ライフサイエンスコーパス: outer

1 ting on co-composted biochar that covers the outer and inner (pore) surfaces of biochar particles usi

2 erent proteins depends on translocons at the outer and inner chloroplast membrane (TOC and TIC, respe

3 sues along with a reduction in the number of outer and inner dynein arms.

4 ner chloroplast membrane) machineries in the outer and inner envelope membranes, respectively.

5 igh electron density region, composed of the outer and inner membranes and the cristae cluster, which

6 is obtained by charge-weighted averaging of outer and inner radii.

7 sis of retinal cells, including those in the outer and inner retinal layers.

8 Only DBDPE showed inhibition of both outer and inner ring deiodination (O and IRD) of T3 and

9 acking cone ERG are truncated with shortened outer and inner segments.

10 Both the outer and inner stratifying dendrites express postsynapt

11 ition-metal-based electrocatalyst through an outer and inner structural control to strengthen the ele

12 Herein, a novel strategy involving outer and inner structural engineering is developed for

13 ar thickness of the superior outer, inferior outer and temporal outer subfields were statistically si

14 lize IFT-B but does not support transport of outer arm dynein into flagella.

15 of gating zone components along the inner-to-outer axis of the ciliary gating zone.

16 Here we compare the cork oak outer bark transcriptome with that of holm oak.

17 ome comparison between cork oak and holm oak outer bark, which unveils new regulatory candidate genes

18 The apolar outer barrel surface with large sidechains is immersed i

19 ecoming appreciable and then dominant in the outer, baryonic regions of the disks of star-forming gal

20 The outer blood-retina barrier is established through the co

21 y differentially contribute to the inner vs. outer blood-retinal barrier function.

22 y, c-di-GMP was found to be localized at the outer boundary of mature colonies in contrast to a unifo

23 tbd7 knockout results in more tightly packed outer bud cells, which display stronger E-cadherin local

24 so revealed that C3P3 enhanced processing of outer capsid mu1 protein to mu1C, a previously described

25 ted with antigen or anti-CD3 antibody in the outer chamber.

26 in the compensation is more significant for outer channels.

27 port machinery, the regulatory kinase at the outer chloroplast membrane 1 (KOC1).

28 s accomplished by the TOC (translocon on the outer chloroplast membrane) and TIC (translocon on the i

29 capsulates one sulfate in its thiourea-based outer cleft, followed by a second encapsulation in its u

30 ion-dependent manner and ultimately promotes outer coat dissociation.

31 and posterior eye segments, but whether the outer coats of these abnormal eyeballs, cornea anteriorl

32 or pool began to subdivide into an inner and outer compartment that began to express markers of smoot

33 to the size of BChE results in a predominant outer complexation of BChE within the dangling chains of

34 ity in the core of their structure while the outer configuration is suitable with aqueous environment

35 incorporating the amino acid arginine in the outer coordination sphere was immobilized on modified ca

36 compositional state of the Earth's core, the outer core composition is close to eutectic in most regi

37 more, the lipid composition of the inner and outer cotyledons differed from each other, a remarkable

38 ressorium, which is used to breach the tough outer cuticle of a rice leaf, enabling the fungus entry

39 Rod basal outer disks displayed excessive outgrowth, and cone oute

40 we observe the dimerization of P. aeruginosa outer domains without any perturbation of the conserved

41 he oral cavity, whereas others innervate the outer ear.

42 e, placing the Sas-6 carboxyl termini at the outer edge of the approximately 60 nm radius cartwheel [

43 tes that the elemental concentrations in the outer endodermis are significantly (p < 0.01) higher tha

44 However, the indigestible outer envelope of the spermatophore delays female remati

45 probing the strong affinity of the inner and outer faces of the gamma-CD for the polyoxometalate surf

46 uteinizing hormone then acts on receptors in outer granulosa cells to rapidly decrease cGMP.

47 in neurons, causes profound hearing loss and outer hair cell degeneration in mice.

48 red explicitly-organ of Corti mechanics, and outer hair cell electro-mechanics.

49 reveals persistent damage to some surviving outer hair cell stereocilia.

50 ate Foxo3 and its transcriptional targets in outer hair cell survival after noise damage.

