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1  mt:lrRNA, which encodes the 16S rRNA of the mitochondrial ribosome.
2 ptidyl transferase center (PTC) of the human mitochondrial ribosome.
3 s previously assigned to be a subunit of the mitochondrial ribosome.
4 of mt-rRNA variations on the function of the mitochondrial ribosome.
5 sis and function of the large subunit of the mitochondrial ribosome.
6 G in both the A- and P-sites of the metazoan mitochondrial ribosome.
7 nd the major binding partner of ATAD3 is the mitochondrial ribosome.
8 n the biogenesis of the large subunit of the mitochondrial ribosome.
9  the respiratory chain are translated by the mitochondrial ribosome.
10 ified as the major acetylated protein in the mitochondrial ribosome.
11 gated if the Oxa1 complex interacts with the mitochondrial ribosome.
12 tion on prokaryotic ribosomes and eukaryotic mitochondrial ribosomes.
13 c ribosomes (80S), as well as other kinds of mitochondrial ribosomes.
14 hile providing insight into the evolution of mitochondrial ribosomes.
15 bditis elegans, and Saccharomyces cerevisiae mitochondrial ribosomes.
16 bditis elegans, and Saccharomyces cerevisiae mitochondrial ribosomes.
17 ts (MRP-S22 through MRP-S36) are specific to mitochondrial ribosomes.
18 present in the 39 S subunits are specific to mitochondrial ribosomes.
19 lude that HLL and HLP encode L14 subunits of mitochondrial ribosomes.
20 re presented as a model system for mammalian mitochondrial ribosomes.
21 ion of mitochondrial encoded mRNAs occurs on mitochondrial ribosomes.
22 he small subunit of either E. coli or bovine mitochondrial ribosomes.
23 ure rRNA and a reduced ratio of cytosolic to mitochondrial ribosomes.
24 or expansion of protein content in mammalian mitochondrial ribosomes.
25 dysfunction in the protein components of the mitochondrial ribosomes.
26 ialized, with an extreme example being their mitochondrial ribosomes.
27 ranslated regions and promote translation on mitochondrial ribosomes.
28 mutations and possessing low affinity toward mitochondrial ribosomes.
29 because of a decrease in fully assembled 55S mitochondrial ribosomes.
30 n a significant inhibition of translation on mitochondrial ribosomes.
31     Very little is known about biogenesis of mitochondrial ribosomes.
32 ify a third gene essential for expression of mitochondrial ribosomes.
33  the Oxa1L-CTT derivatives bind to mammalian mitochondrial ribosomes.
34 in targets the peptidyltransferase center of mitochondrial ribosomes.
35  the protein-rich small subunit of mammalian mitochondrial ribosomes.
36 le of assembly proteins in the biogenesis of mitochondrial ribosomes.
37 k interactions with the large subunit of the mitochondrial ribosome (39S) (K(d) = 1.5 muM).
38                                The mammalian mitochondrial ribosomes (55S) differ unexpectedly from b
39 remodeling during the evolution of mammalian mitochondrial ribosomes (55S).
40                                The ancestral mitochondrial ribosome (70S) underwent major structural
41 hondrial DNA-encoded proteins synthesized by mitochondrial ribosomes also contain polyproline stretch
42 logy to proteins uL30m and mL63 in mammalian mitochondrial ribosomes also suggests a plausible evolut
43             We propose that mS38 confers the mitochondrial ribosome an intrinsic capacity of translat
44 nthesis by the reversible acetylation of the mitochondrial ribosome and characterize MRPL10 as a nove
45 ation, 17q gain, and increased expression of mitochondrial ribosome and electron transport-associated
46 hondrial rRNA levels, proper assembly of the mitochondrial ribosome and hence for mitochondrial trans
47 est regulatory mechanisms for assembling the mitochondrial ribosome and illustrate dynamic changes in
48 (mt) shifts the equilibrium between the 55 S mitochondrial ribosome and its subunits toward subunit d
49                                              Mitochondrial ribosome and mitochondria-associated genes
50 analyses define the interactome of the human mitochondrial ribosome and reveal novel assembly factors
51 -purified with the small, 28S subunit of the mitochondrial ribosome and the endogenous protein co-fra
52 rose gradients with the large subunit of the mitochondrial ribosome and the monosome.
