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1 educed mitochondrial DNA content and reduced mitochondrial mRNA.
2 rry out guide-RNA-dependent U-insertion into mitochondrial mRNA.
3 ct the insertion and deletion of uridines in mitochondrial mRNAs.
4 s required throughout the life cycle of most mitochondrial mRNAs.
5 ression relies on mitoribosomes to translate mitochondrial mRNAs.
6 r element by Rmd9 confers stability to yeast mitochondrial mRNAs.
7 generate open reading frames in trypanosomal mitochondrial mRNAs.
8 required for U-insertion/deletion editing of mitochondrial mRNAs.
9 he leaderless or nearly leaderless nature of mitochondrial mRNAs.
10 ng and thereby generate mature forms of some mitochondrial mRNAs.
11  for correcting the coding sequences of many mitochondrial mRNAs.
12 affinity to 5'-untranslated regions of yeast mitochondrial mRNAs.
13 ation phenomenon required for translation of mitochondrial mRNAs.
14 ement to facilitate degradation of T. brucei mitochondrial mRNAs.
15  specific for the 5'-untranslated regions of mitochondrial mRNAs.
16 equences in 5'-untranslated regions of yeast mitochondrial mRNAs.
17 is required for 5' end processing of several mitochondrial mRNAs.
18 eletion of uridines at specific sites within mitochondrial mRNAs.
19 eotide sequence present in all S. cerevisiae mitochondrial mRNA 5'-UTLs that is a potential rRNA bind
20 mLRPPRC1 and causes non-uniform increases of mitochondrial mRNAs, accumulation of some unprocessed mi
21                         The interaction with mitochondrial mRNAs also produces a dramatic inhibition
22 asts showed decreased steady-state levels of mitochondrial mRNAs, although the length of poly(A) tail
23  significantly higher levels of steady-state mitochondrial mRNA and butyrate-induced p21(WAF1/Cip1) a
24                                              Mitochondrial mRNA and rRNA levels are reduced in rpm2-1
25                                Expression of mitochondrial mRNA and transcription of mitochondrial RN
26                            The expression of mitochondrial mRNA and tRNA was dependent upon LRPPRC le
27 rotein that associates with both nuclear and mitochondrial mRNAs and as such is a potential candidate
28 oteins, and (b) selected transcriptional and mitochondrial mRNAs and proteins in human muscle.
29                  The mitoribosome translates mitochondrial mRNAs and regulates energy conversion that
30 -dependent degradation pathway for T. brucei mitochondrial mRNAs and reveal an unprecedented role for
31 ciable effects on the steady-state levels of mitochondrial mRNAs and rRNAs.
32  transport profiles of mitochondrial and non-mitochondrial mRNA, and differences in transport paramet
33 es short and long A-tails typically found in mitochondrial mRNAs, and decreases the abundance of neve
34 ifically to 5'-untranslated regions of yeast mitochondrial mRNAs, and transcripts containing these re
35 rance, perhaps involved in recruiting unique mitochondrial mRNAs; and it has a polypeptide exit tunne
36                                      Several mitochondrial mRNAs are affected by interferon treatment
37                                    Mammalian mitochondrial mRNAs are basically leaderless, having few
38 l process in kinetoplastid parasites whereby mitochondrial mRNAs are modified through the specific in
39 A-containing cargoes, including granules and mitochondrial mRNA, are transported within neuronal proj
40 RBP SYNJ2BP retains specific nuclear-encoded mitochondrial mRNAs at the OMM during translation stress
41 LRPPRC in post-transcriptional regulation of mitochondrial mRNAs between tissues.
42 specifically removes poly(A) extensions from mitochondrial mRNAs both in vitro and in mitochondria of
43 is and proteomics, that byps are retained in mitochondrial mRNAs but not translated.
44 osoma brucei inserts and deletes uridines in mitochondrial mRNAs by a series of enzymatic steps that
45 diting in Trypanosomatids creates functional mitochondrial mRNAs by extensive uridylate (U) insertion
46      RNA editing produces mature trypanosome mitochondrial mRNAs by uridylate (U) insertion and delet
47 ce for binding of 5'-untranslated regions of mitochondrial mRNAs by yeast mitochondrial NADP+-specifi
48 hetic neurons to include the nuclear-encoded mitochondrial mRNA coding for COXIV.
49 lleviation of catalytic inhibition of IDH by mitochondrial mRNA correlates with the property of allos
50 uding binding and regulating nuclear-encoded mitochondrial mRNAs, coupled with a role in mitigating p
51 ia, or that a mechanistically unique type of mitochondrial mRNA editing has evolved within the dinofl
52                                              Mitochondrial mRNA editing in trypanosomatid parasites i
53                                     Although mitochondrial mRNA editing is widespread in some eukaryo
54                             In kinetoplastid mitochondrial mRNA editing, post-transcriptional inserti
55 hic Parkinson's disease (IPD), expression of mitochondrial mRNA encoding the ND1 subunit of mitochond
56 despite the previously observed increases in mitochondrial mRNAs encoding electron transport chain (E
57   Brar et al. reveal a novel mechanism where mitochondrial mRNAs escape global translational repressi
58            Although no consistent effects on mitochondrial mRNA expression were observed, complementa
59  and that NF-kappa B can negatively regulate mitochondrial mRNA expression.
60                                The levels of mitochondrial mRNAs for subunits I and II of cytochrome
61 hen subjected to poly(A) tail-length assays, mitochondrial mRNAs from affected individuals were shown
62         The m.14484T > C mutation may affect mitochondrial mRNA homeostasis, supported by reduced lev
63 RSF2P95H/+ mutation disrupts the splicing of mitochondrial mRNAs, impairs mitochondrial complex I fun
64 rized the transport of mitochondrial and non-mitochondrial mRNA in differentiated axons and dendrites
65 ate uridine (U) addition/deletion editing of mitochondrial mRNAs in kinetoplastid protozoa.
