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1 l residents and the scientific community off-guard.
2 corded their foraging behaviour during chick guarding.
3  to modulate aggression associated with mate guarding.
4  fluids and represent forms of chemical mate guarding.
5 pective cohort study of the US Army National Guard (2009-2014).
6 hrorynchus) is Askari wa kifaru, the rhinos' guard [6].
7                          As compared to nest guards, A. cerana foragers produced 3.38 fold higher lev
8 ctive contribution through which hepatocytes guard against aberrant cytosolic RLR-RNA-sensing pathway
9 ring the ongoing SARS-CoV-2 pandemic, and to guard against airborne transmitted diseases.
10 hip to help maintain glucose homeostasis and guard against hypoglycemia.
11                             Thus, efforts to guard against inbreeding effects in populations of endan
12   The uterus is a remarkable organ that must guard against infections while maintaining the ability t
13  distributions of parameters that can better guard against misinterpretation of results, as compared
14 nes to access social support, which may help guard against negative effects of in-person social depri
15  a three-dimensional (3D) optical lattice to guard against on-site interaction shifts.
16 lls serve as sentinels in barrier tissues to guard against previously encountered pathogens.
17  between polymorphic alleles, Dmc1 must also guard against recombination between divergent sequences.
18                                           To guard against spurious association, we controlled for po
19 indings are replicated before publication to guard against subsequent replication failures.
20 ceptor, supports circadian clock function to guard against the detrimental effects of circadian stres
21 at propagate by sexual reproduction actively guard against the fertilization of an egg by multiple sp
22 gnizing issues that need to be considered to guard against time-driven confounders.
23  through extensive sensitivity analyses that guard against various model assumption violations.
24 GCR are physiologically relevant events that guard against wasteful oxygen consumption and inappropri
25                       The germline genome is guarded against invading foreign genetic elements by sma
26 , we hypothesize that global p53 activity is guarded against loss of any one regulatory partner, allo
27 cin appears to be widespread and needs to be guarded against with scepticism and rigor.
28  Pak2 as an important signaling molecule for guarding against aberrant immune responses through regul
29 perature and the retention of bodily fluids, guarding against external stresses and mediating the sen
30 matically analyzing nongenetic data sets and guarding against false positives.
31 nuously balance Hsf1 and Ifh1 activity, thus guarding against proteotoxic stress during ribosome asse
32 our initial hypothesis that H223 protonation guards against early refolding.
33 choice, 53BP1 functions as a DSB escort that guards against illegitimate and potentially tumorigenic
34               This perpetual changing of the guard allows the pathogen to remain one step ahead of th
35 hree male strategies - multiple mating, mate guarding and paternal care - in response to partner avai
36 ng a discrete transition between continence (guarding) and micturition (augmenting) reflexes.
37                      The visual prognosis is guarded, and eyes may require multiple surgeries to pres
38 ion(s) such as sight hunting, scent hunting, guarding, and companionship.
39 ations such as sight hunting, scent hunting, guarding, and companionship.
40 As) are a class of small noncoding RNAs that guard animal genomes against mutation by silencing trans
41 e effective than non-lethal strategies, with guard animals showing the most potential among the non-l
42                   Passive mechanisms of mate guarding are used by males to promote sperm precedence w
43  high-throughput screening, revealing CRISPR GUARD as a rapidly implementable strategy to improve the
44                             Optimism remains guarded as additional evidence accumulates.
45 ide RNA Assisted Reduction of Damage (CRISPR GUARD) as a method for protecting off-targets sites by c
46 l interactions between entering foragers and guards at the hive entrance.
47 ance defensive signalling by also attracting guard bees and that the visual movements of appropriate
48 ces between African and European forager and guard bees are depleted in widely conserved genes, indic
49  brachial artery (BAO) induces increased paw-guarding behaviors, mechanical hypersensitivity, and dec
50 In summary, we identified a "changing of the guards" between small RNA types that may systemically af
51 e SLIM by rf fields in conjunction with a DC guard bias, enabling essentially lossless TW transmissio
52  and aggregation of proteins unless they are guarded by chaperone systems.
53 cently described cellular processes that are guarded by the host.
