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1 ard and reverse genetics for the study of As hyperaccumulation.
2  extremely high level of Cd tolerance and Cd hyperaccumulation.
3 n grown under conditions that favored AdoMet hyperaccumulation.
4 rtmentation of AdoMet as well as the mode of hyperaccumulation.
5 CsGSTF1 as being associated with anthocyanin hyperaccumulation.
6 s gene expression, a known hallmark of metal hyperaccumulation.
7 echanisms associated with hypertolerance and hyperaccumulation.
8  into phylogenetic patterns of trace element hyperaccumulation.
9  vital role in homeostasis of nickel ions in hyperaccumulation.
10 c acid and citric acid involvement in nickel hyperaccumulation.
11 nd whether associated partners may affect Se hyperaccumulation.
12 egrade starch during the night, resulting in hyperaccumulation.
13 se results demonstrate a role for NAS2 in Zn hyperaccumulation also under near-natural conditions.
14 ever, no correlation was observed between Se hyperaccumulation and ATPS, APR, and SAT activities in s
15 sis pathway, gsh2 mutants exhibited gamma-EC hyperaccumulation and GSH deficiency.
16 le contribution to zinc, cadmium, and nickel hyperaccumulation and hypertolerance were predicted.
17                             Mechanisms of Se hyperaccumulation and its adaptive significance appear t
18 derstanding of the mechanisms of heavy metal hyperaccumulation and tolerance and as a source of genes
19 lation and tolerance in plants and algae, Se hyperaccumulation, and ecological and evolutionary aspec
20 of ScATM1, abrogate intra-mitochondrial iron hyperaccumulation, and restore mitochondrial respiratory
21             Diseases characterized by copper hyperaccumulation are currently challenging to identify
22 ing of the traits and mechanisms involved in hyperaccumulation are needed so that phytoextraction can
23 rate that both good biomass yields and metal hyperaccumulation are required to make the process effic
24 ce signalling through ROS and that, as metal hyperaccumulation became effective as a form of elementa
25 tists focused on the mechanisms of Cd and Zn hyperaccumulation but did not take into consideration th
26 tutive zinc/cadmium (Zn/Cd) tolerance and Zn hyperaccumulation but high intraspecific variability in
27 kely selection pressure for the evolution of hyperaccumulation, but few have tested the origin(s) of
28                   Hence, BSD2 prevents metal hyperaccumulation by exerting negative control over the
29                                      Arsenic hyperaccumulation can be engineered in A. thaliana by kn
30 1 under the LOB promoter, indicating that BR hyperaccumulation contributes to the lob mutant phenotyp
31 sights garnered from molecular mechanisms of hyperaccumulation, domestication and agronomic developme
32                          Here we show that a hyperaccumulation effect can allow efficient enrichment
33   The basis of the nutrient-dependent AdoMet hyperaccumulation effect is discussed in relation to hom
34 llow us to alter the expression of candidate hyperaccumulation genes and thus dissect the molecular a
35                                              Hyperaccumulation has evolved independently in at least
36 ilitated by molecular dissection of plant Zn hyperaccumulation (i.e., the ability of certain plants t
37 lation, but few have tested the origin(s) of hyperaccumulation in a phylogenetic context.
38                               To achieve Phe hyperaccumulation in a plant system, we simultaneously d
39 s belong to the same species and that nickel hyperaccumulation in A. serpyllifolium appears to repres
40                                  However, Se hyperaccumulation in Astragalus is not driven by an over
41  one of the main transporters involved in Cd hyperaccumulation in N. caerulescens and copy number var
42 ot seem to be much ecotypic variation for Zn hyperaccumulation in N. caerulescens.
43 ability of contaminants can sometimes induce hyperaccumulation in normal plants, but may produce unde
44 n of the molecular mechanisms involved in As hyperaccumulation in P. vittata using gametophytes as an
45 eview what is known about evolution of metal hyperaccumulation in plants and describe a population-ge
46                 In this work, engineering Cu-hyperaccumulation in plants was approached.
47 ions into the basic mechanisms underlying As hyperaccumulation in plants.
48  our understanding of the evolution of metal hyperaccumulation in plants.
49 on the evolutionary history of selenium (Se) hyperaccumulation in Stanleya (Brassicaceae).
50 esults give insight into the evolution of Se hyperaccumulation in Stanleya and suggest that Se tolera
51 e organic Se are likely prerequisites for Se hyperaccumulation in Stanleya.
52 t in the epidermal storage cells where metal hyperaccumulation in T. caerulescens occurs.
