ライフサイエンスコーパス: blob

1 an unusual ocean warming event known as "The Blob".

2 ed actin structures with low mobility (actin blobs).

3 es along their surface and a neck behind the blob.

4 ontribute equally to the North Atlantic cold blob.

5 ose relation between pinwheel centers and CO blobs.

6 ation pinwheels, and cytochrome oxidase (CO) blobs.

7 approximately twice as many pinwheels as CO blobs.

8 labeled cells partially overlapped with the blobs.

9 l area (MT) and their relationship to the CO blobs.

10 ompared to the positions of the overlying CO blobs.

11 on of MT-projecting cells with the overlying blobs.

12 elation between the cell distribution and CO blobs.

13 labeled cells that were aligned with the CO blobs.

14 coincided with cytochrome oxidase (CO)-rich blobs.

15 form unambiguous clusters that coincide with blobs.

16 t with larger subdomains that go well beyond blobs.

17 ions, ND blobs were larger than the deprived blobs.

18 olution, image noise and overlap between the blobs.

19 V2 at 4 weeks of age labeled neurons around blobs.

20 fically, our results show that within the CO blobs: 1) all K cell axons contain glutamate, and the va

21 Unlike the original Blob, Blob 2.0 peaked in the summer, a season when little is k

22 We show that Blob 2.0 primarily results from a prolonged weakening of

23 ors in equal proportions, as were the random blobs; (4) 'anti-symmetric' - symmetric blobs were of op

24 l precursors (gem, zic2) requires the Acidic blob (AB) region in the N-terminal portion of the protei

25 data as pictures and clusters the pixels as blobs according to the brightness of each pixel to gener

26 lob/peak detection, baseline correction, and blob alignment.

27 cts content complexity to simple moving grey blobs, allowing objective mechanistic investigation.

28 y ligands for each detected electron density blob along with interactive 3D visualizations.

29 erblobs are "X-like" linear systems, whereas blobs also receive nonlinear "Y-like" M input.

30 own to be crucial for maintaining these warm blobs, also causing abnormally cold temperatures over No

31 : First, the guest molecules concentrate in "blobs", amorphous clusters involving multiple guest mole

32 inance and local-contrast "gain control", a "blob analysis" step to differentiate between cells, vess

33 ) tissue-level mitotic region selection, (3) blob analysis, and (4) cell-level refinement.

34 In squirrel monkeys, both blob and interblob regions of V1 contributed equally to

35 a heterogeneous pattern of terminations from blob and interblob regions within DM.

36 Both the Blob and record-low CSL can be attributed to wind change

37 e emergent dynamics of the living functional blob and robophysical model can inform the design of add

38 r color representation that switches between blobs and a combined blob/interblob system based on the

39 color-activated regions (cytochrome oxidase blobs and bridges) of primary visual cortex (V1), wherea

40 eta neurons have dense axonal arbors in both blobs and interblobs but not layer 4B.

41 ionship to the pattern of cytochrome oxidase blobs and interblobs in a manner suggesting a heterogene

42 The cytochrome oxidase (CO) blobs and interblobs in layer 3B of primate visual corte

43 Our results suggest that both the blobs and interblobs project to the thin stripes and cal

44 In layer 2/3, both blobs and interblobs receive M and P input, but the P in

45 d lateral connections, the thalamic pathway, blobs and interblobs, and the innate lineage-specific in

46 l amounts of labeled cells were found in the blobs and interblobs.

47 lower 4Calpha and 4Cbeta and axons targeting blobs and interblobs.

48 The earlier hypothesis that CO blobs and pinwheel centers are coterminous remains the o

49 o account for the claimed misalignment of CO blobs and pinwheel centers.

50 rce of potential predictability for the warm blobs and temperature fluctuations over North America.

51 ferential selective constrainton hydrophobic blobs and that SNPs splitting a long hydrophobic blob or

52 the first and second retention times of two blobs and the Pearson's correlation coefficient of the t

53 vious report of specific connections between blobs and thin stripes, which is parallel to the connect

54 rgence of blob/interblob information in L2/3 blobs and, possibly, some V2 stripes.

