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1 e peroxisomal fatty acid (FA) beta-oxidation spiral.
2 tic field control of the incommensurate spin spiral.
3 self-association of LANA into supermolecular spirals.
4 cteristic shapes, including rods, cocci, and spirals.
5 ically-driven bending into multi-turn inward spiraling.
6 at preferentially induced radial (<10 Hz) or spiral (10-20 Hz) hallucinations in a behavioral experim
7 ), whereas more artifacts were observed with spiral 4D flow (kappa = 0.30 and 0.20).
8                      For portal venous flow, spiral 4D flow was in better agreement with 2D cine phas
9                  Inspired by the Archimedean spiral, a new integrated design of micropseudocapacitors
10 ctively evaluated and underwent a high-pitch spiral acquisition CT scan.
11 tion - 80x0.5 mm, scanning range in a single spiral acquisition from the skull to the proximal femora
12                                              Spiral adenosine stress cardiovascular magnetic resonanc
13 or was assessed using accelerometry, digital spiral analysis, and a standard clinical rating scale at
14  of theoretical plates as compared to the 3D spiral and 2D serpentine columns, respectively.
15 e in the peak capacity as compared to the 3D spiral and 2D serpentine columns, respectively.
16 dose-matched delayed contrast agent-enhanced spiral and axial abdominal EID and PCD scans were acquir
17 inal vessels showed good equivalence between spiral and Cartesian 4D flow techniques (lower bound of
18                          We propose that the spiral and dense coat organize the cytoadherence structu
19 e subgroups of retinal ganglion cells (RGC), spiral and vestibular ganglia, inner ear and vestibular
20 formed rings of variable size, ellipses, and spirals and also arcs that could be assembly products.
21 ions in the number and shapes of dislocation spirals and different layer stackings that are determine
22                               Both standard (spiral) and triggered CT scans were used to reconstruct
23  3D printed in titanium as 2D serpentine, 3D spiral, and 3D serpentine columns, of equal length and i
24  the mitochondrial fatty acid beta-oxidation spiral, and thus is important for energy metabolism.
25 laments, whereas Shs1-capped rods form arcs, spirals, and rings.
26 lic interconnects, springs, and freestanding spiral architectures on flexible and rigid substrates.
27                                          The spirals are shown to be springs whose bending drives mem
28 l structure by locating the Scutum-Centaurus spiral arm as it passes through the far side of the Milk
29 nd a tertiary protostar is coincident with a spiral arm in the outer disk at a separation of 183 astr
30 ay, we detected a pair of trailing symmetric spiral arms in the protoplanetary disk surrounding the y
31  an emission gap closer to the star than the spiral arms.
32 DNA, via a set of pre-sensor 1 hairpins that spiral around the translocation substrate.
33 ynamin family, which polymerize into helical spirals around such necks.
34 alpha-ARNT and HIF-1alpha-ARNT, wherein ARNT spirals around the outside of each HIF-alpha subunit.
35 dules of neighbouring protomers, and a quasi-spiral arrangement of DNA binding elements that circumna
36 trophoblast (CTB) invasion of the uterus and spiral arteries is often shallow.
37 ells invade the decidua and remodel maternal spiral arteries to establish adequate nutrition during g
38 oblasts invading the maternal uterus and its spiral arteries.
39                                     Decidual spiral arteriole (SpA) remodeling is essential to ensure
40 ure displaying poor trophoblast invasion and spiral artery development in the maternal decidua, accom
41 utrophils, or blockade of TNF-alpha improves spiral artery remodeling and rescues pregnancies.
42 tional zone, smaller placentas, and impaired spiral artery remodeling with fetal growth restriction.
43 atural killer (uNK) cells, and impairment of spiral artery remodeling.
44 ng to shallow uterine invasion and deficient spiral artery remodeling.
45 dm1/Blimp1 is essential for specification of spiral artery trophoblast giant cells (SpA-TGCs) that in
46                                     One such spiral assembly was solved as a crystal structure of 3.7
47 -wide activity arises from a low-dimensional spiral attractor.
48                   In this work, we propose a spiral blade plasmonic vortex lens (SBPVL) that offers u
49                                              Spiral-bound flip cards and download pdf surround HOTV a
50 plasma gondii, the apical complex includes a spiral cap of tubulin-rich fibers called the conoid.
