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1 oacyl-tRNAs (aa-tRNAs) onto the ribosome for protein biosynthesis.
2 the main target for antibiotics that inhibit protein biosynthesis.
3 at is dependent on TNF signaling and de novo protein biosynthesis.
4 ntegration at the translocon during membrane protein biosynthesis.
5 t dissociate into subunits in order to begin protein biosynthesis.
6 havior of incomplete chains generated during protein biosynthesis.
7 eins, and enzymes involved in amino acid and protein biosynthesis.
8 nce of molecular chaperones participating in protein biosynthesis.
9 metabolism and cell wall, nucleic acid, and protein biosynthesis.
10 ting can modulate mRNA function and rates of protein biosynthesis.
11 may selectively and differentially modulate protein biosynthesis.
12 l hemoglobin, far more than they require for protein biosynthesis.
13 mechanisms to ensure quality control during protein biosynthesis.
14 he other route to this essential compound in protein biosynthesis.
15 has been shown to block translocation during protein biosynthesis.
16 in the ribosome is a fundamental step during protein biosynthesis.
17 st suggests that organisms minimize costs of protein biosynthesis.
18 cyl groups mimic a chemistry found in modern protein biosynthesis.
19 ion of proteins involved in cytoskeleton and protein biosynthesis.
20 ll cycle progression and on nucleic acid and protein biosynthesis.
21 lidinones are potent inhibitors of bacterial protein biosynthesis.
22 lationship between amino-acid metabolism and protein biosynthesis.
23 ons with mRNA, tRNA and other ligands during protein biosynthesis.
24 ptidyl-tRNA hydrolysis during termination of protein biosynthesis.
25 onment during 2 h of inhibition of host cell protein biosynthesis.
26 genes proposed to be involved in iron-sulfur protein biosynthesis.
27 ty of the TFEB protein and altered lysosomal protein biosynthesis.
28 d suggest a role for ubiquitination early in protein biosynthesis.
29 receptor chimaera in the absence of de novo protein biosynthesis.
30 ource of GTP for translational elongation in protein biosynthesis.
31 al subunits, and reduced activity of plastid protein biosynthesis.
32 here they served as precursors for bacterial protein biosynthesis.
33 conserved process for secretory and membrane protein biosynthesis.
34 and the second, more potent as inhibitors of protein biosynthesis.
35 otein S6 was also modulated by inhibition of protein biosynthesis.
36 eIF3 plays a key role in protein biosynthesis.
37 so activated by reduction in the accuracy of protein biosynthesis.
38 ant life employs the same 20 amino acids for protein biosynthesis.
39 the E1 molecule and then utilize tyrosine in protein biosynthesis.
40 r a spring between these two proteins during protein biosynthesis.
41 ative activity, and amino acid transport and protein biosynthesis.
42 nsensitive to cycloheximide, an inhibitor of protein biosynthesis.
43 some of which encode proteins that modulate protein biosynthesis.
44 0 inhibition because of their high amount of protein biosynthesis.
45 ly linked to ribosomes and are implicated in protein biosynthesis.
46 ly to be important for optimizing functional protein biosynthesis.
47 olved in gametogenesis while down-regulating protein biosynthesis.
48 ment, cell invasion, antigenic variation and protein biosynthesis.
50 that post-translational modifications during protein biosynthesis along secretory pathways play criti
51 ddition to their essential catalytic role in protein biosynthesis, aminoacyl-tRNA synthetases partici
52 by upregulation of enzymes involved in both protein biosynthesis and biosynthetic pathways, as well
55 amino acids are the basic building blocks of protein biosynthesis and contribute to many other metabo
56 ng quality control processes associated with protein biosynthesis and cotranslational folding (CTF).
58 is maintained and regulated by the rates of protein biosynthesis and degradation in living systems.
59 olved in signal transduction, transcription, protein biosynthesis and degradation, and cell motility,
60 assessed by measuring adhesive strength, and protein biosynthesis and deposition were determined by i
62 ks-1/S6 kinase or in ife-2/eIF4E also reduce protein biosynthesis and extend lifespan, but only rsks-
69 ncentrate iron in iron-oxy minerals for iron-protein biosynthesis and protection against oxy radical
71 nificant over-representation of genes in the protein biosynthesis and stress response categories.