54      Generally, we found that nests were not guarded by the same male for the whole provisioning seas
55                                     RIN4 is 'guarded' by several independently evolved NLRs from vari
56 tamembrane domain acts as a master regulator guarding cadherin stability.
57     While DELLA had no effect on ABA levels, guard cell ABA responsiveness was increased in S-della a
58 ces stomatal closure via QUAC1/ALMT12 and/or guard cell ABA synthesis.
59 o red light is correlated with a decrease in guard cell abscisic acid content and an increase in jasm
60 to darkness is mediated by reorganisation of guard cell actin filaments, a process that is finely tun
61 pecies Kalanchoe fedtschenkoi, we found that guard cell anion channel activity, recorded under voltag
62  the hormone that leads to the activation of guard cell anion channels by the protein kinase OPEN STO
63 the molecular basis for circadian control of guard cell aperture, we used large-scale qRT-PCR to comp
64 ic Gbeta subunit, AGB1, is required for four guard cell Ca(o) responses: induction of stomatal closur
65  extracellular ATP and of leaf mesophyll and guard cell chloroplasts during light-to-low-intensity bl
66 bitors and suggest a mechanism through which guard cell CO2 signaling controls plant water management
67 H LEAF TEMPERATURE 1 (HT1)-a central node in guard cell CO2 signaling-and that MPK12 functions as an
68          This process is mainly regulated by guard cell control of the stomatal aperture, but recent
69 tants to explore the impact of clustering on guard cell dynamics, gas exchange, and ion transport of
70 ulose and xyloglucan are required for normal guard cell dynamics.
71 ls and stomatal responses require reversible guard cell elongation and contraction.
72 mechanical, pectin-based pinning down of the guard cell ends, which restricts increase of stomatal co
73                    High temperature promotes guard cell expansion, which opens stomatal pores to faci
74  digesting enzymes, coupled with bioassay of guard cell function) plus modeling lead us to propose th
75 highlight the role of polar reinforcement in guard cell function, which simultaneously improves our u
76                            The regulation of guard cell genes involved in controlling stomatal moveme
77                 We show that a range of core guard cell genes, including SPCH/MUTE, SMF, and FAMA, ma
78 cal link between OsGRXS17, the modulation of guard cell H2O2 concentrations, and stomatal closure, ex
79 ]i oscillations and analyze their origins in guard cell homeostasis and membrane transport.
80 tool with which to explore the links between guard cell homeostasis, stomatal dynamics, and foliar tr
81 nel by the protein kinases OPEN STOMATA1 and GUARD CELL HYDROGEN PEROXIDE-RESISTANT1 (GHR1) in Xenopu
82 ctors can utilize intrinsic HDAC activity to guard cell identity by repressing lineage-inappropriate
83  tissue, and that H3K27me3 dynamics regulate guard cell identity.
84 ing potassium (K(+) ) nutrition and a robust guard cell K(+) inward channel activity is considered cr
85 e xyloglucan, stomatal apertures, changes in guard cell length, and cellulose reorganization were abe
86 s, promotes rosette expansion, and modulates guard cell mechanics in adult plants.
87 y, CO2, and light, but without connection to guard cell mechanics.
88  profiling and identification of Arabidopsis guard cell metabolic signatures in response to red light
89 ints to multiple processes and plasticity in guard cell metabolism that enable these cells to functio
90 rther exploring and potentially manipulating guard cell metabolism to improve plant water use and pro
91 eview some of the osmoregulatory pathways in guard cell metabolism, genes and signals that determine
92                       Therefore, analysis of guard cell metabolites is fundamental for elucidation of
93                      The red-light-modulated guard cell metabolome reported here provides fundamental
94 indings reveal that high temperature-induced guard cell movement requires components involved in blue
95  than the wild type, reduced light-dependent guard cell opening, and reduced water loss, with aw havi
96                 Moreover, the differences in guard cell oscillator function may be important for the
97  misexpressed CCA1 Our results show that the guard cell oscillator is different from the average plan
98 onsistent with a disabled active response of guard cell osmotic pressure.
