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1 ylus keniensis) and invertebrate (a guild of symbiotic Acacia ants) animal species in a semi-arid Ken
2 mbiotic larval stage (32-49% higher) and the symbiotic adult life stage (51% higher).
3               Analyzing genetic diversity of symbiotic algae across >5,000 km of the PAG, the Gulf of
4 coral animal in concert with its unicellular symbiotic algae and a wide diversity of closely associat
5 phs, such as plants and mycorrhizal fungi or symbiotic algae and corals, underpin the functioning of
6 zed the contribution of both animal host and symbiotic algae to thermal tolerance in corals that have
7 enetic divergence in both the coral host and symbiotic algae.
8 tion are potential negative ramifications of symbiotic alliances.
9 AraC-like transcription factor CuxR in plant symbiotic alpha-proteobacteria.
10 critical roles in the nitrogen cycle through symbiotic and asymbiotic biological fixation of nitrogen
11  of Bradyrhizobium have been shown to be non-symbiotic and do not possess the ability to form nodules
12 s a versatile fungus with saprophytic, plant symbiotic and insect pathogenic lifestyle options.
13 t of an operational SOS response in presumed symbiotic and parasitic bacteria hints at an intermediat
14 small molecule signals is important for both symbiotic and pathogenic relationships, but is often poo
15 how human neutrophils interact with both the symbiotic and the dysbiotic oral community; an understan
16 ydrogen metabolism, probably associated with symbiotic and/or fermentation-based lifestyles.
17 ccurate differentiation between the healthy (symbiotic) and unhealthy (dysbiotic) microbial state has
18 role of this Amadori compound in pathogenic, symbiotic, and opportunistic bacteria.
19 these different-yet highly complementary and symbiotic-approaches with the view that increased synerg
20     Here we modelled the global diversity of symbiotic arbuscular mycorrhizal (AM) fungi using curren
21 cement can happen even in the most intricate symbiotic arrangements and that preexisting horizontally
22                                    A complex symbiotic association between legumes and nitrogen-fixin
23                              Especially, the symbiotic association between legumes and Rhizobium bact
24 proaches will improve understanding of these symbiotic associations and, in the long term, their usef
25 uscular mycorrhizas (AM) are the most common symbiotic associations between a plant's root compartmen
26                                              Symbiotic associations in the rhizosphere between plants
27 ty makes this kinase a putative regulator of symbiotic associations involving nutrient acquisition.
28 a presents a particularly large diversity of symbiotic associations that has frequently undergone shi
29 mponent that aid in plant defense and enable symbiotic associations with rhizobia.
30 ction as effector proteins that may regulate symbiotic associations.
31 oblem because of their inherent capacity for symbiotic atmospheric nitrogen fixation, which provides
32                                              Symbiotic bacteria and mucosal immunoglobulins have co-e
33 reased cellulose degrading activity and that symbiotic bacteria are a rich biochemical and enzymatic
34                                              Symbiotic bacteria assist in maintaining homeostasis of
35                                              Symbiotic bacteria decreased plant defenses in all Solan
36 teraction between the host immune system and symbiotic bacteria determines their cooperative rather t
37                          Although engineered symbiotic bacteria have been shown to render mosquitoes
38 icrobial gut symbionts and demonstrates that symbiotic bacteria in the gut lumen appear to function a
39  which may contribute to the biogeography of symbiotic bacteria in the gut.
40 ir free-living relatives, mutualistic insect symbiotic bacteria inhabit a static environment where th
41                  Our relationship with these symbiotic bacteria is especially important during the ea
42 were more abundant in predatory mites, while symbiotic bacteria prevailed in prey mites.
43                                              Symbiotic bacteria products are known to modulate differ
44           In addition to metabolic benefits, symbiotic bacteria provide the host with several functio
45 ny insect species harbor obligate, heritable symbiotic bacteria that provision essential nutrients an
46 inate from the microbiome, the consortium of symbiotic bacteria that reside within all animals.
47                        Thus, the presence of symbiotic bacteria that suppress plant defenses might he
48                               The ability of symbiotic bacteria to inhibit pathogen colonization is m
49                               Recognition of symbiotic bacteria via the nucleotide-binding oligomeriz
50 l have orthologs in other phytopathogenic or symbiotic bacteria, and are involved in the modulation a
51 yotes commonly host communities of heritable symbiotic bacteria, many of which are not essential for
52             Most animals host communities of symbiotic bacteria.
53 late the growth of trout total skin and gill symbiotic bacteria.