53 and physiological processes underlying metal hyperaccumulation in T. caerulescens.
54 en suggested to play an important role in Zn hyperaccumulation in T. goesingense.
55 ction in zinc and cadmium hypertolerance and hyperaccumulation in the extremophile plant species Arab
56 ar physiology and molecular biology to Zn/Cd hyperaccumulation in the intact plant, T. caerulescens s
57 ACR3 expression with HAC1 mutation led to As hyperaccumulation in the shoots, whereas combining HAC1
58 onses in plants, is a strong predictor of Ni hyperaccumulation in the six diverse Thlaspi species inv
59 ed a critical role in the evolution of metal hyperaccumulation in the Thlaspi genus.
60 stand the role of free histidine (His) in Ni hyperaccumulation in Thlaspi goesingense, we investigate
61 and molecular basis of nickel (Ni)/zinc (Zn) hyperaccumulation in Thlaspi; however, the molecular sig
62                                        Metal hyperaccumulation is an uncommon but highly distinctive
63               In mature sbe2a leaves, starch hyperaccumulation is greatest in visibly senescing regio
64        These observations suggest that metal hyperaccumulation is incompatible with defence signallin
65                    To investigate whether Se hyperaccumulation is ubiquitous in S. ericoides or restr
66 y was to investigate how plant selenium (Se) hyperaccumulation may affect ecological interactions and
67 een pathogen resistance and Ni tolerance and hyperaccumulation may have played a critical role in the
68  arsenate, consistent with other known metal hyperaccumulation mechanisms in plants.
69 iously characterized maize leaf carbohydrate hyperaccumulation mutants.
70 cled unattached kinetochores, similar to the hyperaccumulation observed of dynamic outer kinetochore
71                                         This hyperaccumulation occurs because the translation of each
72                                              Hyperaccumulation of 6:2 FTSA, defined as tissue/soil co
73 h decreased cyclin D1 proteolysis and, thus, hyperaccumulation of active cyclin D1.CDK4 (cyclin-depen
74                                          The hyperaccumulation of AdoMet was a robust phenomenon when
75                                        Thus, hyperaccumulation of arf3a and ectopic accumulation of m
76                The sota mutant plants showed hyperaccumulation of aromatic amino acids accompanied by
77                                              Hyperaccumulation of As by plants has been identified as
78 in-accumulating regions in leaves due to the hyperaccumulation of carbohydrates.
79                      Our study confirmed the hyperaccumulation of Cd and Zn for each metallicolous po
80 growth and sterile, which is associated with hyperaccumulation of cellular acetate and decreased accu
81    Genetic suppressor analysis revealed that hyperaccumulation of copper and cadmium in bsd2 mutants
82 acking superoxide dismutase and also lead to hyperaccumulation of copper ions.
83 tone modifications that are required for the hyperaccumulation of Crb2 at DSBs.
84  cha1Delta strain to high serine resulted in hyperaccumulation of endogenous serine and in turn a sig
85 ncluding the reduction of lignin content and hyperaccumulation of flavonoids and p-coumarate esters.
86 '-hydroxylase (C3'H) lead to reduced lignin, hyperaccumulation of flavonoids, and growth inhibition i
87  cycle enzyme fumarate hydratase (FH) causes hyperaccumulation of fumarate.
88 nstitutive activation of cAPK suppresses the hyperaccumulation of glycogen in a pho85 mutant.
89  in the increase in phosphate scavenging and hyperaccumulation of glycogen in nutrient-rich condition
90 h defects on a variety of carbon sources and hyperaccumulation of glycogen in rich medium high in Pi.
91                                              Hyperaccumulation of glycogen in the pho85 strains is in
92          Disruption of PCL8 and PCL10 caused hyperaccumulation of glycogen, activation of glycogen sy
93 ells with disrupted PHO85 genes, we observed hyperaccumulation of glycogen, activation of glycogen sy
94 d levels of metabolites such as glucose-6-P, hyperaccumulation of glycogen, and activation of glycoge
95 ant to inhibition by phosphorylation, caused hyperaccumulation of glycogen.
96 , lactate or glycerol as a carbon source and hyperaccumulation of glycogen.
97 tion of PKA in a pho85 mutant suppresses the hyperaccumulation of glycogen.
98                      Loss of VRN1 results in hyperaccumulation of H2A.Z, more dynamic nucleosomes and
99                                              Hyperaccumulation of iron in opt3-2 resulted in the form
100 f CYP94B3 function in cyp94b3 mutants causes hyperaccumulation of JA-Ile and concomitant reduction in
101  quantitative mass spectrometry demonstrated hyperaccumulation of Lys63 chains in the insoluble fract
102 c transmission reduced AZ seeding and caused hyperaccumulation of material at existing AZs.
