The human intronless melanocortin 4-receptor gene is NMD insensitive
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NMD resulting from encephalomyocarditis virus IRES-directed translation initiation seems to be restricted to CBP80/20-bound mRNAA 3' UTR sequence stabilizes termination codons in the unspliced RNA of Rous sarcoma virus.FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlationMechanism of escape from nonsense-mediated mRNA decay of human beta-globin transcripts with nonsense mutations in the first exonA nuclear translation-like factor eIF4AIII is recruited to the mRNA during splicing and functions in nonsense-mediated decayIntegration of splicing, transport and translation to achieve mRNA quality control by the nonsense-mediated decay pathway.A truncated Kv1.1 protein in the brain of the megencephaly mouse: expression and interaction.Organizing principles of mammalian nonsense-mediated mRNA decayMutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humansGenetic variants in ALDH1B1 and alcohol dependence risk in a British and Irish population: A bioinformatic and genetic study.Out-of-frame T cell receptor beta transcripts are eliminated by multiple pathways in vivoThe uORF-containing thrombopoietin mRNA escapes nonsense-mediated decay (NMD).Transcripts expressed using a bicistronic vector pIREShyg2 are sensitized to nonsense-mediated mRNA decay.Multifaceted Regulation of Gene Expression by the Apoptosis- and Splicing-Associated Protein Complex and Its Components.Preventing dangerous nonsense: selection for robustness to transcriptional error in human genes.Towards characterization of palmoplantar keratoderma caused by gain-of-function mutation in loricrin: analysis of a family and review of the literature.Nonsense-mediated decay in genetic disease: friend or foe?Directional next-generation RNA sequencing and examination of premature termination codon mutations in endoglin/hereditary haemorrhagic telangiectasiaA whole-genome analysis of premature termination codons.The mammalian nonsense-mediated mRNA decay pathway: to decay or not to decay! Which players make the decision?NMD: RNA biology meets human genetic medicine.The structure and function of the rous sarcoma virus RNA stability element.Mechanism, factors, and physiological role of nonsense-mediated mRNA decay.Characterization of the melanocortin-4-receptor nonsense mutation W16X in vitro and in vivo.Nonsense-mediated mRNA decay (NMD) mechanisms.A single-nucleotide deletion leads to rapid degradation of TAP-1 mRNA in a melanoma cell line.Internal ribosome entry sequence-mediated translation initiation triggers nonsense-mediated decay.An intron is required for dihydrofolate reductase protein stability.
P2860
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P2860
The human intronless melanocortin 4-receptor gene is NMD insensitive
description
2002 nî lūn-bûn
@nan
2002 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
The human intronless melanocortin 4-receptor gene is NMD insensitive
@ast
The human intronless melanocortin 4-receptor gene is NMD insensitive
@en
The human intronless melanocortin 4-receptor gene is NMD insensitive
@nl
type
label
The human intronless melanocortin 4-receptor gene is NMD insensitive
@ast
The human intronless melanocortin 4-receptor gene is NMD insensitive
@en
The human intronless melanocortin 4-receptor gene is NMD insensitive
@nl
prefLabel
The human intronless melanocortin 4-receptor gene is NMD insensitive
@ast
The human intronless melanocortin 4-receptor gene is NMD insensitive
@en
The human intronless melanocortin 4-receptor gene is NMD insensitive
@nl
P2093
P356
P1476
The human intronless melanocortin 4-receptor gene is NMD insensitive
@en
P2093
Andreas E Kulozik
Gabriele Neu-Yilik
Katja S Brocke
P356
10.1093/HMG/11.3.331
P407
P577
2002-02-01T00:00:00Z