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1 ly to be important for optimizing functional protein biosynthesis.
2 olved in gametogenesis while down-regulating protein biosynthesis.
3 ment, cell invasion, antigenic variation and protein biosynthesis.
4 oacyl-tRNAs (aa-tRNAs) onto the ribosome for protein biosynthesis.
5 the main target for antibiotics that inhibit protein biosynthesis.
6 at is dependent on TNF signaling and de novo protein biosynthesis.
7 ntegration at the translocon during membrane protein biosynthesis.
8 t dissociate into subunits in order to begin protein biosynthesis.
9 havior of incomplete chains generated during protein biosynthesis.
10 eins, and enzymes involved in amino acid and protein biosynthesis.
11 nce of molecular chaperones participating in protein biosynthesis.
12 lised by the cell to optimise the outcome of protein biosynthesis.
13  into cellular responses to impaired plastid protein biosynthesis.
14 ting can modulate mRNA function and rates of protein biosynthesis.
15 l hemoglobin, far more than they require for protein biosynthesis.
16  mechanisms to ensure quality control during protein biosynthesis.
17 he other route to this essential compound in protein biosynthesis.
18 has been shown to block translocation during protein biosynthesis.
19 in the ribosome is a fundamental step during protein biosynthesis.
20 st suggests that organisms minimize costs of protein biosynthesis.
21 cyl groups mimic a chemistry found in modern protein biosynthesis.
22 RF through which DENR acts to regulate CLOCK protein biosynthesis.
23 ll cycle progression and on nucleic acid and protein biosynthesis.
24 lidinones are potent inhibitors of bacterial protein biosynthesis.
25 lationship between amino-acid metabolism and protein biosynthesis.
26 ons with mRNA, tRNA and other ligands during protein biosynthesis.
27 ptidyl-tRNA hydrolysis during termination of protein biosynthesis.
28 llular accumulation of DOX and inhibition of protein biosynthesis.
29 onment during 2 h of inhibition of host cell protein biosynthesis.
30 genes proposed to be involved in iron-sulfur protein biosynthesis.
31 d suggest a role for ubiquitination early in protein biosynthesis.
32  receptor chimaera in the absence of de novo protein biosynthesis.
33 ource of GTP for translational elongation in protein biosynthesis.
34 ognate amino acid and provide substrates for protein biosynthesis.
35 thways related to mitochondrial function and protein biosynthesis.
36 ve understanding of productive and erroneous protein biosynthesis.
37 and organoids, NLE1 was limiting for de novo protein biosynthesis.
38 airing nucleolar protein quality control and protein biosynthesis.
39 binding to the ribosome and interfering with protein biosynthesis.
40 ns but are typically not incorporated during protein biosynthesis.
41  govern ribosome biogenesis and to fine-tune protein biosynthesis.
42              Ribosomes are the workplace for protein biosynthesis.
43 t into its functioning during suppression of protein biosynthesis.
44  changed cell geometry or upon inhibition of protein biosynthesis.
45 at must be resolved to explain the origin of protein biosynthesis.
46 ting conserved molecular mechanisms, such as protein biosynthesis.
47 slation elongation is a crucial phase during protein biosynthesis.
48 d genetic code with up to 256 new codons for protein biosynthesis.
49 ant life employs the same 20 amino acids for protein biosynthesis.
50  metabolism and cell wall, nucleic acid, and protein biosynthesis.
51  may selectively and differentially modulate protein biosynthesis.
52  for efficient translation initiation during protein biosynthesis.
53 ion of proteins involved in cytoskeleton and protein biosynthesis.
54 ty of the TFEB protein and altered lysosomal protein biosynthesis.
55 al subunits, and reduced activity of plastid protein biosynthesis.
56 here they served as precursors for bacterial protein biosynthesis.
57 conserved process for secretory and membrane protein biosynthesis.
58 and the second, more potent as inhibitors of protein biosynthesis.
59 otein S6 was also modulated by inhibition of protein biosynthesis.
60                     eIF3 plays a key role in protein biosynthesis.
61 so activated by reduction in the accuracy of protein biosynthesis.
62 the E1 molecule and then utilize tyrosine in protein biosynthesis.
63 r a spring between these two proteins during protein biosynthesis.
64 ative activity, and amino acid transport and protein biosynthesis.
65 nsensitive to cycloheximide, an inhibitor of protein biosynthesis.
66  some of which encode proteins that modulate protein biosynthesis.
67 0 inhibition because of their high amount of protein biosynthesis.
68 ly linked to ribosomes and are implicated in protein biosynthesis.
