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1 anually tri-folded with the endothelial side inward.
2 strate area to a continuous 2D curl of plane inward.
3 l. (2015) shed light on how these cells move inward.
4 is transmitted from the extracellular domain inward.
5 omes with the unoccupied terminal end facing inward.
6 where one points outward and the other three inward.
7 ts formed farther from the star and migrated inwards.
8 ased peer review tends to drive radiologists inward, against each other, and against practice leaders
9  by VMAT out of the vesicle lumen coupled to inward amphetamine transport.
10 cted motor, which then pulls the sliding MTs inward and clusters them at the poles.
11  D1/D5 receptors), caused inhibition of both inward and outward currents by approximately 60% and app
12 f mGluR1 and mGluR5 resulted in a mixture of inward and outward currents mediated by a nonselective c
13 e "knock-on" mechanism of permeation in both inward and outward directions, and there is no similar l
14 overning the complex temporal progression of inward and outward gas fluxes to and from the silage int
15 n silver to specific superimpositions of the inward and outward surface plasmon profiles for the two
16 parently by placing its methyl group further inward and receiving stronger water repulsion.
17 2 directed outwards, whereas A63 is directed inwards and anchored by stacking and hydrogen-bonding in
18 II)4L4 tetrahedra, one with ligands puckered inward, and the other outward.
19 embrane domains (TMDs), which switch between inward- and outward-facing (IF, OF) orientations.
20 tons and triggers alternating access between inward- and outward-facing conformations of the substrat
21 te (ABC) transporter that alternates between inward- and outward-facing conformations to capture and
22 trates across membranes by switching between inward- and outward-facing conformations.
23 s involve cycling between conformations with inward- and outward-facing substrate-binding sites in re
24           The crystal structures of MalFGK2, inward- and outward-facing, show that the transporter is
25 tching sequences or to pump liquids radially inward, as well as the complete pre-storage and release
26 light-activated proton pump recruited a slow inward ASIC current, which required molecular proximity
27 A drop in extracellular pH induces transient inward ASIC currents (IASICs) in postsynaptic MNTB neuro
28 triders rotate the curved tips of their legs inward at a relatively low descending velocity with a fo
29 s' cast by the molecular clouds as they move inward at about 300 kilometres per second towards the ac
30 energy reached approximately 60 meV and then inward at higher energies.
31 ocations in the nucleosome linkers to induce inward (AT-IN) and outward (AT-OUT) bending of the linke
32 esis that Kir2 currents non-linearly balance inward background cation currents, accounting for two le
33 at Kir2 currents non-linearly counterbalance inward background cation currents, such as K2P1 currents
34                      KEY POINTS: Outward and inward background currents across the cell membrane bala
35  postulates that ILVs form individually from inward budding of the endosomal limiting membrane, plant
36                                   Subsequent inward budding of the endosomal membrane generates multi
37 cytosis (CME) involves nanoscale bending and inward budding of the plasma membrane, by which cells re
38 etinopathy, but specifically confined in the inward bulge of the staphyloma and secondary to excessiv
39 t on SD OCT (P < .001) were noted inside the inward bulge of the staphyloma between eyes with and wit
40 ch-clamp experiments clearly showed that the inward Ca(2+) current was absent.
41     It is concluded that D550Y/Q917H reduced inward Ca(2+) currents through a defect in the cell surf
42 at the cardiac plasma membrane, and thus the inward calcium current, through a complex pathway involv
43 ellular calcium concentrations and increased inward cation currents.
44 ls that divide by constriction of the cortex inward, cells of land plants divide by initiating a new
45 (+) ) nutrition and a robust guard cell K(+) inward channel activity is considered critical for plant
46 commonly known to function as a light-driven inward chloride pump.
47 me function as outward proton pumps, some as inward chloride pumps, whereas others function as light
48 d Cl channel (ANO2) to elicit, unusually, an inward Cl current.
49             Hence the olfactory response has inward CNG and Cl components that are in rapid successio
50 surement demonstrated lumenal narrowing from inwards collapse of hyalinized arteriolar walls unable t
51 nd the P1 active site in PDX1.3 have adopted inward conformations consistent with a catalytically pri
52 teraction sites, whereas inward-occluded and inward conformations present only a single beta-d-glucos
53 e silver element, accompanied by outward and inward counterion fluxes.