99                   FOCL1-GFP localizes to the guard cell outer cuticular ledge and plants lacking FOCL
100                  The regulation of the GORK (Guard Cell Outward Rectifying) Shaker channel mediating
101  Arabidopsis plants overexpressing circGORK (Guard cell outward-rectifying K(+) -channel) were hypers
102 ata and developed a biomechanical model of a guard cell pair.
103 ctance measurements using intact plants, and guard cell patch-clamp experiments were performed.
104 e the possible origins of sucrose, including guard cell photosynthesis, and discuss new evidence that
105 dence that HG delivery and modification, and guard cell pressurization, make functional contributions
106 ic signatures in response to ABA in B. napus guard cell protoplasts.
107 layers to the increasingly complex system of guard cell regulation.
108 of protoplasts, firmly establishing a direct guard cell response to red light.
109 -induced stomatal opening arises from direct guard cell sensing of red light versus indirect response
110 re reject cycadalean affinities, whereas its guard cell shape and stomatal ledges are angiospermous.
111 ew functional role of small GTPase, NOG1, in guard cell signaling and early plant defense in response
112 evidence that the regulatory patterns of key guard cell signaling genes are linked with the character
113                  Specially, NOG1-2 regulates guard cell signaling in response to biotic and abiotic s
114 etabolites is fundamental for elucidation of guard cell signaling pathways.
115 posttranslational modifications to fine-tune guard cell signaling.
116                A lack of correlation between guard cell size and DNA content, lack of arabinans in ce
117                         Evidence from fossil guard cell size suggests that polyploidy in Sequoia date
118                        Our results show that guard cell starch degradation has an important role in p
119 cs to define the mechanism and regulation of guard cell starch metabolism, showing it to be mediated
120                         Diel rescheduling of guard cell starch turnover in K. fedtschenkoi compared w
121  transport, metabolism, and signaling of the guard cell to define the water relations and transpirati
122 bryophyte monophyly and demonstrate that the guard cell toolkit is more ancient than has been appreci
123 no effect on the induction of heat-sensitive guard cell transcripts, supporting the existence of an a
124 by a dynamic, mechanistic model that assumes guard cell turgor changes in concert with leaf turgor in
125 n in the proteins responsible for regulating guard cell turgor.
126 ends on changes in osmolyte concentration of guard cell vacuoles, specifically of K(+) and Mal(2-) Ef
127 tic solutes that drive reversible changes in guard cell volume and turgor.
128      Combined experimental data (analysis of guard cell wall epitopes and treatment of tissue with ce
129      Hence, PME34 is required for regulating guard cell wall flexibility to mediate the heat response
130                  Restoration of PME6 rescues guard cell wall pectin methyl-esterification status, sto
131  these results provide new insights into how guard cell walls allow stomata to function as responsive
132 chanisms for how stomatal pores form and how guard cell walls facilitate dynamic stomatal responses r
133 e signals suggesting that the flexibility of guard cell walls is impaired.
134 opening, we have generated SGC (specifically guard cell) Arabidopsis (Arabidopsis thaliana) plants in
135 s well as diel changes in their abundance in guard cell-enriched epidermis and mesophyll cells from l
136               We have characterized FOCL1, a guard cell-expressed, secreted protein with homology to
137  transport across the membrane system of the guard cell.
138                                 Although the guard-cell-signaling pathway coupling blue light percept
139    Expressing S-della under the control of a guard-cell-specific promoter was sufficient to increase
140 ) was overexpressed under the control of the guard-cell-specific promoter, GC1.
141 ary cells (SCs) flanking two dumbbell-shaped guard cells (GCs)-is linked to improved stomatal physiol
142                                  We measured guard cells across the genera with stomata to assess dev
143              A new study makes it clear that guard cells also metabolise starch to accelerate opening
144  Stomatal pores are formed between a pair of guard cells and allow plant uptake of CO2 and water evap
145  localized synthesis of stilbenes in stomata guard cells and cell walls is induced by P. viticola inf
146                                              Guard cells and epidermal cells of hornworts show striki
147 (2)-induced activation of Ca(2+) channels in guard cells and is required for stomatal closure.
148 receptor JAZ2 is constitutively expressed in guard cells and modulates stomatal dynamics during bacte
149 he increased number of small cells below the guard cells and of fully developed stomata indicated tha
150 ne localization patterns when imaged in both guard cells and pollen.