103 f transgenic chloroplasts as bioreactors for hyperaccumulation of membrane proteins for biotechnologi
104 l mutants exhibited reduced levels of JA and hyperaccumulation of OPC-8:0.
105 t incorporates the light requirement and the hyperaccumulation of photoassimilates.
106 ationally lipoylated mitochondrial proteins, hyperaccumulation of photorespiratory Gly, and reduced a
107 poylation of mitochondrial proteins, and the hyperaccumulation of photorespiratory intermediates, gly
108 f different genotypes of annual ryegrass for hyperaccumulation of Pi in their shoots, Gulf and Urugra
109 trogen-acquisition mechanisms in the arsenic hyperaccumulation of Pteris vittata, and provide valuabl
110 duction of esterified suberin components and hyperaccumulation of putative suberin precursors in the
111                            Together with the hyperaccumulation of reactive oxygen species (ROS), ndl1
112         The latter class of mutations led to hyperaccumulation of repair intermediate Mlh1-Pms1 foci
113        Through genetic analysis we show that hyperaccumulation of Rum1 contributes to re-replication
114 y play an important signaling role in the Se hyperaccumulation of S. pinnata, perhaps by constitutive
115 osensitivity that occurs in conjunction with hyperaccumulation of salicylic acid (SA).
116 mutant's growth defects, suggesting that the hyperaccumulation of salicylic acid is unlikely to be re
117 g irreversible replication fork collapse and hyperaccumulation of ssDNA.
118 ant energy and carbon reserve in plants, and hyperaccumulation of TAG in vegetative tissues can have
119                       Detrimental effects of hyperaccumulation of the aromatic amino acid phenylalani
120 ial nutrient for life, but at the same time, hyperaccumulation of this redox-active metal in biologic
121  in CDPK2 deficient parasites results in the hyperaccumulation of this sugar polymer.
122 lso altered so that it largely overrides the hyperaccumulation of transcripts, and as a consequence,
123 rkat T cells, avicin G treatment resulted in hyperaccumulation of ubiquitinated proteins in S. pombe
124 displayed increased tolerance to and reduced hyperaccumulation of Zn, and limited accumulation of Cd,
125 understanding the mechanisms responsible for hyperaccumulation of Zn, Cd, Ni and As by plants.
126                      Mapping the trait of Na-hyperaccumulation onto the phylogenetic relationships be
127 metals and thus could be a key player in the hyperaccumulation phenotype expressed in T. caerulescens
128            We therefore conclude that the Ni hyperaccumulation phenotype in T. goesingense is not det
129 ericoidesPR population may contribute to the hyperaccumulation phenotype.
130 bidopsis, QUIRKY, had a similar carbohydrate hyperaccumulation phenotype.
131 uppress the arsenate sensitivity and arsenic hyperaccumulation phenotypes of yeast (Saccharomyces cer
132  a mutualism system for beneficial fungi and hyperaccumulation plants, which facilitates high-efficie
133                     The study of these metal hyperaccumulation processes at the cellular level in T.
134                                  Although Se hyperaccumulation protects plants from herbivory by some
135                                       Nickel hyperaccumulation reverses this pathogen hypersensitivit
136                                              Hyperaccumulation tends to negatively affect Se-sensitiv
137 S2-RNAi lines, however, did not reach the Zn hyperaccumulation threshold.
138  and PDF2.3) as possible contributors to the hyperaccumulation/tolerance phenotype.
139 d correlation with Zn(2+), Cd(2+), or Ni(2+) hyperaccumulation/tolerance.
140 us studies have indicated that the Zn and Cd hyperaccumulation trait exhibited by this species involv
141 ility and therefore may contribute to the Se hyperaccumulation trait; however, it is not sufficient t
142                      We could not detect Dup hyperaccumulation using mutations in the CRL4(Cdt2) comp
143 o investigate the mechanisms responsible for hyperaccumulation, using natural hyperaccumulators as mo
144 is the key plant characteristic required for hyperaccumulation; vacuolar compartmentalization appears
145                                         True hyperaccumulation was found in three taxa within the S.
146                                           Se hyperaccumulation was found to positively correlate with
147  responsible for selenium (Se) tolerance and hyperaccumulation were studied in the Se hyperaccumulato
148  manganese absorption could induce manganese hyperaccumulation when ZIP14 is inactivated.
149  ZNT1 does not directly participate in metal hyperaccumulation within the leaf.

 
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