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1  estimated to constitute <0.02% of the total chloroplast protein.
2  plant PII-like protein is a nuclear-encoded chloroplast protein.
3 here it accounted for up to 15% of the total chloroplast protein.
4 bunit IV of the cytochrome b6/f complex, and chloroplast proteins.
5 ps cooperating in the rapid replenishment of chloroplast proteins.
6 ion, and glycosylation, in the regulation of chloroplast proteins.
7 -responsive genes encoding mitochondrial and chloroplast proteins.
8 hared by promoters of nuclear-genes encoding chloroplast proteins.
9 cific DNA affinity chromatography from total chloroplast proteins.
10 hloroplast development and reduced levels of chloroplast proteins.
11 or embryo-defective (emb) mutants altered in chloroplast proteins.
12 rone homolog genes (CGE) in moss that encode chloroplast proteins.
13 and b suggesting a role in the expression of chloroplast proteins.
14 als modulate expression of nuclear genes for chloroplast proteins.
15 uired to maintain nuclear gene expression of chloroplast proteins.
16 ent but did not require ATP, GTP, or soluble chloroplast proteins.
17 ed with the stabilities of two other soluble chloroplast proteins.
18 -silico analysis of selected nuclear-encoded chloroplast proteins (132 proteins) was performed.
19 ns and also interacts with MYOSIN-RESEMBLING CHLOROPLAST PROTEIN, a proposed structural protein influ
20 anslating ribosomes, ultimately compromising chloroplast protein abundance and thus plant growth and
21                     The Arabidopsis thaliana chloroplast protein ACCELERATED CELL DEATH2 (ACD2) modul
22 ng, reduced chloroplast translation, reduced chloroplast protein accumulation, and elevated chloropla
23 t rRNA processing and a drastic reduction in chloroplast protein accumulation.
24 e identification of specific DNA variants of chloroplast proteins allows discriminating individuals a
25  of the expression of nuclear genes encoding chloroplast proteins allows for metabolic adjustment in
26 ondrial protein to replace the function of a chloroplast protein and illustrates the plasticity of th
27 1 mutants have altered levels of a subset of chloroplast proteins and display abnormal chloroplast de
28  field of posttranslational modifications of chloroplast proteins and points out the importance of th
29 gy in the proteolytic regulation of specific chloroplast proteins, and how dynamic control of chlorop
30 ombinant CPE cleaves in the absence of other chloroplast proteins, and this activity depends on metal
31 of 1,105 proteins were assigned as potential chloroplast proteins, annotated for function, and quanti
32 ic analysis indicated that nuclear genes for chloroplast proteins are down-regulated, and proteins me
33                                         Most chloroplast proteins are imported from the cytosol throu
34                                         Most chloroplast proteins are imported from the cytosol via m
35                              Nucleus-encoded chloroplast proteins are imported via multiprotein trans
36                                         Most chloroplast proteins are nucleus-encoded and imported fo
37  our understanding of the mechanism by which chloroplast proteins are sorted and transported via the
38                                         Most chloroplast proteins are synthesized in the cytosol and
39                                         Most chloroplast proteins are synthesized in the cytosol as h
40              The majority of nucleus-encoded chloroplast proteins are targeted to the organelle by di
41 he Arabidopsis Thf1 gene encodes an imported chloroplast protein, as shown by in vitro import and loc
42                  The accumulation of several chloroplast proteins, as well as most of the chloroplast
43 plasts, involving regulatory nucleus-encoded chloroplast proteins, as well as nucleocytosolic photore
44 tion of starch granules consistent with some chloroplast proteins being decreased.
45 lar mechanisms underlying the trafficking of chloroplast proteins between the intracellular compartme
46 n vitro analyses reveal different aspects of chloroplast protein biogenesis.