66 nscriptional process that creates functional mitochondrial mRNAs in Kinetoplastids.
67                               Translation of mitochondrial mRNAs in Saccharomyces cerevisiae depends
68 dence of extensive substitutional editing of mitochondrial mRNAs in the dinoflagellate species Pfiest
69                                          The mitochondrial mRNAs in the yeast Saccharomyces cerevisia
70 nd deletion RNA editing generates functional mitochondrial mRNAs in Trypanosoma brucei Editing is cat
71                                              Mitochondrial mRNAs in Trypanosoma brucei undergo extens
72 nd deletion RNA editing generates functional mitochondrial mRNAs in Trypanosoma brucei.
73  the U insertion and deletion RNA editing of mitochondrial mRNAs in trypanosomes.
74 actions between 3' processing and editing of mitochondrial mRNAs in trypanosomes.
75 DNA shuffling, we have mapped the termini of mitochondrial mRNAs in wheat, a monocot, and compared th
76 translational termination of nuclear-encoded mitochondrial mRNAs, including complex-I 30kD subunit (C
77 protein complex called the editosome cleaves mitochondrial mRNA, inserts or deletes uridine nucleotid
78 ethyltransferase, demonstrates that m(1)A in mitochondrial mRNA interferes with translation.
79             Maturation of Trypanosoma brucei mitochondrial mRNA involves massive posttranscriptional
80                                          The mitochondrial mRNA is modified by oligo- or polyadenylat
81        Uridine insertion/deletion editing of mitochondrial mRNAs is a characteristic feature of kinet
82 xamining the developmental timing of altered mitochondrial mRNA levels, we also reveal transcript-spe
83 n vivo selection that links cell survival to mitochondrial mRNA localization.
84 l disorders, our findings reveal a defect of mitochondrial mRNA maturation associated with human dise
85  uridylate insertion or deletion cycles is a mitochondrial mRNA maturation process catalyzed by multi
86  levels and half-lives of a subset of mature mitochondrial mRNAs: ND2, ND3, CYTB, COX2, and ATP8/6.
87                     Northern analyses of six mitochondrial mRNAs (normalized to mtDNA) reveal that tr
88                                          The mitochondrial mRNA of the parasitic protozoa Trypanosoma
89                                      Several mitochondrial mRNAs of the kinetoplastid protozoa do not
90               The coding sequence of several mitochondrial mRNAs of the kinetoplastid protozoa is cre
91               The coding sequence of several mitochondrial mRNAs of the kinetoplastid protozoa is cre
92 in vitro but did not affect the stability of mitochondrial mRNAs or alter the expression of nuclear g
93 ase did not affect the number or sequence of mitochondrial mRNA poly(A) tails, where unexpectedly we
94 c variations in the LRPPRC gene, involved in mitochondrial mRNA polyadenylation and translation.
95 to stabilize mitochondrial mRNAs, to promote mitochondrial mRNA polyadenylation, and to coordinate mi
96                  Furthermore, within the non-mitochondrial mRNA pool, we observed two distinct popula
97 essing and degradation, miRNA biogenesis and mitochondrial mRNA processing, systematically decoding t
98     Dramatically elevated levels of the COX2 mitochondrial mRNA-specific translational activator prot
99 arization, an apparently critical element of mitochondrial mRNA stability and quality control.
100    These findings demonstrate the control of mitochondrial mRNA synthesis by a protein that has an es
101         Patient fibroblasts have a defect in mitochondrial mRNA synthesis, but no mtDNA deletions or
102 ocesses such as kinetoplast DNA replication, mitochondrial mRNA synthesis, glycosyl phosphatidylinosi
103 d and has features that allow it to regulate mitochondrial mRNA synthesis.
104 e second pathway results in slow turnover of mitochondrial mRNA (t(1/2) of approximately 3 h) and is
105 increased the levels of mutant COX3 and COX2 mitochondrial mRNAs that were destabilized by mutations
106 brucei editosome catalyzes the maturation of mitochondrial mRNAs through the insertion and deletion o
107 f(5)C) (refs.(2-4))-drive the translation of mitochondrial mRNA to power metastasis.
108 ivators, suggesting an organized delivery of mitochondrial mRNAs to the translation system.
109 echanistically, CBFB enhanced the binding of mitochondrial mRNAs to TUFM, a mitochondrial translation
110  the post-transcriptional level to stabilize mitochondrial mRNAs, to promote mitochondrial mRNA polya
111 iting is a process that creates translatable mitochondrial mRNA transcripts from cryptogene encoded R
112 ments indicate a role for MRB1590 in editing mitochondrial mRNA transcripts, in particular the transc
113 logically targeted through the inhibition of mitochondrial mRNA translation in vivo.
114 e caused primarily by inhibition of the COX1 mitochondrial mRNA translation, a finding confirmed by l
115                  In Trypanosoma brucei, most mitochondrial mRNAs undergo editing, and 3' adenylation
116                  In Trypanosoma brucei, most mitochondrial mRNAs undergo internal changes by RNA edit
117 dine insertion/deletion (U-indel) editing of mitochondrial mRNA, unique to the protistan class Kineto
118                                        Human mitochondrial mRNAs utilize the universal AUG and the un
119  suppress cbp1 ts alleles and stabilize many mitochondrial mRNAs, was also isolated.
120   By contrast, depletion of Not1 solubilizes mitochondrial mRNAs, which are rendered insoluble upon N
121 l ribosomes to facilitate the translation of mitochondrial mRNAs, which lack typical anti-Shine-Dalga

 
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