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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

25 Many neurons were tuned for numerosities irrespective of the physical

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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