151 ase gene, PME6, which is highly expressed in guard cells and required for stomatal function.
152 n involves limited separation between sister guard cells and stomatal responses require reversible gu
153  was observed in the whole stomatal complex (guard cells and subsidiary cells), root vasculature, and
154      Although it has long been observed that guard cells are anisotropic due to differential thickeni
155                                    The focl1 guard cells are larger and less able to reduce the apert
156                                     Stomatal guard cells are pairs of specialized epidermal cells tha
157              Here, we show that the walls of guard cells are rich in un-esterified pectins.
158                                     Stomatal guard cells are widely recognized as the premier plant c
159                         Starch is present in guard cells at the end of night, unlike in the rest of t
160 ether pore formation is an outcome of sister guard cells being pulled away from each other upon turgo
161 e [ADGase]) or retain starch accumulation in guard cells but are starch deficient in mesophyll cells
162 diating a massive K(+) efflux in Arabidopsis guard cells by the phosphatase AtPP2CA was investigated.
163 blished that the circadian oscillator within guard cells can contribute to long-term WUE.
164                                              Guard cells collapse inwardly, increase in surface area,
165 pare circadian oscillator gene expression in guard cells compared with the "average" whole-leaf oscil
166 hat has been implicated in anionic flux from guard cells controlling the stomatal aperture.
167 utside inwardly and continues to do so after guard cells die and collapse.
168 tomic force microscopy, that although mature guard cells display a radial gradient of stiffness, this
169                                              Guard cells dynamically adjust their shape in order to r
170             In silico analysis revealed that guard cells express all the genes required for beta-oxid
171 b1 and Glb2 scavenge NO produced in stomatal guard cells following ABA supply; plants overexpressing
172  meeting these challenges and to engineering guard cells for improved water use efficiency and agricu
173                                              Guard cells form stomatal pores that optimize photosynth
174    Here, we characterize transcriptomes from guard cells in C3 Tareneya hassleriana and C4 Gynandrops
175 predominantly in the phloem-loading zone and guard cells in leaves, root vasculature, and shoot apica
176                       Decreased flavonols in guard cells in the anthocyanin reduced (are) mutant and
177 ion across the bundle sheath, mesophyll, and guard cells in the C4 leaf.
178 to the characteristic patterning of stomatal guard cells in the context of a growing leaf.
179                              The position of guard cells in the epidermis is ideally suited for cellu
180   Further, upon initiation of reprogramming, guard cells induce H3K27me3-mediated repression of a reg
181                             The shape of the guard cells influenced the rapidity of response and the
182 it, the capacity for lateral displacement of guard cells into neighboring epidermal cells, are crucia
183 mponent of phototropin signaling in stomatal guard cells is discussed.
184  leaves, suggesting that the SA signaling in guard cells may be independent from other cell types.
185                                              Guard cells of are show greater ABA-induced closure than
186 photosynthesis were more highly expressed in guard cells of C4 compared with C3 leaves.
187 +) (K(+) (in) ) channels was impaired in the guard cells of cipk23 mutants, whereas activation of the
188                Reductions in LD abundance in guard cells of the lycophyte Selaginella suggest that TA
189 dants, higher levels of ROS were detected in guard cells of the tomato are mutant and lower levels we
190 plants where ABA biosynthesis was rescued in guard cells or phloem companion cells of an ABA-deficien
191 epted that differential radial thickening of guard cells plays an important role in the turgor-driven
192                                              Guard cells shrink and close stomatal pores when air hum
193                                     Stomatal guard cells surround pores in the epidermis of plant lea
194 ynthetic, light-gated K(+) channel BLINK1 in guard cells surrounding stomatal pores in Arabidopsis to
195 he regulatory networks and ion fluxes in the guard cells surrounding the stomatal pore [2].
196  but not JA-dependent response, is faster in guard cells than in whole leaves, suggesting that the SA
197  across the plasma and vacuolar membranes of guard cells that drive stomatal movements and the signal
198 tails of the local separation between sister guard cells that give rise to the stomatal pore or how f
199              Stomata are defined by pairs of guard cells that perceive and transduce external signals
200        Each stomate is bordered by a pair of guard cells that shrink in response to drought and the a
201  on changes in turgor pressure acting within guard cells to alter cell shape [1].
