Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
about
Development of a single vector system that enhances trans-splicing of SMN2 transcriptsMolecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha (PPARalpha)-regulated peroxisomal acyl-CoA thioesterasesWhen proteome meets genome: the alpha helix and the beta strand of proteins are eschewed by mRNA splice junctions and may define the minimal indivisible modules of protein architecture.New high-technology products for the treatment of haemophilia.Exon exchange approach to repair Duchenne dystrophin transcriptsTrans-splicing into highly abundant albumin transcripts for production of therapeutic proteins in vivo.Trans-splicing-mediated improvement in a severe mouse model of spinal muscular atrophy.Selective modification of alternative splicing by indole derivatives that target serine-arginine-rich protein splicing factors.Correction of aberrant FGFR1 alternative RNA splicing through targeting of intronic regulatory elements.Complementary intron sequence motifs associated with human exon repetition: a role for intragenic, inter-transcript interactions in gene expression.Reprogramming of tau alternative splicing by spliceosome-mediated RNA trans-splicing: implications for tauopathies.Complex spliceosomal organization ancestral to extant eukaryotes.Molecular imaging of gene expression in living subjects by spliceosome-mediated RNA trans-splicingTargeted genetic repair: an emerging approach to genetic therapy.Ribozyme-mediated revision of RNA and DNAGene therapy progress and prospects: reprograming gene expression by trans-splicing.Splicing regulators: targets and drugsSplicing therapeutics in SMN2 and APOB.IL-33 isoforms: their future as vaccine adjuvants?Expression analysis and functional activity of interleukin-7 splice variants.De novo assembly and characterization of breast cancer transcriptomes identifies large numbers of novel fusion-gene transcripts of potential functional significanceCorrection of tau mis-splicing caused by FTDP-17 MAPT mutations by spliceosome-mediated RNA trans-splicing.Optimization of trans-Splicing for Huntington's Disease RNA Therapy.Design and characterization of a twin ribozyme for potential repair of a deletion mutation within the oncogenic CTNNB1-ΔS45 mRNA.Molecular barcoding of viral vectors enables mapping and optimization of mRNA trans-splicing.RNA Structure Design Improves Activity and Specificity of trans-Splicing-Triggered Cell Death in a Suicide Gene Therapy Approach.SHIP1 Deficiency in Inflammatory Bowel Disease Is Associated With Severe Crohn's Disease and Peripheral T Cell Reduction.
P2860
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P2860
Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
description
2003 nî lūn-bûn
@nan
2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
@ast
Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
@en
type
label
Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
@ast
Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
@en
prefLabel
Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
@ast
Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
@en
P2860
P356
P1476
Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing
@en
P2093
Mariano A Garcia-Blanco
P2860
P304
P356
10.1172/JCI200319462
P407
P577
2003-08-01T00:00:00Z