ライフサイエンスコーパス: septum

1 in removal with maximal rates in the lateral septum.

2 o exert focal pressure upon the intra-atrial septum.

3 rotein FtsK may license recombination at the septum.

4 affected by muscimol inactivation of medial septum.

5 e nasal bone process and cartilaginous nasal septum.

6 tures, cranial base synchondroses, and nasal septum.

7 de medially through formation of a cell wall septum.

8 on unidirectional regulation via the medial septum.

9 ed in the anterior left ventricular wall and septum.

10 ns (CVOs), olfactory bulbs, hippocampus, and septum.

11 cell separation with a thinner and defective septum.

12 ortices (eddies) on the upstream side of the septum.

13 ddy-trapped nuclei function to reinforce the septum.

14 th of the cell in the absence of a completed septum.

15 point-source release, but again, not to the septum.

16 trongly influenced by inputs from the medial septum.

17 e lateral wall, but not the interventricular septum.

18 peptidoglycan-like sacculus and/or division septum.

19 nd is concentrated at the poles and division septum.

20 ablation at the left side of the ventricular septum.

21 system depend on the integrity of the medial septum.

22 y mechanism for cholinergic functions of the septum.

23 pha by a short truncated stalk with a single septum.

24 a, of which some are attached to hyphae by a septum.

25 rongly curved leading edge of the developing septum.

26 e divisome, allowing cells to synthesise the septum.

27 rons receive GABAergic input from the medial septum.

28 at interrupted PG synthesis destabilizes the septum.

29 ic cells in the DG and project to the medial septum.

30 rtrophy involving the basal interventricular septum.

31 dial versus longitudinal PG insertion at the septum.

32 xtended anteriorly into the interventricular septum.

33 orsal and intermediate region of the lateral septum.

34 ith activity patterns governed by the medial septum.

35 a local role for MGP in the developing nasal septum.

36 rs during the development of the ventricular septum.

37 poptotic chondrocytes in the calcified nasal septum.

38 years, prior sinonasal surgery and S-shaped septum.

39 arently being prevented by the intermuscular septum.

40 n of peptidoglycan remodeling at the forming septum.

41 venous approach through the interventricular septum.

42 te cell wall synthesis and hydrolysis at the septum.

43 s 923 +/- 12 ms; P < 0.005; interventricular septum 1003 +/- 31 vs 974 +/- 21 ms, P < 0.05; entire LV

44 Cardiac hypertrophy (interventricular septum, 12+/-4 [7-23] mm; left ventricular posterior wal

45 imal left ventricular thickness in the basal septum (19-31 mm), severe basal LVOTO (70-120 mm Hg), an

46 nts, most commonly involving the left atrial septum (32/43; 74.4%).

47 nstrated (1) a single LV breakthrough at the septum (38+/-15 ms post-QRS onset); (2) prolonged right-

48 cardioversion before PVAI and posterior wall/septum ablation while in sinus rhythm (group 1), versus

49 autonomous manner, with cells separated by a septum able to maintain different MT dynamics.

50 ns in the anterodorsal region of the primate septum (ADS) are primarily devoted to processing uncerta

51 atrophy of subcortical structures (striatum, septum, amygdala).

52 th pulmonary atresia with intact ventricular septum and 28 with virtual atresia) underwent RV decompr

53 s, 480 (62%) for TGA with intact ventricular septum and 298 (38%) for TGA with ventricular septal def

54 nt in 79% of patients with ATTR (70% sigmoid septum and 30% reverse septal contour), whereas symmetri

55 at are sealed with a silicone cap and Teflon septum and allow syntheses to be performed on a 2-6 mL s

56 ytocin receptor (OTR) binding in the lateral septum and amygdala.

57 rns revealed collection due to a hemivaginal septum and an absent ipsilateral kidney; thus, establish

58 depress cortical function, including lateral septum and anterior hypothalamus.

59 SpoIIIAH interact across the double membrane septum and are thought to assemble into a channel that s

60 rng10Delta and rga7Delta result in defective septum and cell lysis during cytokinesis.

61 s of EGFP(+) cells in epithelia of the nasal septum and conchae.

