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1 ased motor mechanism that resides in the OHC lateral wall.
2 membrane protein highly expressed in the OHC lateral wall.
3 e of sheet orientation in the late-activated lateral wall.
4 e and retained the geometry of the infarcted lateral wall.
5 and subepicardial ROIs were placed on the LV lateral wall.
6 ns and actually twisted clockwise at the AVV lateral wall.
7 olic kinase activity in the late-contracting lateral wall.
8  mammalian hearing and originates within its lateral wall.
9 eter of the PM was 22% of that of the intact lateral wall.
10  for electromotile force coupling in the OHC lateral wall.
11 s the second reduced counts primarily in the lateral wall.
12 types in the organ of Corti and the cochlear lateral wall.
13 dence of pedicle screw breach in the pedicle lateral wall.
14 ebral ventricle walls, mainly located in the lateral wall.
15 quires the metabolic support of the cochlear lateral wall.
16 esses in the cochlea, including the cochlear lateral wall.
17 in part because it is softer than the mature lateral wall.
18 l ganglion neurons, or cells of the cochlear lateral wall.
19 ade peptidoglycan in the division septum and lateral wall.
20 neurons, and, finally, the fibrocytes in the lateral wall.
21  dilatation, a thinned septum, and thickened lateral wall.
22 regions, whereas 84% of LV leads were in the lateral wall.
23 ficantly less at the flow divider versus the lateral wall.
24 tiating fibrocytes and marginal cells in the lateral wall.
25 the RV free wall, ventricular septum, and LV lateral wall.
26 rominence and central region in the cochlear lateral wall.
27  for interactions between the bundle and the lateral wall.
28 on of new peptidoglycan into portions of the lateral wall.
29 all sheet extension was >2 times that in the lateral wall (0.22+/-0.12 versus 0.09+/-0.06).
30 g (IVS, 0.009 +/- 0.002 mL.min-1.g-1.beat-1; lateral wall, 0.005 +/- 0.001 mL.min-1.g-1.beat-1; P = .
31 basal and midcavity septum compared with the lateral wall (11.0+/-1.4 versus 10.1+/-1.3 mm; P<0.001).
32 ); at 21 to 28 days, the difference was 50% (lateral wall, 14 +/- 6%; IVS, 28 +/- 6%; P = .0001).
33 H levels were significantly increased in the lateral wall 2 and 4 h post-exposure and returned to nor
34  followed by the tongue (57%), oropharyngeal lateral wall (49%), and epiglottis (26%).
35  was required for tether formations from OHC lateral wall (499 +/- 152 pN) than from OHC basal end (1
36 r each patient, located at the extreme basal lateral wall (8 of 11 patients) and other regions (9 of
37 our LV ROIs (anterior, posterior, septal and lateral wall, 99 +/- 2, 94 +/- 5, 94 +/- 4 and 97 +/- 3%
38 in septum showed exaggerated loading and the lateral walls a low load.
39 V2.7m8) and the other targeting the cochlear lateral wall (AAV8BP2).
40                                              Lateral wall ablation was performed either by creating a
41 ia characteristics, resulting in a defective lateral wall, abnormal neuroblast migration and differen
42                                      The OHC lateral wall above the nuclear level is composed of the
43 found that deletion of Panx1 in the cochlear lateral wall almost abolished ATP release under physiolo
44 nt tether length, was 3.71 pN/microm for OHC lateral wall and 4.57 pN/microm for OHC basal end.
45 ochlear potential generation in the cochlear lateral wall and caused outer hair cell electromotor pro
46 ween the mitral valve annulus pACC at the LV lateral wall and mean LAP.
47 of Corti and modiolar core, by L-NAME in the lateral wall and modiolar core, and by NAC in all three
48 inantly in the basal-midventricular inferior-lateral wall and papillary muscles.
49 ted nonlinear capacitance resided in the OHC lateral wall and was not detected at the apical cuticula
50 orientation (anterior, posterior, medial, or lateral wall), and proximity/relationship to the major p
51 erenol stimulation in DHF (both anterior and lateral walls), and CRT substantially improved both.
52 A is present in the neurosensory epithelium, lateral wall, and spiral limbus of the cochlea, with hig
53 heterogeneity (>10 fold) comparing septum to lateral walls, and enhanced growth and metabolic kinase
54 lume of the tongue, parapharyngeal fat pads, lateral walls, and soft palate) was similar between subj
55                                          The lateral walls are affected most by strain, and the septa
56 t all primary, coarse-grained platy calcitic lateral walls are covered by fine-grained fibrous aragon
57 d C(peak) increase with the logarithm of the lateral wall area (A(LW)) and determine from the functio
58 omputer simulation model showed that the hot lateral wall artifact found in SPECT myocardial perfusio
59 d, reconstructed SPECT images showed the hot lateral wall artifact with a mean septal-to-lateral wall
60 hing caused an additional 9% decrease in the lateral wall as a result of the adjacent lung-lateral wa
61 tially linked to beta(1-3)glucan, and in the lateral wall, attached in part to beta(1-6)glucan.
