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1 ole and the methyl terminal located near the equator).
2 tial history of fossil sampling north of the equator.
3  frequent in countries more distant from the equator.
4 e neutron star, is moving toward the stellar equator.
5 pped the spindle pole from moving toward the equator.
6  three nonrandom positions around the pollen equator.
7  attached triazolyl ammonium group along its equator.
8 ed by substantial range shifts away from the equator.
9 d to place cytokinetic nodes around the cell equator.
10 n for why biodiversity increases towards the equator.
11 in the Northern Hemisphere than south of the equator.
12  thick spanning the EOM origins to the globe equator.
13 s three planets are aligned with the stellar equator.
14 ity of ecological interactions closer to the equator.
15 cillations back and forth across the spindle equator.
16 /- 11 kilometers northward of the geographic equator.
17 s assemble and chromosomes are pushed to the equator.
18 e that an ecosystem is located closer to the Equator.
19 d for localization of myosin at the cellular equator.
20 n antiparallel "barrel" array at the spindle equator.
21 les and along a diffuse cortical band at the equator.
22 cle and initiate differentiation at the lens equator.
23 e and movement toward both the poles and the equator.
24 e in the northern North Atlantic towards the Equator.
25 voir of factors (including FGF) for the lens equator.
26 efore cytokinesis, then elevated only at the equator.
27 es S) (p < 0.001), and remained low near the equator.
28 ation of the small GTPase, RhoA, at the cell equator.
29 tastrophe frequencies, decreasing toward the equator.
30  aseismic section of the megathrust near the equator.
31 bers develop in a shear zone paralleling the equator.
32 eturns cold deep waters southward across the Equator.
33 e there is no variation in day length at the Equator.
34 ee species in Amazonian rainforests near the Equator.
35 y pushing chromosome arms toward the spindle equator.
36  (32)P-gamma-ATP, was detectable only at the equator.
37 ous cavity through a scleral incision at the equator.
38 red at nearly every division septum and cell equator.
39 nificantly correlated with distance from the equator.
40 valents had positions at or near the spindle equator.
41 nt pathways that transported aurora B to the equator.
42  on opposite sides of the eye's midline, the equator.
43  to define EOM tendons anterior to the globe equator.
44 es of movements that bring it to the spindle equator.
45 destabilized and aurora B dispersed from the equator.
46 longitude and concentrated near the magnetic equator.
47 udinal range of species decreases toward the equator.
48 ed with latitude both north and south of the equator.
49 des Mountains of South America straddles the equator.
50 quator and is thinnest just posterior to the equator.
51 s did not show appreciable movement from the equator.
52 ega with radius across the tachocline at the equator.
53  approximately 11 sites around each cellular equator.
54 celerating the zonal wind component near the equator.
55 it encountered as it was moved away from the equator.
56 ly reoriented actin filaments along the cell equator.
57 on of spindle microtubules that point to the equator.
58  436b is nearly perpendicular to the stellar equator.
59 lows from the Galapagos Archipelago near the Equator.
60 maining stable along range edges nearest the equator.
61 at Gef3 colocalizes with septins at the cell equator.
62 proximal chromosomes specifically toward the equator.
63  as cell shape and cortical flows toward the equator.
64 ople currently living in Africa south of the Equator.
65 cts with small particles as it traversed the equator.
66 d on average around six degrees north of the Equator.
67 reased latitudinal range sizes closer to the equator.
68  Asians living at latitudes distant from the equator.
69 7), representing oblique imaging of the lens equator.
70 t the clonal borders, giving rise to ectopic equators.
71 Myo2 appears in cytokinetic nodes around the equator 10 min before spindle pole body separation (cell
72 lantic oceans, confined to a strip along the equator (30 degrees N and 30 degrees S).
73  compared across latitudes, ranging from the equator (+5 degrees N) to the subtropics (-35 degrees S)
74 and most were located between the macula and equator (70%).
75 mm, and were mostly located posterior to the equator (91%).
76                  These factors make Saturn's equator a natural laboratory to test models of jets in g
77 ter cells, they align at the mitotic spindle equator, a process known as chromosome congression.
78  congression of chromosomes near the spindle equator, a process mediated by dynamic kinetochore micro
79  its surface warming occurs mostly along the Equator, a region without TC activity.
80          A metaphase position at the spindle equator, according to the model, requires equal numbers
81 s when a chromosome is left near the spindle equator after anaphase onset (lagging chromosome).
