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1 n RPL23 and regulating its assembly into the 60S ribosomal subunit.
2 ict the antiassociation factor eIF6 from the 60S ribosomal subunit.
3 e cytoplasm until its incorporation into the 60S ribosomal subunit.
4 leus, and promotes hYVH1 partitioning to the 60S ribosomal subunit.
5 nt ITS2 rRNA processing and synthesis of the 60S ribosomal subunit.
6 RNA makes up the major mass and shape of the 60S ribosomal subunit.
7 for cell proliferation and biogenesis of the 60S ribosomal subunit.
8 A maturation or with decreased levels of the 60S ribosomal subunit.
9 the biogenesis and the nuclear export of the 60S ribosomal subunit.
10 ulatory region located on the surface of the 60S ribosomal subunit.
11 13a was phosphorylated and released from the 60S ribosomal subunit.
12 g site connected to the GTPase center in the 60S ribosomal subunit.
13  and 5.8S rRNAs and in the biogenesis of the 60S ribosomal subunit.
14 ghly conserved role in the maturation of the 60S ribosomal subunit.
15 se domain were primarily associated with the 60S ribosomal subunit.
16 o ensure proper construction of the NPET and 60S ribosomal subunits.
17 NAs, leading to the formation of the 40S and 60S ribosomal subunits.
18 n Rkm1 and prevented from loading to the pre-60S ribosomal subunits.
19 cific factors required for the maturation of 60S ribosomal subunits.
20 unnel (NPET) is a major functional center of 60S ribosomal subunits.
21 ed structure that binds to 80S ribosomes and 60S ribosomal subunits.
22 tructure of the RQC complex bound to stalled 60S ribosomal subunits.
23 ether with Ltn1 and the AAA-ATPase Cdc48, to 60S ribosomal subunits.
24 ing and maturation steps for construction of 60S ribosomal subunits.
25 ernal T-shaped structure (TSS) that binds to 60S ribosomal subunits.
26  critical for late cytoplasmic maturation of 60S ribosomal subunits.
27 M directs the nuclear export of both 40S and 60S ribosomal subunits.
28  a late, cytosolic step of the biogenesis of 60S ribosomal subunits.
29 the Obg family involved in the biogenesis of 60S ribosomal subunits.
30  and Bop1 is necessary for the biogenesis of 60S ribosomal subunits.
31 e it physically interacts with Rat1p and pre-60S ribosomal subunits.
32 at eIF6 is not required for the stability of 60S ribosomal subunits.
33 ormation and deficiency of newly synthesized 60S ribosomal subunits.
34 se cells leads to a deficit in the cytosolic 60S ribosomal subunits.
35  it is an essential gene required for stable 60S ribosomal subunits.
36 volved in the biogenesis and/or stability of 60S ribosomal subunits.
37  for a late step in biogenesis of the large (60S) ribosomal subunit.
38 NF90 as components of precursors to 60S (pre-60S) ribosomal subunits.
39 ation (UFMylation) facilitates the rescue of 60S ribosomal subunits (60S) that are released after rib
40  fivefold and reduces steady-state levels of 60S ribosomal subunits, 80S ribosomes, and polysomes.
41 of the anti-association factor eIF6 from the 60S ribosomal subunit, a key step in the translational a
42  mutant 25S ribosomal RNAS (rRNAs) in mature 60S ribosomal subunits, a process that requires ubiquiti
43 els but does result in a decrease in 40S and 60S ribosomal subunit abundance.
44 d Lsg1p, that are found associated with free 60S ribosomal subunits affinity purified with the nuclea
45 itiation complex, followed by joining of the 60S ribosomal subunit and formation of the 80S complex.
