about
AceView: a comprehensive cDNA-supported gene and transcripts annotationRBM6-RBM5 transcription-induced chimeras are differentially expressed in tumoursInfluence of XPB helicase on recruitment and redistribution of nucleotide excision repair proteins at sites of UV-induced DNA damageSOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic developmentA new MIF4G domain-containing protein, CTIF, directs nuclear cap-binding protein CBP80/20-dependent translationMutation of SALL2 causes recessive ocular coloboma in humans and miceARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomaliesA competition between stimulators and antagonists of Upf complex recruitment governs human nonsense-mediated mRNA decayLoss-of-function mutations in the keratin 5 gene lead to Dowling-Degos diseaseMutational analysis of human eIF4AIII identifies regions necessary for exon junction complex formation and nonsense-mediated mRNA decay.Competency for nonsense-mediated reduction in collagen X mRNA is specified by the 3' UTR and corresponds to the position of mutations in Schmid metaphyseal chondrodysplasiaHuman eukaryotic release factor 3a depletion causes cell cycle arrest at G1 phase through inhibition of the mTOR pathwaySplicing remodels messenger ribonucleoprotein architecture via eIF4A3-dependent and -independent recruitment of exon junction complex componentsThe canonical UPF1-dependent nonsense-mediated mRNA decay is inhibited in transcripts carrying a short open reading frame independent of sequence contextThe shuttling protein Npl3 promotes translation termination accuracy in Saccharomyces cerevisiae.The ubiquitin-proteasome system and nonsense-mediated mRNA decay in hypertrophic cardiomyopathyDoes constructive neutral evolution play an important role in the origin of cellular complexity? Making sense of the origins and uses of biological complexityNuclear mRNA degradation pathway(s) are implicated in Xist regulation and X chromosome inactivationMutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humansAxial Spondylometaphyseal Dysplasia Is Caused by C21orf2 MutationsDoes enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse linesEndangered species hold clues to human evolutionA probabilistic classifier for olfactory receptor pseudogenesInhibition of Nonsense-mediated mRNA Decay by the Natural Product Pateamine A through Eukaryotic Initiation Factor 4AIIIGene variants in noncoding regions and their possible consequences.Beta1 integrin-mediated adhesion signalling is essential for epidermal progenitor cell expansion.The hierarchy of exon-junction complex assembly by the spliceosome explains key features of mammalian nonsense-mediated mRNA decay.Relaxed functional constraints on triplicate α-globin gene in the bank vole suggest a different evolutionary history from other rodents.XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients.Future alternative therapies for β-thalassemia.Natural selection retains overrepresented out-of-frame stop codons against frameshift peptides in prokaryotes.Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells.Splice isoforms of the polyglutamine disease protein ataxin-3 exhibit similar enzymatic yet different aggregation properties.Genome-wide functional analysis of human 5' untranslated region introns.Is there a classical nonsense-mediated decay pathway in trypanosomes?When a ribosome encounters a premature termination codon.A role for nonsense-mediated mRNA decay in plants: pathogen responses are induced in Arabidopsis thaliana NMD mutants.Toward a rationale for the PTC124 (Ataluren) promoted readthrough of premature stop codons: a computational approach and GFP-reporter cell-based assayThe application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genesmRNA surveillance and endoplasmic reticulum quality control processes alter biogenesis of mutant GABAA receptor subunits associated with genetic epilepsies.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Nonsense-mediated mRNA decay in mammals.
@ast
Nonsense-mediated mRNA decay in mammals.
@en
type
label
Nonsense-mediated mRNA decay in mammals.
@ast
Nonsense-mediated mRNA decay in mammals.
@en
prefLabel
Nonsense-mediated mRNA decay in mammals.
@ast
Nonsense-mediated mRNA decay in mammals.
@en
P356
P1476
Nonsense-mediated mRNA decay in mammals.
@en
P304
P356
10.1242/JCS.01701
P407
P577
2005-05-01T00:00:00Z