51 es an intensive electromagnetic field into a spiral capacitive gap (around 200 mum), which provides s
52 a counter-rotating cell boundary layer, with spiral cell orientation within the vortex.
53 re is chiral, consisting of interpenetrating spiral chains of hydrogen-bonded water molecules and rot
54 core structure in which five subunits form a spiral chamber that binds the clamp at its base in a twi
55 i chip containing two series-coupled, square spiral channels 4.2 cm and 2.8 cm long and 250 mum x 140
56 w silica spheres (smHSSs) using microfluidic spiral channels with enhanced mixing performance, introd
57 o optically control the direction, speed and spiral chirality of such waves in cardiac tissue.
58 itute a group that appears to have lost both spiral cleavage and centrosomes.
59                    In addition to exhibiting spiral cleavage and early cell fate determination, troch
60 lida, Macrostomorpha, and Polycladida) share spiral cleavage and entolecithal eggs with other lophotr
61            Lecithoepitheliata have primitive spiral cleavage but derived ectolecithal eggs.
62 y countercurrent chromatography (LSRCCC) and spiral-coil LSRCCC.
63 at a higher flow rate, as compared to the 3D spiral column, provided a 58% reduction in the analysis
64 e cooperation among genetic strangers in the spiraling competition between increasingly large groups
65                        Through a marriage of spiral computed tomography (CT) and graphical volumetric
66 r preoperative abdominal or thoracoabdominal spiral computed tomography images.
67 rbors hundreds of microns along the cochlear spiral, contacting many outer hair cells (OHCs).
68 ize and axon outgrowth, are graded along the spiral contour of the cochlea.
69 cause the tissue at the anatomically defined spiral core would already be weakly conducting, and a fu
70 by destroying the electrical activity at the spiral core.
71                                          The spiraling cost of new drugs mandates a fundamentally dif
72  Gravitational forces are expected to excite spiral density waves in protoplanetary disks, disks of g
73 ue that the observed spirals trace shocks of spiral density waves in the midplane of this young disk.
74                              Meanwhile, this spiral design can be engineered into arbitrary microshap
75 ral surface of LES are arranged in a helical/spiral fashion.
76 rtex and continuously proceeds outwards in a spiraling fashion.
77                                   Unilateral spiral fiber neuron ablations shift the directionality o
78    By in vivo calcium imaging, we found that spiral fiber neurons are active in response to aversive
79                    These results reveal that spiral fiber neurons are essential for the function of t
80  directionality of escapes and indicate that spiral fiber neurons excite the M-cell in a lateralized
81 -latency escapes, supporting the notion that spiral fiber neurons help activate M-cell-mediated start
82 ike M-cell ablations, bilateral ablations of spiral fiber neurons largely eliminate short-latency esc
83 s composed of excitatory interneurons called spiral fiber neurons, which project to the M-cell axon h
84 shear scrolling method generates Archimedean spiral fibers that demonstrate exotic, telescoping elong
85 e RecA (Rad51) protein that assembles into a spiral filament on DNA and mediates genetic exchange.
86  the mechanical properties of the mysterious spiral filaments formed by the yeast ESCRT-III protein S
87 2/CHMP4B spontaneously forms single-stranded spiral filaments.
88 eover, it was found that juice produced with spiral-filter press demonstrates a higher retention of p
89 s demonstrates the advantage of the use of a spiral-filter press in comparison with belt press in the
90  disadvantages of the innovative, low-oxygen spiral-filter press system were studied in comparison wi
91            First, the system parameters of a spiral-filter press were optimised with the aim of produ
92  a higher juice yield could be achieved with spiral-filter press.
93 gen) levels in the extraction chamber of the spiral-filter press.
94 onsisted of (1) shredding, (2) pressing with spiral-filter technology including a vacuumised extracti
95 , which utilises internal ridge(s) to induce spiral flow.
96 nts: a highly curved 800-residue N-terminal 'spiral', followed by a 400-residue low-curvature 'bridge
97                 This converts the hub into a spiral form that can release or gain CaMKII dimers.
98           Plates with triangular dislocation spirals form noncentrosymmetric stacking that gives rise
99 inescence, plates with hexagonal dislocation spirals form the bulk 2H layer stacking commonly observe
100                                AF-initiating spirals formed at the site showing the greatest rate-dep
101                         The CM site contains spiral-fractured bone and molar fragments, indicating th
102 demonstrated quantitative stability during a spiral functional MRI sequence.