55 lously salty water that originated from the "Blob" and encountered several mesoscale eddies, whose su

56 tmospheric and oceanographic anomalies, the "Blob" and extreme El Nino Southern Oscillation (ENSO).

57 Using software that was developed to detect "blobs" and report their intensity, we were able to quant

58 steady filament section, a growing spherical blob, and an intermediate matching zone.

59 a from pneumatically tangled filaments, worm blobs, and bird nests along with additional numerical si

60 bulk, capture and absorption of surrounding blobs, and oriented attachment of other crystals.

61 Encoding across the cortex has a blob-and-pinwheel-type geometry of PDs.

62 the STM tip) the images changed to pairs of "blobs," apparently reflecting the attachment points of t

63 The blobs appear at a higher frequency than previously obser

64 45, the same age at which cytochrome oxidase blobs appear, presumably signaling the differentiation o

65 ng; however, no CO+ or PV+ or CB+ patches or blobs are found in V1.

66 These blobs are in dynamic equilibrium with the dilute solutio

67 In the low temperature states the blobs are interpermeable, the polymer does not conform t

68 Individual neurons in the blobs are not tuned to orientation, and populations of n

69 ophobic blob or joiningtwo short hydrophobic blobs are particularly likely to be disease associated.

70 The blobs are placed at a distance xi0 between their centers

71 More probable regions are screened based on blob area and then analysed at cell-level by developing

72 Stimuli consisted of colored Gaussian-blobs arranged either mirror-symmetrically or quasi-rand

73 or faces and face-like configurations (three blobs arranged like an upside-down triangle).

74 ated with oil or via direct contact with oil blobs as depicted in the figure.

75 led cells was more than twice as high in the blobs as that in the interblobs, and most of the cluster

76 iguously by the presence of a tall spherical blob at the DNA intersections.

77 ated by a crumpled globule build of Gaussian blobs at longer distances.

78 At high temperatures the blobs become spatially separated leading to a fractal cr

79 sional, soft, and shape-shifting "blob." The blob behaves as a living material capable of mitigating

80 Unlike the original Blob, Blob 2.0 peaked in the summer, a season when littl

81 by layers IIIa/b and Cytochrome Oxidase (CO)-blobs boundaries in the human primary visual cortex.

82 hibit different synaptic relationships to CO blob cells.

83 At any time t, several VF frequency blobs coexisted in the field of view, and the number of

84 Measurements showed that the location of the blobs coincided with the positions of the inserts.

85 hese cells consistently projected outside CO blob columns in all layers.

86 roject to thin stripes while neurons outside blob columns project to thick and pale stripes, suggesti

87 idase (CO) stripes in area V2: neurons in CO blob columns project to thin stripes while neurons outsi

88 blob, and blob/interblob borders showed that blob columns tended to have about 1.5 times more MT-proj

89 in which thin stripes receive V1 inputs from blob columns, and thick and pale stripes receive common

90 tem by demonstrating four V1-to-V2 pathways: blob columns-to-thin stripes, blob/interblob border colu

91 ubpopulation to reside predominantly outside blob columns; however, unlike previous descriptions of l

92 n both normal and strabismic monkeys: (1) CO-blob compartment neurons showed a more pronounced bias f

93 We outline the important properties of the blob complex and sketch the proof of a generalization of

94 e "blob complex." Fixing an n-category , the blob complex associates a chain complex B(*)(W;C) to any

95 The blob complex has a very natural definition in terms of h

96 oms for higher categories, and describe the "blob complex." Fixing an n-category , the blob complex a

97 o-step process, wherein metastable amorphous blobs condense from the gas phase, before evolving into

98 l-length PC1 appeared as two unequally sized blobs connected by a 35 nm string.