51 ected in the entire lateral wall of cochlear outer hair cells and had an intermediary distribution (b

52 s mechanoelectrical transduction currents in outer hair cells and hence cochlear amplification is gre

53 his observation accords with the function of outer hair cells and lends support to the recent hypothe

54 These include the cochlear outer hair cells and their singular feature, somatic ele

55 The ability of Anc80L65 to target outer hair cells at high rates, a requirement for restor

56 ner hair cells are of linear shape, those of outer hair cells exhibit a distinctive V-shape.

57 of all inner hair cells and the majority of outer hair cells in an adult cochlea via virus injection

58 Outer hair cells in the cochlea have a unique motility i

59 he organ of Corti complex felt by individual outer hair cells varies along the cochlear length.

60 In this case, the absence of outer hair cells would be compatible with overexposure t

61 nario where the singular organization of the outer hair cells' cortical cytoskeleton may have emerged

62 taV giant spectrin, a major component of the outer hair cells' cortical cytoskeleton.

63 ently expanded to the entire lateral wall in outer hair cells.

64 majority of unique residues align along the outer helical ridge.

65 ions between solvated cations present at the outer Helmholtz plane and adsorbed species having large

66 rease in the concentration of cations at the outer Helmholtz plane with increasing cation size.

67 nt and the macular thickness of the superior outer, inferior outer and temporal outer subfields were

68 tromeres supports functional assembly of the outer kinetochore but is unable to correct errors in kin

69 components, which form part of a trypanosome outer kinetochore complex.

70 sister kinetochores, representing the final outer kinetochore component recruited prior to anaphase

71 During chromosome segregation, outer kinetochore components track depolymerizing ends o

72 new family of proteins distantly related to outer kinetochore proteins Ndc80 and Nuf2.

73 Meiosis requires transient removal of the outer kinetochore, the complex that connects microtubule

74 tes of Mps1-regulated phosphorylation at the outer kinetochore.

75 is counteracted, we compare the roles of two outer-kinetochore bound phosphatases and find that BubR1

76 These bacteria form a mat-like photoactive outer layer around an otherwise unconsolidated core.

77 RACs have a highly ordered structure with an outer layer of condensed heterochromatin, an inner layer

78 escence quenching of the free aptamer in the outer layer of unmodified reduced graphene (rGO; sensing

79 taken to investigate the effect of the PDMS outer layer on the uptake rate of analytes during the ma

80 The outer layer proteins, VP4 (cleaved to VP8* and VP5*) and

81 Escape into the cytosol and outer-layer shedding depend on interaction of a hydropho

82 the pretreatment led to depectination of the outer layers thereby exposing xylan polymers and increas

83 tive cell wall components (especially of the outer layers) vary when the fungus senses changes in the

84 ion, we show that coupling may extend to the outer leaflet of the plasma membrane by examining the fl

85 ion with the GM1 ganglioside receptor in the outer leaflet of the plasma membrane in intestinal (HT-2

86 and phosphatidylserine (PS) exposure on the outer leaflet of the plasma membrane preceded loss of PM

87 membranes and, most interestingly, with the outer leaflet of the plasma membrane, suggesting a role

88 phosphatidylserine (PtdSer) exposure on the outer leaflet of transduced cells triggers their engulfm

89 lipid bilayer with lipopolysaccharide in the outer leaflet.

90 a unique lipid bilayer containing LPS in its outer leaflet.

91 proximately 1:1 if only the PG lipids in the outer leaflets of membranes are accessible to daptomycin

92 differences in tension between the inner and outer leaflets of the membrane contribute to this proces

93 nd 2, observed in the OCT, correspond to the outer limiting membrane and the cone ellipsoids, respect

94 effect on functional expression of the renal outer medullary potassium channel.

95 antibiotic that permeabilizes the bacterial outer membrane (OM) and has been used to treat these inf

96 The defining feature of the mycobacterial outer membrane (OM) is the presence of mycolic acids (MA

97 plex assembles beta-barrel proteins into the outer membrane (OM) of Gram-negative bacteria.

98 The outer membrane (OM) of Gram-negative is a unique lipid b

99 in-related protein 1 (Drp1) on mitochondrial outer membrane (OMM).

100 ays into mitochondria use translocons on the outer membrane (TOM) and inner membrane (TIM).