54 hosts of CPB by chemical elicitors and their symbiotic bacteria.
55 es which inject and feed on entomopathogenic symbiotic bacteria.
56 arbours complex communities of commensal and symbiotic bacterial microorganisms.
57  Bacteroides thetaiotaomicron is a human gut symbiotic bacterium that utilizes a myriad of host dieta
58                 We show that a single sponge symbiotic bacterium, Entotheonella sp., constitutes the
59 ermeable channel is known to be required for symbiotic Ca(2+) oscillations, but the calcium channels
60 bia are released from infection threads into symbiotic cells of nodules.
61 onal reprogramming in the differentiation of symbiotic cells.
62  To facilitate the molecular analysis of the symbiotic characteristics of such legumes, we took an in
63  system to control bioluminescence and other symbiotic colonization factors.
64  bacteria undergo during the early stages of symbiotic colonization.
65                         The gut harbors many symbiotic, commensal, and pathogenic microbes that break
66 zobial strain, suggesting its involvement in symbiotic communication.
67  animals studied to date are associated with symbiotic communities of microorganisms.
68  the result of a shift of the oral bacterial symbiotic community to a dysbiotic more complex communit
69                                     The core symbiotic community was composed of Alphaproteobacteria
70 ll focus on determining the function of this symbiotic community, and how it may change during ANG de
71 thetic efficiency was consistently lower for symbiotic compared to autonomous algae, suggesting nutri
72                  Individual genomes in these symbiotic complexes differ dramatically in relative abun
73 blished databases of adult and larvae of the symbiotic coral Acropora millepora, revealing both share
74 rs of the Cryptochiridae are small, fragile, symbiotic crabs that live in domiciles in modern corals.
75  to all previously known Cycloclasticus, the symbiotic Cycloclasticus appears to lack the genes neede
76 h similarities between the genes used by the symbiotic Cycloclasticus to degrade short-chain alkanes
77 h chronic skin GVHD and confirm parallel but symbiotic developmental pathways of Th22 and Th17 differ
78 ain promotes colonization of the host by the symbiotic dinoflagellate Symbiodinium minutum.
79       The coral holobiont includes the host, symbiotic dinoflagellates (Symbiodinium spp.), and a div
80             Symbioses between cnidarians and symbiotic dinoflagellates (Symbiodinium) are ecologicall
81 ntially expressed genes (DEGs) for endophyte-symbiotic (E+) vs endophyte-free (E-) clones in leaf bla
82 umen appear to function as partners both for symbiotic EAA supplementation and for digestion of insol
83  gut symbionts also function as partners for symbiotic EAA supplementation is important because the q
84  reduced by competition for nitrogen between symbiotic ectomycorrhizal fungi that associate with plan
85                                Stress in the symbiotic environment may arise from three sources: host
86 mphasizes the role of stress as a cue in the symbiotic environment of plants and animals.
87                     This review examines the symbiotic, evolutionary, proteomic and genetic basis for
88    With the objective of identifying Frankia symbiotic factors we present a novel approach based on b
89  gatekeeper mutants failed to restore proper symbiotic features in a symrk null mutant where rhizobia
90  conserved throughout evolution(5) and their symbiotic functions preserved, at least between monocot
91 S production in bryophytes could result from symbiotic fungal and bacterial partners that could also
92 lase DWARF14-LIKE (D14L) are involved in pre-symbiotic fungal perception.