99 In contrast, blobs corresponding to the deprived columns were smaller

100 ese animals, ocular dominance stripes and CO blobs corresponding to the nasal retina stained more int

101 With restricted lesions, blobs corresponding to the ND columns had sizes similar

102 E tiling arrays in the presence of simulated blobs covering between 1 and 9% of the array area.

103 ome oxidase (CytOx) blob spatial density and blob cross-sectional area of deprived (D) and nondeprive

104 ualization, detection and removal of various blob defects from the .CEL files of different types of A

105 rrays, MAT), we found that even the smallest blob defects significantly decreased the sensitivity and

106 Plastic changes in blobs described here occur much earlier than previously

107 as been used to overcome these challenges in blob detection.

108 this research, we propose a joint constraint blob detector from U-Net, a deep learning model, and Hes

109 es the gap between classical computer vision blob detectors, such as Difference of Gaussians (DoG) fi

110 The Blob developed in the NE Pacific during the winter of 20

111 The location of CO blobs did not relate in a systematic way to maps of orie

112 We hypothesize that the collective blob displays rudimentary differentiation of function ac

113 The blob distance and similarity are the Euclidean distance

114 sumably signaling the differentiation of the blob-dominated and interblob-dominated streams in the pr

115 was characterized by the formation of small blobs for the short insert (60 bp) and clear loops and o

116 mistries allowed formulating a mechanism for blob formation.

117 The life span of frequency blobs from birth to either annihilation or breakup to an

118 to overcome these problems and identify true blobs from noisy medical images.

119 is cooling, known as the North Atlantic cold blob, has been hypothesized to arise from reduced polewa

120 EP), identified here and previously as 'warm blobs', have devastating impacts on regional ecosystems.

121 K LGN layers and CO blobs, however, are also well developed in nocturnal pri

122 hed as an assembly of densely packed fractal blobs, i.e., regions of size xi, where the fiber concent

123 V1, such as the cytochrome oxidase (CO) rich blobs in cortical layer III, synthesize new output pathw

124 We measured Layer III blobs in CytOx-reacted tangential sections of flat-mount

125 romatic processing given reports that the CO blobs in diurnal primates contain cells selective for co

126 lob columns, as projecting selectively to CO blobs in L2/3, suggesting convergence of blob/interblob

127 yer 4Calpha project axons to layer 4B and CO blobs in layer 2/3, thus relaying M input to these regio

128 in layer 4C and the cytochrome oxidase-rich blobs in layer 2/3.

129 The average size of glaucomatous blobs in layers 2 and 3 of V1 cortex was reduced by half

130 reduction in the size of cytochrome oxidase blobs in layers 2 and 3 of V1 cortex.

131 al whether the cytochrome oxidase (CO)-dense blobs in primate primary visual cortex (V1) and CO-dense

132 tightly colocalized with cytochrome oxidase blobs in V1 and with thin stripes in V2.

133 ionship between each labeled cell and the CO blobs in V1 were analyzed quantitatively.

134 diabetes, 51% (31) observed dark "spots" or "blobs" in the entoptic field corresponding to retinal de

135 of cytochrome oxidase (CytOx)-rich patches (blobs) in the striate cortex (V1) of normally sighted Ho

136 urbulent filaments in fusion plasmas, called blobs, in a high-frequency video obtained from Gas Puff

137 The blobs include clusters of condensin proteins and exclude

138 images, particularly small objects known as blobs, include low image resolution, image noise and ove

139 preferentially underneath cytochrome oxidase blobs, indicating that MT-projecting neurons of both typ

140 The polymers are composed of blobs, inside which the radius of gyration of a polymer

141 surface equally divided into compartments of blob, interblob, and blob/interblob borders showed that

142 ions from the deeper layers to the overlying blob/interblob architecture is less clear.

143 o-V2 pathways: blob columns-to-thin stripes, blob/interblob border columns-to-thick stripes, interblo

144 interblob projecting to pale stripes and the blob/interblob border region projecting to thick stripes

145 ed into compartments of blob, interblob, and blob/interblob borders showed that blob columns tended t

146 CO blobs in L2/3, suggesting convergence of blob/interblob information in L2/3 blobs and, possibly,

147 n that switches between blobs and a combined blob/interblob system based on the spatial content of th

148 ordered proteins; the size and shape of each blob is extracted from MD simulation of the real protein

149 of chromotopic maps, expressed by a uniform blob-like architecture of hue responses within each area

150 ondenses during the late S phases to produce blob-like chromosomes.