101 machine that spans both plasma membrane and outer membrane and actively extrudes substrates, includi

102 anion channel 1 (VDAC1) on the mitochondrial outer membrane and inhibited its opening.

103 with integral proteins of the mitochondrial outer membrane and is important for the structure-inspir

104 sis, we show that Kdo-N3 is localized to the outer membrane and specifically incorporates into rough

105 ent imaging of the dynamics of the bacterial outer membrane as cells divide.

106 amyloid fibres, which translocate across the outer membrane as unfolded amyloid precursors through a

107 A crown-like structure outside the outer membrane capping the secretin was found not to be

108 All mitochondrial outer membrane channels known to date are beta-barrel me

109 ng of pre-integration forms of a hyperstable outer membrane complex and reveals a key driving force f

110 rating lipopolysaccharide, a major bacterial outer membrane component) and induce a comparable degree

111 We conclude that the mitochondrial outer membrane contains a considerably larger variety of

112 ide-like sequence (C10OOc12O) that inflicted outer membrane damage at a low micromolar range, whereas

113 omplex-forming effector at the mitochondrial outer membrane during Coxiella infection.

114 Recognition of compatible receptors leads to outer membrane exchange among clonemates and fitness con

115 We analyzed outer membrane fractions of yeast mitochondria and ident

116 This pathway may link outer membrane fusion to lipids homeostasis.

117 ntly trigger disruption of the mitochondrial outer membrane in cells dependent on Bfl-1, but not in c

118 In bacteria such as Escherichia coli, the outer membrane is a unique asymmetric lipid bilayer with

119 defatted cells were similar, indicating that outer membrane lipids govern overall hydrophobicity.

120 In this work, we characterize PelC, an outer membrane lipoprotein essential for Pel production.

121 he peptidoglycan synthase PBP1A requires the outer membrane lipoprotein LpoA for constructing a funct

122 molecules are unable to rapidly traverse the outer membrane of Gram-negative bacteria and accumulate

123 recently identified the Borrelia burgdorferi outer membrane protein (OMP) BB0406 and found that the g

124 Here, we demonstrate that A. marginale outer membrane protein A (AmOmpA; AM854) contributes to

125 Outer membrane protein A (OmpA) is a porin involved in A

126 An anti-outer membrane protein A (OmpA) polyclonal antibody prev

127 in, MlaC, ferries lipids between MlaD and an outer membrane protein complex.

128 ssing three peptides AHC (ApoB100, HSP60 and outer membrane protein of chlamydia pneumonia) in stabil

129 Typhimurium porins including outer membrane protein OmpD, which induce both IgG1 and

130 OmpA is an outer membrane protein present in the R. rickettsia, the

131 MAM-7 that was previously reported to be an outer membrane protein.

132 assive immunizations with antisera targeting outer membrane proteins (OMPs) have shown encouraging re

133 esponsible for the biogenesis of beta-barrel outer membrane proteins (OMPs) in Gram-negative bacteria

134 by cell-surface macromolecules (likely to be outer membrane proteins and pili) which, upon contacting

135 e Bam complex assembles a great diversity of outer membrane proteins into a membrane without an obvio

136 rial depolarization and proteasome-dependent outer membrane rupture.

137 tion operates independently of activation of outer membrane stress pathways.

138 ncovalent protein interactions that link the outer membrane to the aqueous periplasmic region.

139 ngococcal serogroup B vaccine (4CMenB) is an outer membrane vesicle and recombinant protein-based vac

140 secreted by H3-T6SS and is incorporated into outer membrane vesicles (OMVs) by directly interacting w

141 n a manner consistent with the production of outer membrane vesicles.

142 MitoNEET is anchored to the mitochondrial outer membrane via its N-terminal alpha helix domain and

143 g the lipid composition of the mitochondrial outer membrane were tested, we did not detect any leakag

144 ane proteins CusA (inner membrane) and CusC (outer membrane).

145 818 proteins into the four subcompartments: outer membrane, inner membrane, intermembrane space, or

146 nsitive Escherichia coli strain with a leaky outer membrane, we identified a mutant with increased re

147 The outer membrane-associated BoMan26B initially acts on the

148 further examine the interaction of PorB with outer membrane-associated proteins, including PorA and R

149 al inner membrane and subsequently binds the outer membrane-derived lipoproteins and LPS to inhibit T

150 noxious compounds that damage the bacterial outer membrane.

