Analysis of a Charcot-Marie-Tooth disease mutation reveals an essential internal ribosome entry site element in the connexin-32 gene.
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Translational control mechanisms in metabolic regulation: critical role of RNA binding proteins, microRNAs, and cytoplasmic RNA granulesSearching for IRESFunctional expression of human α9* nicotinic acetylcholine receptors in X. laevis oocytes is dependent on the α9 subunit 5' UTR.Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila.IRES-mediated translation of the carboxy-terminal domain of the horizontal cell specific connexin Cx55.5 in vivo and in vitro.Characterization of the internal IRES element of the zebrafish connexin55.5 reveals functional implication of the polypyrimidine tract binding protein.Irresistible IRES. Attracting the translation machinery to internal ribosome entry sitesInternal ribosomal entry site (IRES) activity generates endogenous carboxyl-terminal domains of Cx43 and is responsive to hypoxic conditions.New ways of initiating translation in eukaryotes?Role of 5'- and 3'-untranslated regions of mRNAs in human diseases.Melanocortin 3 receptor has a 5' exon that directs translation of apically localized protein from the second in-frame ATG.Post-transcriptional regulation of connexins.Translational control in endothelial cells.Complete eradication of xenograft hepatoma by oncolytic adenovirus ZD55 harboring TRAIL-IETD-Smac gene with broad antitumor effectMolecular genetics of X-linked Charcot-Marie-Tooth disease.Acute downregulation of Cx43 alters P2Y receptor expression levels in mouse spinal cord astrocytes.Redefining the structure of the mouse connexin43 gene: selective promoter usage and alternative splicing mechanisms yield transcripts with different translational efficiencies.Mutations in noncoding regions of GJB1 are a major cause of X-linked CMT.Secondary RNA structure and nucleotide specificity contribute to internal initiation mediated by the human tau 5' leader.Different mechanisms preserve translation of programmed cell death 8 and JunB in virus-infected endothelial cells.Translational control of Scamper expression via a cell-specific internal ribosome entry site.Translational control of SEPT9 isoforms is perturbed in disease.Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A Neuropathy.Restoration of functional gap junctions through internal ribosome entry site-dependent synthesis of endogenous connexins in density-inhibited cancer cellsA single internal ribosome entry site containing a G quartet RNA structure drives fibroblast growth factor 2 gene expression at four alternative translation initiation codons.A novel mutation in the nerve-specific 5'UTR of the GJB1 gene causes X-linked Charcot-Marie-Tooth disease.Genetic variants in mRNA untranslated regions.Connexins: Synthesis, Post-Translational Modifications, and Trafficking in Health and Disease.Altered expression of melanocortin-1 receptor (MC1R) in a yellow-coloured wild raccoon dog (Nyctereutes procyonoides).
P2860
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P2860
Analysis of a Charcot-Marie-Tooth disease mutation reveals an essential internal ribosome entry site element in the connexin-32 gene.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Analysis of a Charcot-Marie-To ...... ement in the connexin-32 gene.
@en
Analysis of a Charcot-Marie-To ...... ement in the connexin-32 gene.
@nl
type
label
Analysis of a Charcot-Marie-To ...... ement in the connexin-32 gene.
@en
Analysis of a Charcot-Marie-To ...... ement in the connexin-32 gene.
@nl
prefLabel
Analysis of a Charcot-Marie-To ...... ement in the connexin-32 gene.
@en
Analysis of a Charcot-Marie-To ...... ement in the connexin-32 gene.
@nl
P2860
P356
P1476
Analysis of a Charcot-Marie-To ...... ement in the connexin-32 gene.
@en
P2093
P2860
P304
34586-34591
P356
10.1074/JBC.M005199200
P407
P577
2000-11-01T00:00:00Z