ライフサイエンスコーパス: septum

1 ith activity patterns governed by the medial septum.

2 ch proteins were recruited to the developing septum.

3 tures, cranial base synchondroses, and nasal septum.

4 peptidoglycan-like sacculus and/or division septum.

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

6 rtrophy involving the basal interventricular septum.

7 dial versus longitudinal PG insertion at the septum.

8 xtended anteriorly into the interventricular septum.

9 and protein-protein interactions across the septum.

10 orsal and intermediate region of the lateral septum.

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

12 rs during the development of the ventricular septum.

13 poptotic chondrocytes in the calcified nasal septum.

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

15 arently being prevented by the intermuscular septum.

16 n of peptidoglycan remodeling at the forming septum.

17 ical structures, including the outflow tract septum.

18 venous approach through the interventricular septum.

19 te cell wall synthesis and hydrolysis at the septum.

20 in removal with maximal rates in the lateral septum.

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

22 rotein FtsK may license recombination at the septum.

23 affected by muscimol inactivation of medial septum.

24 e nasal bone process and cartilaginous nasal septum.

25 de medially through formation of a cell wall septum.

26 on unidirectional regulation via the medial septum.

27 ed in the anterior left ventricular wall and septum.

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

29 molecules and deposits them at the division septum.

30 egates along an axis parallel to the closing septum.

31 w,2) (conducted by K(V)2.1) in both apex and septum.

32 nucleus of the stria terminalis, and lateral septum.

33 uration on vasopressors and midline shift at septum.

34 all synthesis to cell wall hydrolysis at the septum.

35 x2 and Nkx2-1 that fuses to form a transient septum.

36 ecifically cholinergic neurons in the medial septum.

37 uring midcell positioning of the cytokinetic septum.

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

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

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

41 n the presence of inhibition from the medial septum; (2) compress learned spike sequences in the form

42 pital discharge (p = 0.019 pineal; p = 0.008 septum), 3 months (p = 0.026; p = 0.007), 6 months (p =

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

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

45 The medial septum, a part of the basal forebrain that innervates th

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

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

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

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

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

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

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

53 MltC and RlpA both localize to the septum and are functionally redundant under normal labor

54 scular system including the aorticopulmonary septum and cardiac ganglion.

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

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

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

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

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

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

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

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

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

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

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

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

67 d its sole identified GABA input, the medial septum and nucleus of the diagonal band (MSDB).

68 iated with increased activity in the lateral septum and preoptic area, demonstrating recruitment of s

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

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

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

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

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

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

75 2 in "limbic" areas such as the hippocampus, septum, and extended amygdala have also been described.

76 o the amygdala, extended amygdala, striatum, septum, and hippocampus of tetrapods.

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

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

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

80 r LV, left atrium (LA), RV, interventricular septum, and LV posterior wall diameters at 18 months (P

81 an z scores for LV, LA, RV, interventricular septum, and LV posterior wall diameters increased over a

82 t atrial systolic diameter, interventricular septum, and LV posterior wall thickness, were positively

83 um, entorhinal cortex and perirhinal cortex, septum, and olfactory system in the initial phase status

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

85 DDD) pacing lead to LV dilatation, a thinned septum, and thickened lateral wall.

86 ts in the endocardial-derived cardiac valve, septum, and vasculature.

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

88 diabetes, hypercoagulability, or hypermobile septum; and medication use (HR, 3.01 [CI, 1.59 to 5.69];

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

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

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

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

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

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

95 specifically in three brain regions: lateral septum, bed nucleus of the stria terminalis, and ventral

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

97 done even in the case of interfering column/septum bleed or simultaneously eluted peaks.

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

99 ls were predominantly located in the lateral septum, but also the hippocampus, anteroventral thalamus

100 subcortical structures including the medial septum, but it is unclear how spatial information from p

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

102 ibition of cholinergic neurons in the medial septum by DREADD (designer receptors exclusively activat

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

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

105 propose that lytic transglycosylases at the septum cleave PG strands that are crosslinked beyond the

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

107 nd limiting for both septal PG synthesis and septum closure in some bacteria, but not in others.