151 cules use the same import channel across the outer membrane.

152 n and thus assists its localization into the outer membrane.

153 and the penetration of the Escherichia coli outer membrane.

154 ndria and chloroplasts is the presence of an outer membrane.

155 nd thereby lifts the cell wall closer to the outer membrane.

156 s responsible for shuttling hopanoids to the outer membrane.

157 uring the first step of LPS transport to the outer membrane.

158 ysaccharide into the external leaflet of the outer membrane.

159 ey of 1,347 CEPs encompassing 90% inner- and outer-membrane and periplasmic proteins of Escherichia c

160 e exhibiting high activity for the bacterial outer-membrane protease (OmpT).

161 In the case of outer-membrane proteins (OMPs), unfolded-state propertie

162 Although cell lysis and outer-membrane vesicle extrusion are possible means by w

163 The assembly of proteins into bacterial outer membranes is a key cellular process that we are on

164 e trafficked between the bacterial inner and outer membranes through the hydrophilic space of the per

165 the periplasmic space between the inner and outer membranes.

166 reagents in the gas phase by ALD to form an outer metal ion bridging group, which can bind a second

167 m the ER to mitochondria and clusters at the outer mitochondrial membrane (OMM).

168 localized tail-anchored (TA) proteins of the outer mitochondrial membrane are cleared by a newly iden

169 y regulates Mitofusin, which is required for outer mitochondrial membrane fusion.

170 regulator) can commit cells to apoptosis via outer mitochondrial membrane permeabilization.

171 The outer mitochondrial membrane protein mitochondrial Rho G

172 Whereas outer mitochondrial membrane-associated degradation is t

173 raction of mislocalized TA proteins from the outer mitochondrial membrane.

174 me biosynthesis during erythropoiesis at the outer mitochondrial membrane.

175 sion requires division of both the inner and outer mitochondrial membranes (IMM and OMM, respectively

176 rgely restricted to members of the inner and outer NPC rings, but it lacks numerous others including

177 Ellipsoid zone (EZ) width (EZW) and outer nuclear layer (ONL) and inner retinal layer (IRL)

178 uclear layer, inner nuclear layer (INL), and outer nuclear layer (ONL) thicknesses; and horizontal ex

179 gnificantly blocked photoreceptor apoptosis, outer nuclear layer (ONL) thinning, and retinal gliosis.

180 outer plexiform, and to a lesser extent the outer nuclear layer.

181 layer, inner plexiform layer, and inner and outer nuclear layers and within the spindle-shaped cell

182 l changes in the separation of the inner and outer nuclear membrane are responsible for the additiona

183 ar cell terminals in separate inner (ON) and outer (OFF) sublayers in response to light intensity inc

184 negative bacteria, a structure comprising an outer (OM) and an inner (IM) membrane, is essential for

185 eir dendritic stratification near either the outer or the inner border of the inner plexiform layer.

186 of the choroid, retinal pigment epithelium, outer part of the retina and the optic nerve head within

187 iffusion through the coating; therefore, the outer PDMS layer influences the uptake rate into the mat

188 mposition and structure of starches from the outer pericarp and core tissues of a golden kiwifruit we

189 Rheological properties of outer pericarp starches were compared with normal maize

190 Compared to the outer pericarp starches, amylose content and enzyme susc

191 beta-limit dextrins (LDs) than those of the outer pericarp starches.

192 hemical properties of starches from core and outer pericarp were studied.

193 created from microtubules originating on the outer periclinal cell face, pointing to a cell-directed,

194 We conclude that the outer planets of the TRAPPIST-1 system are capable of re

195 radiation environments of the exoplanets and outer planets.

196 inner nuclear layer (T6 and N6 sectors), and outer plexiform layer (S6 sector), as well as the overal

197 inner plexiform layer neurites, and varicose outer plexiform layer neurites all bear spines, that som

198 ner plexiform layer appears earlier than the outer plexiform layer, synaptic proteins, and ribbons ar

199 , efficiently reaching the inner nuclear and outer plexiform, and to a lesser extent the outer nuclea

200 ingly, the directionality and/or velocity of outer polar nuclear migration into the hair outgrowth al

201 -selective tarantula toxin that binds to the outer pore of the channel.