82 s failed to align efficiently at the spindle equator after simultaneous perturbation of Kid and NuMA
83 orts monooriented chromosomes to the spindle equator along kinetochore fibers of already bioriented c
84 indle midzone and became concentrated at the equator along midzone microtubules.
85 d chromosomes could glide toward the spindle equator alongside kinetochore fibers attached to other a
86 g for key factors, such as distance from the equator, altitude, climate and physicochemical soil prop
87 the Pacific temperature contrast between the equator and 32 degrees N has evolved from approximately
88 se positions near the equator or between the equator and a pole.
89 ce of misorientation relative to the spindle equator and abnormal oscillatory behavior.
90  fluorescence in the choroid extended to the equator and adjacent sclera.
91  glaucoma were excised 3 mm posterior to the equator and affixed to an inflation chamber.
92 pture mechanism: type 2 nodes diffuse to the equator and are captured by stationary type 1 nodes.
93 s, sister chromatids congress to the spindle equator and are subsequently segregated via attachment t
94 sin were broadly distributed around the cell equator and assembled into a contractile ring through st
95    Such changes are most pronounced near the equator and at high latitudes and are a substantial frac
96 ized throughout the spindle, sparsely at the equator and at higher concentrations near the poles.
97 ficient to generate furrows at both the cell equator and cell poles, in both metaphase and anaphase.
98 s could explain how birds cross the magnetic equator and deal with declination.
99 s richness of herbivores were highest at the equator and decreased with increasing latitude, both nor
100 ric currents constantly flowing out from the equator and entering the anterior and posterior poles.
101 n both HNLC and oligotrophic waters near the Equator and further south, whereas nitrogen and zooplank
102 ye thins progressively from the fovea to the equator and is thinnest just posterior to the equator.
103 One cline was generated by high UVR near the equator and led to the evolution of dark, photoprotectiv
104 n Z (MapZ) forms ring structures at the cell equator and moves apart as the cell elongates, therefore
105 greatest at reef ecosystems proximate to the equator and northern-most locations, showing little sync
106             The RVPT was located between the equator and ora serrata in all patients.
107 ng effects (>0.3 W m(-2)) are found near the Equator and over tropical continents.
108 ng controlled cortical disassembly along the equator and possibly global cortical contraction.
109 onent vanishes were used to map the magnetic equator and reveal an offset of 484 +/- 11 kilometers no
110  meridional temperature gradient between the equator and subtropics was greatly reduced, implying a v
111 on subunits (n = 15) or at sites between the equator and the extracellular domain in the alpha-subuni
112                                    The Sun's equator and the planets' orbital planes are nearly align
113 t microscopy (IFM) located MreCD(Spn) to the equators and septa of dividing cells, similarly to the P
114 orthern hemisphere, approximately 1 near the equator, and </=1 in the southern hemisphere.
115 es generate strands spread widely beyond the equator, and growing strands depend on random encounters
116             Of tumors located in the macula, equator, and periphery, 15 (36.6%), 26 (36.6%), and 13 (
117  or inclined with respect to the host star's equator, and the population of giant planets orbiting cl
118 xhibiting lagging chromosomes at the spindle equator, and this percentage was enhanced to 17.55% afte
119 ick spanning the orbit from origins to globe equator, and used as indicators of contractility.
120 es at centrosomes and spreads to the spindle equator; and (b) any remaining cytoplasmic cyclin B is d
121 d that the collective subunit motions at the equator are asymmetric during the AChR gating isomerizat
122 y occur because many countries closer to the equator are caught in the gap between the demise of trad
123  central claim that "countries closer to the equator are generally more violent." We point to the lac
124 ying mixing across density surfaces near the Equator are less than 10% of those at mid-latitudes for
125  We document that shorter distances from the equator are linked to higher national narcissism levels,
126 sembly and disassembly of the CR at the cell equator are poorly understood.
127 nward by 3.0 millimeters, and sites near the equator are pulled northward by 1.5 millimeters.
128 AC) model proposes that MTs nucleated at the equator are slid outward by the cooperative actions of t
129   The mean position of the ITCZ north of the Equator arises primarily because the Atlantic Ocean tran
130  southern tip of Africa and moves toward the equator as a western boundary current.
131 cline and the N/P ratio increases toward the equator as average temperature and growing season length
132 ng a special case and latitudes north of the equator as being pivotal in the evolution of highly spec
133  specifies a broad band of cortex around the equator as the division site.