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

109 We find this secretion event is linked to septum completion and forestalled when the process is sl

110 o the cytokinesis site that is degraded upon septum completion but stabilized when septation is aberr

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

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

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

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

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

116 previously established model to study atrial septum defects, displayed polydactyly or hypodactyly.

117 previously established model to study atrial septum defects, which displayed polydactyly or hypodacty

118 Delay of septum degradation requires Fir1, an intrinsically disor

119 d, its role as a spatiotemporal landmark for septum deposition is not widely discussed.

120 mechanisms of spatiotemporal coordination of septum deposition with actomyosin ring constriction are

121 yeast, proper furrow formation also requires septum deposition.

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

123 fects were observed in BFCNs from the medial septum diagonal band and horizontal diagonal band, but n

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

125 Models of path integration use medial septum/diagonal band of Broca (MSDB)-dependent MEC grid-

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

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

128 rgic, or glutamatergic neurons in the medial septum/diagonal band of Broca does not affect modulation

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

130 r discrimination identified the dorsolateral septum (DLS) as a relay of the dentate gyrus-CA3 circuit

131 orally regulates membrane traffic to promote septum-driven cytokinesis in fission yeast.

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

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

134 adult male Wistar rats, silencing the medial septum during recall did not affect avoidance memory exp

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

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

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

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

139 dispersal, CR assembly and constriction, and septum formation [4, 5].

140 l division complexes, suffered from aberrant septum formation and exhibited enhanced cellular autolys

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

142 Septum formation and resolution into distinct trachea an

143 Thus, inhibition of Cdc15-scaffolded septum formation at cell poles is a key Pom1 mechanism t

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

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

146 4 phosphatase functions in cell division and septum formation in F. graminearum, likely by counteract

147 ring constriction occurs simultaneously with septum formation in fungi.

148 Z and EzrA are localized at midcell, and the septum formation is initiated but unable to progress to

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

150 Scd1 promotes normal septum formation, andscd1Deltacells display aberrant sep

151 ater to the ingressing membrane and promotes septum formation.

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

153 ng sporulation, an asymmetrically-positioned septum generates a larger mother cell and a smaller fore

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

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

156 Forty-six patients with LVH (LV septum >11 mm) and elevated cardiac biomarkers (N-termin

157 office vaginoscopy revealed that the vaginal septum had not reformed nor was any vaginal stenosis not

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

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

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

161 regions and circuits, including the lateral septum, hypothalamus, amygdala, bed nucleus of the stria

162 that is selectively degraded in its primary septum immediately after its completion by secreted enzy

163 The medial septum implements cortical theta oscillations, a 5-12 Hz

164 rent slow-release dispensers, a small rubber septum impregnated with the chemical was as effective as

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

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

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

168 of vaginoscopic incision of oblique vaginal septum in adolescents with Obstructed hemi-vagina and ip

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

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

171 urrents in cholinergic neurons of the medial septum in mGluR5 KO mice.

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

173 ircumventricular regions of the habenula and septum in mice.

174 ecorded from rat CA1 and caudodorsal lateral septum in rat during a rewarded navigation task and comp

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

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

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

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

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

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

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

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

183 ome must be translocated across the division septum into the forespore by the DNA translocase SpoIIIE

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

185 Thus, the septum is critical for sustaining precise theta phase co

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

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

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

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

190 Instead, the septum is uniformly and only slightly thinned as it curv

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

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

193 P=0.013) and a difference between membranous septum length and implantation depth (DeltaMSID) >=3 mm

194 Conversely, membranous septum length and implantation depth alone were not asso

195 r the left coronary cusp, but not membranous septum length nor implantation depth alone, are predicti

196 ding valve implantation depth and membranous septum length, an anatomic surrogate of the distance bet

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

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

199 The lateral septum (LS) has been implicated in anxiety and fear modu

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

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

202 The lateral septum (LS) plays an important role in regulating aggres

203 ed the role of DH projections to the lateral septum (LS), a brain region implicated in cocaine seekin

204 bcortical brain regions, such as the lateral septum (LS), a structure that plays important roles in r

205 receptor (OXTR) system, through the lateral septum (LS), contributes to social behavior, which is di

206 The lateral septum (LS), which is innervated by the hippocampus, is

207 region involved in aggression is the lateral septum (LS).