62 ural bead columns were inserted into the mid-lateral wall between the PMs.
63 ateral wall as a result of the adjacent lung-lateral wall boundary.
64 the septal ring and scattered foci along the lateral wall, but mutants have no phenotypic change.
65 eart and around the circumference toward the lateral wall, but not the interventricular septum.
66 s is markedly upregulated selectively in the lateral wall by noise exposure, presumably in response t
67                                   IVS and LV lateral wall circumferential strain (CS) were both reduc
68        We selectively labeled and imaged the lateral wall components in the isolated guinea pig OHC u
69 ional LV ischemia involving the inferior and lateral walls confers increased likelihood of RV dysfunc
70 cal vent insertion (49%), in the inferior or lateral wall consistent with infarction (5%), or in othe
71                               With RBBB, the lateral wall contracts early so that biventricular (BiV)
72 ions in the mechanical properties of the OHC lateral wall could play a role in the modulation of OHC
73 id not show hot lateral wall (mean septal-to-lateral wall count ratio = 1.04) and the ratios changed
74 the filling of the left lung (mean septal-to-lateral wall count ratio = 1.05).
75 id not show hot lateral wall (mean septal-to-lateral wall count ratio = 1.07).
76  lateral wall artifact with a mean septal-to-lateral wall count ratio of 0.86.
77 ups persisted for IVS CS (P<0.01) but not LV lateral wall CS (P=0.09).
78                       Although IVS CS and LV lateral wall CS correlated with pulmonary artery systoli
79 oherence interferometry through the cochlear lateral wall demonstrates that the time difference betwe
80                 Subsequently, attachments to lateral walls disappear and attachments to microtubule e
81  provide durability and may contact with the lateral wall either to give additional anchoring of the
82 ere approximately 2 times higher than in the lateral wall (epicardium, 0.14+/-0.07 versus 0.05+/-0.03
83 was more pronounced in the right ventricular lateral wall, expressed by worsening in longitudinal str
84 ope and is determined by the balance between lateral wall extension and synthesis of peptidoglycan at
85  in patients without MVP with basal inferior-lateral wall fibrosis (n=20).
86  pocket of 0.5 L volume was punched into the lateral wall for each control trial.
87  PBP3, PBP5 and PBP4a, and possibly PBP4, in lateral wall growth.
88 nvolved the subepicardial layer inferior and lateral wall in 154 patients (41%; IL group), the midwal
89 T is achieved over a fairly broad area of LV lateral wall in both nonfailing and failing hearts, with
90 uld have subsequently expanded to the entire lateral wall in outer hair cells.
91 y less at the flow divider compared with the lateral wall in the DES group (0.07 mm [interquartile ra
92 reater at the flow divider compared with the lateral wall in the DES group (uncovered: 40% [IQR 16% t
93 direction through an opening in the cochlear lateral wall in this study.
94 (P < 0.0032) and ventral displacement of the lateral walls in the mid- and caudal regions (P < 0.0001
95 beling in tanycytes of the ventral floor and lateral walls in the tuberal and mammillary recess porti
96 PBP3 and PBP4a localized specifically to the lateral wall, in distinct foci, whereas PBP1 and PBP2b l
97 of the molecular and ionic substrates of the lateral wall, including those necessary for electromotil
98                    The outer hair cell (OHC) lateral wall is a unique trilaminate structure consistin
99                                      The OHC lateral wall is a unique trilaminate structure consistin
100  side of the nostril sulcus representing the lateral wall is funnel-like.
101 vide on the mechanical properties of the OHC lateral wall is important for understanding the mechanis
102     Electromechanical coupling in the cell's lateral wall is modeled in terms of linear constitutive
103 ration of contraction of both the septum and lateral wall is shorter in obstructed patients with the
104 stable for generations while material in the lateral walls is diluted by growth and turnover.
105                        Regional inferior and lateral wall ischemia was greater among patients with RV
106 e cytoskeletal framework associated with the lateral wall known as the cortical lattice.
107             Recurrent conduction through the lateral wall lesions was associated with intraprocedural
108                                           RV lateral wall longitudinal strain (LS) and interventricul
109                                           RV lateral wall LS and IVS LS, but not LV lateral wall LS,
110 2+/-3.9%, P=0.002, respectively), whereas LV lateral wall LS was preserved.