54 th AP phases 1 and 2 that was followed by an inward current (-0.42 +/- 0.03 pA pF(-1); n = 21) during
55 tion passively imports protons generating an inward current (IH), which may be exacerbated in NKA-sub
56 itive and voltage-dependent Na(+) persistent inward current (NaPIC).
57 Pinacidil failed to activate current and the inward current activated by elevated [K(+) ]o was insens
58 y terminus of the peptide, which triggers an inward current concomitant with calcium influx.
59 and had significantly larger menthol-induced inward current densities than medium-large cells, most o
60           PDM also attenuated the PM-induced inward current during co-application, providing further
61 sinhibition) combined with an increase in an inward current from excitatory synapses.
62                                         This inward current has two components: a canonical transient
63          Similarly, although 5-HT induced an inward current in both control and HFD gastric nodose ne
64                        Alkaline pH evokes an inward current in nociceptive neurons, which is primaril
65 s activity as a SERT substrate, 4-MEC evoked inward current in SERT-expressing Xenopus oocytes, where
66 respond to the application of glutamate with inward current mediated by Ca(2+)-permeable AMPARs.
67 so poorly coupled, enabling local Ca-induced inward current of sufficient source strength to overcome
68 ry current-a nonrectangular self-terminating inward current produced in optical stimulation due to Ch
69 f firing rate corresponded with an increased inward current that was blocked by TPQ.
70  which displayed a hyperpolarization-induced inward current that was enhanced by cGMP as well as cAMP
71 on of SAN pacemaker activity by allowing net inward current to flow during the diastolic depolarizati
72 m of many itch receptors, where they mediate inward current to trigger action potentials in primary a
73 ltage clamp experiments showed activation of inward current when extracellular K(+) ([K(+) ]o ) was i
74             Spontaneous Ca release activates inward current which depolarizes membrane potential (Vm)
75 ficantly decreased firing rate and increased inward current within SCN neurons in a GIRK-dependent ma
76 duced current IMI (a nonlinear voltage-gated inward current) that effectively acted as a negative lea
77 nd that despite evoking a similar excitatory inward current, activation of NMDARs resulted in a large
78 e from caged glutamate generated a transient inward current, as expected for the electrogenic inward
79 eptor and is mediated by a voltage-dependent inward current.
80  currents increases, while the open time for inward currents (Cl(-) efflux) is constant irrespective
81  evoked rapidly activating and desensitizing inward currents (peak 18 +/- 3 pA/pF at -60 mV) in healt
82  not known although activation of persistent inward currents (PICs) might be involved.
83  repolarization represents a balance between inward currents (primarily through calcium and sodium ch
84 eration of extrasynaptic NMDAR-mediated slow inward currents (SICs) in neighboring neurons, which can
85 th single-channel conductances of 20 pS for inward currents and 80 pS for outward currents.
86                                         Both inward currents and 5-HT release were inhibited by Piezo
87 hermore, capsaicin-induced spontaneous pain, inward currents in DRG neurons, and synaptic currents in
88 how that activation of NMDARs evoked similar inward currents in MNCs of sham and renovascular hyperte
89 -d-aspartate receptor (NMDAR)-dependent slow inward currents in neurons.
90 BAB receptor agonist baclofen also inhibited inward currents induced by CIM0216 in DRG neurons, and n
91                                              Inward currents observed during exposure to NH4Cl were d
92 d for two bacterial Na(v) channels to induce inward currents of K+ ions.
93  Many chimeras have stronger light-activated inward currents than the three parents, and some have un
94                          Additionally, tonic inward currents were also detected, but only in the stri
95                                  P2X7R-gated inward currents were suppressed in the contralateral hip
96  that activation of Piezo2 by force leads to inward currents, 5-HT release and an increase in mucosal
97  by enhancing subthreshold voltage-activated inward currents.
98    Conduction velocities were slowest at the inward curvature into the isthmus entrance (0.28+/-0.2 m
99 mical analyses show OsSWEET2b in an apparent inward (cytosolic) open state forming homomeric trimers.