62 at the GABAergic innervation from the medial septum and diagonal band complex contributes to temporal

63 GABAergic projections from the medial septum and diagonal band complex exclusively innervate G

64 The medial septum and diagonal band of Broca (MS-DBB) has an essent

65 ut to the hippocampus arises from the medial septum and diagonal band of Broca (MS-DBB), and we inves

66 pulation of neurons in the medial BF (medial septum and diagonal band of Broca) of macaque monkeys en

67 ed by a loss of effective contraction in the septum and free wall, coupled with reduced basal longitu

68 (SCN) that paralleled changes in the medial septum and hippocampus, but not in other neural structur

69 ore dense ascending NI projections to medial septum and hippocampus.

70 es reduces the thickness of interventricular septum and interstitial fibrosis and increases anterior

71 dem to degrade peptidoglycan in the division septum and lateral wall.

72 ion, but abnormal upper longitudinal vaginal septum and lower vaginal agenesis.

73 ssociated significant bowing (>15 mm) of the septum and mild obliteration of the right ventricular ca

74 f the mitral valve leaflets, and interatrial septum and mild pericardial effusion.

75 nchymal cushion that later gives rise to the septum and mitral and tricuspid valves.

76 Whereas some variations, e.g., the septum and morphology of the sinus, have been extensivel

77 licated terminus region is released from the septum and recoils to the center of a sister nucleoid.

78 ded all cases of TGA with intact ventricular septum and TGA with ventricular septal defect performed

79 stress reduced hippocampal correlations with septum and thalamus and increased correlations with amyg

80 rea of the contact between the hypertrophied septum and the anterior leaflet of the mitral valve.

81 engulfment in which the junction between the septum and the lateral cell wall moves around the foresp

82 rtilage, failure of fusion between the nasal septum and the secondary palate, and higher levels of ph

83 ut from the rostral BF, including the medial septum and the vertical and horizontal limbs of the diag

84 ar septal defect, 238 (59.5%) with an intact septum, and 9 (2.3%) with a Taussig-Bing anomaly, were f

85 minantly from the prefrontal cortex, lateral septum, and amygdala.

86 is expressed in the basal forebrain, in the septum, and in some amygdalar nuclei in the adult rodent

87 re cell clusters within the amygdala, medial septum, and inferior raphe.

88 , nucleus incertus, supramammillary nucleus, septum, and laterodorsal tegmental nucleus.

89 ctions to ventral hippocampus, ventrolateral septum, and LHb originated from the dorsocaudal IP.

90 ction, myocardial delayed enhancement of the septum, and mediastinal lymphadenopathy should raise the

91 ction, myocardial delayed enhancement of the septum, and mediastinal lymphadenopathy were more often

92 es a strong cholinergic innervation from the septum, and muscarinic acetylcholine receptors (mAChRs)

93 res such as PFO size, associated hypermobile septum, and presence of a right-to-left shunt at rest ha

94 risk markers of large PFO size, hypermobile septum, and presence of right-to-left shunt at rest are

95 he RV insertion points, the interventricular septum, and the left ventricular lateral wall, reproduci

96 ventral midbrain that project to the lateral septum, and we reveal essential roles for Neurod1 and Ne

97 was patchy with a predilection for the basal septum, anterior wall, and perivalvular regions.

98 In select cases, the basal septum appears compartmentalized as the stimulated wavef

99 selective cholinergic lesions of the medial septum area (MS) or nucleus basalis magnocellularis (NBM

100 ta throughout the right ventricular wall and septum, as well.

101 ring sliding from cell poles, which prevents septum assembly at the ends of cells with a displaced nu

102 nisms such as a ParAB Brownian ratchet and a septum-associated FtsK motor.

103 mentous fungus Aspergillus nidulans SPBs and septum-associated MTOCs were described.

104 Testing different septum-associated proteins for a role in sMTOC function,

105 mbe eMTOCs, A. nidulans sMTOCS are permanent septum-associated structures.

106 thus facilitating placement of the division septum at the midcell.

107 nsities of terminals were encountered in the septum, bed nucleus of the stria terminalis, substantia

108 es communicating channels that penetrate the septum between adjacent cells.