53 s was 1.10 +/- 0.01 x 10(-7) cm(2) s(-1) for mitochondrial ribosomes and 1.72 +/- 0.03 x 10(-7) cm(2)
54   The three core subunits are synthesized on mitochondrial ribosomes and inserted into the inner memb
55 e C-terminal tail of Oxa1L (Oxa1L-CTT) binds mitochondrial ribosomes and is believed to coordinate th
56 l features that are characteristic solely of mitochondrial ribosomes and other features that are char
57 ked the putative zinc transporter SLC30A9 to mitochondrial ribosomes and OxPhos integrity and establi
58 mino acid tail of Oxa1L (Oxa1L-CTT) binds to mitochondrial ribosomes and plays a role in the co-trans
59  reviews the distinctive properties of human mitochondrial ribosomes and ribosomal proteins, and the
60                                              Mitochondrial ribosomes and translation factors co-purif
61 ransiently, via RNA, with editing complexes, mitochondrial ribosomes, and several ancillary factors t
62         Because the protein:RNA ratio in the mitochondrial ribosome (approximately 69:approximately 3
63 MPV17L2 proteins of the small subunit of the mitochondrial ribosome are trapped in the enlarged nucle
64                        The extra proteins in mitochondrial ribosomes are 'new' in the sense that they
65          The ribosomal RNA components of the mitochondrial ribosomes are coded for by mitochondrial D
66                                              Mitochondrial ribosomes are functionally specialized for
67                                        Human mitochondrial ribosomes are highly divergent from all ot
68                              Cytoplasmic and mitochondrial ribosomes are necessary for two compartmen
69                                       Bovine mitochondrial ribosomes are presented as a model system
70 s highlighting the cytosolic rather than the mitochondrial ribosome as the primary drug target.
71  provide a checkpoint for proper 28S and 55S mitochondrial ribosome assembly.
72 l protein synthesis associated with impaired mitochondrial ribosome assembly.
73 cytosolic ribosome and for the A1555G mutant mitochondrial ribosome associated with hypersusceptibili
74 n C7orf30 is, on the contrary, essential for mitochondrial ribosome biogenesis and mitochondrial tran
75 ate that this is one mechanism to coordinate mitochondrial ribosome biogenesis and transcription in h
76                                              Mitochondrial ribosome biogenesis is therefore critical
77 les in inflammation and infection processes, mitochondrial ribosome biogenesis, and regulation of apo
78 e ribosomal subunit in a process crucial for mitochondrial ribosome biogenesis.
79         We propose that Mtg2p is involved in mitochondrial ribosome biogenesis.
80  that POLRMT associates with h-mtTFB1 in 28S mitochondrial ribosome complexes that are stable in the
81  the intricate oxidative phosphorylation and mitochondrial ribosome complexes was evident.
82                                              Mitochondrial ribosomes comprise the most diverse group
83 ty and that the decreased specificity toward mitochondrial ribosome confers the lowered cytotoxicity.
84         This finding suggests that mammalian mitochondrial ribosomes contain several novel proteins.
85                                    Mammalian mitochondrial ribosomes contain two prokaryotic-like rRN
86 , MT-RNR2) mitochondrial RNA subunits of the mitochondrial ribosome encoded within mitochondrial DNA
87                                   Therefore, mitochondrial ribosomes engage with the OXA1L-insertase
88  stimulate mitochondrial Met-tRNA binding to mitochondrial ribosomes, exhibiting a 50-fold preference
89 specific antibodies are present in a petunia mitochondrial ribosome fraction.
90 ple of a ribosomal protein that is shared by mitochondrial ribosomes from lower and higher eukaryotes
91            Sucrose gradient sedimentation of mitochondrial ribosomes from temperature-sensitive mtg3
92             Our Drosophila studies show that mitochondrial ribosome function is necessary for synapse
93 auses maternally inherited deafness disrupts mitochondrial ribosome function, in part, via increased
94 iae GTPase Mtg2p (Yhr168wp) is essential for mitochondrial ribosome function.
95                                              Mitochondrial ribosomes had a particle composition of 75
96                                    The human mitochondrial ribosome has 29 distinct proteins in the s
97 of the large subunit (39 S) of the mammalian mitochondrial ribosome has been achieved by carrying out
98 of the small subunit (28 S) of the mammalian mitochondrial ribosome has been achieved by carrying out
99                                   The bovine mitochondrial ribosome has been developed as a model sys
100 in detail, their mechanism of action against mitochondrial ribosomes has yet to be explored.
101 s of association with mtDNA nucleoids and/or mitochondrial ribosomes in cell fractionation studies.
102  to an increase in translational activity of mitochondrial ribosomes in Sirt3(-/-) mice.
103                           IF-2mt can bind to mitochondrial ribosomes in the absence of GTP, initiator
104 s and mitigates toxicity linked to mammalian mitochondrial ribosome inhibition.
105                        Here we show that the mitochondrial ribosome is a neurodevelopmentally regulat
106 hout functional METTL15, the assembly of the mitochondrial ribosome is decreased, with the late assem
107 mammalian mitochondrial ribosomes, the human mitochondrial ribosome is one of the most protein-rich r
108                                          The mitochondrial ribosome is responsible for the biosynthes
109                  The binding of Oxa1L-CTT to mitochondrial ribosomes is an enthalpy-driven process wi
110 bosome profiling, we show that inhibition of mitochondrial ribosomes is similarly context-specific-CH
111                                    Mammalian mitochondrial ribosomes lack several of the major RNA st
112 protein that interacts specifically with the mitochondrial ribosome large subunit 16 S rRNA.