134 -range signaling during the formation of the equator, as defined by the presence of an organized arra
135 o warm water parcels that travel towards the Equator at shallow depths and then resurface in the east
136 mpanied a northward shift of Earth's thermal equator at the onset of an abrupt climate change 14.6 ky
137 on interpolar MTs move away from the spindle equator at the same rate as the poles, consistent with M
138 creases with mean temperature and toward the equator, because P is a major limiting nutrient in older
139 he congression of chromosomes to the spindle equator before the cell initiates anaphase.
140  than in the tropics, with distance from the equator being the best predictor of phylogenetic communi
141  per year, in a belt concentrated around the equator beneath the Atlantic hemisphere.
142 required to enrich ring proteins at the cell equator but instead regulate formation of a compact matu
143 pensis) that breed, only 25 km apart, on the equator but out of phase with each other.
144 nce in two Peruvian populations close to the equator but with disparate degrees of urbanization.
145 ce distinct energy barriers to gating at the equator (but not elsewhere), and that the collective sub
146 lowing chromosomes to persist at the spindle equator, but consist of tubulin subunits that continuall
147 CENP-E-free chromosomes moved to the spindle equator, but their kinetochores bound only half the norm
148 ization of Ect2 is spatially confined to the equator by centralspindlin, Ect2's spindle midzone ancho
149 certainty of 10% with that observed near the equator by Mariner 10.
150 mation is mediated by RhoA activation at the equator by the centralspindlin complex and midzone micro
151 lity in nitrate concentration on and off the equator can be explained by upwelling rate, with slower
152         Local release of blebbistatin at the equator caused localized accumulation of equatorial acti
153  that cortical flow converging upon the cell equator compresses the actomyosin network to mechanicall
154 owth rates and dynamics at the poles and the equator, consistent with spindle microtubules of mixed p
155 the higher Src family kinase activity at the equator contributes to the higher degree of protein phos
156 yes with intravitreal implants placed at the equator delivered Gd-DTPA throughout the vitreous cavity
157                                These ectopic equators distort a mosaic analysis of these genes and le
158 romagnetic dipole is moving toward the Sun's Equator during a solar cycle.
159 or activation of myosin binding sites at the equator during anaphase.
160  to align mitotic chromosomes at the spindle equator during cell division, but how it accomplishes th
161 nchorage of the contractile ring at the cell equator during cytokinesis in animals and fungi, respect
162 ubules focuses myosin activation to the cell equator during cytokinesis.
163                   Mto1 targeting to the cell equator during division depends on direct interaction wi
164 ytokinesis, MLCK was enriched at the spindle equator during late metaphase, and was maximally activat
165 ill maintained their position at the spindle equator during metaphase and segregated properly during
166  Earth's history, was nearly bisected by the Equator during the late Palaeozoic and early Mesozoic er
167 poorly sampled xeric belt that straddled the Equator during the Permian period differed markedly from
168 e flow, including a sign-change close to the equator, even at asymptotically low viscosity.
169 degrees S to 32 degrees S latitudes favoring equator-facing slopes, which are times and places with p
170  resides in the vegetation and soil near the Equator for a shorter time than at latitudes north of 75
171 enlargement in the dorsal eye due to ectopic equator formation.
172 naphase; among these, those aimed toward the equator grew longer, and their tips coincided with corti
173 that the present salinity gradient along the Equator has developed relatively recently.
174 tance are, on average, located closer to the equator, have more challenging climates (e.g., higher te
175  we propose a new Bond number defined by the equator height and optical resolution to represent the m
176                        Verifying the droplet equator height is a key parameter, we propose a new Bond
177  was located far south of Jupiter's magnetic equator in a region where the radial component of the ma
178 gatively regulated Rac1 activity at the cell equator in anaphase.
179  'bullseye') increases with proximity to the Equator in both hemispheres, and larger bullseyes are as
180 ty that organizes chromosomes at the spindle equator in C. albicans to overcome fundamental noisiness
181 whereas these filaments dissociated from the equator in control cells during late cytokinesis, they p
182 a broad band of nodes that forms at the cell equator in fission yeast cytokinesis.
183 ork of dynamic microtubules to find the cell equator in preparation for division signals.
184  block chromosome congression to the spindle equator in prometaphase, or segregation to the poles in
185 ed, wetter conditions developed north of the equator in response to high summer insolation and increa
186 cultivated tomato beyond its origin near the equator in South America, and they provide a compelling
187 reconstructions of the region straddling the equator in the Early Permian but is at odds with its nor
188 iquids have flowed on the surface at Titan's equator in the past, to date, liquids have only been con
189  in-phase precipitation reduction across the equator in the tropical Americas associated with Heinric
190 ing in the same geographical location at the equator indicated that race is a significant risk factor
191 preading East Pacific Rise just North of the Equator initiated at a melt-rich segment about 5 kilomet
192 ct that a northward shift of Earth's thermal equator, initiated by an increased interhemispheric temp
193 he congression of chromosomes to the spindle equator involves the directed motility of bi-orientated
194                                          The equator is established in at least two steps: photorecep
195 ng a small circle tilted with respect to the equator is found to correspond to a southern-hemisphere
196 new insights into how RhoA activation at the equator is initiated and maintained.