72 o the Kozak consensus sequence for mammalian protein biosynthesis and the 3'-UTR demonstrated three c
73 thesis of aromatic amino acids essential for protein biosynthesis and the production of a wide array
74 ted functions were over-represented in loopy proteins, biosynthesis and energy metabolism were under-
75 g the kinases PIM2 and DYRK3, which regulate protein biosynthesis, and a number of genes in cilium bi
77 ntral metabolism, including gluconeogenesis, protein biosynthesis, and purine/pyrimidine synthesis wa
79 ve effect of CHES1, indicating that PIM2 and protein biosynthesis are important targets of the antipr
80 e proteins (SvsR) is presumed to function in protein biosynthesis, because it exhibits a high degree
81 bit bacterial growth and cell-free ribosomal protein biosynthesis but also harbors an orthogonal func
82 t affected by cycloheximide, an inhibitor of protein biosynthesis, but is affected by proteasome inhi
84 he A-tRNA entrance corridor, thus inhibiting protein biosynthesis by blocking the binding site of the
85 minoacyl-tRNA synthetases play a key role in protein biosynthesis by catalyzing the specific aminoacy
86 y activates GADD34, which promotes ER client protein biosynthesis by dephosphorylating phospho-Ser 51
87 ropose that oxazolidinones inhibit bacterial protein biosynthesis by interfering with the binding of
88 transport particle, and may control storage protein biosynthesis by regulating one or more processes
90 ossibility that small molecules can regulate protein biosynthesis by selectively binding to mRNA.
91 These findings suggest that inhibition of protein biosynthesis can alter degradation of some prote
93 and cellular growth, indicating that reduced protein biosynthesis can confer a suppressive effect on
96 ipts proved time-, dose-, nitric oxide-, and protein biosynthesis-dependent but glucose independent.
97 e the first committed step in O-glycosylated protein biosynthesis, determine sites of O-glycosylation
98 ghly significant number of genes involved in protein biosynthesis displayed an increase in transcript
99 critical transitions in progression include protein biosynthesis, E26 transformation-specific (ETS)
101 tics to identify genes co-occurring with the protein biosynthesis enzyme SepCysS, which converts phos
102 idant defense enzymes, molecular chaperones, protein biosynthesis enzymes, and trafficking and degrad
103 th conditions of mammalian mRNAs that encode protein biosynthesis factors and contain hallmark 5'-ter
105 for physiological disorders associated with protein biosynthesis, folding, trafficking, and membrane
106 work of molecular interactions that balances protein biosynthesis, folding, translocation, assembly/d
107 romolecular assembly that is responsible for protein biosynthesis following genetic instructions in a
108 lta strains and that the stress response and protein biosynthesis gene categories were coordinately r
109 lthough correct tRNA 3' ends are crucial for protein biosynthesis, generation of mature tRNA 3' ends
112 1, lamin B1, vimentin, and beta-actin) or in protein biosynthesis (glutamyl-prolyl-transfer RNA synth
113 ion in one or more of the steps that control protein biosynthesis has been associated with alteration
116 esis in the panicle of adult plants, whereas protein biosynthesis in adult leaves was 8-fold lower th
117 somes, the essential organelles required for protein biosynthesis in all cells, cause tissue-specific
118 Despite the broad requirement of GlyRS for protein biosynthesis in all cells, mutations in this gen
123 expression elicits a sustained repression of protein biosynthesis in cells responding to stress.
