ライフサイエンスコーパス: be tuned for

1 We find that many MT neurons are tuned for 3-D surface orientation, and that tilt and

2 l (object-related) pathway of visual cortex, were tuned for 3D orientation--that is,for specific slan

3 tion of functional nanoparticles (FNPs) that are tuned for a specific application is an area of immen

4 e studies show that visual motion processing is tuned for accuracy under naturalistic conditions, but

5 as a platform to build prochelators that can be tuned for activation in the reducing environment of c

6 Furthermore, the drug ratios in cb-ApDCs can be tuned for an enhanced synergistic effect without the

7 substrate surface, whose hydrophilicity can be tuned for an improved device response.

8 In the future, our platform can be tuned for any biological application of interest, off

9 as the distributed activity of neurons that are tuned for both the direction and speed of target mot

10 ave almost unlimited sequence space, and can be tuned for broad-spectrum or specific activity against

11 Together, PM is tuned for cardinal orientations, high SFs, and low sp

12 spatial scales, whereas the visual periphery is tuned for coarse spatial scales, in line with the nat

13 suggest a mechanism by which the hydroxylase is tuned for converting hispidin into the fungal lucifer

14 roduces the vision that SPION properties can be tuned for desirable dielectric heating and magnetic r

15 he simplicity with which the same device can be tuned for different applications simply by controllin

16 Proprioceptive feedback must be tuned for different behavioural contexts(3-6), but th

17 metal cations, enabling their properties to be tuned for different biomedical applications.

18 s with ion-transporting side chains that can be tuned for different electrolytes.

19 It can be tuned for different modes of operation.

20 ariations between Aux/IAA family members may be tuned for differential transcriptional repression and

21 nd visual posterior sylvian area (VPS), that are tuned for direction of self-motion in both visual an

22 ermitting the same canonical microcircuit to be tuned for diverse computational tasks.

23 from readily accessible monomers, which can be tuned for drug encapsulation and which retain good ce

24 ems from elements whose combination need not be tuned for dynamic stability.

25 o better understand how this protein machine is tuned for enzymatic cellulose solubilization.

26 The electronic structure can be tuned, for example, by changing the group IVA element

27 wavelength of lasing [Formula: see text] can be tuned, for example, by chemical composition.

28 crystallites in the combined population may be tuned, for example, to optimize packing of particles.

29 These novel structures can be tuned for excellent conductivity; versatile mechanica

30 intracellular Ca(2+) and that Ca(2+) gating is tuned for fast responses in neuronal BKCa-Cav complex

31 nlinear interaction terms (1f1 +/- 1f2) that were tuned for flanker orientation and position in adult

32 Os, and how this distribution must therefore be tuned for genomes of vastly different sizes.

33 with a conventional helicase mechanism that is tuned for great efficiency and specificity for G4s.

34 the design of origami-like modular units can be tuned for high structural performances and various st

35 cations but an intra-scan overlap method can be tuned for highest performance and is recommended when

36 the degradability of these polymers needs to be tuned for improved localized intratumoral gene delive

37 e interpret as a "noise width," available to be tuned for increased foraging efficiency.

38 erfacial and electrostatic forces, which can be tuned, for instance, by choosing different media to c

39 ICX neurons are tuned for interaural time difference (ITD), the owl'

40 ase-separated 2D reaction scaffolds that can be tuned for interfacial catalysis.

41 These scaffolds can be tuned for MAGL-selective or dual MAGL-FAAH inhibition

42 Every aspect of the Gemini Planet Imager has been tuned for maximum sensitivity to faint planets near

43 We conclude that enzymatic constants are tuned for metabolic remodeling.

44 ally linked to somatotopy, such that neurons were tuned for motion toward their preferred surround vi

45 ns in the Drosophila brain, called pC2, that are tuned for multiple temporal aspects of one mode of t

46 Many neurons were tuned for numerosities irrespective of the physical

47 These colorimetric sensors can be tuned for numerous vapour sensing scenarios in confin

48 thesize that assembly kinetics and stability are tuned for optimal viral replication, not maximal ass

49 cs images have many parameters which need to be tuned for optimal detection.

50 erophilic complex affinity, which appears to be tuned for optimal function.

51 The hyPAD can be tuned for optimal performance by adjusting the applie

52 evels of plasticity allow neural circuits to be tuned for optimal performance.

53 l allow the cyclic depsipeptide structure to be tuned for optimum selectivity.

54 nds on receptive field spatial phase), which is tuned for orientation, and a phase-nonspecific compon

55 Most, however, were tuned for orientation and binocular disparity and w

56 ed foundations on how these interactions can be tuned for outstanding DRM performance.

57 er many critical advantages, and systems can be tuned for performance, recyclability, selectivity, ai

58 s been uniquely customized with shading that is tuned for pockets and cavities of a user-defined size

59 We find that although both populations are tuned for posterior motion, they can be distinguishe

60 of a number of kinetic adaptations, myosin V is tuned for processive movement on actin and will be ca

61 This approach can be tuned for production of branched hydrocarbons and aro

62 any neurons in the lateral prefrontal cortex were tuned for quantity irrespective of the exact physic

63 We propose that subclass-1 myosin-Is are tuned for rapid sliding, whereas subclass-2 isoforms

64 e cell type in the body, the astrocyte, that is tuned for rapid detection of physiological changes in

65 his review, we describe how the ILs and DESs are tuned for RCC and specifically address the CO(2) che

66 at connections between layer 4 and layer 2/3 are tuned for reliable transmission of spatially distrib

67 ell-resolved peaks, the laser wavelength can be tuned for selective ionization of targeted molecules.

68 These conductances are tuned for specific activity patterns but might also

69 rtant for understanding how diverse kinesins are tuned for specific cellular functions.

70 nments, suggesting Snf2 family motor domains are tuned for specific tasks.

71 majority of neurons in primary visual cortex are tuned for stimulus orientation, but the factors that

72 responses of individual neurons is found to be tuned for stimulus features and proposed to be used a

73 We found that PSS neurons, like MT neurons, were tuned for stimulus motion and showed strong suppres

74 ing how fetal versus adult receptor isoforms are tuned for synapse development versus the all-or-none

75 rotemporal tuning in which the posterior STG is tuned for temporally fast varying speech sounds that

76 spectral modulation) while the anterior STG is tuned for temporally slow varying speech sounds that

77 r rapid sliding, whereas subclass-2 isoforms are tuned for tension maintenance or stress sensing.

78 reviously found that many macaque V4 neurons are tuned for the curvature and object-centered position

79 e demonstrate that excitation and inhibition are tuned for the same direction, but differ in relative

80 in and that L-selectin bonds with PSGL-1 may be tuned for the compressive forces characteristic of le

81 he versatile reactivity of the thioacids can be tuned for the conversion of carboxylic acids into cor

82 , and exhibit a range of activities that can be tuned for the optimal performance of a broad range of

83 The deubiquitinase TRABID/ZRANB1 is tuned for the recognition and cleavage of K29 and K33

84 Reafferent responses were tuned for the amount of stimulus translation, and,

85 ework for understanding how diverse kinesins are tuned for their specific cellular roles.

86 mechanics metadynamics simulations, that it is tuned for transglycosylation (DeltaG() = 12 kcal/mol)

87 ng that rates of ptRNA processing by RNase P are tuned for uniform specificity and consequently optim

88 tiple available cores and processors and can be tuned for various memory settings.

89 The ESI interface and the ITMS were tuned for various parameters, and data acquisition

90 ld organization ensures that most MT neurons are tuned for velocity but do not tend to respond to amb