109 ed to complete the division, leaving a clear septum between the two daughter liposomes.

110 n the basal left ventricle, particularly the septum, but also basal inferior wall and subaortic mitra

111 embryonic cells of the cortex, striatum, and septum, but this lineage relationship is lost before E15

112 scovered that PBP4 is active not only at the septum, but unexpectedly at the peripheral wall as well.

113 se receptors were knocked out in the lateral septum by infusion of recombinant adeno-associated viral

114 Intact or highly restricted intra-atrial septum can be reliably diagnosed in the human fetus as e

115 ction of the ring is to spatially coordinate septum cell wall assembly.

116 ich contractile forces of the ring shape the septum cell wall by stimulating the cell wall machinery

117 othalamus from somatostatin-positive lateral septum cells evokes food approach without affecting food

118 d nucleus of the stria terminalis to lateral septum circuit.

119 nd how Z-ring contraction limits the rate of septum closure during cytokinesis in Escherichia coli ce

120 Surprisingly, septum closure rate was robust to substantial changes in

121 ase (P<0.001) and in the basal and midcavity septum compared with the lateral wall (11.0+/-1.4 versus

122 condary septum formation and correct primary septum completion.

123 CpoB localizes to the septum concurrent with PBP1B-LpoB and Tol at the onset o

124 hat in the absence of a functional ring, the septum continues to ingress but in a disorganized and as

125 campus, paraventricular thalamus and lateral septum correlated with genotype-related differences in b

126 Furthermore, multiple nodule with fibrous septum could suggest subtype AB.

127 ich was explained by opposite changes in the septum (decrease) and lateral (increase) wall.

128 th pulmonary atresia with intact ventricular septum deemed suitable for RV decompression have a high

129 inding revealed before closing a ventricular septum defect; - 1 patient during follow-up performed 2

130 evelopment, carbohydrate metabolism, cardiac septum development and glucose metabolism.

131 eurons) across its different regions (medial septum, diagonal band, magnocellular preoptic area, and

132 Aergic and cholinergic neurons in the medial septum-diagonal band of Broca (MSDB) have been associate

133 (mPSCs) was substantially blunted for medial septum/diagonal band (MS/DB) neurons in brain slices on

134 ptogenetic protein oChIEF-tdTomato in medial septum/diagonal band of Broca cholinergic neurons using

135 The medial septum/diagonal band of Broca complex (MSDB) is a key st

136 itter acetylcholine, derived from the medial septum/diagonal band of Broca complex, has been accorded

137 RV/(left ventricle + septum) did not rise directly in proportion to RV systol

138 d and apical portion of the interventricular septum dissecting into the basal part.

139 tarting at early anaphase and spreads to the septum during and after ring constriction.

140 es of cross-linking in S. aureus: one at the septum during cell division, and another at the peripher

141 B appears to co-ordinate PG synthesis at the septum during division and at the side-wall during elong

142 Autologous native cartilage from the nasal septum, ear, or rib is the standard material for surgica

143 itically, at P12, inactivation of the medial septum eliminates theta in both structures.

144 Inhibitory inputs from the lateral septum enable separate signalling by lateral hypothalamu

145 pn(KO) mutant they commonly deviate into the septum even in the absence of a muscular VSD.

146 in each of three subdivisions of the lateral septum, females had greater CRF2 binding than males as j

147 Myofibers in the ventricular septum follow a stereotypical pattern that is disrupted

148 Strikingly, proteins involved in septum formation (the chitin synthase Chs2) and/or its c

149 ning in the cell middle, before the start of septum formation and anchorage to the cell wall.

150 d beta(1,3)glucan is essential for secondary septum formation and correct primary septum completion.

151 C14 is required for normal cell division and septum formation and FgCdc14 possesses phosphatase activ

152 shape, suggesting that SspA plays a role in septum formation and spore maturation.

153 are in the same genetic pathways to regulate septum formation and/or cell separation.

154 alysis, and that its biochemical activity in septum formation can be provided by PBP 3.

155 vesicle traffic during polarized growth and septum formation during cytokinesis.

