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1 he 16 S rRNA core of the large mitochondrial ribosome subunit.
2 ouridine residues within helix 69 of the 50S ribosome subunit.
3 repressor Armitage--and proteins of the 60S ribosome subunit.
4 cessing, and assembly of the large and small ribosome subunits.
5 rate limiting for the efficient assembly of ribosome subunits.
6 , and assembled with ribosomal proteins into ribosome subunits.
7 ovided evidence for the presence of SecY and ribosome subunits.
8 ing that results in production of proper 30S ribosome subunits.
9 at, following its synthesis on mitochondrial ribosomes, subunit 6 of the ATPase (Atp6p) can be cross-
10 ry site (IRES), which directly binds the 40S ribosome subunit and is a target for candidate therapeut
12 7-cognate codons in high-abundance mRNAs for ribosome subunits and energy metabolism, congruent with
14 associates with a class of mRNAs that encode ribosome subunits and precursors to snoRNAs involved in
15 ion, the ribosomal proteins of the small 30S ribosome subunit, and minor ribosome-associated proteins
16 y understood form of initiation in which 40S ribosome subunits are loaded onto mRNA through interacti
17 increased ribosome density, consistent with ribosome subunit assembly for initiation, the first step
19 messenger RNA synthesis and processing, and ribosome subunit biogenesis, take place within the nucle
21 ciation of cap-binding factors and the small ribosome subunit but before formation of the 80S ribosom
22 tightly associated with some of the free 40S ribosome subunits, but it was not present in the 80S poo
23 n requires ribosomal RNA methylation in both ribosome subunits by TlyA (Rv1694), an enzyme with dual
26 ally occurs by 5'-processive scanning of 40S ribosome subunits from the m7GTP-cap to the initiating A
28 ping, involves discontinuous scanning by 40S ribosome subunits, in which large segments of the 5' non
31 of the RBD to 23S rRNA in the late stages of ribosome subunit maturation would position the ATP-bindi
32 ffect steady-state levels of large and small ribosome subunits, monoribosomes, and polyribosomes.
35 beyond that required for the typical rate of ribosome-subunit production and accumulate in the nucleo
36 ng, nucleophosmin-mediated nuclear export of ribosome subunits, protein synthesis levels, and cell gr
37 Tsc1 promoted the nuclear export of maturing ribosome subunits, providing a mechanistic link between
38 It was shown decades ago that purified 30S ribosome subunits readily interconvert between "active"
39 t that late steps in maturation of the large ribosome subunit rRNAs employ mechanisms that are evolut
40 or 4E (eIF4E), diminishes phosphorylation of ribosome subunit S6, and phosphorylates translation init
41 f tRNA from the A to the P site as the small ribosome subunit spontaneously rotates back from the hyb
42 omplex known to be related to arrangement of ribosome subunits that exhibit extremely high gene expre
43 hibited dramatic reductions in levels of 60S ribosome subunits under non-permissive conditions as wel
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