202 The Yersinia outer protein J (YopJ) family of bacterial effectors dep

203 Correct outer protein shell assembly is a prerequisite for virio

204 involving the central breast and right upper outer quadrant.

205 The outer radius is the atomic (covalent) radius, and the in

206 differentiation of ASCs within the inner and outer regions of the biphasic scaffolds.

207 on PKM2 deletion, PKM1 is upregulated in the outer retina and there is increased expression of genes

208 h led to chronic degenerative changes in the outer retina of these mice.

209 Detection of abnormal flow in the outer retina served as candidate CNV with OCTA.

210 yolk lesions," the OCT showed a cleft in the outer retina, creating an apical and basal separation of

211 ermediates to the apical side to nourish the outer retina.

212 Outer retinal and renal glomerular functions rely on spe

213 c candidates were proposed: complete RPE and outer retinal atrophy (cRORA), incomplete RPE and outer

214 lete RPE and outer retinal atrophy, complete outer retinal atrophy, and incomplete outer retinal atro

215 retinal atrophy (cRORA), incomplete RPE and outer retinal atrophy, complete outer retinal atrophy, a

216 mplete outer retinal atrophy, and incomplete outer retinal atrophy.

217 s study proposes a new interpretation of the outer retinal bands that leads to a more accurate interp

218 in the OCT represent, especially over the 4 outer retinal bands.

219 through regressing lesions revealed altered outer retinal layers and choroidal hypertransmission.

220 ly by the OPL without any involvement of the outer retinal layers and RPE.

221 umulation leads to a clear separation of the outer retinal layers.

222 Outer retinal thickness at the foveal center increased b

223 antibodies in 25 cases of acute zonal occult outer retinopathy (AZOOR) identified using the classific

224 viable cells throughout and spheres with an outer rim of viable cells but necrotic cells centrally.

225 th few macrophages and viable cells at their outer rim.

226 ct pirouette mechanism for automerization of outer ring carbons in phenanthrene, a reaction demonstra

227 a tractor mechanism involving the inner and outer root sheaths.

228 The photoreceptor outer segment (OS) is a unique modification of the prima

229 ntal extent of the ONL and the photoreceptor outer segment (POS) interdigitation zone (IZ).

230 s, all-trans-retinal, is released in the rod outer segment by photoactivated rhodopsin after light ex

231 Photoreceptor outer segment degeneration was evident, with a significa

232 of key photoreceptor genes underlies delayed outer segment elongation and possibly mispositioning of

233 omes in building the elaborate photoreceptor outer segment filled with hundreds of tightly packed "di

234 Measurements of the rod outer segment photocurrent in transgenic mice, which hav

235 ubstantial as the desensitization of the rod outer segment photocurrent.

236 afish also showed mislocalisation of certain outer segment proteins (rhodopsin, opn1lw, opn1sw1, GNB3

237 re absent, thereby preventing trafficking of outer segment proteins to their destination.

238 r-specific knock-out mice, the photoreceptor outer segment structure was severely impaired at 4 weeks

239 Ca(2+) ions have distinct roles in the outer segment, cell body, and synaptic terminal of photo

240 of Ca(2+) regulate phototransduction in the outer segment, metabolism in the cell body, and neurotra

241 ide of the inner segment, directly below the outer segment.

242 accumulates either in the cone cell body or outer segment.

243 icalis, these processes are connected to the outer-segment membrane by links composed of protocadheri

244 in in the form of phagocytized photoreceptor outer segments (OS).

245 ed progressive degeneration of photoreceptor outer segments (OSs) and increased apoptosis of retinal

246 (RPE) is the clearance of shed photoreceptor outer segments (POS) through a multistep process resembl

247 Outer segments appeared rapidly at postnatal day six and

248 G protein-coupled receptor found in the rod outer segments in the retina, which triggers a visual re

249 Phagocytosis of daily shed photoreceptor outer segments is an important function of the retinal p

250 al retina at postnatal day 6 (P6) and older, outer segments were absent, thereby preventing trafficki

251 isks displayed excessive outgrowth, and cone outer segments were curved, with lamellae of heterogeneo

252 he identification of small fragments of cone outer segments within the RPE led us to characterize the

253 livered M-opsin localizes in the dorsal cone outer segments, and co-localizes with S-opsin in the ven

254 nal defects in phagocytosis of photoreceptor outer segments.