47 -responsive genes encoding mitochondrial and chloroplast proteins but have little effect on more cons
48  occurs in both nuclear- and plastid-encoded chloroplast proteins, but the physiological significance
49 mplex regulatory network systems controlling chloroplast proteins by a range of posttranslational mod
50                              Nucleus-encoded chloroplast proteins can be transported via the secretor
51 ports the concept that peptides derived from chloroplast proteins can function as regulators of plant
52            Consequently, N termini of mature chloroplast proteins cannot be accurately predicted.
53                 Loss of CGEP upregulated the chloroplast protein chaperone machinery and 70S ribosoma
54 ed comparative native gel electrophoresis of chloroplast protein complexes followed by protein mass s
55                      Here we report that the chloroplast proteins COR15A and COR15B are necessary for
56                    The thioredoxin-regulated chloroplast protein CP12 forms a multienzyme complex wit
57                                          The chloroplast protein CSP41a both binds and cleaves RNA, p
58                                Certain other chloroplast proteins decline with age coordinately with
59                     Although the pathways of chloroplast protein degradation and the types of chlorop
60 ysis and mass spectrometry identified mainly chloroplast proteins differentially expressed between th
61  with reductions in the accumulation of some chloroplast proteins, directly or indirectly.
62              Once inside the organelle, many chloroplast proteins engage one of four additional prote
63            An extensive overview of BS and M chloroplast protein expression and homeostasis machineri
64 e excision repair of oxidized pyrimidines in chloroplast protein extracts of Arabidopsis thaliana.
65 o DNA replication using a partially purified chloroplast protein fraction.
66 ting as a molecular chaperone and protecting chloroplast proteins from thermal aggregation and inacti
67           Genetic evidence suggests that the chloroplast protein GUN1 integrates signals derived from
68 l proteomes showed that many nuclear encoded chloroplast proteins have alternatively processed N-term
69 romal chaperones, suggesting an imbalance in chloroplast protein homeostasis and a well-coordinated n
70 ysically interacts with proteins involved in chloroplast protein homeostasis based on coimmunoprecipi
71               To extend our understanding of chloroplast protein import and the role played by the im
72 y is shown to control TOC protein levels and chloroplast protein import and to influence photosynthet
73 of the putative Arabidopsis homologs for the chloroplast protein import apparatus has revealed many q
74 in pea (Pisum sativum) as a component of the chloroplast protein import apparatus.
75                                 We have used chloroplast protein import assays as a means to identify
76 genetic attributes of Chlamydomonas to study chloroplast protein import by creating a series of delet
77  work showed that SP1-mediated regulation of chloroplast protein import contributes to the organellar
78  GTPases, we provide new insights of how the chloroplast protein import cycle may be regulated.
79 ve begun to take a genetic approach to study chloroplast protein import in Chlamydomonas reinhardtii
80 usly unrecognized roles in the regulation of chloroplast protein import in response to developmental,
81 s was developed to explore the regulation of chloroplast protein import in vivo using two independent
82                This work characterizes a new chloroplast protein import intermediate which has comple
83 roplast proteins, and how dynamic control of chloroplast protein import is critically important for p
84 derived energy long known to be required for chloroplast protein import is delivered via the Hsp70 ch
85                    Our results indicate that chloroplast protein import is responsive to environmenta
86  of two nuclear-encoded preproteins with the chloroplast protein import machinery at three stages in
87  protein (IAP) 100, a 100-kDa protein of the chloroplast protein import machinery of peas.
88  of complex chloroplasts provide barriers to chloroplast protein import not present in the simpler do
89 en demonstrated to be an intermediate in the chloroplast protein import pathway in vitro.
90 isible, 1 MDa complex-subunit abundance, and chloroplast protein import phenotypes.
91                                              Chloroplast protein import presents a complex membrane t
92  suggest that even severely impaired in vivo chloroplast protein import probably does not limit the a
93                                       In the chloroplast protein import system, a heat shock protein
94  dehydrogenase was shown to be important for chloroplast protein import, and it has been proposed to
95 ure applications of this system to analyzing chloroplast protein import, and provide valuable insight
96 at the three components may cooperate during chloroplast protein import.
97                                           In chloroplasts, protein import is accomplished by the TOC
98 ion arises from changes in the abundances of chloroplast proteins in Emiliania huxleyi strain CCMP 15
99 art at least to de novo protein synthesis of chloroplast proteins in the sea slug.
100          While the import of nuclear-encoded chloroplast proteins is relatively well studied, the tar
101                              Biosynthesis of chloroplast proteins is to a large extent regulated post
102 hagy, including impacts on lipid droplet and chloroplast protein levels.