100  Individuals with AN (n=28) showed localized inward deformations of the thalamus relative to healthy
101 .5), encoded by the SCN5A gene, conducts the inward depolarizing cardiac Na(+) current (INa) and is v
102 ubstrate-type releaser at DAT that evoked an inward depolarizing current and calcium influx, whereas
103                                           In inward destruction, species loss is almost proportional
104 th a distinct splitting margin (stage 1), an inward detached crescentic flap lying on the anterior le
105 d by the intermediate Ag20 shell, preventing inward diffusion of the surface Au atoms.
106  of palladium phosphide and consequently the inward diffusion of vacancies and their coalescence into
107 )Ab in the presence of applied forces in the inward direction, but not in the outward direction.
108                                              Inward displacement of TM2 might alter the sidechain env
109    Our mechanics analysis revealed that such inward expansion is enabled by the much stiffer lithiate
110 ry of SERT is thought to proceed through the inward facing conformation.
111 avity in what could be a stabilization of an inward facing conformation.
112 otide-free state, with hydrolysis driving an inward facing conformation.
113 acochaperone noribogaine, which binds to the inward facing conformation.
114 ations, unlike K(+), are unable to enter the inward facing sites in the dephosphorylated enzyme.
115 The dephosphoenzyme contains Na(+) selective inward facing sites, whereas the phosphoenzyme contains
116 avoring outside facing sites and disfavoring inward facing sites.
117 suppressor mutations, which trap SERT in the inward facing state, or (ii) by the pharmacochaperone no
118 sted to adopt different conformations in the inward facing, outward facing and amphetamine-bound stat
119 hanism, making iterative transitions between inward-facing (E1) and outward-facing (E2) conformations
120 used to resolve the backbone dynamics in the inward-facing (IF) and outward-facing (OF) states by ana
121 has an enhanced solvent accessibility in the inward-facing (relative to the outward-facing) form.
122 ads to the activation of two cytoplasmically inward-facing channels: the plasma membrane, Cch1p, and
123 ructure of the uracil transporter UraA in an inward-facing conformation allowed us to identify the an
124  the glucose EIIC superfamily, bcChbC in the inward-facing conformation and bcMalT in the outward-fac
125 gent-solubilized TmrAB in a nucleotide-free, inward-facing conformation by single-particle electron c
126                                 Recently, an inward-facing conformation of LeuT was solved revealing
127                      In this study, an open, inward-facing conformation of Pho84 was used to study th
128 ectrogenic binding of K(+) or of H(+) to the inward-facing conformation of SERT in (i) cancelling out
129 ubstrate to LeuT, promotes an outward-closed/inward-facing conformation of the transporter and increa
130     The SUR1-ABC core is found in an unusual inward-facing conformation whereby the two nucleotide bi
131 -binding domains of the transporter adopt an inward-facing conformation with the two nucleotide-bindi
132               The structure shows UapA in an inward-facing conformation with xanthine bound to residu
133 nd ADP reveal an unprecedented closed and an inward-facing conformation, respectively.
134 nd the crystal structure of MsbA in the open inward-facing conformation.
135 ited to a series of crystal structures in an inward-facing conformation.
136 inding site when the transporter rests in an inward-facing conformation.
137       Crystal structures in the outward- and inward-facing conformations of a glutamate transporter h
138 7, suggesting that Mhp1 adopts predominantly inward-facing conformations.
139                  Furthermore, simulations of inward-facing LeuT with Na(+) ions and substrate bound s
140 urrent Pho84 transport model is based on the inward-facing occluded crystal structure of the Pho84 ho
141 , indicating that the transporter lies in an inward-facing open conformation.
142 rd-facing occluded with substrate bound, and inward-facing open).
143 tal structures of outward-facing Sav1866 and inward-facing Pgp.
144 rmation until maltose triggers return to the inward-facing state for substrate and Pi release.
145 onal transition from an outward-facing to an inward-facing state of the transporter.
146 conformational change in Pho84 from an open, inward-facing state to an occluded state.
147  noribogaine (a DAT ligand selective for the inward-facing state) and/or pifithrin-mu (an HSP70 inhib
148 In our structure, TmrAB adopts an asymmetric inward-facing state, and we show that the C-terminal hel
149 +) binding by facilitating transition to the inward-facing state.
150 sporter Can1 is promoted by transition to an inward-facing state.
151 lobal (transition between outward-facing and inward-facing states) scales.
152 ng structural isomerization from outward- to inward-facing states.
153 d at residues selected to track the putative inward-facing to outward-facing transition.