151 etrix oligonucleotide microarrays often have blob-like image defects that will require investigators

152 the torus is strikingly heterogeneous, with blob-like Mbp-size domains that undergo major dynamic re

153 Mine waste dumps consist of individual, blob-like spoil piles, each with unique geological and g

154 ically driven translocation of polypeptides, blob-like structures typically form inside nanopores, of

155 ted chromosomes emerge as intact, compacted, blob-like structures, decorated with native proteins fro

156 ting unidirectional elongation and promoting blob-like tissue expansions.

157 observations show a rapid resurgence of the Blob-like warm sea surface temperature (SST) anomalies t

158 ent dynamics facilitates directed persistent blob locomotion.

159 The "blob mechanism" unveiled in this work synthesizes elemen

160 Brochard and de Gennes' blob model for tube geometry fits the data, with a simpl

161 d by Cu(2+) and Ni(2+) with the fluorescence blob model showed that d(blob) was equal to the Debye le

162 The "nodes-links-blobs" model predicts a power-law approach to the percol

163 MK) near the null-point and constant outflow blobs not only along the outer spine but also along the

164 eads to a morphological instability, causing blobs of iron-rich liquid to penetrate the oxide.

165 and the K pathway in the cytochrome oxidase blobs of layer 2/3.

166 ls send axons to the cytochrome oxidase (CO) blobs of layer III and to layer I of primary visual cort

167 referentially distributed within the CO-rich blobs of layers V-VI.

168 ntration of cytochrome oxidase in patches or blobs of primate striate cortex has never been explained

169 t-wavelength cones to the cytochrome-oxidase blobs of primay visual cortex (V1), the dorsal-most pair

170 - symmetric blobs were of one color, random blobs of the other color(s); (2) 'random-segregated' - a

171 ities between K axon circuitry within the CO blobs of the three primate species examined also could i

172 uitry related to the K pathway within the CO blobs of two diurnal primates (macaque monkeys and squir

173 GC(2)MS then aligns the blobs of two GCxGC/TOF-MS data sets according to their d

174 y projections to the cytochrome oxidase (CO) blobs of V1 suggest involvement in chromatic processing

175 f labeled neurons were in cytochrome oxidase blobs of V1, many labeled neurons were located in interb

176 d conceptualization, which first identifies "blobs" of 4-15 residues representing local globular regi

177 regime characteristic of a chain of swollen blobs on long length scales and a high-force, salt-valen

178 s had an asymmetric loop, a large asymmetric blob or a spur-like projection at the appropriate positi

179 eurons, regardless of their soma location in blob or interblob columns, as projecting selectively to

180 s and that SNPs splitting a long hydrophobic blob or joiningtwo short hydrophobic blobs are particula

181 entation domains and cytochrome oxidase (CO) blobs or interblobs, CO blobs tended to prefer lower SFs

182 mature pattern of CO patches (also known as blobs or puffs) was visible, aligned with the ocular dom

183 the percentage of plasmids containing loops, blobs or spurs, consistent with the known effects of mon

184 ack any obvious modular arrangement, such as blobs or stripes, which are found in some primates and c

185 O-compartment as the injection site (blob-to-blob, or interblob-to-interblob) was moderately strong (

186 Within V1 no PV+ patches, CO blobs, or patchy distribution of CB+ neuropil that might

187 on resulted in large, irregularly shaped oil blobs over time, the deformation of which without fragme

188 lar ruler to measure the average distance (d(blob)) over which electron transfer takes place between

189 4C beta and were coarser than the overlying blob pattern in the same animal.

190 e processing workflow of GC(2)MS consists of blob/peak detection, baseline correction, and blob align

191 timulus as meaningful (as a face vs as shape blobs) predicts subsequent visual memory even when match

192 quencies and reduced the number of frequency blobs progressing to a single frequency.

193 The blob regime identified from an analysis of blob trajecto

194 other V2 thin stripes and neurons in the CO blob regions of V1.