156 dynamics of glucan synthases for successful septum formation in cytokinesis.

157 4 phosphatase functions in cell division and septum formation in F. graminearum, likely by counteract

158 indings prompt not only a partial rethink of septum formation in S. pneumoniae, but consideration of

159 Interaction with FtsZ required for septum formation is one of the host interventions for in

160 What keeps Chs3 inactive until secondary septum formation remains unknown.

161 Scd1 promotes normal septum formation, andscd1Deltacells display aberrant sep

162 ater to the ingressing membrane and promotes septum formation.

163 ck in the completion, but not initiation, of septum formation.

164 ogy consistent with the inhibition of normal septum formation.

165 g cleavage-furrow ingression through primary septum formation.

166 to help ensure that the cytokinetic division septum forms only at the mid-cell position.

167 In this process, the septum generates less than one hemisphere of each daught

168 us aureus undergoes cytokinesis, it builds a septum, generating two hemispherical daughters whose cel

169 shapes, we show that the ring promotes local septum growth in a curvature-dependent manner, allowing

170 ch BFCNs and some GABA neurons in the medial septum had been destroyed by mu P75-saporin, human MGE-l

171 6 mm cartilage biopsy sample from the nasal septum harvested under local anaesthesia during collecti

172 ctions from the nucleus incertus (NI) to the septum have been implicated in the modulation of hippoca

173 Fetal interventions targeting the atrial septum have used a direct approach through the atrial wa

174 re pulmonary atresia with intact ventricular septum (hazard ratio [HR]: 3.64, 95% confidence interval

175 We observe that the septum hole and ring are circular and centered in wild-t

176 way ablation was accomplished from the right septum in 110 patients, and from the left septum in 3 pa

177 tional target sites at the right ventricular septum in 2 patients (22%) and at the epicardium in 1 pa

178 ht septum in 110 patients, and from the left septum in 3 patients, in the atypical group.

179 e cells, showing that it is recruited to the septum in a manner dependent on wall teichoic acid.

180 ular septal wall thickness (interventricular septum in diastole Z value, +0.45 +/- 0.49, P < 0.001) a

181 al YFP-QueE fusion localizes to the division septum in filamentous cells, suggesting QueE blocks sept

182 prevent abnormal mineralization of the nasal septum in Mgp(-/-);Hyp compound mutants.

183 ircumventricular regions of the habenula and septum in mice.

184 ctivity was recorded at the left side of the septum in proximity to the His-bundle.

185 rojection from the hippocampus to the medial septum in rats, and thereby simulate hippocampal input o

186 peptidoglycan synthesis is restricted to the septum in spherical bacteria, and instead indicate the p

187 day 10, 28.7% +/- 5.2 on day 20; P < .001 vs septum) in areas of in Eu-HP-DO3A-labeled cell grafts.

188 ne expression of whole septum (LS and medial septum) in selectively bred maternal mice.

189 rtion of cells projecting selectively to the septum; in turn, EBGNs were targeted by septal and entor

190 tal diagonal band and areas of the posterior septum including the septofimbrial and triangular septal

191 ion yeast scaffold molecule Sid4 anchors the septum initiation network to the spindle pole body (SPB,

192 -long timescale, and was dependent on medial septum inputs.

193 creases in the thickness of interventricular septum, interstitial fibrosis, and phosphorylated p38 mi

194 ing division for reshaping the flat division septum into a curved surface.

195 By integrating a small triangular septum into the waveguide plate, we are able to direct t

196 Aneurysm of the muscular interventricular septum is a rare entity as compared to the membranous pa

197 venous approach through the interventricular septum is feasible in patients.

198 Targeting specific sites of the interatrial septum is followed by an increase in heart rate and atri

199 PG synthesis at the cell division septum is necessary for constructing new poles of progen

200 divisome and work together to synthesize the septum is not well understood.