113 ses in the monosome and both subunits of the mitochondrial ribosome, leading to impaired protein synt
114                    The Leishmania tarentolae mitochondrial ribosome (Lmr) is a minimal ribosomal RNA
115                                    The human mitochondrial ribosome (mitoribosome) and associated pro
116                                The mammalian mitochondrial ribosome (mitoribosome) and its associated
117  present cryo-EM structures of the human 55S mitochondrial ribosome (mitoribosome) and the mitoriboso
118 c concept that postulates a key role for the mitochondrial ribosome (mitoribosome) in aminoglycoside
119 vity via metabolism-dependent changes in the mitochondrial ribosome (mitoribosome) in S. cerevisiae.
120                     The RNA component of the mitochondrial ribosome (mitoribosome) is reduced in size
121                                          The mitochondrial ribosome (mitoribosome) is responsible for
122                                          The mitochondrial ribosome (mitoribosome) synthesizes 13 pro
123  as the model organism and characterized its mitochondrial ribosome (mitoribosome) using cryo-EM.
124 proteins comprising the large subunit of the mitochondrial ribosome (mitoribosome).
125                                              Mitochondrial ribosomes (mitoribosomes) are essential, a
126                                    Mammalian mitochondrial ribosomes (mitoribosomes) are responsible
127                                The mammalian mitochondrial ribosomes (mitoribosomes) are responsible
128                                              Mitochondrial ribosomes (mitoribosomes) are tethered to
129                      Biogenesis of mammalian mitochondrial ribosomes (mitoribosomes) involves several
130                                              Mitochondrial ribosomes (mitoribosomes) perform protein
131                                              Mitochondrial ribosomes (mitoribosomes) play a central r
132                                              Mitochondrial ribosomes (mitoribosomes) synthesize prote
133 ypeptides synthesized within mitochondria on mitochondrial ribosomes (mitoribosomes) with over 70 pol
134 horylation (OXPHOS) system is carried out by mitochondrial ribosomes (mitoribosomes).
135 ied 13 proteins that cofractionated with the mitochondrial ribosome, most of which play a role in tra
136 e of the unusual proteins contained in human mitochondrial ribosomes, MRPS29.
137 al component of the 28S small subunit of the mitochondrial ribosome (mS25).
138 berrant assembly of the large subunit of the mitochondrial ribosome (mt-LSU).
139 lly associates with the large subunit of the mitochondrial ribosome (mt-LSU).
140 the additional and/or larger proteins of the mitochondrial ribosome must compensate for the shortened
141 ce that assembly of the small subunit of the mitochondrial ribosome occurs at the nucleoid.
142                                              Mitochondrial ribosomes of Trypanosoma brucei are compos
143 rthermore, unlike cytoplasmic ribosomes, the mitochondrial ribosome possesses intersubunit bridges co
144                                      Using a mitochondrial ribosome profiling and mitochondrial poly(
145                                              Mitochondrial ribosome profiling confirmed stalled trans
146                                              Mitochondrial ribosome profiling uncovered mitoribosome
147 predicted by variation in TFAM, histone, and mitochondrial ribosome protein abundance.
148  down electron transfer chain element cco-1, mitochondrial ribosome protein S5 mrps-5, and antibiotic
149       Interaction of oxazolidinones with the mitochondrial ribosomes provides a structural basis for
150 itochondrially-encoded RNA components of the mitochondrial ribosome require various post-transcriptio
151 sed and increased abundance of plastidic and mitochondrial ribosomes, respectively.
152 tudies with both Escherichia coli and bovine mitochondrial ribosomes revealed that the f(5)C(34) faci
153        Knockdown of specific subunits of the mitochondrial ribosome reverses PLK1-inhibitor induced a
154 ribosomes and a cryo-EM map of the mammalian mitochondrial ribosome show that (i) the overall structu
155 A methyltransferase required for small (28S) mitochondrial ribosome subunit assembly.
156 fications of the 16 S rRNA core of the large mitochondrial ribosome subunit.
157 ere we show that, following its synthesis on mitochondrial ribosomes, subunit 6 of the ATPase (Atp6p)
158                                              Mitochondrial ribosomes synthesize a subset of hydrophob
159 e identify diverse types of nonstop mRNAs on mitochondrial ribosomes that are resistant to translatio
160                         Typical of mammalian mitochondrial ribosomes, the human mitochondrial ribosom
161                              We propose that mitochondrial ribosomes themselves recognize a common fe
162 ped as a model system for the study of human mitochondrial ribosomes to address several questions rel
163 LRMT interacts directly with h-mtTFB1 in 28S mitochondrial ribosomes to augment its 12S rRNA methyltr
164 didates for mitochondrial disease, since the mitochondrial ribosome translates mRNAs for the 13 essen
165 MPV17L2 contributes to the biogenesis of the mitochondrial ribosome, uniting the two subunits to crea
166 A calculated hydration factor of 3.3 g/g for mitochondrial ribosomes was also obtained utilizing a ca
167  molecular weight and buoyant density of rat mitochondrial ribosomes were determined.
168 , the physiochemical properties of rat liver mitochondrial ribosomes were examined and compared with
169 e found in the mammalian and D. melanogaster mitochondrial ribosomes while C. elegans has two S18 hom
170  to the small (28S) subunit of the mammalian mitochondrial ribosome with K(d) values similar to that

 
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