| scholarly article | Q13442814 |
| P50 | author | Zofia M Chrzanowska-Lightowlers | Q39034391 |
| P2093 | author name string | Robert N Lightowlers | |
| Richard J Temperley | |||
| Paul M Smith | |||
| Sara H Seneca | |||
| P2860 | cites work | Identification and cloning of human mitochondrial translational release factor 1 and the ribosome recycling factor | Q22008466 |
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| Sequence and organization of the human mitochondrial genome | Q27860659 | ||
| Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA | Q27860870 | ||
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| Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria | Q28201407 | ||
| Mitochondrial respiratory-chain diseases | Q29614474 | ||
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| Making sense of mimic in translation termination | Q33338049 | ||
| The RNase P associated with HeLa cell mitochondria contains an essential RNA component identical in sequence to that of the nuclear RNase P. | Q33966946 | ||
| An mRNA surveillance mechanism that eliminates transcripts lacking termination codons | Q34120142 | ||
| Quality control of mRNA function | Q34156109 | ||
| Epidemiology and treatment of mitochondrial disorders | Q34386766 | ||
| Blue Native electrophoresis to study mitochondrial and other protein complexes | Q34675865 | ||
| Mitochondrial encephalomyopathies | Q35085834 | ||
| Class-1 translation termination factors: invariant GGQ minidomain is essential for release activity and ribosome binding but not for stop codon recognition | Q39229931 | ||
| Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis | Q40723426 | ||
| In vivo labeling and analysis of human mitochondrial translation products | Q41244321 | ||
| A bacterial RNA that functions as both a tRNA and an mRNA. | Q41710118 | ||
| Mutations in the highly conserved GGQ motif of class 1 polypeptide release factors abolish ability of human eRF1 to trigger peptidyl-tRNA hydrolysis. | Q43206485 | ||
| Post-transcriptional addition of polyadenylic acid to mitochondrial RNA by a cordycepin-insensitive process | Q43643234 | ||
| Human polynucleotide phosphorylase, hPNPase, is localized in mitochondria. | Q54523690 | ||
| A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis | Q71345252 | ||
| Studies on mitochondrial oxidative phosphorylation in permeabilized human skin fibroblasts: application to mitochondrial encephalomyopathies | Q72799018 | ||
| Interaction of mitochondrial elongation factor Tu with aminoacyl-tRNA and elongation factor Ts | Q73763064 | ||
| The epidemiology of pathogenic mitochondrial DNA mutations | Q74159368 | ||
| Decreased ATP synthesis is phenotypically expressed during increased energy demand in fibroblasts containing mitochondrial tRNA mutations | Q77892921 | ||
| P433 | issue | Pt 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 725-731 | |
| P577 | publication date | 2004-02-01 | |
| P1433 | published in | Biochemical Journal | Q864221 |
| P1476 | title | Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codons | |
| P478 | volume | 377 |
| Q33506537 | A unique genetic code change in the mitochondrial genome of the parasitic nematode Radopholus similis |
| Q38920032 | Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation |
| Q33300478 | Broad genomic and transcriptional analysis reveals a highly derived genome in dinoflagellate mitochondria |
| Q33316556 | Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency. |
| Q42806022 | Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206. |
| Q44673190 | Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches |
| Q34772842 | HMRF1L is a human mitochondrial translation release factor involved in the decoding of the termination codons UAA and UAG. |
| Q57910058 | Human Mitochondrial mRNAs Are Stabilized with Polyadenylation Regulated by Mitochondria-specific Poly(A) Polymerase and Polynucleotide Phosphorylase |
| Q37693914 | Identification of a novel human nuclear-encoded mitochondrial poly(A) polymerase |
| Q35840151 | Mitochondrial poly(A) polymerase and polyadenylation |
| Q40226349 | Plant mitochondrial genes can be expressed from mRNAs lacking stop codons. |
| Q24303855 | Stable PNPase RNAi silencing: its effect on the processing and adenylation of human mitochondrial RNA |
| Q35781669 | Translation of nonSTOP mRNA is repressed post-initiation in mammalian cells |
| Q35170120 | Turnover of ATP synthase subunits in F1-depleted HeLa and yeast cells |
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