111    RV lateral wall LS and IVS LS, but not LV lateral wall LS, correlated with pulmonary artery systol
112      Comparisons of the transcriptome in the lateral wall (LW) with other cochlear regions in a mouse
113 thout left lung wrap-around did not show hot lateral wall (mean septal-to-lateral wall count ratio =
114 ients, reconstructed images did not show hot lateral wall (mean septal-to-lateral wall count ratio =
115                        Participants received lateral wall, medial wall, 2.5 wall, or 3 wall decompres
116 duces an electromechanical response in their lateral wall membrane.
117 mesenchymal cells differentiate to shape the lateral wall, modiolus and pericochlear spaces.
118 tality was increased in patients with severe lateral wall motion abnormalities (p = 0.05), ST-segment
119 F at presentation, length of stay, prior MI, lateral wall motion abnormality at presentation, and pea
120 m -20.4 +/- 9.6% to -30.5 +/- 14.0%, whereas lateral wall motion occurred earlier with no net magnitu
121  decrease in systolic wall thickening in the lateral wall occurred compared with the interventricular
122 duction of a localized cell expansion in the lateral wall of a root epidermal cell.
123 cells, whereas it was detected in the entire lateral wall of cochlear outer hair cells and had an int
124 ior alveolar artery (PSAA) is located on the lateral wall of maxillary sinus and may become injured d
125 cified pseudoaneurysm arising from the right lateral wall of the abdominal aorta with the neck of the
126                                          The lateral wall of the avian braincase, which is indicative
127                                          The lateral wall of the braincase lies along a boundary in t
128 pulations of mesoderm, will give rise to the lateral wall of the braincase.
129 r may determine the final composition of the lateral wall of the braincase.
130 eactivity is present in the spiral ganglion, lateral wall of the cochlea, and organ of Corti, all tar
131 e mammalian subventricular zone (SVZ) of the lateral wall of the forebrain ventricle retains a popula
132 ventricular zone (SVZ), lies adjacent to the lateral wall of the lateral ventricle and is responsible
133 ration of neuronal precursors throughout the lateral wall of the lateral ventricle in the adult mamma
134                                          The lateral wall of the lateral ventricle in the human brain
135 e present in the brains, particularly in the lateral wall of the lateral ventricle of juvenile (3-mon
136                          Whole mounts of the lateral wall of the lateral ventricle stained for the ne
137 the subventricular zone (SVZ) throughout the lateral wall of the lateral ventricle.
138 orm regenerative units (pinwheels) along the lateral wall of the lateral ventricle.
139             We show here that the SVZ of the lateral wall of the lateral ventricles in adult mice is
140  ependymal cells during the formation of the lateral wall of the lateral ventricles in the brain.
141           It is the subependymal zone of the lateral wall of the lateral ventricles.
142 cell niche that lies along the length of the lateral wall of the lateral ventricles.
143 art failure induced by rapid pacing from the lateral wall of the left ventricle (220 +/- 9 bpm for 26
144  AVL, V5, and V6 accurately demonstrated the lateral wall of the left ventricle (p < 0.0001).
145 laris (SV) is a stratified epithelium in the lateral wall of the mammalian cochlea, responsible for b
146 his study is to compare the thickness of the lateral wall of the maxillary sinus (TLWMS) and the thic
147 r superior alveolar artery that supplies the lateral wall of the maxillary sinus.
148  collected an additional five swabs from the lateral wall of the mid-vagina.
149 vely flat central ulcer on the right postero-lateral wall of the midesophagus below the level of the
150                                          The lateral wall of the mouse subventricular zone harbors ne
151 taining cells fated to form a portion of the lateral wall of the neural tube at essentially all rostr
152 n kinase type IV-were immunolocalized to the lateral wall of the OHC.
153             The time to peak velocity in the lateral wall of the patients, as compared with that in t
154                  Lesions were present in the lateral wall of the RA (six of seven maps) and in the LA
155 in six cases, three involving lesions in the lateral wall of the RA and three involving the LA septum
156 y, temporary pacing leads were placed in the lateral wall of the right atrium and at the roof of the
157 ricle (P=0.021), and conduction delay to the lateral wall of the systemic ventricle (P=0.01) were ass
158 ose with lower SVEF, conduction delay to the lateral wall of the systemic ventricle, and those with a
159 ateral ventricle on images that depicted the lateral wall of the ventricle.
160 se that forms U-shaped patterns facing outer lateral walls of epidermis and cortex cells.
161        Human chromosomes attach initially to lateral walls of microtubules.
162 aining nucleation complexes localized to the lateral walls of pre-existing CMTs.
163 ns, localizes peptidoglycan synthesis in the lateral walls of rod-shaped cells.
164  of the CD1b heavy chain in the superior and lateral walls of the A' pocket.
165 ained and some IcsA is distributed along the lateral walls of the bacillus.