103 oxidase is nuclear encoded, similar to other chloroplast proteins localized in the lumen.
104 complished through stabilizing the conserved chloroplast protein MORF2, which is degraded during immu
105 s motivated an extensive characterization of chloroplast protein N termini in Arabidopsis (Arabidopsi
106        UV cross-linking assays revealed that chloroplast proteins of 37 and 38 kDA bind specifically
107 hibits reduced import of two nucleus-encoded chloroplast proteins of different import profiles.
108                              Nucleus-encoded chloroplast proteins of vascular plants are synthesized
109 amydomonas reinhardtii cells depleted of the chloroplast protein PGRL1 was rescued by the introductio
110                                      Euglena chloroplast protein precursors are transported as integr
111                                  All Euglena chloroplast protein precursors have functionally similar
112 independent loci (PPR30 and mTERF9) encoding chloroplast proteins predicted to be involved in post-tr
113                    An important regulator of chloroplast protein production is the downstream box (DB
114                      Under stress, intensive chloroplast protein remodeling and degradation can occur
115      Here, we report the identification of a chloroplast protein required for Rubisco accumulation in
116            We describe here the diversity of chloroplast proteins required for embryo development in
117  cpRNPs CP31A and CP29A (for 31 kD and 29 kD chloroplast protein, respectively), associate with large
118 at the tRNA deficiencies lead to compromised chloroplast protein synthesis and the observed whole-pla
119 ing a maize (Zea mays L.) gene (Zmeftu1) for chloroplast protein synthesis elongation factor, EF-Tu,
120 under long-term treatment with lincomycin, a chloroplast protein synthesis inhibitor.
121                          While regulation of chloroplast protein synthesis is of central importance,
122 f illumination, carbon source, and levels of chloroplast protein synthesis on trans-acting proteins t
123 ted by the finding that loss of RH50 renders chloroplast protein synthesis sensitive to erythromycin
124 the presence of cycloheximide indicated that chloroplast protein synthesis was broadly reduced in the
125 ersely, photosynthetic proteins and those of chloroplast protein synthesis were significantly lower i
126 tudy the role of initiation codon context in chloroplast protein synthesis, we mutated the three nucl
127 found in all cells except those deficient in chloroplast protein synthesis.
128 center protein of photosystem II or impaired chloroplast protein synthesis.
129  and biochemical approaches for the study of chloroplast protein targeting.
130 sence of Rubisco activase, a nuclear-encoded chloroplast protein that consists of two isoforms arisin
131        Rubisco activase is a nuclear-encoded chloroplast protein that is required for the light activ
132 results suggest that DCP68 is a bifunctional chloroplast protein that participates in reductive sulfu
133    Arabidopsis FZO-LIKE (FZL) was shown as a chloroplast protein that regulates chloroplast morpholog
134  (Nicotiana tabacum) and identified a set of chloroplast proteins that are likely degraded by Clp.
135         The fibrillins are a large family of chloroplast proteins that have been linked with stress t
136                              Nucleus-encoded chloroplast proteins that reside in the thylakoid lumen
137                     Similar to the authentic chloroplast protein, the reconstituted alpha/beta 14-mer
138 n used to elucidate the function of numerous chloroplast proteins, the characterization of essential
139 and tatC, which are likely to be involved in chloroplast protein translocation.
140  would be a useful model system for studying chloroplast protein transport.
141 genes involved in chlorophyll catabolism and chloroplast protein turnover were subdued in bzip60-2, a
142                                         Most chloroplast proteins undergo N-terminal maturation, but
143 luding plastid biogenesis, proteostasis, the chloroplast Protein Unfolding Response, and metabolism,
144                                   While most chloroplast proteins use N-terminal transit peptides to
145 ermined the localizations of 1,034 candidate chloroplast proteins using fluorescent protein tagging i
146                                         Many chloroplast proteins were less abundant in the first eme
147 chloroplast genes and nuclear genes encoding chloroplast protein, which sheds light on the understand
148  182-amino-acid-long putative precursor of a chloroplast protein with high sequence similarity to evo
149 wild-type fusion protein was associated with chloroplasts, proteins with transit peptide deletions re

 
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