201 After division is completed and the dividing septum is thinned, the mother cell engulfs the forespore

202 entetate dimeglumine in the interventricular septum, left ventricular (LV) free wall and encompassing

203 including thickening of the interventricular septum, left ventricular volume reduction, left ventricu

204 Basal septum LS, the combined average LS of basal and mid inte

205 e recently examined gene expression of whole septum (LS and medial septum) in selectively bred matern

206 glutamatergic synaptic inputs to the lateral septum (LS) and optogenetic activation of vHPC projectio

207 ng effects on neural activity in the lateral septum (LS) are both necessary and sufficient to cause s

208 Lateral septum (LS) has re-emerged as an important structure in

209 Lateral septum (LS) is a brain region critically involved with a

210 acid (GABA) neurotransmission in the lateral septum (LS) is implicated in modulating various behavior

211 Lesioning the lateral septum (LS) is known to cause "septal rage," a phenotype

212 The lateral septum (LS) is thought to suppress fear and anxiety thro

213 lutamate/GABA-glutamine cycle in the lateral septum (LS) of postpartum female mice.

214 ghly diffuse cell walls (particularly at the septum), marked alterations in fatty acid composition an

215 ocardial pacing through the interventriuclar septum may offer a simpler solution.

216 GABAergic projection neurons from the medial septum (MS) as the major afferents to dentate PV interne

217 The medial septum (MS) is required for theta rhythmic oscillations

218 The medial septum (MS) is strongly linked to locomotor behavior, an

219 ved auditory input primarily from the medial septum (MS), rather than AC.

220 (n=8), lateral RV (n=44), RV apex (n=61), RV septum (n=29), LV apex (n=12), LV midlateral wall (n=17)

221 Formation of a division septum near a randomly chosen pole during sporulation in

222 basal left ventricular summit in 4, and LVOT septum near the His bundle in 1.

223 left ventricular summit, and rarely the LVOT septum near the His bundle.

224 The presence of neither a hypermobile septum nor a right-to-left shunt at rest was detected mo

225 on of synaptic circuits involving the medial septum of mice, we have identified postsynaptic cortical

226 ovoid shape, was localized at the poles and septum of pneumococcal chains of ovoid, nonseparated bac

227 with the nucleation of the inclusions at the septum of the cells, showing an intricate and original c

228 protein localized to a ring adjacent to the septum on each end of the rod-shaped cell.

229 uired to recruit SpoIIIAH to the sporulation septum on the mother cell side; however, the mechanism b

230 embranous bones and enlargement of the nasal septum or defects in vomeronasal cartilage.

231 elease of excess cell wall material from the septum or newly born cell poles.

232 lly, we found that some EBGNs located in the septum or the entorhinal cortex also displayed a long-ra

233 Injection of anterograde tracers into medial septum, or triangular septal and septofimbrial nuclei, r

234 known to govern cell wall hydrolysis at the septum, our findings indicate that FtsEX acts on FtsA to

235 llosum, arachnoid cyst, abnormalities of the septum pellucidum and the fornix.

236 itary, absent pituitary infundibulum, absent septum pellucidum, migration anomalies, and hemispheric

237 sotopic N2O laser analyzer through a syringe septum port.

238 at the division site before FtsZ and guides septum positioning in pneumococcus.

239 ly required for the survival of this lateral-septum projecting neuronal subset during development.

240 the division site, and timely recruitment of septum protein Bgs1.

241 In the septum, regional work was indeed increased in MI rats co

242 ssemble into the divisome and synthesize the septum remains poorly understood.

243 erivative tissues, such as the ovule and the septum, resulting in a split gynoecium and no observable

244 lionic eminences and adjacent regions of the septum, resulting in an approximately 30% increase in ad

245 Anterograde axonal tracing from the septum revealed extensive innervation of the hippocampus

246 (55% women; age, 18-76 years), free wall and septum RVLS (6 segments) and free wall RVLS (3 segments)

247 er positioning against the right ventricular septum (RVS) using a preshaped guiding catheter, driven

248 ver, the precise contributions of the medial septum's cholinergic neurones to these functions remain

249 The muscular ventricular septum separates the flow of oxygenated and de-oxygenate

250 The septum, shared between ventricles and affected by septal

251 n having some similarity to the B. anthracis septum site-determining protein MinD and a C-terminal do

252 sion protein SspA-mCherry localized first to septum sites, then subsequently around the surface of th

253 This is the first evidence for a septum-specific protein, Spa10, as anchor for a specific

254 , and reticular formation, hypothalamus, and septum/striatum of the left hemisphere was correlated wi

255 zation of these receptors within the lateral septum, suggesting that not only different neurotransmit

256 Z-rings, leading to the frequent abortion of septum synthesis, which in turn results in the productio

257 formed Z-rings is crucial for completion of septum synthesis.