46 ric protein of about 26 kDa, can bind to the 60S ribosomal subunit and prevent its association with t
47 tion initiation factor 6 (eIF6) binds to the 60S ribosomal subunit and prevents its association with
48 t a 2.5-A structure of the Trypanosoma cruzi 60S ribosomal subunit and propose a model for the stepwi
49 epletion of Dbp3p results in a deficiency of 60S ribosomal subunits and a delayed synthesis of the ma
50 r 6 (eIF6) is essential for the synthesis of 60S ribosomal subunits and for regulating the associatio
51 that specifically and stably associates with 60S ribosomal subunits and nucleoli and is incorporated
52 a significant role in the binding of Ltn1 to 60S ribosomal subunits and that NTD mutations causing de
53  regions of FMR1 that mediate its binding to 60S ribosomal subunits and the interactions among the FM
54 size the 25S and 5.8S rRNA components of the 60S ribosomal subunit, and exonucleolytic 5' processing
55 les colocalized with poly(A+) mRNA, with the 60S ribosomal subunit, and with elongation factor 1alpha
56   We directly tracked the CrPV IRES, 40S and 60S ribosomal subunits, and tRNA using single-molecule f
57 ex process in which initiator tRNA, 40S, and 60S ribosomal subunits are assembled by eukaryotic initi
58                       In eukaryotes, 40S and 60S ribosomal subunits are assembled in the nucleus and
59                       In eukaryotes, 40S and 60S ribosomal subunits are assembled in the nucleus from
60 strate that structural domains of eukaryotic 60S ribosomal subunits are formed in a hierarchical fash
61  colocalization of NPM with maturing nuclear 60S ribosomal subunits, as well as newly exported and as
62             In Saccharomyces cerevisiae, the 60S ribosomal subunit assembles in the nucleolus and the
63 leles of rRNA-processing factors that affect 60S ribosomal subunit assembly accumulated Rpl11b-GFP in
64 ile the protein composition of various yeast 60S ribosomal subunit assembly intermediates has been st
65 iogenesis, we examined in detail one step in 60S ribosomal subunit assembly-processing of 27SA(3) pre
66 bm3 might enhance the association of 40S and 60S ribosomal subunits at 32 degrees C.
67  of the ubiquitin-like (Ubl) protein UFM1 to 60S ribosomal subunits at the RTJ.
68                          L22, a component of 60S ribosomal subunits, binds three sites on EBER-1, and
69  predominantly nucleolar and is required for 60S ribosomal subunit biogenesis and possibly for transl
70 UCE) localizes to the nucleolus and promotes 60S ribosomal subunit biogenesis.
71 ak5, Mtr4, Drs1, Spb4, and Dbp9) involved in 60S ribosomal subunit biogenesis.
72  ski6-2 mutant has normal amounts of 40S and 60S ribosomal subunits but accumulates a 38S particle co
73 NX increased the content of not only 40S and 60S ribosomal subunits but also 80S monosomes and polyso
74 xpressed in yeast cells associates with free 60S ribosomal subunits but not with 80S monosomes or pol
75 dimented through sucrose gradients with free 60S ribosomal subunits but not with 80S monosomes or pol
76 uring events during the biogenesis of large (60S) ribosomal subunits, but their precise molecular fun
77 ted in a selective reduction in the level of 60S ribosomal subunits, causing a stoichiometric imbalan
78 led that the RQC forms a stable complex with 60S ribosomal subunits containing stalled polypeptides a
79                 Nuclear export of the large (60S) ribosomal subunit depends on the adapter protein Nm
80 n of any steps prior to the rejoining of the 60S ribosomal subunit during the entire translation init
81           A selective autophagic pathway for 60S ribosomal subunits elicited by nitrogen starvation i
82         The FXR proteins are associated with 60S ribosomal subunits even in cells that lack FMR1 and
83 23p-mediated nuclear import of the essential 60S ribosomal subunit export factor, Nmd3p, and a DeltaR
84 releases ubiquitinated nascent proteins from 60S ribosomal subunits for proteasomal degradation.
85 protein Nmd3 is an adaptor for export of the 60S ribosomal subunit from the nucleus.
86          Here, by isolating late cytoplasmic 60S ribosomal subunits from Sbds-deleted mice, we show t
87      We found that L13a is released from the 60S ribosomal subunit in response to infection by respir
88  developed to follow the localization of the 60S ribosomal subunit in S. cerevisiae.
89  that a fraction of Rbm3 was associated with 60S ribosomal subunits in an RNA-independent manner.
90 g of pre-rRNA, and maturation of cytoplasmic 60S ribosomal subunits in KRAS mutant lung cancer cells.
