerging role for protein-protein interactions.T-cell receptor sequences that elicit strong down-regulation of premature termination codon-bearing transcripts.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.Periaxin mutations cause a broad spectrum of demyelinating neuropathies.Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type V.Nuclear export of mRNA.Multifunctional regulatory proteins that control gene expression in both the nucleus and the cytoplasm.Identification and characterization of RED120: a conserved PWI domain protein with links to splicing and 3'-end formation.Molecular heterogeneity of familial porphyria cutanea tarda in Spain: characterization of 10 novel mutations in the UROD gene.Quality control of gene expression in the nucleus.Deep brain stimulation modulates nonsense-mediated RNA decay in Parkinson's patients leukocytesNonsense-mediated mRNA decay in Saccharomyces cerevisiae: a quality control mechanism that degrades transcripts harboring premature termination codons.A Hox gene mutation that triggers nonsense-mediated RNA decay and affects alternative splicing during Drosophila development.Efficient downregulation of immunoglobulin mu mRNA with premature translation-termination codons requires the 5'-half of the VDJ exonEffects of length and location on the cellular response to double-stranded RNA.Use of an in vivo reporter assay to test for transcriptional and translational fidelity in yeast.Identification of novel splice variants and exons of human endothelial cell-specific chemotaxic regulator (ECSCR) by bioinformatics analysis.Regulation of natural mRNAs by the nonsense-mediated mRNA decay pathway.Complex alternative splicing of the hKLK3 gene coding for the tumor marker PSA (prostate-specific-antigen).Unspliced Rous sarcoma virus genomic RNAs are translated and subjected to nonsense-mediated mRNA decay before packaging.Drosophila ribosomal proteins are associated with linker histone H1 and suppress gene transcription.Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation.RNA polymerase errors cause splicing defects and can be regulated by differential expression of RNA polymerase subunits.The odd coupling
P2860
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P2860
mRNA quality control: Marking the message for life or death.
description
2001 nî lūn-bûn
@nan
2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի փետրվարին 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
mRNA quality control: Marking the message for life or death.
@ast
mRNA quality control: Marking the message for life or death.
@en
mRNA quality control: Marking the message for life or death.
@nl
type
label
mRNA quality control: Marking the message for life or death.
@ast
mRNA quality control: Marking the message for life or death.
@en
mRNA quality control: Marking the message for life or death.
@nl
prefLabel
mRNA quality control: Marking the message for life or death.
@ast
mRNA quality control: Marking the message for life or death.
@en
mRNA quality control: Marking the message for life or death.
@nl
P1433
P1476
mRNA quality control: Marking the message for life or death
@en
P2093
Lykke-Andersen J
P304
P356
10.1016/S0960-9822(01)00036-7
P407
P577
2001-02-01T00:00:00Z