154    Here we present crystal structures of the inward-facing, intermediate, and outward-facing states o
155 of the binding site to the cytoplasmic side (inward-facing, open NBD conformation).
156 en [nucleotide binding domains (NBDs) apart; inward-facing] and closed (NBDs close; outward-facing) c
157               Hyperpolarizing HCs stimulated inward feedback currents in cones that averaged 8-9 pA a
158 ectivity, where TWIK-1 displays robust Na(+) inward flux in response to subphysiological K(+) concent
159 , the overlapping tissue showed a contracted inward fold at its peripheral edge with scar tissue); 1
160 upiter and Saturn, in which Jupiter migrates inward from a > 5 astronomical units (AU) to a approxima
161 ultaneously: The frozen phase boundary moves inward from the droplet free surface toward the droplet-
162 y, is highest when habitable area disappears inward from the edge of a region, lower when it disappea
163 bly supplied these sediments, which advanced inward from the wall, infilling both the crater and an i
164  gaze and retraction of the eye on attempted inward gaze.
165 ward, outward-occluded, inward-occluded, and inward GLUT1 conformations.
166                                       4) The inward GLUT1 conformer presents overlapping endofacial W
167 the inner membrane, cell wall synthesis, and inward growth of the outer membrane.
168 treadmilling, which guides and regulates the inward growth of the septal wall.
169 rofile, whereas its metabolite PM induced an inward hDAT current consistent with a DAT substrate prof
170 ier model in an outward (OWF) and develop an inward (IWF) facing model employing an integrated experi
171                         Both the outward and inward K(+) currents shifted Veq K(+) consistent with K(
172  membrane invagination, which grows radially inward like the shutter of a camera.
173 leosome proximity in the AT-IN arrays due to inward linker DNA bending.
174                                         This inward-looking threat from parochialism occurs just as t
175      This process induces cargo crowding and inward membrane buckling, followed by constriction of th
176 e from endolysosomal Ca(2+) stores activates inward membrane currents and depolarizes the beta cell t
177                                    Jupiter's inward migration entrained s greater, similar 10-100 km
178  There is debate whether in situ assembly or inward migration is the dominant mechanism of the format
179                                         This inward migration of GJ 436b could have triggered the atm
180                                              Inward motion of Arg664 allows it to interact with the g
181          We show that phosphorylation favors inward motion of Arg664, while simultaneously favoring o
182 ntally, and validate theoretically, that the inward motion of the phase boundary near the substrate d
183 nhibitory inputs directionally selective for inward motion opposing the excitation.
184                                              Inward movement is driven by the matrix-localized, Hsp70
185 rd current, as expected for the electrogenic inward movement of co-transported Na(+) In contrast, glu
186 of the open structure reflecting in part the inward movement of Glu-216 to form a hydrogen bond with
187 o GPCR deactivation that is characterized by inward movement of the TM6 intracellular end.
188 ment of K(+) induces filter opening, whereas inward movement promotes inactivation.
189               These are reflected in reduced inward Na(+) and outward K(+) currents.
190                 We found that a dominance of inward Na-Ca exchanger current (I(NCX)) over Ca-dependen
191  LCR signal activating an earlier and larger inward NCX current.
192       All restored teeth initially exhibited inward (negative) cuspal flexure due to polymerization s
193 protein, as well as a mechanically-sensitive inward non-selective cation current characteristic of Pi
194 d its structure in a novel conformation, apo inward-occluded and a new nucleotide-bound state, high-e
195 ucose and maltose interaction sites, whereas inward-occluded and inward conformations present only a
196 llus halodurans, have been resolved in novel inward-occluded states, with the extracellular vestibule
197 ns, the so-called outward, outward-occluded, inward-occluded, and inward GLUT1 conformations.
198 buted to decreasing current density radially inward on the silicon surface exposed to Triton((R)) X-1
199  mediating the conformational switch between inward-open and outward-open states necessary for drug e
200 or substrate translocation by stabilizing an inward-open conformation.
201  7, and 11 form an extracellular gate in the inward-open conformation.
202 ral intermediate preceding transition to the inward-open conformation.
203 ed phosphorylation and agents that stabilize inward-open conformations (e.g., 5-HT, ibogaine) increas
204 ported here spontaneously adopt occluded and inward-open conformations.