208 ar hypothalamus (PVH) to the ventral lateral septum (LSv) that shows a scalable regulation on feeding

209 l malformation syndromes including urorectal septum malformation, caudal regression, vertebral-anal-c

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

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

212 The medial septum (MS) is critical in theta generation by two possi

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

214 Medial septum (MS) lesions lead to perseverative, inflexible-ty

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

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

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

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

219 e, we describe a novel population of lateral septum neurons expressing neurotensin (LS(Nts)) in mice

220 culus homologs, hypothalamus, preoptic area, septum, nucleus of the diagonal band of Broca, and main

221 homologs receive differential input from the septum, nucleus of the diagonal band of Broca, preoptic

222 focal localization of MmpL3 at the poles and septum of actively-growing bacilli where the synthesis o

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

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

225 eptidoglycan hydrolase CbpD that targets the septum of S. pneumoniae cells to show that class A PBPs

226 antly impact the contamination of the rubber septum of the aflibercept vial.

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

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

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

230 ation sequence to early activation of the LA septum or roof during distal CS pacing were the end poin

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

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

233 ing global cerebral autoregulation (p = 0.01 septum; p = 0.05 pineal) and cerebral autoregulation asy

234 sotopic N2O laser analyzer through a syringe septum port.

235 tants with greater errors in size sensing or septum positioning paradoxically appear to behave as bet

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

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

238 n was performed in both atria by interatrial septum puncture, with irrigated conventional catheter an

239 zes to the pole, and redirecting HspX to the septum radically disrupts the normal polar localization

240 LV) endocardial side of the interventricular septum, referred to as LV septal (LVs) pacing, was demon

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 icate that cholinergic neurons in the medial septum represent a key cell type involved in sensorimoto

244 rated that cholinergic neurons in the medial septum represent a key cell-type involved in sensorimoto

245 cells lacking these factors, the asymmetric septum retracts, resulting in forespore cytoplasmic leak

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

247 (55% women; age, 18-76 years), free wall and septum RVLS (6 segments) and free wall RVLS (3 segments)

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

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

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

251 DD pacing, whereas with AAI pacing, the thin septum showed exaggerated loading and the lateral walls

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

253 factory bulb, all pallial divisions, lateral septum, suprachiasmatic nucleus, prethalamic and thalami

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

255 R) constriction with membrane ingression and septum synthesis.

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

257 sal tongue epithelium have perturbed lingual septum tendon formation and disrupted intrinsic muscle p

258 f the brain, especially in the hypothalamus, septum, thalamic reticular nucleus, certain cortices and

259 coupled with deposition of an extracellular septum that is selectively degraded in its primary septu

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

261 albindin-expressing cells within the lateral septum, the brain region in which GLP-1R is most highly

262 o actively move proteins around the division septum, thereby distributing peptidoglycan synthesis and

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

264 correlation with diastolic interventricular septum thickness in those athletes.

265 ndex, parasternal long axis interventricular septum thickness, and mean left ventricular wall thickne

266 rdiac hypertrophy, as indicated by increased septum thickness.

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

268 is and coordinating the inward growth of the septum to form the new poles of the daughter cells(4).

269 xpression heterogeneity (>10 fold) comparing septum to lateral walls, and enhanced growth and metabol

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

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

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

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 patocytes, ECs, and stage-matched MCs, i.e., septum transversum mesenchyme (STM), in 2D cultures.

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

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

279 for PG synthesis localizes mid-cell, at the septum, under the control of a multiprotein complex call

280 Vaginoscopic incision of the oblique vaginal septum using a "No-Touch" technique is a safe, minimally

281 vaginoscopic incision of the oblique vaginal septum using a "No-touch" technique over an 8-year perio

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

283 th pulmonary atresia with intact ventricular septum vary widely.

284 tion in the medial amygdala, ventral lateral septum, ventromedial hypothalamus, and hypothalamic para

285 T1 and ECV values were increased in the septum versus the free wall.

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

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

288 adolescents with OHVIRA the oblique vaginal septum was incised successfully without any intraoperati

289 The atrioventricular septum was mapped via EAM, and His bundle (HB) electrogr

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

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

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

293 ), the lateral wall was more loaded, and the septum was unloaded.

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

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

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

297 of the multiple planes perpendicular to the septum which divide the cell in two identical halves can

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

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

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

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