69 lterations delimit the cellular capacity for protein biosynthesis, accelerate growth and drive diseas
70 ti-gene operons, thus coordinating ribosomal protein biosynthesis across multiple operons.
71         Protein degradation, in synergy with protein biosynthesis, allows cells to respond to various
72 that post-translational modifications during protein biosynthesis along secretory pathways play criti
73 ddition to their essential catalytic role in protein biosynthesis, aminoacyl-tRNA synthetases partici
74                                  We revealed protein biosynthesis and altered translation elongation
75  by upregulation of enzymes involved in both protein biosynthesis and biosynthetic pathways, as well
76 I- and Pol II-transcribed genes required for protein biosynthesis and cell cycle progression.
77 nscriptional pattern suggestive of increased protein biosynthesis and cellular proliferation.
78 gh its highly context-specific regulation of protein biosynthesis and classifies PLAG1 among a rare s
79 amino acids are the basic building blocks of protein biosynthesis and contribute to many other metabo
80 ng quality control processes associated with protein biosynthesis and cotranslational folding (CTF).
81      A link was recently established between protein biosynthesis and cytokine signal transduction.
82                             The induction of protein biosynthesis and decrease in protein catabolism
83  is maintained and regulated by the rates of protein biosynthesis and degradation in living systems.
84 olved in signal transduction, transcription, protein biosynthesis and degradation, and cell motility,
85 involving a tight control of many aspects of protein biosynthesis and degradation.
86 assessed by measuring adhesive strength, and protein biosynthesis and deposition were determined by i
87 s to the up-regulation of genes essential to protein biosynthesis and energy production.
88 ks-1/S6 kinase or in ife-2/eIF4E also reduce protein biosynthesis and extend lifespan, but only rsks-
89                                              Protein biosynthesis and extracellular secretion are ess
90 transcription of genes involved in secretory protein biosynthesis and granule-vesicle formation.
91          Ribotoxins are potent inhibitors of protein biosynthesis and inactivate ribosomes from a var
92 onine (HHT) is a first-in-class inhibitor of protein biosynthesis and is FDA-approved for the treatme
93 ed, RRE RNA secondary structure prevents Ant protein biosynthesis and lytic development.
94  amino acid implicated in energy metabolism, protein biosynthesis and neurotransmission.
95 ycle, starch biosynthesis, lipid metabolism, protein biosynthesis and processing.
96 ncentrate iron in iron-oxy minerals for iron-protein biosynthesis and protection against oxy radical
97 egulation of genes involved in all stages of protein biosynthesis and ribosome biogenesis during both
98                                    Moreover, protein biosynthesis and rRNA production were decreased
99 nificant over-representation of genes in the protein biosynthesis and stress response categories.
100 he roles of tRNA(Glu) at the intersection of protein biosynthesis and tetrapyrrole biosynthesis.
101 o the Kozak consensus sequence for mammalian protein biosynthesis and the 3'-UTR demonstrated three c
102 fficient mRNA splicing is a prerequisite for protein biosynthesis and the eukaryotic splicing machine
103 thesis of aromatic amino acids essential for protein biosynthesis and the production of a wide array
104                          NLE1 limits de novo protein biosynthesis and the tumorigenic potential of ad
105 ted functions were over-represented in loopy proteins, biosynthesis and energy metabolism were under-
106 g the kinases PIM2 and DYRK3, which regulate protein biosynthesis, and a number of genes in cilium bi
107 ases in genes regulating membrane integrity, protein biosynthesis, and apoptosis.
108            It downregulates RNA translation, protein biosynthesis, and metabolism in high-risk women'
109 ntral metabolism, including gluconeogenesis, protein biosynthesis, and purine/pyrimidine synthesis wa
110 ated with apoptosis, mitochondrial function, protein biosynthesis, and RNA binding.
111            The expression of several HS core proteins, biosynthesis, and modification enzymes was inc
112 he UPR activation, and attenuation of myelin protein biosynthesis; and resulted in late-onset, progre
113 ve effect of CHES1, indicating that PIM2 and protein biosynthesis are important targets of the antipr
114 ses like DNA replication, RNA synthesis, and protein biosynthesis are located inside the "cytoplasm"
115 e proteins (SvsR) is presumed to function in protein biosynthesis, because it exhibits a high degree
116 bit bacterial growth and cell-free ribosomal protein biosynthesis but also harbors an orthogonal func
117 t affected by cycloheximide, an inhibitor of protein biosynthesis, but is affected by proteasome inhi
118 gonist exposure and stimulation of secretory protein biosynthesis by agonist.