93 species, yet interactions between plants and symbiotic fungi (mutualists and potential pathogens) aff
94         Applying the species pool concept to symbiotic fungi facilitated a better understanding of ho
95 1 is required to initiate Ca(2+) spiking and symbiotic gene expression in Medicago truncatula roots i
96 t spread by horizontal transfer of a few key symbiotic genes, converting soil bacteria into legume sy
97                        Here we show that the symbiotic genomic idiosyncrasies of ectomycorrhizal basi
98                 We report that selective gut symbiotic gram-negative bacteria were able to disseminat
99                    We previously showed that symbiotic gut bacteria from CPB larvae suppressed jasmon
100                                              Symbiotic gut microbiota is essential for human health,
101                                          The symbiotic gut microbiota play pivotal roles in host phys
102 y plants (UHb) overexpressing the barley non-symbiotic hemoglobin gene HvHb1 that oxidizes NO to NO3(
103 showed that T6SS loci are also widespread in symbiotic human gut bacteria of the order Bacteroidales,
104 identify plant genes required for successful symbiotic infection, we screened an ethyl methanesulfona
105                                          The symbiotic interaction between legume plants and rhizobia
106                                          The symbiotic interaction between legumes and nitrogen-fixin
107  is still a poorly characterized step of the symbiotic interaction, as only a few of the genes induce
108 n also is accumulated during early phases of symbiotic interaction, but the pathways involved have no
109     Other 45 were upregulated throughout the symbiotic interaction, from rhizosphere colonization to
110  to both NF and CK signals critical for this symbiotic interaction.
111 olus vulgaris)-Rhizobium tropici (Rhizobium) symbiotic interaction.
112 hich play a key role in the rhizobium-legume symbiotic interaction.
113 nd drought tolerance; and (3) CO2 effects on symbiotic interactions and eco-evolutionary feedbacks.
114 a widely spread perennial herb used to study symbiotic interactions and physiological mechanisms unde
115 lant hormones regulating shoot branching and symbiotic interactions with arbuscular mycorrhizal fungi
116 ous stages of macronutrient deficiencies and symbiotic interactions with rhizobia and mycorrhiza were
117                              Legumes develop symbiotic interactions with rhizobial bacteria to form n
118 In legume plants, low-nitrogen soils promote symbiotic interactions with rhizobial bacteria, leading
119 g of tissues as well as for host-parasite or symbiotic interactions.
120 ism and cellular physiology, morphology, and symbiotic interactions.
121 tent with a role in fungal morphogenesis and symbiotic interface differentiation, CAZymes over-expres
122 t is essential for the formation of a stable symbiotic interface in both AM and rhizobium symbiosis.
123 Our results show that vesicle traffic to the symbiotic interface is specialized and required for its
124 s a mutual symbiosis that involves a complex symbiotic interface over which nutrients are exchanged b
125 ovides a model for nutrient exchanges at the symbiotic interface, which may guide future experiments.
126  the intracellular fungus from the apoplatic symbiotic interface.
127                        We envisage that the "symbiotic layout" of VisANT can be employed as a general
128 ck of nucleotide biosynthesis capacity and a symbiotic lifestyle.
129 of T. gelatinosa, and perhaps related to its symbiotic lifestyle.
130 also established many novelties due to their symbiotic lifestyle.
131 gration with a bacterial biofilm to obtain a symbiotic-like hybrid - the fabric provides structural f
132 NF induction of the EARLY NODULIN11 (ENOD11) symbiotic marker, while a CK-degrading enzyme (CYTOKININ
133                                              Symbiotic microbes impact the severity of a variety of d
134 in host defense, but less is known about how symbiotic microbes mediate pathogen-induced damage to ho
135               There is growing evidence that symbiotic microbes play key roles in host defense, but l
136  exchange, as cues for cellular responses in symbiotic microbes.
137 nodules, specialized plant organs containing symbiotic microbes.
138 system to accommodate invasive structures of symbiotic microbes.
139                                              Symbiotic microbial communities are critical to the func
140 dy describes a mechanism by which the insect symbiotic microbiome offsets gut immunity to achieve hom
141 ic metals, sponges lack organs but harbour a symbiotic microbiome performing various functions.
142 ect of pathogenic bacteria on a host and its symbiotic microbiota is vital and widespread in the biot
143              Consequently, reconstitution of symbiotic microbiota or IL-1alpha ablation markedly amel
144 alterations caused by pathogenic bacteria on symbiotic microbiota using C. elegans as the model speci
145                                 The trillion symbiotic microorganisms inhabiting the mammalian gastro
146 m pathogens is crucial for plants that allow symbiotic microorganisms to infect and colonize their in
147                         These data support a symbiotic model of collective invasion where phenotypica
148   Comparative analyses of wild-type (WT) and symbiotic mutants in Nod factor receptor5 (nfr5), Nodule
149 nt growth phenotypes seen between WT and the symbiotic mutants in nonsupplemented soil were retained
150 t the root-associated community shift in the symbiotic mutants is a direct consequence of the disable
151 dance can help improve the representation of symbiotic N fixation in Earth System Models.