166 n irreplaceable role in the extension of the lateral walls of the cell.
167 g chamber by unfolding helices that form the lateral walls of the chamber.
168              Transversal shear stress on the lateral walls of the foot processes was prominently incr
169 l canal, at the polar ends of the VW, at the lateral walls of the GCs and at the periclinal cell wall
170 ntraoperative tissue (n = 43) samples of the lateral walls of the human lateral ventricles.
171 en the greater palatine foramina (GPFd), the lateral walls of the nasal cavity (NCd), and the infraor
172 itions of the greater palatine foramina, the lateral walls of the nasal cavity, and the infraorbital
173 s located in the adhesions of the medial and lateral walls of the rostral LVs upregulated parvalbumin
174 ependymal cells that line the bottom and the lateral walls of the third ventricle.
175  CT caused a major artifactual defect in the lateral wall on the PET image.
176 etimes with irregular distribution along the lateral wall or a preference for the septum.
177           The incidence of oscillopsia after lateral wall orbital decompression was 35% when patients
178                   Prior tumor resection with lateral wall osteotomy and failure to adhere to all prot
179                   Prior tumor resection with lateral wall osteotomy, delay in IACC implementation or
180 m stretch was significantly increased in the lateral walls (P < 0.023) in a ventral-lateral direction
181 ltivariable analysis, inducible inferior and lateral wall perfusion defects increased the likelihood
182  mutant (or depletion of all three isoforms) lateral wall PG synthesis was impaired and the cells bec
183                         We conclude that the lateral wall PM is more compliant than the CL/SSC comple
184 ided septal flash with simultaneous RV basal lateral wall prestretch/late activation.
185 al activation (right-sided septal flash), RV lateral wall prestretch/late contraction, postsystolic s
186 g" strains were significantly greater at the lateral wall, regardless of short-axis level, whereas E(
187 ndividuals and the presence of oropharyngeal lateral-wall related obstruction; it was also associated
188 loaded chamber (containing the electromotile lateral wall) relative to the lower portion (containing
189 ventricular septum, and the left ventricular lateral wall, reproducing the pattern of fibrosis found
190    This type of asymmetric mineralization of lateral walls results from the vertical arrangement of t
191                                      (2) All lateral wall right atrial activation can be uniform duri
192 icular, we sought an explanation for the hot lateral wall seen in SPECT images from normal female and
193                                     Vertical lateral walls separating autozooid chambers have aragoni
194     In nonstented coronary bifurcations, the lateral wall showed significantly greater intima as well
195             Optimal CRT was achieved from LV lateral wall sites, slightly more anterior than posterio
196 d to affect both the motor protein and other lateral wall stiffness components.
197                                 We find that lateral wall stiffness, defined by the surface modulus,
198  cells by stereocilia displacement and/or by lateral wall stretching result in a frequency-dependent
199 e of the different functional regions (e.g., lateral wall, synaptic basal pole) of the polarized cell
200 dibular symphysis area, and thickness of the lateral wall (T-LW) of the maxillary sinus.
201                          The maxillary sinus lateral wall tends to increase in thickness from the sec
202 rotease activity was higher in the infarcted lateral wall than in the remote, uninjured septum on ex
203  includes taste buds, papilla epithelium and lateral walls that extend into underlying connective tis
204 d flow per beat between the left ventricular lateral wall (the site of stimulation) and the IVS was f
205        As compared with the intensity at the lateral wall, the intensities of prestin labeling at the
206 of the present study is to examine the sinus lateral wall thickness (LWT) of atrophic posterior maxil
207 5%) thicker LV walls with a normal septal-to-lateral wall thickness ratio.
208 also indicate that lipid peroxidation in the lateral wall tissues does not influence permanent thresh
209 formed in the organ of Corti, but not in the lateral wall tissues.
210      LVLWS/LVSWS was more robust than the LV lateral wall to LV septal wall ratio of early diastolic
211 rial lines were created in the posterior and lateral walls using low- and high-energy settings, respe
212 ctions in tongue fat and pterygoid and total lateral wall volumes.
213 end-systole and post-end-systole in inferior-lateral wall was frequent in patients with fibrosis (81
214 hereas during dyssynchrony (DDD pacing), the lateral wall was more loaded, and the septum was unloade
215  ablation procedure, conduction block in the lateral wall was verified in 10 of 14 patients using 1 o
216 ession analysis the volume of the tongue and lateral walls was shown to independently increase the ri
217 rimitral ATs had larger areas of AAPs on the lateral wall whereas patients with roof-dependent ATs ha
218 ling was found at the outer layer of the OHC lateral wall, which was further evidenced by use of a hy
219  to shift and rotate in the plane of the OHC lateral wall with a dynamics tightly regulated by membra

 
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