202 ) increases reactive oxygen species (ROS) in guard cells to close Arabidopsis (Arabidopsis thaliana)
203  negative regulator of GA signaling, acts in guard cells to promote stomatal closure and reduce water
204        The importance of ABA biosynthesis in guard cells versus vasculature for whole-plant stomatal
205              Stomata are formed by a pair of guard cells which have thickened, elastic cell walls to
206 division to differentiate highly specialized guard cells while maintaining a stem cell population [1,
207 dest alteration of Ca transient frequency in guard cells, associated with the absence of Ca-induced s
208 Mal inhibited the anion current of Kalanchoe guard cells, both in wild-type and RNAi mutants with imp
209 The accumulation of flavonol antioxidants in guard cells, but not surrounding pavement cells, was vis
210                                     In plant guard cells, extracellular calcium (Ca(o) ) is as strong
211 ntified 390 distinct metabolites in B. napus guard cells, falling into diverse classes.
212 time-dependent outward potassium currents in guard cells, higher rates of water loss through transpir
213 d an elevation in H2O2 production within the guard cells, increased sensitivity to ABA, and a reducti
214 l responsible for the release of malate from guard cells, is essential for efficient stomatal closure
215 e main inward rectifying channels present in guard cells, mediating K(+) influx into these cells, res
216 uate the current literature on metabolism in guard cells, particularly the roles of starch, sucrose,
217 nase inhibition decreases FRET efficiency in guard cells, providing direct experimental evidence that
218 inating from the appressoria formed over the guard cells, was thought to require light to induce natu
219                                              Guard cells, which flank the stomata, undergo adjustment
220 ith the turgor pressure of the epidermis and guard cells, which ultimately determine stomatal pore si
221 the expression of other transporter genes in guard cells, which ultimately led to improved growth.
222 We quantified 223 metabolites in Arabidopsis guard cells, with 104 found to be red light responsive.
223 f stiffness, this is not present in immature guard cells, yet young stomata show a normal opening res
224 ll pores on plant leaves and stems formed by guard cells.
225 on of NCED3, a key step of ABA synthesis, in guard cells.
226  which is expressed in expanding tissues and guard cells.
227 ced by abscisic acid and highly expressed in guard cells.
228  (C3 plants), bundle-sheath (C4 plants), and guard cells.
229 hich is one of the phototropin substrates in guard cells.
230 y a reduced accumulation of K(+) ions in the guard cells.
231 n of signal amplification and specificity in guard cells.
232 rimary and specialized metabolic pathways in guard cells.
233 ith its putative paralog SINE2, expressed in guard cells.
234 regulation of salicylic acid (SA) pathway in guard cells.
235 dynamics, gas exchange, and ion transport of guard cells.
236 efense and is linked to hormone signaling in guard cells.
237 g autonomous red light signaling pathways in guard cells.
238 xpression from bundle sheath to mesophyll to guard cells.
239 he activity of AtCLCa in vivo in Arabidopsis guard cells.
240 idence that basal SnRK2 activity prevails in guard cells.
241 in N. benthamiana leaf cells and Arabidopsis guard cells.
242 tion induces LCBK1 expression, especially in guard cells.
243 to plants increased flavonol accumulation in guard cells; however, no flavonol increases were observe
244 their hosts, wherein specific host proteins 'guard' central cellular processes and trigger inflammato
245     Within the circulatory system, platelets guard circulating tumor cells (CTCs) from immune elimina
246  liquid chromatography (LC)-MS, the use of a guard column (i.e., fast chromatography) may be sufficie
247                         Thus, Rcr3 acts as a guarded decoy in this interaction, trapping the fungus i
248 Finally, we create an online tool for CRISPR GUARD design.
249                 Innate lymphoid cells (ILCs) guard epithelial tissue integrity during homeostasis, bu
250                  PRINCESS leverages Software Guard Extensions (SGX) and hardware for trustworthy comp
251 y checkpoint (SAC), a signaling network that guards fidelity of chromosome segregation.