152  mechanisms and optimize N uptake as well as symbiotic N fixation in roots.
153 lant interactions with mycorrhizal fungi and symbiotic N-fixing microbes.
154 ist on low-input agriculture, enabled by the symbiotic N2 -fixation these legumes perform in associat
155                                              Symbiotic N2 fixation (SNF) brings nitrogen into ecosyst
156 creasing drought frequency, which may affect symbiotic N2 fixation (SNF), a process that facilitates
157                                          Non-symbiotic N2 fixation appears to be the major source of
158 approach to estimate the contribution of non-symbiotic N2 fixation is robust because it focuses on gl
159 mber of transgenic nodules was increased and symbiotic N2 fixation per nodule was elevated, indicatin
160 ism and partitioning processes in support of symbiotic N2 fixation.
161 genus of Actinobacteria abundant in soil and symbiotic niches, the ability to rapidly degrade cellulo
162                             Trees capable of symbiotic nitrogen (N) fixation ('N fixers') are abundan
163                                              Symbiotic nitrogen (N)-fixing trees can drive N and carb
164                                The rarity of symbiotic nitrogen (N)-fixing trees in temperate and bor
165                         Iron is critical for symbiotic nitrogen fixation (SNF) as a key component of
166                                              Symbiotic nitrogen fixation (SNF) occurs in specialized
167 hotosynthesis, induction of root nodules and symbiotic nitrogen fixation and denitrification.
168 f nodule cells and a substantial decrease in symbiotic nitrogen fixation and plant growth.
169 exploring the miR172-mediated improvement of symbiotic nitrogen fixation in common bean, the most imp
170  Iron (Fe) is an essential micronutrient for symbiotic nitrogen fixation in legume nodules, where it
171 nt species with the conspicuous capacity for symbiotic nitrogen fixation in root nodules, specialized
172 has roles within the community not including symbiotic nitrogen fixation.
173  an indirect effect resulting from abolished symbiotic nitrogen fixation.
174  cap and signal motile rhizobia required for symbiotic nitrogen fixation.
175 um cofactor of nitrogenase, is essential for symbiotic nitrogen fixation.
176                             Establishment of symbiotic nitrogen-fixation in legumes is regulated by t
177  a test case, we applied this algorithm to a symbiotic nitrogen-fixing bacterium, Sinorhizobium melil
178                                              Symbiotic nitrogen-fixing trees are thought to provide m
179                             The formation of symbiotic nodule cells in Medicago truncatula is driven
180                  Cytokinins are required for symbiotic nodule development in legumes, and cytokinin s
181 for receptor-mediated cytokinin signaling in symbiotic nodule organogenesis.
182 hylation was found in only a small subset of symbiotic nodule-specific genes, including more than hal
183 f soil and in the iron-rich environment of a symbiotic nodule.
184                                Initiation of symbiotic nodules in legumes requires cytokinin signalin
185 s of postembryonic organs, lateral roots and symbiotic nodules.
186 cibacteria have small genomes and a presumed symbiotic or parasitic lifestyle, but the difficulty in
187 trition to relationships that are commensal, symbiotic, or parasitic.
188                      Antioxidant activity of symbiotic organisms known as lichens is an intriguing fi
189           Food webs are replete with similar symbiotic organisms, and we suspect the predator catalys
190  when using metagenomic DNA from inseparable symbiotic organisms, RADseq loci may belong to any numbe
191 d pectinase expression to be enriched in the symbiotic organs, consistent with enzymatic buildup in t
192 the first evidence (to our knowledge) on the symbiotic origins of eukaryotic cells based on the "thir
193                     Although over 95% of the symbiotic pairs are economically harmless, there are als
194 study elucidates the evolutionary history of symbiotic palaemonids based on a phylogenetic analysis o
195 signal molecules is a key step to select the symbiotic partner.
196 xpression in the presence and absence of the symbiotic partner.
197  to the striking difference in the choice of symbiotic partners by Mexican and Brazilian Mimosa speci
198  meliloti symbiosis, incompatibility between symbiotic partners frequently occurs, leading to the for
199                       They are also critical symbiotic partners in the health of their hosts.
200 and can be used to reinforce the behavior of symbiotic partners that can learn and remember them effe
201  seas is complicated by interactions between symbiotic partners that define stress responses and the
202 lutionary rates in both, rather than single, symbiotic partners.