103                                       Unlike spiral galaxies such as the Milky Way, the majority of t
104  similar densities to star clusters in giant spiral galaxies.
105            Proper structural organization of spiral ganglion (SG) innervation is crucial for normal h
106 tion was seen in satellite cells surrounding spiral ganglion (SG) neurons from postnatal month 1 onwa
107 bular and cochlear sensory epithelia and the spiral ganglion - by measuring electrophysiological prop
108 through anatomically distinct populations of spiral ganglion afferent neurons.
109 t on their postsynaptic targets, the type II spiral ganglion afferents.
110 uitment into both the sensory epithelium and spiral ganglion and also resulted in diminished survival
111 f Tg-mtTFB1 mice implicated apoptosis in the spiral ganglion and stria vascularis because of mitochon
112                                              Spiral ganglion cell (SGC) degeneration was prevented du
113 ans of a cochlear implant requires a healthy spiral ganglion cell population.
114                                The remaining spiral ganglion cells (type IIs) are unmyelinated and co
115       Our injections also transduced 10% of spiral ganglion cells and a much larger fraction of thei
116 he electrical responsiveness of BDNF-treated spiral ganglion cells is preserved during this period as
117  strikingly, significant degeneration of the spiral ganglion cells of the auditory nerve.
118                  We have shown that cochlear spiral ganglion cells secrete OPG at high levels and lac
119                                          The spiral ganglion is a compelling model system to examine
120 ocalize with the Schwann cell marker Krox20, spiral ganglion marker NF200, nor glial fibrillary acidi
121              Prph((-/-)) mice lacked type II spiral ganglion neuron innervation of the outer hair cel
122                   Optogenetic stimulation of spiral ganglion neurons (SGNs) activated the auditory pa
123                                      Type II spiral ganglion neurons (SGNs) are small caliber, unmyel
124                                The mammalian spiral ganglion neurons (SGNs) are specialzed bipolar ne
125                                              Spiral ganglion neurons (SGNs) receive input from cochle
126                                              Spiral ganglion neurons (SGNs) relay acoustic code from
127 synapses between inner hair cells (IHCs) and spiral ganglion neurons (SGNs) that carry acoustic infor
128             For sounds of a given frequency, spiral ganglion neurons (SGNs) with different thresholds
129 c) contributes to the proper organization of spiral ganglion neurons (SGNs) within the Rosenthal's ca
130 Such injury can also lead to degeneration of spiral ganglion neurons (SGNs), but this occurs over a p
131 eloping murine cochlea, where two classes of spiral ganglion neurons (SGNs), type I and type II, navi
132  the radiation beam was directed towards the spiral ganglion neurons (SGNs), whereas little responses
133 y cells in the cochlea, i.e., hair cells and spiral ganglion neurons (SGNs), with a focus on their to
134 ed into a mini-burst of action potentials in spiral ganglion neurons (SGNs).
135 eripheral auditory fibers (PAFs) and loss of spiral ganglion neurons (SGNs).
136  cells directly in the sensory epithelium or spiral ganglion neurons (SGNs).
137 mechanosensory hair cells (HCs) and afferent spiral ganglion neurons (SGNs).
138 IHCs), and was lacking from the postsynaptic spiral ganglion neurons (SGNs).
139  and also resulted in diminished survival of spiral ganglion neurons after hair cell death.
140  show that alpha2delta3 mRNA is expressed in spiral ganglion neurons and auditory brainstem nuclei an
141 n binaural transduction of inner hair cells, spiral ganglion neurons and vestibular hair cells.
142      Inner hair cells, auditory synapses and spiral ganglion neurons are all present after noise expo
143 reduces the spontaneous activity of IHCs and spiral ganglion neurons in the developing cochlea and pr
144         In vivo recordings from postsynaptic spiral ganglion neurons showed a use-dependent reduction
145 nnervation of the inner hair cells by type I spiral ganglion neurons was normal.
146 no evident pathology among supporting cells, spiral ganglion neurons, or cells of the cochlear latera
147 physical properties of the auditory neurons (spiral ganglion neurons, SGNs) stimulated in electrical
148                                           In spiral ganglion neurons, the primary afferents in the co
149  encoding of sound onset in the postsynaptic spiral ganglion neurons.
150 wave I latency, consistent with apoptosis of spiral ganglion neurons.