255 increased structural instability of the rod outer segments.

256 itating rhodopsin transport to photoreceptor outer segments.

257 glycolytic pathway impacted the size of the outer segments.

258 The major outer sheath protein (MOSP) is a prominent constituent o

259 rlapping grounding zone wedges (GZWs) on the outer shelf of the Whales Deep Basin.

260 ic model for calcium concentration regulated outer shell assembly.

261 ithin a hollow cavity surrounded by a porous outer shell have received tremendous research interest o

262 d metal shell, whereby the morphology of the outer shell is determined by the concentration of metall

263 tect their genomes by packaging them into an outer shell or capsid of virus-encoded proteins.

264 tect their genomes by packaging them into an outer shell or capsid of virus-encoded proteins.

265 O2 creates a hollow nanostructure with Li2O outer-shell and Li2O2 inner-shell surfaces.

266 Outer-shell s(0)/p(0) orbital mixing with d(10) orbitals

267 e alloys (including quasicrystals) formed in outer space in a complex, multi-stage process.

268 oyable applications, both in terrestrial and outer-space structures, as well as morphing devices.

269 ive theoretical treatment of the kinetics of outer sphere electrochemical reactions.

270 and quantum-chemical calculations suggest an outer sphere electron transfer from the COF to the co-ca

271 analysis of the voltammetric response of an outer sphere redox couple can be used to track changes i

272 t-energy structure calculated to be an As-up outer-sphere complex.

273 ectrostatic interactions may assemble stable outer-sphere ion clusters in organic solutions, elucidat

274 Here, we characterize trefoil-shaped outer-sphere lanthanide chloride and nitrate ion cluster

275 oxidation and generally considered to be an outer-sphere oxidant.

276 ere Rb(+) slowly transforms to a less stable outer-sphere Rb(+).

277 perometry and cyclic voltammetry of an ideal outer-sphere redox probe, reversible ferrocene methanol

278 Outer-sphere reductive single electron transfer (OS-SET)

279 lop a single germ tube that emerges from the outer spore wall in a process called outgrowth.

280 lf the product of the Coriolis parameter and outer storm size.

281 Outer stratifying cells make up on average 60% of the me

282 e melanopsin-expressing cells (or 80% of the outer stratifying cells) have their soma displaced to th

283 theory calculations show that the inner and outer structural engineering contributing to the synergi

284 superior outer, inferior outer and temporal outer subfields were statistically significant (p = 0.03

285 filters and fibrous filters with a sievelike outer surface and a fibrouslike porous substrate.

286 ment epithelium-derived factor (PEDF) on the outer surface of exosomes.

287 erent molecular units can be anchored on the outer surface of MOF NPs in a self-assembly process gene

288 -shaped spikes extending up to 6 nm from the outer surface of the capsid shell.

289 tically disordered regions (in the inner and outer surface of the Fe3O4 shell) and spins located in t

290 istance of the repeat region, exposed on the outer surface of the sporozoites, combined with the flex

291 by simple impregnation is oriented along the outer surface of ZIF-8 (Au25 (SG)18 /ZIF-8).

292 luorescence assays that combined monoclonal (outer surface protein A) and polyclonal antibodies were

293 ieves a minimal IR emissivity (10.1%) on the outer surface that effectively suppresses heat radiation

294 TPase recruitment of mTORC1 to the lysosomal outer surface, enabling activation of mTOR by the Ras ho

295 ve sites in the interior tubular vessels and outer surfaces for ultrasensitive detection of NA in liv

296 The outer T=13 shell protein P8 consists of two alpha-helica

297 anslocate aminoglycerophospholipids from the outer to the inner leaflet of the plasma membrane.

298 % of the co- variability (below 5 km) in the outer tropical (10-25 degrees N) central Pacific Ocean,

299 The outer wall is composed of a separate extended network of

300 Further, site-specific degradation of the outer ZN matrix and release of transfection competent CS