ライフサイエンスコーパス: blob

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

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

3 ompared to the positions of the overlying CO blobs.

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

5 elation between the cell distribution and CO blobs.

6 labeled cells that were aligned with the CO blobs.

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

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

9 ose relation between pinwheel centers and CO blobs.

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

11 approximately twice as many pinwheels as CO blobs.

12 labeled cells partially overlapped with the blobs.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 45, the same age at which cytochrome oxidase blobs appear, presumably signaling the differentiation o

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

40 These blobs are in dynamic equilibrium with the dilute solutio

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

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

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

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

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

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

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

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

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

50 hibit different synaptic relationships to CO blob cells.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 The blob distance and similarity are the Euclidean distance

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

125 4C beta and were coarser than the overlying blob pattern in the same animal.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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