258 he NI resulted in retrograde labeling in the septum that was concentrated in the horizontal diagonal

259 provide gamma-rhythmic inputs to the lateral septum; these inputs are causally associated with improv

260 correlation with diastolic interventricular septum thickness in those athletes.

261 tween J-point elevation and interventricular septum thickness suggests a possible mechanistic role of

262 acid (18:2n6) and diastolic interventricular septum thickness.

263 rdiac hypertrophy, as indicated by increased septum thickness.

264 Contrary to this, we found the nasal septum to be abnormally mineralized and shortened in Mgp

265 -dependent manner, allowing even a misshapen septum to grow into a more regular shape.

266 croscopy in strains with a thick sporulation septum to investigate the architecture and function of t

267 e anterior hypothalamus and then the lateral septum to modulate aggression associated with mate guard

268 ly encode hippocampal feedback, enabling the septum to monitor ongoing patterns of activity in the hi

269 in the small cell by transfer from the polar septum to the adjacent cell pole where SpoIIE is protect

270 monstrate that top-down projections from the septum to the hypothalamus control food intake negativel

271 atheter, driven through the interventricular septum to the LVS.

272 cending projection from medial and posterior septum to the NI that provides a "feedback loop" to modu

273 eviously uncharacterized projection from the septum to the NI, which may provide feedback modulation

274 waveguide outputs varies exponentially with septum translation offset and that nearly 100% transmiss

275 proepicardial organ on the right side of the septum transversum caudal to the developing heart.

276 have conditionally inactivated Gata4 in the septum transversum mesenchyme and its derivatives by usi

277 s of Gata4 in the hepatic endoderm or in the septum transversum mesenchyme remains to be determined.

278 e position of the proepicardial organ on the septum transversum.

279 ic bud and in the adjacent mesenchyme of the septum transversum.

280 cular development, we show that extracardiac septum transversum/proepicardium (ST/PE)-derived endothe

281 em into four easily recognized groups: nasal septum variations, middle turbinate variations, uncinate

282 th pulmonary atresia with intact ventricular septum vary widely.

283 open-cell design stent into the fetal atrial septum via a percutaneous access route through the fetal

284 itudinal peak systolic strain (LSsys) in the septum was assessed by 2-dimensional speckle tracking im

285 We found that the division septum was built at discrete sites that moved around the

286 Once exposed, the newly formed septum was found to be stiffer than the surrounding, old

287 ents) or right side (36%) of the interatrial septum was observed to be responsible for >/=80% of the

288 EGM assessment of the left interventricular septum was performed during RV basal septal pacing in 40

289 t the junction of the right ventricle to the septum was respectively observed in 11 (31%) versus 10 (

290 Deviated nasal septum was the most frequent variation in patients with

291 k of aggressiveness, and nodule with fibrous septum were evaluated in low (A, AB) versus high risk (B

292 or pulmonary atresia with intact ventricular septum were included from 4 pediatric centers.

293 Inferior and anterior walls and septum were maximally involved, whereas inferolateral an

294 scopy established that LtgA localizes to the septum, whereas LtgD is localized around the cell.

295 idline of the ventral aspect and ventricular septum, which are vessel populations primarily derived f

296 f trabeculae into the developing ventricular septum, which has been hypothesized to be the mechanisti

297 es strong descending inputs from the lateral septum, which is connected, in turn, with cortical netwo

298 he small capacitance of the 50 mum thick SU8 septum, which is only thinned around the aperture, and u

299 ral crest lineage results in increased nasal septum width, delayed palatal shelf development, and sub

300 strain/strain rate, predominantly within the septum, with relationships to invasive hemodynamics, rig