203 sal mechanisms that drive the recruitment of symbiotic partners.
204 ing interdependencies within this uncultured symbiotic partnership are poorly understood.
205  investigate the role of diverse and mutable symbiotic partnerships in increasing corals' ability to
206 the origins and evolutionary trajectories of symbiotic partnerships remains a major challenge.
207       Organisms across the tree of life form symbiotic partnerships with microbes for metabolism, pro
208 t also impede the establishment of essential symbiotic partnerships.
209 and how its biosynthesis is regulated by the symbiotic pathway.
210 ymbiosis, we tested for correlations between symbiotic persistence and legume distribution, climate,
211 nction to include the negative regulation of symbiotic persistence in host-strain interactions.
212 annual temperatures are associated with high symbiotic persistence in legumes.
213 reads are normal, whereas rhizobia and their symbiotic plant cells become necrotic immediately after
214 s in the formation of root nodules, in which symbiotic plant cells host and harbor thousands of nitro
215 its within the microbial community, a common symbiotic plasmid allows all Rhizobium species to engage
216                                 However, the symbiotic plasmids are extremely similar, with high rate
217 diated by cell-associated matrices including symbiotic polysaccharide (Syp) and cellulose.
218 econd clade, the species use a Nod-dependent symbiotic process and some of them display a profuse ste
219  dynamics of fixers and non-fixers along the symbiotic process in the Cupriavidus taiwanensis-Mimosa
220 rized by the use of a unique Nod-independent symbiotic process.
221 nts of the Nod-dependent and Nod-independent symbiotic processes, and for comparative analysis of ste
222 tructures and were produced by two different symbiotic Pseudonocardia spp. from ants in the genus Apt
223 lated by DOES NOT MAKE INFECTIONS 2, the key symbiotic receptor kinase of the common symbiosis signal
224 racts with and is phosphorylated by the LYK3 symbiotic receptor kinase, negatively regulates rhizobia
225 eraction with and phosphorylation by two key symbiotic receptor kinases, and downstream signaling via
226                                          The symbiotic receptor-like kinases nodulation receptor-like
227 ting proteins have been identified for these symbiotic receptor-like kinases, very little is known ab
228 ntial phosphorylation targets for both these symbiotic receptor-like kinases.
229  to map the phosphorylation site(s) of plant symbiotic receptor-like kinases.
230            In order to better understand the symbiotic relationship and cellular cross-talk between H
231 lement each other to cooperatively shape the symbiotic relationship between commensal bacteria and ma
232 les and SWRs and provide novel evidence of a symbiotic relationship between non-REM and REM stages of
233                                To maintain a symbiotic relationship between the host and its resident
234 my scientific career entailed dissecting the symbiotic relationship between two membrane transporters
235 al microbiome and immune system are in close symbiotic relationship in health.
236 e mechanisms for planted soybean that have a symbiotic relationship with bacteroids in their root nod
237 ccess atmospheric di-nitrogen (N2) through a symbiotic relationship with rhizobia that reside within
238                                  It shares a symbiotic relationship with the bacterium Xenorhabdus ne
239 lved multiple means by which to maintain its symbiotic relationship with the microbiota.
240 ingly, CLK1 overcomes this dilemma through a symbiotic relationship with the serine-arginine protein
241 organisms have co-evolved with the host in a symbiotic relationship.
242   Here I discuss examples of these addictive symbiotic relationships and how they are a likely outcom
243 is reveals numerous instances in which these symbiotic relationships are established by alternative,
244                                              Symbiotic relationships can shape the evolution of the p
245                                              Symbiotic relationships encompass different lifestyles,
246                                              Symbiotic relationships promote biological diversificati
247 genome-scale data from organisms involved in symbiotic relationships remains challenging.