151   To understand better the sophistication of spiral ganglion response properties, we compared somatic
152 t of the rat AN projecting from the cochlear spiral ganglion to brainstem cochlear nuclei.
153                 PLP1(+) glial cells from the spiral ganglion were identified as neural progenitors, w
154  may set the "address" of neurons within the spiral ganglion, allowing them to elaborate the appropri
155 is sufficient to attract leukocytes into the spiral ganglion, and that fractalkine signaling plays a
156 ed macrophages were also observed within the spiral ganglion, but their numbers remained elevated for
157 e type II proximal, radial process, near the spiral ganglion, in agreement with the high voltage thre
158 vating the organ of Corti originate from the spiral ganglion, roughly 95% of which innervate exclusiv
159 thods to co-culture neural stem cell-derived spiral ganglion-like neurons (ScNs) and mouse auditory c
160 rine and terrestrial organisms (for example, spiralling gastropod shells).
161                                          The spiral geometry of the scours suggests that they were ca
162 se conclusions, an enhanced configuration of spiral graft is proposed and compared against convention
163 oposed and compared against conventional and spiral grafts to reaffirm its potential benefits.
164 sm resulting in the narrow pith cavity, weak spiral growth but increased vascular bundle of the thick
165 wall variant with narrow pith cavity, mildly spiral growth, and flat and enlarged SAM, including thos
166  Although ESCRT-III subunits polymerize into spirals, how individual ESCRT-III subunits are activated
167 ering in the presence of moving gratings and spirals, hummingbirds lost positional stability and resp
168                                              Spiral images were scored for image quality (Wilcoxon si
169 ress mediate tissue and cell damage that can spiral in a cycle of inflammation and more oxidative str
170 d on the identification of the blood flow as spiral in the whole arterial system and is believed to i
171  functional MRI studies was performed with a spiral in-and-out gradient echo sequence.
172 ow-dimensional, periodic, decaying orbit - a spiral - in which it behaved as a true attractor, conver
173  in the morphology of membrane-bound dynamin spirals, indicating that the PH domain regulates membran
174 nar capacitors with vacuum gaps of 60 nm and spiral inductor coils of micron pitch we realize microwa
175 y secretions using closed-loop separation of spiral inertial microfluidics (C-sep).
176 ome size minimization include tightly packed spirals inferred to be DNA, few densely packed ribosomes
177  the ipso carbon of the aryl group to give a spiral intermediate, and then migration of the keto carb
178                                   This death spiral is fueled by specialized proteins and error-prone
179 e-initiating heminodes in the distal osseous spiral lamina, NaV1.1 partly overlapped NaV1.6 and ankyr
180 e magnetic-field-driven flop of conical spin spirals leads to the simultaneous reversal of magnetizat
181 ke form that wraps around the cell body in a spiral-like fashion and enables the cell to escape by a
182 ilament executes a polymorphic change into a spiral-like form that wraps around the cell body in a sp
183 s that many of them are not closed but have "spiral-like" morphologies.
184 odel (TM-A model), the TM is attached to the spiral limbus (as in wild-type animals); in the second m
185 el (TM-D model), the TM is detached from the spiral limbus (mimicking the cochlea of Otoa(EGFP/EGFP)
186  Various graphene patterns, including texts, spirals, line arrays, and integrated circuit patterns, w
187 erromagnetic ferroelectrics are conical spin spiral magnets with a simultaneous reversal of magnetiza
188 ary flow instabilities for low-aspect ratio, spiral microchannels, with improved flow models for desi
189 stigation of sorting live HT-29 cells in the spiral microfluidic channel indicated that the distribut
190 e position and diameter of microspheres in a spiral microfluidic channel under various flow rates.
191 ch are then sorted by flowing them through a spiral microfluidic channel.
192                Based on inertial focusing in spiral microfluidic channels, I-SELEX enables stringent
193 s for the production and use of a label-free spiral microfluidic device to allow size-based isolation
194                                The described spiral microfluidic devices can be produced at an extrem
195 tic fields because, owing to Lorentz forces, spiral modes orbit decreases in diameter pulling the cha
196 neage of bacteria most known for their long, spiral morphology.