205 nsport of 5-HT, which increases the level of inward-open SERT and may lead to unwinding of the TM5 he
206  coli BAM complex in two distinct states: an inward-open state and a lateral-open state.
207  compounds bind in the central cavity of the inward-open state of hGLUT1, and all binding sites overl
208 ith the conformational transition toward the inward-open state, a role that is likely to be shared ac
209 s relative to the Gate domains may access an inward-open state.
210 oning of the N terminus and transition to an inward-open state.
211 utward-open, outward-partially occluded, and inward-open states of the transport cycle.
212 lized in outward-open, outward-occluded, and inward-open states.
213 ions match crystal structures, including our inward-open structure.
214      Here, we present three inhibitor-bound, inward-open structures of WT-hGLUT1 crystallized with th
215 centrations that induced outward opening and inward opening, respectively, as measured by the accessi
216 modynamic coupling between Na(+) release and inward-opening, and identifies diverse, yet well-defined
217 ntial motifs regardless of whether they face inward or outward from histone octamers along the DNA he
218 ll four azaphosphatrane (+)P-H vectors point inward, or else where one points outward and the other t
219 RET to monitor intersubunit rotation and the inward/outward movement of the L1 stalk of the large rib
220  flicker) and symmetrically moving patterns (inwards, outwards, random directions) with and without p
221 etres, whose orbits do not decay appreciably inward over 4.5 billion years, contribute at most about
222 GLAST expressions and attenuated the peak of inward potassium current.
223 ASK-1, GS and GLAST expressions and enhanced inward potassium currents compared with those in the COH
224 s triggered by edge cooling and large-scale, inward propagating avalanches.
225 rectification behavior of AM2 (i.e., why the inward proton flux is allowed when the pH is low in vira
226 e creation of a light-driven, single-photon, inward proton transporter.
227 ces outward pushing forces to antagonize the inward pulling forces from kinesin-14 or dynein.
228 phasizes that measured intrinsic properties (inward rectification and external [K] dependence) and lo
229                 The results demonstrate that inward rectification depends on a single amino acid (Ala
230                                 However, the inward rectification of GABA-induced transport currents
231 es of quasi-instantaneous activation, strong inward rectification, depended on the external [K(+)], a
232 m conductance predominantly mediated by K(+) inward rectifier (Kir)2.1, which was blocked by the NMDA
233  at depolarized membrane potentials, whereas inward rectifier channels conduct greater current at hyp
234                              G protein gated inward rectifier K(+) (GIRK) channels open and thereby s
235                              Although strong inward rectifier K(+) (Kir) channels have been reported
236                                              Inward rectifier K(+) channel subfamily 2 (Kir2) channel
237                                    ABSTRACT: Inward rectifier K(+) channel subfamily 2 (Kir2) channel
238           In the present study, we show that inward rectifier K(+) channel subfamily 2 isoform 1 (Kir
239                      We explored the role of inward rectifier K(+) conductances in colonic ICC that m
240                                 In contrast, inward rectifier K(+) current and L-type Ca(2+) channels
241 onents of transient outward K(+) current and inward rectifier K(+) current, along with corresponding
242 ic and functional data showing that the K(+) inward rectifier KAT1 (K(+)Arabidopsis thaliana 1) chann
243 leads to the activation of G-protein-coupled inward rectifier potassium (GIRK) channels and hyperpola
244                              G protein gated inward rectifier potassium (GIRK) channels are gated by
245  = 0.2 muM), small-molecule inhibitor of the inward rectifier potassium (Kir) channel and diuretic ta
246     Emerging evidence suggests that mosquito inward rectifier potassium (Kir) channels represent viab
247                    Endothelial cells express inward rectifier potassium (Kir) channels, but their rol
248 nding partners, kainate receptor GluR6/7 and inward rectifier potassium channel Kir2.1, closely assoc
249 ed rectifier potassium current (IKr) and the inward rectifier potassium current (IK1) were also downr
250 ly non-selective members of the prokaryotic 'inward rectifier' subfamily of K(+) channels.
251 y-which activates capillary endothelial cell inward-rectifier K(+) (KIR2.1) channels to produce a rap
252  containing the ABC transporter SUR1 and the inward-rectifier K(+) channel Kir6.2, in the presence of
253           The defining structural feature of inward-rectifier potassium (Kir) channels is the unique
254 rent at physiological conditions is strongly inward rectifying and predominantly carried by chloride.