248 Several clades of angiosperms have developed symbiotic relationships with actinorhizal bacteria that
249 diverse group of plants that forms elaborate symbiotic relationships with mycorrhizal fungi, and incl
250  legume to study the establishment of binary symbiotic relationships with nitrogen-fixing rhizobia th
251      Given that nearly all tree species form symbiotic relationships with one of two types of mycorrh
252                   Moreover, soybean can form symbiotic relationships with Rhizobium bacteria to fix a
253        Fungus-growing ants engage in complex symbiotic relationships with their fungal crop, speciali
254 ep environments, suggests a broader range of symbiotic relationships within AOM consortia than previo
255                     But while promoting such symbiotic relationships, plants must restrict the format
256 clade of legumes, indicating a host-specific symbiotic requirement for Mn(2+) transport.
257                      These two pre-infection symbiotic responses have been used in combination to sho
258  unable to nodulate, but still exhibit early symbiotic responses including rhizobial infection.
259 roduce, followed by the activation of either symbiotic responses that promote microbial colonization
260 support that MtCEP1 modulates EIN2-dependent symbiotic responses.
261 r nuclear Ca(2+) oscillations and subsequent symbiotic responses.
262                                              Symbiotic rhizobia in legumes account for a large portio
263                          In this context the symbiotic roles of iron trichloride and oxygen in the gu
264  demonstrate uncoupling of symbiosis and the symbiotic root developmental signalling during pre-symbi
265 carboxymethylcellulase, and Cel5A), from the symbiotic rumen Bacteroidetes Prevotella bryantii B14.
266 f the poplar rhizosphere showed evidence for symbiotic sharing of nutrients between the plant and the
267 o our knowledge, a novel common component of symbiotic signaling integrating signal perception throug
268 ependent increase in nodulation requires the symbiotic signaling pathway and ETHYLENE INSENSITIVE2 (E
269 + genotypes included orthologs to some known symbiotic signaling pathway genes, such as NFR5, NSP2, N
270        Different deficiencies at upstream of symbiotic signaling pathway were revealed in the two nod
271       In conclusion, the biologically active symbiotic signals secreted by Frankia appear to be chemi
272  promote ENOD11 expression in the absence of symbiotic signals.
273 nts, and the mechanism of iron uptake within symbiotic soybean root nodules is unknown.
274                                              Symbiotic species are no longer able to degrade plant ce
275 ance hole size barely changes in specialized symbiotic species, but evolves rapidly once symbiosis wi
276 mostly free-living shrimp, albeit with a few symbiotic species.
277 t that NCR peptides are host determinants of symbiotic specificity in M. truncatula and possibly in c
278 800, that has evolved the ability to control symbiotic specificity.
279 nscription factors may have implications for symbiotic stability, endophyte distribution in the plant
280 ion pattern intermediate between the typical symbiotic state and the aposymbiotic state.
281 sses apparently only occur from a generalist symbiotic state.
282 e regulatory protein NF-kappaB and cnidarian symbiotic status.
283 rge and primarily parasitic communities, and symbiotic sternorrhynchans as examples of generally smal
284 at host-associated niches have selected some symbiotic Streptomyces for increased cellulose degrading
285 basidiomycete Hebeloma cylindrosporum before symbiotic structure differentiation with Pinus pinaster.
286 udy provides the first evidence of extensive symbiotic supplementation of EAA by microbial gut symbio
287  Specifically, we have limited insights into symbiotic syntroph and methanogen ('syntrophy') acid deg
288 norhizobium meliloti and Medicago truncatula symbiotic system, we previously described several natura
289 ively may contribute to the stability of the symbiotic system.
290 ta and shearinines in the fungus-growing ant symbiotic system.
291                                         Both symbiotic systems are lineage specific and differ in the
292  genes in symbiotic systems, 136 fungi-fungi symbiotic systems were built up by co-culturing seventee
293 nvestigate the expression of silent genes in symbiotic systems, 136 fungi-fungi symbiotic systems wer
294  expect it to be applicable to other similar symbiotic systems, especially other nodule-forming legum
295 olecules, which can be transposable to other symbiotic systems.
296 s that have shaped evolution of this complex symbiotic trait.
297 mploys the promoter of RAM1 as integrator of symbiotic (transmitted via CCaMK and CYCLOPS) and hormon
298       For example, Late Triassic corals have symbiotic values, which tie photosymbiosis to major cora
299 disposed to different ecological strategies (symbiotic versus free-living lifestyles) depending on th
300    In essence, she presented a comprehensive symbiotic view of eukaryotic cell evolution (eukaryogene

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