197 e having a 'right-handed' (counterclockwise) spiralling morphology is induced by L-enantiomers of Asp
198 two types of magnetoelectric effect-electron spiral motion and magnon-drag thermopower-as well as enh
199                     Our results suggest that spiral motion patterns that emerge in spatio-temporal op
200  accelerated electrons experience collective spiral motions, which leads to elliptically polarized sy
201 del, a new class of self-similar logarithmic spirals observed in a large zone of the parameter space.
202 ossible establishment of a self-perpetuating spiral of events that maintains or prolongs the pro-cata
203 ocirculatory flow may interrupt the downward spiral of injury toward progressive kidney failure and s
204                                          The spiral of one TOR interacts with the bridge of another,
205 quality control and precipitating a downward spiral of the cell's ability to maintain protein homeost
206                                    Polymeric spirals of crescent-shaped BAR-domain superfamily protei
207 i stacked BChl molecules in cylinders and/or spirals of different size.
208 ow that Cdt1 stabilizes MCM in a left-handed spiral open at the Mcm2-5 gate.
209 consisted of small, tortuous vessels with a "spiral" or "corckscrew" aspect.
210 can be used to study different types of spin spiral order and resulting multiferroic effects.
211                          As the pitch of the spiral order varies across the 3d transition metal compo
212 spin interaction which is essential for spin spiral order.
213 scissors game has a replicator equation that spirals out to the boundary, space stabilizes the system
214    We discovered that the growth displayed a spiral pattern and pith played an important role in prom
215   These individual carpels are arranged in a spiral pattern on the subtending stem tip, the receptacl
216 viewed a genuine static image of a radial or spiral pattern without any flicker.
217 ajority of MSTd neurons respond optimally to spiral patterns, rather than to the radial expansion pat
218 , geometric hallucinations such as radial or spiral patterns.
219 int unprecedented high values of OAM, namely spiral phase mirrors, to generate photons with more than
220 te OAM control of neutrons using macroscopic spiral phase plates that apply a 'twist' to an input neu
221 rection of propagation, effected by multiple spiral phase plates, and the conservation of topological
222 rown alga, Sargassum muticum, which exhibits spiral phyllotaxis (137.5 degrees angle) and an unlinked
223 itive beam steering device that integrates a spiral plasmonic antenna with a subwavelength metallic w
224 stants that exceed the length of the distal, spiral process, enabling spatial summation from widespre
225 h the high voltage threshold measured in the spiral process.
226           A high-resolution variable-density spiral pulse sequence with a novel density compensation
227 ration recovery interleaved variable-density spiral pulse sequence.
228 ows for a direct visualization of arrhythmic spiral re-entry and represents a revolutionary tool to a
229 te these secondary flows in low aspect ratio spiral rectangular microchannels and define their develo
230 cale nucleotide-driven motions of the ATPase spiral relative to the planar proteolytic base.
231 veguide cross-section of the silicon nitride spiral resonator is designed to possess small and flatte
232  multi split ring resonators, and (ii) multi spiral resonators.
233 nm) transforms the films from flat sheets to spiral ribbons, which subsequently translate large dista
234 state of ATP and are associated with an open spiral ring formation that is vital for asymmetric subun
235 les and show that, surprisingly, Min-protein spiral rotations govern the larger part of the geometric
236 amber parameters: pole-to-pole oscillations, spiral rotations, and traveling waves.
237 spiratory tracking and the other with use of spiral sampling and a breath hold.
238          The combination of highly efficient spiral sampling with dynamic compressed sensing results
239 velocity scanning and beam path corrections, spiral scan images are shown to exhibit less scan distor
240                                     Although spiral scanning avoids the sudden changes in the beam lo
241 e deviations, i.e. image distortions, we use spiral scanning paths, allowing precise control of a sub
242         The human inner ear has an intricate spiral shape often compared to shells of mollusks, parti
243                     Helicobacter pylori is a spiral-shaped Gram-negative bacterium that colonizes the
244 boundaries of the three ocean basins, before spiraling southeastward and upward through the Antarctic
245 s present a three dimensional view showing a spiralling southward path, with enhanced upwelling by ed
246 i) excitation of a new spin-wave mode with a spiral spatial profile originating from a gyrotropic rot
247 emerge from an enhanced coupling to residual spiral spin fluctuations and their concomitant suppressi
248  magnetic diffraction technique, we reveal a spiral spin order in MnP and trace its pressure evolutio
249 sine triphosphatases (ATPases) form a closed spiral staircase encircling an unfolded substrate, direc
250 nits, which complements the well-established spiral-staircase topology of the 26S ATPases.