252 ican red squirrels (Tamiasciurus hudsonicus) guard food hoards, an extended phenotype that typically
253 ersus 40% eyes, provided no safety margin to guard foveola in 17% versus 33%, and did not entirely co
254 restriction of resident genomic parasites to guard genome integrity.
255 report here our discovery of a new member in guarding genome stability at replication forks.
256                                        Royal Guard has the potential to improve malaria vector contro
257     Thus, the FoxA factors act continuously, guarding hepatic enhancer activity throughout adult life
258                         Furthermore, loss of guard HF cycling suggests that in this particular hair t
259  and is required for zigzag hair bending and guard HF cycling.
260 lution of maternal care, in the form of nest guarding, in a single population of long-tailed sun skin
261                                         Male guarding increases provisioning of nests because females
262                  In laboratory assays, Royal Guard induced > 80% mortality and > 90% blood-feeding in
263 es through the pyriproxyfen component; Royal Guard induced 83% reduction in oviposition and 95% reduc
264                                        Royal Guard is a new insecticide-treated bed-net incorporated
265 ugh, we found that paternity of offspring by guard males is extraordinarily low (10% of offspring).
266 rection in the sensor is reversed before the guard/marker segments escape.
267 n this and other moth species, chemical mate guarding may also impose selection pressure on the long-
268 ast exposure in a sample of Florida National Guard members (1,443 deployed to Operation Enduring Free
269 ested convergence between the MPK3- and MPK4-guarding modules.
270 terized cellular proliferation and apoptosis guards (NF-kappaB, Bcl-2 and p53) in these NPs-treated c
271 st that the complement system utilizes C3 to guard not only extracellular but also the intracellular
272 ship to attract females to enter a nest they guard or cuckoldry during which they steal fertilization
273 exam showed diffuse tenderness without mass, guarding or rebound while reminder of physical exam was
274 or different tasks such as hunting, herding, guarding, or companionship.
275              However, we show that long-term guarding performed by a single male does increase patern
276 e insurgent group, on Myanmar police, Border Guard Police, and military posts, killing 12 security pe
277 ence included but were not limited to Border Guard Police, Myanmar military, and Rakhine extremists.
278 ildren and systemic mastocytosis with a more guarded prognosis in adults who may also harbor other ge
279          Carcinoma of the gall bladder has a guarded prognosis with predominant sites of involvement
280                                       CRISPR GUARD reduces off-target mutagenesis while retaining on-
281 ternal urethral sphincter (EUS) contraction (guarding reflex) to maintain continence.
282 evoked tonic EUS activity, indicative of the guarding reflex, that was proportional to the urethral f
283                    We confirm that oxpeckers guard rhinos and the importance of depredation, not soci
284                                 The use of a guard ring electrode in the detector reduces the crystal
285 st Practice Advice 10: Celiac serology has a guarded role in the detection of continued intestinal in
286 hus, the way we move unmasks one of our well-guarded secrets: how much we value the thing we are movi
287 from the principal flow stream by immiscible guard segments, typically a fluorocarbon (FC) liquid, of
288 rowth factor-beta (TGF-beta) signals in safe-guarding specific Treg cell functions.
289 e Fe-S cluster enzyme GRXS17 is an essential guard that protects proteins against moderate heat stres
290 nnervating neurons (~100 neurons/mouse) that guard the airways against assault.
291  to break regulatory mechanisms that usually guard the host against autoimmune diseases.
292            Specifically, we find that ravens guard their caches against discovery in response to the
293 F programs, and thus how parents' ability to guard their children's health is affected by structural
294 d short palindromic repeat (CRISPR)-Cas loci guard their hosts with an adaptive immune system against
295 esistant An. gambiae sl in Cove Benin, Royal Guard through the pyrethroid component induced comparabl
296 nition receptor that normally functions as a guard to trigger capase-1 inflammasome assembly in respo
297 chemical toggle switch that acts as a sizer, guarding transitions into and exit from a phase of cell-
298 stetric and newborn care and capable of safe-guarding uncomplicated births.
299 es (Helogale parvula) [5]; sentinels (raised guards) use various vocalisations to provide social info
300  outcome in Nocardia endophthalmitis is very guarded when presenting vision is poor.

 
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