125 cific RNA structures that regulate ribosomal protein biosynthesis in E. coli are narrowly distributed
126 r, these studies have shown that acute phase protein biosynthesis in enterocytes is regulated by infl
128 Inhibition was observed without effects on protein biosynthesis in general or PrP-sen biosynthesis
129 e study of interactions between DNA, RNA and protein biosynthesis in order to develop a more comprehe
132 defense system in the plant kingdom, wherein protein biosynthesis in short, procumbent glandular tric
133 ependent increase in myocardial TNF mRNA and protein biosynthesis in the heart as well as in cultured
135 hanism mediated by ERs, and de novo mRNA and protein biosynthesis, in a sex- and region-dependent man
136 gth, taken as models for different stages of protein biosynthesis, in the absence and presence of the
137 air one or more steps of tRNA maturation and protein biosynthesis including 5'-end-processing, post-t
138 acterial metabolism as well as mitochondrial protein biosynthesis, induce neutrophil chemotaxis, the
139 In this study, we found that inhibition of protein biosynthesis induced phosphorylation/activation
141 activates cell death only in the presence of protein biosynthesis inhibitors, which presumably block
145 vents, indicating that, while the process of protein biosynthesis is orthologous, its constituents ar
147 veals that RNA-based regulation of ribosomal protein biosynthesis is used in nearly all eubacterial p
148 (aa-tRNA) formation, an essential process in protein biosynthesis, is generally achieved by direct at
149 in a predicted C-terminal helical region for protein biosynthesis, localization, and interaction with
151 growth arrest, and suggest that restraining protein biosynthesis may be important in the prevention
156 ), matrix formation (n = 25), metabolism and protein biosynthesis (n = 27), cell signaling (n = 21),
157 anobacteria, plastids (chloroplasts) perform protein biosynthesis on bacterial-type 70S ribosomes.
160 oes not interfere with receptor binding or F protein biosynthesis or transport but prevents F protein
162 d several molecular 'programs' implicated in protein biosynthesis, oxidative-stress responses and NF-
163 n mechanisms that exist at every step of the protein biosynthesis pathway, such as alternative splici
164 l understanding of lipid synthesis, membrane protein biosynthesis, phospholipid and membrane protein
165 cellular transport, phospholipid metabolism, protein biosynthesis, protein localization, protein meta
167 ree-dimensional mRNA structure and regulates protein biosynthesis rates raises the possibility that s
168 limits of our knowledge regarding ribosomal protein biosynthesis regulation outside of E. coli, and
171 cell line up-regulated processes, including protein biosynthesis, responses to stress and responses
172 ing study, we show that H-MM is defined by a protein biosynthesis signature that is primarily driven
173 into two broad categories; those that affect protein biosynthesis/stability and traffic to the cell s
175 The alpha-helical motif was not required for protein biosynthesis, tetrameric subunit assembly, tetra
178 is proteolytically processed by furin during protein biosynthesis, the S2' site is cleaved upon viral
180 id residues are bound to the ribosome during protein biosynthesis, these small proteins do not fold u
182 entails the manipulation of essential HIV-1 protein biosynthesis through unnatural amino acid (UAA*)
184 egradation and calls for caution in blocking protein biosynthesis to study the half-life of proteins.
187 e proteins for methoxymalonyl-S-acyl carrier protein biosynthesis (Ttm-ABCDE), eight proteins for dia
188 sduction, vesicular and molecular transport, protein biosynthesis, ubiquitination, and neuronal survi
189 mportant for bacterial growth and functional protein biosynthesis under certain conditions and is qui
190 s in ubiquitin-dependent protein catabolism, protein biosynthesis, vesicle trafficking and the respon
191 this transporter (and other factors) in heme protein biosynthesis, we developed plasmids that produce
193 r necrosis factor-alpha (TNF-alpha) mRNA and protein biosynthesis were examined in adult feline myoca
197 In addition, other proteins involved in protein biosynthesis were shown to be associated with ri
198 ould represent an early intermediate in MoFe protein biosynthesis where the P-cluster precursors have
199 gy is regulated by processes occurring after protein biosynthesis, which are critical for both channe
200 thionine by methionyl-tRNA synthetase during protein biosynthesis, which results in the formation of
201 metabolism accommodated different levels of protein biosynthesis while maintaining a consistent rate
203 many studies have correlated deregulation of protein biosynthesis with cancer, it remains to be estab
204 r corroborated by showing that inhibition of protein biosynthesis with cycloheximide prior to 3-AP an
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