255                                              Inward rectifying currents (IKir) had the canonical feat
256 ells of SUR1 null islets have an upregulated inward rectifying K+ current that helps to compensate fo
257                                              Inward rectifying potassium (Kir) channels play a centra
258 ncodes the GABAB R-coupled G protein-coupled inward rectifying potassium channel subunit 2 (GIRK2) ch
259 with that wave leads to the activation of an inward rectifying potassium conductance in microglia.
260                                          The inward-rectifying K(+) channel AKT1 constitutes an impor
261 tant, indicating that ZxAKT1 functions as an inward-rectifying K(+) channel.
262 ract with and suppress the activities of the inward-rectifying K(+) channels KAT1 and KC1.
263 selective inactivation of current carried by inward-rectifying K(+) channels of tobacco (Nicotiana ta
264 d signaling pathway that selectively targets inward-rectifying K(+) channels.
265 sal CA1 neurons and that a G-protein-coupled inward-rectifying potassium channel mediated regulation
266 xpression of specific BacNav orthologues, an inward-rectifying potassium channel, and connexin-43 in
267  potassium channel TRESK (2-pore-domain weak inward-rectifying potassium channel-related spinal cord
268 wer, acts via 5HT2A receptors to suppress an inward-rectifying potassium conductance in FSIs.
269  DMEK tissue, trifolded with the endothelium inward, reduces surgical trauma to donor cells and facil
270 hanism that couples the transport-associated inward release of the Na(+) ion from the Na2 site to int
271 d, but over a range of transmural pressures, inward remodelling occurred after T3-SCI with a 40% redu
272 dy demonstrates profibrosis and hypertrophic inward remodelling within the largest cerebral artery af
273 ctivation loop first opens up followed by an inward rotation of the alphaC-helix, takes place via a d
274 ormation, protecting nucleosomal DNA with an inward rotational setting, even though such DNA is, on a
275 To reinvestigate this phenomenon, we studied inward short-circuit currents (Isc) in tracheal mucosa f
276 hat are slow near the cortex and fast on the inward side of the subcortical microtubule layer.
277 s, and the asymmetric freezing dynamics with inward solidification causing not fully frozen mass to b
278 pneumatically-driven bending into multi-turn inward spiraling.
279 had started from the outside, then proceeded inward, suggesting that the size of the newly formed bon
280 ng the peak of the population discharge, the inward synaptic current was essentially mediated by glut
281 lular Cl(-) with gluconate(-) diminishes the inward tail current (Cl(-) efflux) at a membrane potenti
282 hat Zn(2+) dissociated more rapidly from the inward- than from the outward-facing state of DAT.
283 rd flow produces a relatively constant force inward, the peak of local contractile forces by CUs scal
284                                 If projected inward, the reaction is slow and not selective.
285 ar surface when CGS21680 is bound, due to an inward tilt of TM2 in that region.
286  narratives than when attention was directed inward to a mental arithmetic task during stimulus prese
287 binding domains, with loop L1 switching from inward to outward conformations with respect to the DNA
288 l gates as the protein transitioned from the inward to outward facing state.
289  as the mutant proteins were driven from the inward to the outward open Na(+)-bound conformation.
290 l that the Core domains of Bor1 have rotated inwards to achieve an occluded state.
291 nsporter facilitates a reorientation from an inward- to outward-facing state.
292 ly, with 5 degrees and 10 degrees LWIs, toes inward ('Toe in'), and toes outward ('Toe out wide').
293 ma toward the dendritic tips than for motion inwards toward the soma.
294 b activates the TRPM4 channel and results in inward transient cation currents that depolarize smooth
295 recruitment of repair proteins; for example, inward translocation of the DNA-end-binding protein Ku w
296  oligopeptide transporters (POTs) couple the inward transport of di- or tripeptides with an inwardly
297 d to Ala, was hyperactive, causing increased inward transport of phosphatidylethanolamine.
298 itro studies have shown that IMDs can induce inward tubulation of liposomes.
299 bit the cancellation between the outward and inward waves.
300      The third uridine is turned outwards or inward, wedging between the other uridines, thus filling
301  localizes to the CUs and subsequently moves inward with the actin flow.

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