91                             The synthesis of 60S ribosomal subunits in Saccharomyces cerevisiae requi
92  revealed a modest increase in the amount of 60S ribosomal subunits in the ydj1-151 strain, consisten
93 ich may account for the selective deficit of 60S ribosomal subunits in these cells.
94                 The biogenesis of the large (60S) ribosomal subunit in eukaryotes involves nucleolar,
95         The FMR1/FXR proteins also contain a 60S ribosomal subunit interaction domain and a protein-p
96 -Diamond syndrome - license entry of nascent 60S ribosomal subunits into active translation by evicti
97  The area surrounding the tunnel exit of the 60S ribosomal subunit is a hub for proteins involved in
98          A factor crucial for modulating the 60S ribosomal subunit is eukaryotic translation initiati
99                                          The 60S ribosomal subunit is one of the bulkiest transport c
100 essing of the ribosomal RNA component of the 60S ribosomal subunit is severely reduced, leading to an
101 ), or a defect in eIF5, proteins involved in 60S ribosomal subunit joining, specifically reduces the
102  that the interaction of the intron with the 60S ribosomal subunit leads to irreversible changes in t
103    Here we show that a specific reduction of 60S ribosomal subunit levels slows aging in yeast.
104                              GNL2 influences 60S ribosomal subunit maturation and global protein synt
105           Thus, our data link defective late 60S ribosomal subunit maturation to an inherited bone ma
106  and controls its assembly necessary for pre-60S ribosomal subunit maturation.
107 hat negatively regulates assembly of the pre-60S ribosomal subunit (MINAS-60).
108  Formation of the earliest precursors of the 60S ribosomal subunit (pre-60S r-particle) is among the
109 f aberrant nascent-chains obstructing large (60S) ribosomal subunits-products of ribosome stalling du
110 ccharomyces cerevisiae gene, which encodes a 60S ribosomal subunit protein required for joining of 40
111  with the ubiquitin-like protein UFM1 on the 60S ribosomal subunit protein RPL26 (also known as uL24)
112  that the addition of an NES directly to the 60S ribosomal subunit protein Rpl3 promotes export.
113 1 is a highly conserved gene which encodes a 60S ribosomal subunit protein that is required for joini
114 ccharomyces cerevisiae gene, which encodes a 60S ribosomal subunit protein.
115 tes, which were accompanied by decreased 40S/60S ribosomal subunit ratios.
116 bited the nuclear export of both the 40S and 60S ribosomal subunits, reduced the available pool of cy
117                         Mutants deficient in 60S ribosomal subunits replicate L-A poorly, but not if
118  In eukaryotes, nuclear export of the large (60S) ribosomal subunit requires the adapter protein Nmd3
119 lation and inhibit the nuclear export of the 60S ribosomal subunit, respectively.
120 lacking PRMT3 showed an accumulation of free 60S ribosomal subunits resulting in an imbalance in the
121 of half-mer polyribosomes, reduced levels of 60S ribosomal subunits resulting in the stoichiometric i
122 tional surveillance, acts as an inhibitor of 60S ribosomal subunit ribophagy and is antagonized by Ub
123 ntify a novel mammalian complex required for 60S ribosomal subunit synthesis, providing further insig
124 omal protein L13a and translocation from the 60S ribosomal subunit to the interferon-gamma-activated
125 protein prevents association between 40S and 60S ribosomal subunits to form 80S ribosomes.
126                                Ltn1 binds to 60S ribosomal subunits to ubiquitylate nascent polypepti
127 tein composition and structure of assembling 60S ribosomal subunits undergo numerous changes as pre-r
128 MINAS-60 increases the amount of cytoplasmic 60S ribosomal subunit, upregulating global protein synth
129  transported to the cytoplasm as part of the 60S ribosomal subunit, using a CRM1-dependent pathway.
130  endoplasmic reticulum (ER) translocon-bound 60S ribosomal subunits via the ribosome-associated quali
131 nucleolar localization, and association with 60S ribosomal subunits were found to map to the amino ac
132 L260c are defective in the maturation of the 60S ribosomal subunit, whereas maturation of the 40S sub
133 f ubiquitinated polypeptides associated with 60S ribosomal subunits, while Dom34-Hbs1 generate 60S-as
134 uires covalent modification of RPL26/uL24 on 60S ribosomal subunits with UFM1.

 
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