251 surements allow us to shed light on Galactic spiral structure by locating the Scutum-Centaurus spiral
252 highly organized knob skeleton composed of a spiral structure coated by an electron-dense layer under
253 cular gas emission that reveal a disk with a spiral structure surrounding the three protostars.
254   However, previous observations that showed spiral structure were not able to probe disk midplanes,
255 DHE-enriched stromal fractions revealed fine spiral structures, similar to bacterial ADHE spirosomes.
256 also creates multiple images of the z = 1.49 spiral supernova host galaxy, and a future appearance of
257  due to an increased number of high-mobility spiral surface modes based on spin-split bands.
258  for its appearance and disappearance during spiral swimming in the natural habitat.
259                                         This spiral system enables us to achieve >/= 85% recovery of
260 ng high-pitch prospectively ECG-gated "Flash Spiral" technique (method A) or retrospectively ECG-gate
261                                         This spiraling tentacle-based grabbing modality, the direct p
262 ons in the circadian clock create a downward spiral that can lead to diabetes and other metabolic dis
263 ymbiotic partners enter into an evolutionary spiral that leads to irreversible codependence and assoc
264 e symptoms enter a seemingly self-propelling spiral that the maladaptive features of a disorder emerg
265  Modern planar inductors consist of metallic spirals that consume significant chip area, resulting in
266 g, while stronger radial threads with weaker spiral threads is better for distributed loading.
267 iodide uptake and a morphological shift from spiral to coccoid form.
268 e and multiple helices, toroids, and conical spirals to structures that resemble spherical baskets, c
269 ut tidally predicted stress fields as Phobos spirals towards Mars.
270                   We argue that the observed spirals trace shocks of spiral density waves in the midp
271  However, outward-bound runs on the circular-spiral track in the dark were associated with backward s
272        During inbound traversals of circular-spiral tracks, angular velocity increases continuously.
273    The nanoparticles followed a right-handed spiral trajectory on the surface of the cell.
274  0 degrees and 180 degrees ; for chest CT, a spiral trajectory with TCM was used.
275 agnetic topology of the alternating-exchange spiral tubes of S = (1/2) (C14H10)(*-) radical anions.
276  as 3D translation and rotation selectivity, spiral tuning, and heading selectivity, can account for
277                                 Dose-reduced spiral unenhanced lung EID and PCD CT examinations were
278 ence the cell swimming direction, within the spiral vortex.
279 d the minimal requirements for alternans and spiral wave break up, namely the kinetics of INa inactiv
280 rved on the surface of the rabbit heart, and spiral wave breakup.
281         Both models produced two-dimensional spiral wave dynamics for that were similar for each pati
282                                              Spiral wave reentry was simulated in monodomain 2-dimens
283 confirmed that localized ablation may anchor spiral wave reentry, producing organized tachycardias.
284  potentials in atrial fibrillation (AF) show spiral wave sources (rotors) in nearly all studies inclu
285   However, it is unclear why ablation near a spiral wave tip would terminate AF and not anchor reentr
286 center for reentry and can anchor an induced spiral wave.
287 t the receiver, which is associated with the spiral wavefront of OAM beams.
288 pm as observed in rabbit myocytes, reentrant spiral waves as observed on the surface of the rabbit he
289 ntrant excitations have been associated with spiral waves circulating around either an anatomically d
290 rotors in high-excitability regions migrated spiral waves to less excitable tissue, where they detach
291  supports the existence of localized rotors (spiral waves) or focal drivers.
292 ny sensory cells at the apex of the cochlear spiral were missing.
293 in more complicated constant linear velocity spirals, where the frequency varies within each scan.
294 s4 create uniform membrane-deforming conical spirals which are assemblies of specific ESCRT-III heter
295 Apaf-1/pc-9 CARD pairs arranged in a shallow spiral with the fourth pc-9 CARD at lower occupancy.
296         The resulting micro-tentacle exhibit spiraling with the final radius as small as ~185 mum and
297                                "Archimedean" spirals, with a constant angular frequency within each s
298 verse osmosis (LRO) and reverse osmosis (RO) spiral-wound membranes showed LRO membrane to be very ef
299                The mechanisms that drive the spiral wrapping of the myelin sheath around axons are po
300 trate the process with linear, circular, and spiral zone plates.

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