119 icrobial peptides (PrAMPs) inhibit bacterial protein biosynthesis by binding to the polypeptide exit
120 he A-tRNA entrance corridor, thus inhibiting protein biosynthesis by blocking the binding site of the
121 minoacyl-tRNA synthetases play a key role in protein biosynthesis by catalyzing the specific aminoacy
122 y activates GADD34, which promotes ER client protein biosynthesis by dephosphorylating phospho-Ser 51
123 ropose that oxazolidinones inhibit bacterial protein biosynthesis by interfering with the binding of
124  transport particle, and may control storage protein biosynthesis by regulating one or more processes
125                Lysyl-tRNAs are essential for protein biosynthesis by ribosomal mRNA translation in al
126 ossibility that small molecules can regulate protein biosynthesis by selectively binding to mRNA.
127    These findings suggest that inhibition of protein biosynthesis can alter degradation of some prote
128 ation that the four fundamental reactions of protein biosynthesis can be RNA-mediated.
129 and cellular growth, indicating that reduced protein biosynthesis can confer a suppressive effect on
130 teins in the dark, suggesting that cell wall protein biosynthesis ceased during the night.
131 ism, ion homeostasis, gene transcription and protein biosynthesis, compatible solute production, horm
132 on of Cox2 levels, a proxy for mitochondrial protein biosynthesis, coupled with the accumulation of t
133 n of transcription (actinomycin D, 4 mum) or protein biosynthesis (cycloheximide, 70 mum).
134 Vs in adipocytes requires continuous RNA and protein biosynthesis de novo.
135 dulin), we outline the general principles of protein biosynthesis, delineate the recognition and degr
136 ipts proved time-, dose-, nitric oxide-, and protein biosynthesis-dependent but glucose independent.
137 e the first committed step in O-glycosylated protein biosynthesis, determine sites of O-glycosylation
138 ghly significant number of genes involved in protein biosynthesis displayed an increase in transcript
139  critical transitions in progression include protein biosynthesis, E26 transformation-specific (ETS)
140                     Movement, cell division, protein biosynthesis, electron transfer against an elect
141 n separate submaps, with pathways related to protein biosynthesis, endoplasmic reticulum retention, e
142 tics to identify genes co-occurring with the protein biosynthesis enzyme SepCysS, which converts phos
143 idant defense enzymes, molecular chaperones, protein biosynthesis enzymes, and trafficking and degrad
144 th conditions of mammalian mRNAs that encode protein biosynthesis factors and contain hallmark 5'-ter
145 ic reticulum (ER) is a central organelle for protein biosynthesis, folding, and traffic.
146  for physiological disorders associated with protein biosynthesis, folding, trafficking, and membrane
147 work of molecular interactions that balances protein biosynthesis, folding, translocation, assembly/d
148 romolecular assembly that is responsible for protein biosynthesis following genetic instructions in a
149 nE gene, which has been reported to uncouple protein biosynthesis from tetrapyrrole biosynthesis in c
150 lta strains and that the stress response and protein biosynthesis gene categories were coordinately r
151 lthough correct tRNA 3' ends are crucial for protein biosynthesis, generation of mature tRNA 3' ends
152 lated in response to DNA damage are numerous protein biosynthesis genes.
153                                    Following protein biosynthesis, glutamic acids on these proteins a
154 1, lamin B1, vimentin, and beta-actin) or in protein biosynthesis (glutamyl-prolyl-transfer RNA synth
155 ion in one or more of the steps that control protein biosynthesis has been associated with alteration
156 ing the process of molecular translation, or protein biosynthesis, has emerged as a major opportunity
157                     Equivalent inhibition of protein biosynthesis in a rabbit reticulocyte system and
158 lation system execute gene transcription and protein biosynthesis in a timely and programmable fashio
159 ity of large cells to scale nucleic acid and protein biosynthesis in accordance with cell volume incr
160 nt increase in myocardial TNF-alpha mRNA and protein biosynthesis in adult cat hearts.
161 esis in the panicle of adult plants, whereas protein biosynthesis in adult leaves was 8-fold lower th
162 somes, the essential organelles required for protein biosynthesis in all cells, cause tissue-specific
163   Despite the broad requirement of GlyRS for protein biosynthesis in all cells, mutations in this gen
164  posttranscriptional networks and suppresses protein biosynthesis in ALL cells.
165  RNA (tRNA) molecules play a crucial role in protein biosynthesis in all organisms.
166 rotein molecules and plays a central role in protein biosynthesis in all organisms.