197 ent of increasing biodiversity from poles to equator is one of the most prominent but least understoo
198 r cell differentiation and elongation at the equator, is disrupted.
199 noise-like plasma waves near the geomagnetic equator known as 'equatorial noise'.
200 in cohorts, individuals living closer to the equator (latitude, 27.47 degrees S) had higher levels of
201 romosomes eventually migrated to the spindle equator, leading to mitotic exit.
202 ere calculated at the cornea, vitreous base, equator, macula, and orbit apex for pressures known to c
203 th and transport angular momentum toward the equator, maintaining the Sun's rapid equatorial rotation
204     A southward migration of Earth's thermal equator may have accompanied the more recent Medieval Wa
205 nd greater phosphorus limitation towards the equator may restrict detritivore-mediated decomposition,
206                    On reefs further from the equator, microbes had more genes encoding chlorophyll bi
207           The human vitreous zonule and lens equator move forward (anteriorly) during accommodation,
208            Centripetal ciliary body and lens equator movements were measured during accommodation in
209                    While accumulating at the equator, myosin filaments disappear from the poles of th
210 mmendations including wider reference to the EQUATOR Network online library (www.equator-network.org/
211 Quality and Transparency of Health Research (EQUATOR) Network.
212 e to the EQUATOR Network online library (www.equator-network.org/).
213 ll-scale channels and dry riverbeds near the equator observed by the Huygens probe at latitudes thoug
214 aged as an open tubular fragment of C60, the equator of C70 fullerene and the unit cycle of a [5,5] a
215 te positioning of the division septum at the equator of Escherichia coli cells requires a rapid oscil
216 regions between the intraocular lens and the equator of the bags were populated by monolayers of epit
217  then associate with type 1 nodes around the equator of the cell during interphase.
218 s are plus ends out and overlap close to the equator of the cell.
219 ndles coalesced into a tight ring around the equator of the cell.
220 y ingression of an acto-myosin furrow at the equator of the cell.
221 tresses were maximum at the contact line and equator of the eye and were parallel to the direction of
222          In vivo, episcleral implants at the equator of the eye did not deliver a significant amount
223  The ability of an episcleral implant at the equator of the eye to deliver drugs to the posterior seg
224 ls that are concentrated in the CMZ near the equator of the eye.
225 ure where the alkylation took place near the equator of the fullerene cage, rather than at the more s
226 ing residues Arg34, Asn69, and Lys134 on the equator of the hexameric protein and a covalent DNA-bind
227 iven fluid circulation from the poles to the equator of the lens.
228 duced concave distortions when viewed at the equator of the liposome.
229            Its components co-localise at the equator of the mitotic spindle and function interdepende
230 osis, chromosomes must become aligned at the equator of the mitotic spindle before segregation.
231 t division septa after FtsZ reappears at the equators of daughter cells.
232 scopy localized PcsB mainly to the septa and equators of dividing cells.
233 n atom resides at a 665 ring junction in the equator on the fullerene cage and that the unpaired elec
234 he literature for a handful of KBOs, and an "equator-on" aspect, we find 1998 SM(165) has axes of len
235 iparallel microtubule overlap at the spindle equator or a key mitotic kinesin.
236 d thereby confine trajectories to either the equator or a meridian of the Bloch sphere.
237 omes had stable metaphase positions near the equator or between the equator and a pole.
238 zonule insertion zone and the posterior lens equator or muscle apex were important for predicting acc
239 ion, accumulate anillin or actin at the cell equator, or undergo equatorial constriction.
240 re significantly more likely to occur in the equator-ora region of the fundus (P < 0.0001), in a diff
241 ring that became tilted relative to Saturn's equator plane in 1983.
242 ance of oceans for climate; indeed, the peak equator-pole ocean heat transport on Earth peaks at almo
243 cond at the equator, predicts an oblateness (equator-pole radius difference) of 7.8 milli-arc seconds
244 approximately 2 kilometers per second at the equator, predicts an oblateness (equator-pole radius dif
245 rain rates at the macula, vitreous base, and equator reached lower values in the vitreous- compared w
246 pic laser coagulation of the entire vascular equator reduces postoperative fetal morbidity in severe
247  means of guiding the chromosome to the cell equator regardless of the initial conditions and uncerta
248 anism by which RhoA is activated at the cell equator remains unknown.