195 of V1 contributed equally to DM, whereas the blob regions provided most of the projections to V1 in o

196 troduced a new software tool, the microarray blob remover (MBR), which allows rapid visualization, de

197 hnical advance in computer vision, to detect blob-shaped objects in contact maps.

198 h experimental trial, observers viewed three blob-shaped objects-the target and two tests-and selecte

199 , and PLA blocks are correlated with the PEG blob size.

200 Blob sizes changed drastically in the region correspondi

201 d to partially molten asthenosphere, fertile blobs, small-scale convection and upwellings driven by c

202 rse of changes of cytochrome oxidase (CytOx) blob spatial density and blob cross-sectional area of de

203 k nurse cell nuclear transitions at the five-blob stage and activate checkpoint controls in the oocyt

204 e cell chromosome reorganization at the five-blob stage and delay production or processing of Grk pro

205 somes, a mitotic-like state called the "five-blob" stage.

206 CO blobs straddled ODC borders in the central visual field,

207 e optical imaging of orientation domains and blob structures, approximately 100-200 micrometer in siz

208 The relative sizes of the two blobs suggested that the smaller one represents the N-te

209 The plasticity of the blob system and that of the ocular dominance columns (OD

210 We found that changes in the blob system were different from that of the ODC.

211 o the brightness of each pixel to generate a blob table.

212 hey have a greater impact on postsynaptic CO blob targets than signals arriving via layer IV from the

213 ochrome oxidase (CO) blobs or interblobs, CO blobs tended to prefer lower SFs than interblobs.

214 ynapse closer to the cell body within the CO blobs than do layer IV axons.

215 of the contiguously hydrophobic sequence (or"blob") that contains the SNP.

216 three-dimensional, soft, and shape-shifting "blob." The blob behaves as a living material capable of

217 specifically focus on the locomotion of the blob to understand how an amorphous entangled ball of wo

218 ly replicating visual percepts ranging from 'blobs' to oriented 'streaks' and 'wedges' depending on t

219 e same CO-compartment as the injection site (blob-to-blob, or interblob-to-interblob) was moderately

220 e blob regime identified from an analysis of blob trajectories agrees with state-of-the-art condition

221 ts suggest that each input pathway to the CO blobs uses a different strategy to contribute to the pro

222 d contributions from cytochrome-oxidase (CO) blob versus interblob neurons.

223 Ocular dominance columns (ODCs), and blob vs. interblob compartments, were revealed by using

224 attern of cytochrome oxidase loss within the blob was uniform, suggesting that all sources of afferen

225 field of view, and the number of coexisting blobs was on average 5.9+/-2.1 (n=8 hearts) as they appe

226 th the fluorescence blob model showed that d(blob) was equal to the Debye length (kappa(-1)).

227 ng that all sources of afferent input to the blobs were affected by experimental glaucoma.

228 presynaptic and postsynaptic profiles in CO blobs were identified with post-embedding immunocytochem

229 Blobs were larger and subjectively darker above and belo

230 With massive lesions, ND blobs were larger than the deprived blobs.

231 each trial; (3) 'non-segregated' - symmetric blobs were of all colors in equal proportions, as were t

232 r arrangements: (1) 'segregated' - symmetric blobs were of one color, random blobs of the other color

233 ndom blobs; (4) 'anti-symmetric' - symmetric blobs were of opposite-color across the symmetry axis.

234 V axons (indirect P and M pathways to the CO-blobs) were labeled by iontophoretic injections of Phase

235 VF consisted of blobs, which are groups of contiguous pixels with a comm

236 we develop a robophysical model of the worm blobs, which displays emergent locomotion in the collect

237 F consists of dynamically changing frequency blobs, which have a short life span and can be modified

238 mantle convection models show that dense TMM blobs with a size of tens of kilometres after the impact

239 oxidase reactivity was uniformly reduced in blobs with input from the glaucomatous eye in a manner c

240 s strong Lyman alpha emission from extended 'blobs' with little or no associated apparent ionizing co