167         All of the products of mitochondrial protein biosynthesis in animals are hydrophobic proteins
168 cations for mRNA decay and the regulation of protein biosynthesis in bacteria.
169                                 They inhibit protein biosynthesis in bacterial pathogens by narrowing
170 expression elicits a sustained repression of protein biosynthesis in cells responding to stress.
171 e partitioning in support of storage oil and protein biosynthesis in developing COS.
172 cific RNA structures that regulate ribosomal protein biosynthesis in E. coli are narrowly distributed
173 r, these studies have shown that acute phase protein biosynthesis in enterocytes is regulated by infl
174 t protein complex required for initiation of protein biosynthesis in eukaryotic cells.
175   Inhibition was observed without effects on protein biosynthesis in general or PrP-sen biosynthesis
176  inactivation reversed attenuation of myelin protein biosynthesis in oligodendrocytes and restored my
177 e study of interactions between DNA, RNA and protein biosynthesis in order to develop a more comprehe
178 e important to fine-tune gene expression and protein biosynthesis in plant cells.
179 e important to fine tune gene expression and protein biosynthesis in plant cells.
180 defense system in the plant kingdom, wherein protein biosynthesis in short, procumbent glandular tric
181 folded or surplus proteins or by-products of protein biosynthesis in the ER and delivers them to 26S
182 ependent increase in myocardial TNF mRNA and protein biosynthesis in the heart as well as in cultured
183  a brief HOCl exposure profoundly suppressed protein biosynthesis in the slices.
184 hanism mediated by ERs, and de novo mRNA and protein biosynthesis, in a sex- and region-dependent man
185 gth, taken as models for different stages of protein biosynthesis, in the absence and presence of the
186 air one or more steps of tRNA maturation and protein biosynthesis including 5'-end-processing, post-t
187 n the Sec translocon and its role in nascent protein biosynthesis, including the correct folding and
188 acterial metabolism as well as mitochondrial protein biosynthesis, induce neutrophil chemotaxis, the
189   In this study, we found that inhibition of protein biosynthesis induced phosphorylation/activation
190                                 Furthermore, protein biosynthesis inhibition increased from 20% under
191 recovery was observed in the presence of the protein biosynthesis inhibitor cycloheximide.
192 activates cell death only in the presence of protein biosynthesis inhibitors, which presumably block
193                Taken together, inhibition of protein biosynthesis is a promising strategy to overcome
194                   Since ribosomally mediated protein biosynthesis is confined to the L-amino acid poo
195                                              Protein biosynthesis is fundamental to cellular life and
196 imulation methods to explore Sec-facilitated protein biosynthesis is hindered by the large system siz
197                                              Protein biosynthesis is inherently coupled to cotranslat
198         Furthermore, efficient inhibition of protein biosynthesis is observed.
199 vents, indicating that, while the process of protein biosynthesis is orthologous, its constituents ar
200                     An indispensable step in protein biosynthesis is the 2(')(3(')) aminoacylation of
201 talytic competency of the ribosome in extant protein biosynthesis is thought to arise primarily from
202 veals that RNA-based regulation of ribosomal protein biosynthesis is used in nearly all eubacterial p
203 (aa-tRNA) formation, an essential process in protein biosynthesis, is generally achieved by direct at
204 in a predicted C-terminal helical region for protein biosynthesis, localization, and interaction with
205            Tet(M) protein interacts with the protein biosynthesis machinery to render this process re
206  growth arrest, and suggest that restraining protein biosynthesis may be important in the prevention
207                        Translation errors in protein biosynthesis may result in low level amino acid
208 of genes in pathways related to RNA, DNA and protein biosynthesis, metabolism and catabolism.
209 the operation of the SBP-single location Chl-protein biosynthesis model.
210                          Whether a change in protein biosynthesis modulates protein degradation has n
211 ), matrix formation (n = 25), metabolism and protein biosynthesis (n = 27), cell signaling (n = 21),
212  enzymes that catalyze the first reaction in protein biosynthesis, namely the charging of transfer RN
213 anobacteria, plastids (chloroplasts) perform protein biosynthesis on bacterial-type 70S ribosomes.
