scholarly article | Q13442814 |
P50 | author | John F Atkins | Q38589745 |
Zoya Ignatova | Q88401015 | ||
P2093 | author name string | Frauke Adamla | |
Rico Schieweck | |||
Paul Saffert | |||
P2860 | cites work | Polyalanine and polyserine frameshift products in Huntington's disease | Q24656119 |
Ribosomal frameshifting in decoding antizyme mRNAs from yeast and protists to humans: close to 300 cases reveal remarkable diversity despite underlying conservation | Q24682819 | ||
RAN translation and frameshifting as translational challenges at simple repeats of human neurodegenerative disorders | Q26823908 | ||
Mechanisms and implications of programmed translational frameshifting | Q26852197 | ||
Autoregulatory frameshifting in decoding mammalian ornithine decarboxylase antizyme | Q28117992 | ||
Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation | Q28246858 | ||
Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed -1 ribosomal frameshifting | Q28258312 | ||
Trinucleotide Repeat Disorders | Q29038716 | ||
Expression levels influence ribosomal frameshifting at the tandem rare arginine codons AGG_AGG and AGA_AGA in Escherichia coli | Q33855616 | ||
Amino acid runs in eukaryotic proteomes and disease associations | Q33897618 | ||
Hungry codons promote frameshifting in human mitochondrial ribosomes | Q34092844 | ||
Human DNA tumor viruses generate alternative reading frame proteins through repeat sequence recoding | Q34383861 | ||
Why base tautomerization does not cause errors in mRNA decoding on the ribosome | Q34489615 | ||
Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders | Q34543709 | ||
Ribosomal frameshifting on MJD-1 transcripts with long CAG tracts | Q34559976 | ||
Low-level expression and reversion both contribute to reactivation of herpes simplex virus drug-resistant mutants with mutations on homopolymeric sequences in thymidine kinase | Q34716802 | ||
Ribosome excursions during mRNA translocation mediate broad branching of frameshift pathways | Q35132310 | ||
Polyglutamine expansion alters the dynamics and molecular architecture of aggregates in dentatorubropallidoluysian atrophy | Q35694039 | ||
An mRNA sequence derived from the yeast EST3 gene stimulates programmed +1 translational frameshifting. | Q35697496 | ||
Dynamic pathways of -1 translational frameshifting | Q35756018 | ||
Autophagy-mediated clearance of huntingtin aggregates triggered by the insulin-signaling pathway | Q36117201 | ||
Programmed translational -1 frameshifting on hexanucleotide motifs and the wobble properties of tRNAs | Q36245899 | ||
Ribosomal frameshifting used in influenza A virus expression occurs within the sequence UCC_UUU_CGU and is in the +1 direction | Q36401203 | ||
An overlapping protein-coding region in influenza A virus segment 3 modulates the host response | Q36554219 | ||
A new kinetic model reveals the synergistic effect of E-, P- and A-sites on +1 ribosomal frameshifting | Q36649698 | ||
RNA pseudoknots and the regulation of protein synthesis | Q37217777 | ||
Protein mistranslation: friend or foe? | Q38229416 | ||
Global and local depletion of ternary complex limits translational elongation | Q41902966 | ||
Programmed -1 frameshifting by kinetic partitioning during impeded translocation | Q42209633 | ||
Degeneracy of the genetic code and stability of the base pair at the second position of the anticodon | Q43058973 | ||
Eukaryotic proteasomes cannot digest polyglutamine sequences and release them during degradation of polyglutamine-containing proteins | Q44833524 | ||
A molecular pathogenesis for transcription factor associated poly-alanine tract expansions | Q45034215 | ||
Depletion of cognate charged transfer RNA causes translational frameshifting within the expanded CAG stretch in huntingtin | Q45291544 | ||
Molecular architecture of CAG repeats in human disease related transcripts | Q45293998 | ||
Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo | Q45294913 | ||
Nuclear targeting of mutant Huntingtin increases toxicity | Q45298981 | ||
Intracellular localization of homopolymeric amino acid-containing proteins expressed in mammalian cells | Q48016847 | ||
A novel programed frameshift expresses the POL3 gene of retrotransposon Ty3 of yeast: frameshifting without tRNA slippage | Q48110364 | ||
Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions. | Q48373564 | ||
A mechanical explanation of RNA pseudoknot function in programmed ribosomal frameshifting | Q48547537 | ||
Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron models. | Q52734262 | ||
Cell Biology. Clogging information flow in ALS. | Q52778504 | ||
Secondary structures and starvation-induced frameshifting | Q74032555 | ||
CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation | Q74171904 | ||
Factors that influence selection of coding resumption sites in translational bypassing: minimal conventional peptidyl-tRNA:mRNA pairing can suffice | Q75224653 | ||
P433 | issue | 35 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 18505-18513 | |
P577 | publication date | 2016-07-05 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | An Expanded CAG Repeat in Huntingtin Causes +1 Frameshifting | |
P478 | volume | 291 |
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