249 Ocean transports energy northward across the Equator, rendering the Northern Hemisphere warmer than t
250            There is strong evidence that the equator represents a unique region that receives cleavag
251 easonal parameter regime for flows above the equator so that rotation is ignored.
252 ses laser coagulation of the entire vascular equator (Solomon technique).
253 s more prevalent in regions further from the equator, suggesting that vitamin D insufficiency may pla
254 s to the north and south of the geographical equator suggests they might be associated with the tops
255 s) appears to increase with proximity to the equator, suicide rates tend to decrease.
256  active Src family kinases was higher at the equator than at the anterior epithelium.
257                            It is at the lens equator that epithelial cells elongate along their apica
258 myosin contractility is greatest at the cell equator, the temporal and spatial cues that direct equat
259 rients within the region of upwelling on the equator, thereby contributing to the sequestration of ca
260 e temperatures to be nearly uniform near the equator, these displacements can grow to extreme distanc
261  all chromosomes have aligned at the spindle equator through attachment of their sister kinetochores
262 ells, we show that myosin accumulates at the equator through stabilization of interactions between th
263  the RV Polarstern in November 2007 from the equator to Cape Town, South Africa and the MV Oceanic II
264 which ranges broadly in the Pacific from the equator to near the Aleutian Islands.
265 mposed on the decline in diversity seen from equator to pole were "hot spots" of enhanced diversity i
266 er maps show an increase in temperature from equator to pole with some evidence for a warm "ring" sur
267         The decline of species richness from equator to pole, or latitudinal diversity gradient (LDG)
268 nctionalized the north pole, south pole, and equator to produce what we call X, Y, and K functionalit
269 the planet, distributed in latitude from the equator to the north pole, and present at most local tim
270 atmospheric heat transport on Earth from the Equator to the poles is largely carried out by the mid-l
271   Recent Ulysses observations from the Sun's equator to the poles reveal fundamental properties of th
272  both to thrive in habitats ranging from the equator to the subarctic and to form large-scale episodi
273            This calibration point implies an Equator-to-pole gradient in sea surface temperatures of
274 the axial dipole prediction of a factor-of-2 equator-to-pole increase in mean field strength, leaving
275  characterized by polar ice sheets and large equator-to-pole temperature gradients, is rooted in envi
276 ric flow that is generally directed from its equator toward its poles at the surface.
277 m the anterior chamber flows around the lens equator toward the cleft.
278 l begins to divide by constricting about its equator, ultimately affording two spherical cells with t
279 ic interaction strength increases toward the equator, using a global experiment with model caterpilla
280 de novo filament assembly occurs at the cell equator via localized myosin II regulatory light chain (
281 e average residential latitude away from the equator was associated with 11% increased odds of XFS (p
282   Every 10 degrees of latitude away from the equator was associated with a mean decrease in UVR troug
283  orbital inclination relative to the Earth's equator was I approximately = 10 degrees.
284 lation between 25(OH)D and distance from the equator was observed across population samples.
285 und which a graft stretching to the temporal equator was rotated.
286 re, greater movement of chromosomes from the equator was usually found in the ask1-1 cells that had l
287 ions, whereas wetter conditions south of the equator were a response primarily to the GHG increase.
288 ace and residence at latitudes closer to the equator were associated with lower rates of affected BSA
289 ina and choroid from the macula and temporal equator were stained with filipin to reveal esterified (
290 ection was higher in trials further from the equator where environmental mycobacteria are less and wi
291 , chromosomes align at the metaphase spindle equator where they oscillate along the pole-pole axis be
292  cells and expression terminates at the lens equator, where epithelial cells terminally differentiate
293 cide with older, low-albedo regions near the equator, where water ice is unstable.
294 function in the precursor cell closer to the equator, which becomes R3.
295 ated with latitude, decreasing closer to the equator, which coincided with a greater than fivefold in
296 violence increase as one moves closer to the equator, which suggests the important role of climate di
297 ubstantially along the direction of the cell equator, while the network contracted laterally along th
298                  Reduced mixing close to the Equator will have to be taken into account in numerical
299 ts, we found increasing predation toward the equator, with a parallel pattern of increasing predation
300 adult eye are aligned at right angles to the equator, with dorsal and ventral ommatidia pointing in o

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