214                                              Protein biosynthesis on the ribosome requires accurate r
215                                              Protein biosynthesis on the ribosome requires repeated c
216 oes not interfere with receptor binding or F protein biosynthesis or transport but prevents F protein
217                                              Protein biosynthesis, or translation, occurs on the ribo
218 d several molecular 'programs' implicated in protein biosynthesis, oxidative-stress responses and NF-
219 n mechanisms that exist at every step of the protein biosynthesis pathway, such as alternative splici
220 l understanding of lipid synthesis, membrane protein biosynthesis, phospholipid and membrane protein
221 cellular transport, phospholipid metabolism, protein biosynthesis, protein localization, protein meta
222 l lack an understanding of the dependence of protein biosynthesis rates on [ATP] and [GTP].
223 ree-dimensional mRNA structure and regulates protein biosynthesis rates raises the possibility that s
224  limits of our knowledge regarding ribosomal protein biosynthesis regulation outside of E. coli, and
225 tion limits tetrapyrrole biosynthesis and/or protein biosynthesis remains poorly understood.
226                                              Protein biosynthesis requires aminoacyl-transfer RNA (tR
227                           Quality control of protein biosynthesis requires ER-retention and ER-associ
228  cell line up-regulated processes, including protein biosynthesis, responses to stress and responses
229 to quantitative or qualitative alteration of protein biosynthesis, secretion, activity, or clearance.
230 ing study, we show that H-MM is defined by a protein biosynthesis signature that is primarily driven
231 m that Aze is misincorporated for Pro during protein biosynthesis, specifically on cytosolically tran
232 into two broad categories; those that affect protein biosynthesis/stability and traffic to the cell s
233                                     Salivary protein biosynthesis starts with the transcription and t
234 The alpha-helical motif was not required for protein biosynthesis, tetrameric subunit assembly, tetra
235                                       During protein biosynthesis the ribosome moves along mRNA in st
236                          After each round of protein biosynthesis, the posttermination complex (PoTC)
237 is proteolytically processed by furin during protein biosynthesis, the S2' site is cleaved upon viral
238               During the elongation cycle of protein biosynthesis, the specific amino acid coded for
239 id residues are bound to the ribosome during protein biosynthesis, these small proteins do not fold u
240 erations of protein degradation may regulate protein biosynthesis through a feedback mechanism.
241  entails the manipulation of essential HIV-1 protein biosynthesis through unnatural amino acid (UAA*)
242                                NX-3 inhibits protein biosynthesis to almost the same extent as the pr
243  now possible to employ in vitro and in vivo protein biosynthesis to elaborate proteins containing a
244  cellular fate of tRNAs can be switched from protein biosynthesis to non-canonical functions.
245 egradation and calls for caution in blocking protein biosynthesis to study the half-life of proteins.
246 min superfamily, the SRP/SR family, and the "protein biosynthesis" translational GTPases.
247                                       Though protein biosynthesis, transport, and quality control in
248 e proteins for methoxymalonyl-S-acyl carrier protein biosynthesis (Ttm-ABCDE), eight proteins for dia
249 sduction, vesicular and molecular transport, protein biosynthesis, ubiquitination, and neuronal survi
250 mportant for bacterial growth and functional protein biosynthesis under certain conditions and is qui
251                      Paradoxically, impaired protein biosynthesis upregulated genes involved in the c
252 s in ubiquitin-dependent protein catabolism, protein biosynthesis, vesicle trafficking and the respon
253 this transporter (and other factors) in heme protein biosynthesis, we developed plasmids that produce
254       To overcome this natural limitation on protein biosynthesis, we have evolved an orthogonal tRNA
255 r necrosis factor-alpha (TNF-alpha) mRNA and protein biosynthesis were examined in adult feline myoca
256                                 LIF mRNA and protein biosynthesis were examined in the adult feline h
257 r processes such as secondary metabolism and protein biosynthesis were generally not affected.
258                 Moreover, TNF-alpha mRNA and protein biosynthesis were observed in myocyte and nonmyo
259      In addition, other proteins involved in protein biosynthesis were shown to be associated with ri
260 ould represent an early intermediate in MoFe protein biosynthesis where the P-cluster precursors have
261                 High ho5C2501 levels reduced protein biosynthesis which however turned out to be bene
262 gy is regulated by processes occurring after protein biosynthesis, which are critical for both channe
263 thionine by methionyl-tRNA synthetase during protein biosynthesis, which results in the formation of
264  metabolism accommodated different levels of protein biosynthesis while maintaining a consistent rate
265                       HP 1 inhibited RNA and protein biosynthesis while not inhibiting DNA biosynthes
266 many studies have correlated deregulation of protein biosynthesis with cancer, it remains to be estab
267 r corroborated by showing that inhibition of protein biosynthesis with cycloheximide prior to 3-AP an
268 have a long history of providing probes into protein biosynthesis, with many of these compounds servi

 
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