ライフサイエンスコーパス: decay rapidly

1 m paradoxical because ancestral correlations decay rapidly.

2 e preservation of soft tissues that normally decay rapidly.

3 redicted level when the synaptic correlation decays rapidly.

4 nels was large immediately after a spike but decayed rapidly.

5 s around the time of encoding, memories will decay rapidly [3, 5, 6, 8].

6 use the soft tissue of the eye and the brain decay rapidly after death, such as within 64 days and 11

7 The potentiation response also decayed rapidly after ethanol removal.

8 contact hypersensitivity responses to hapten decayed rapidly after manufacture.

9 The bulk phase thylakoid PMF decays rapidly after the termination of actinic illumina

10 proposed in which fluorescent exciton states decay rapidly and irreversibly to dark exciplex states.

11 des of recombinant pox boosted CTL responses decayed rapidly and were comparable to those of the DNA-

12 The light intensity decays rapidly and the weak light lasts for hours.

13 ating-the initial high discharge rate, which decays rapidly, and the change of contrast gain with tim

14 he photoexcited perylene-monoimide dye (PMI) decays rapidly ( approximately 3.5 ps) and predominantly

15 eptide-MHC complexes produce a response that decays rapidly as peptide is washed away.

16 of proteins within known regulatory pathways decays rapidly as the path length between two proteins i

17 ecause the DEP force generated by electrodes decays rapidly away from the electrodes, DEP-based micro

18 ile thicker films can improve stability, DMI decays rapidly away from the interface.

19 Human thrombin-activated fVIII (fVIIIa) decays rapidly because of first-order dissociation of th

20 tween nearby PPC neurons was much weaker and decayed rapidly beyond approximately 200 mum.

21 LD decayed rapidly, declining to background levels in appro

22 plasmic Na is submaximal, Na/K pump currents decay rapidly during extracellular K application and mul

23 s, like nanos, is a maternal transcript that decays rapidly during early development.

24 The ferryl complex forms and decays rapidly enough to be on the catalytic pathway.

25 lk utilization is logistic, that is the yolk decays rapidly for a period of time before leveling out.

26 The autofluorescence decayed rapidly from the baseline immediately after 20-m

27 as low, with an average pairwise r2 of 0.30, decaying rapidly from approximately 0.50 to approximatel

28 that the preintegration state is labile and decays rapidly (half-life = 1 day) following the entry o

29 majority of wild barley loci, intralocus LD decays rapidly, i.e., at a rate similar to that observed

30 p by correlational selection are expected to decay rapidly (ie, within a few generations), unless cor

31 e between neuronal circuits, and its effects decay rapidly if stimulation is discontinued.

32 we had previously identified: Class I, which decay rapidly in exponential and stationary phase of gro

33 an, chick, and zebrafish Bmp2 synthetic RNAs decay rapidly in extracts from cells not expressing Bmp2

34 .4, Kv3.3, and Kv3.4) generate currents that decay rapidly in the open state because an N-terminal ba

35 show that pH gradients across such membranes decay rapidly in the presence of alkali-metal cations, b

36 ollateral-CA1 tetanic long-term potentiation decayed rapidly in acute hippocampal slices from beta-ad

37 Ca2+ channel activity decayed rapidly in excised patches, and recovered on add

38 A small group of C(8-10) and C(20) HOMs decayed rapidly in hydrated particles, on a time scale a

39 HIV-1 RNA levels and total HIV-1 DNA levels decayed rapidly in patients during receipt of suppressiv

40 in basal dendrites of hippocampal field CA1 decayed rapidly in slices prepared from 7- to 10-month-o

41 3'UTRs; c-myc mRNA, containing a class I ARE decayed rapidly in the same cells.

42 Levels of linear nonintegrated HIV-1 DNA decayed rapidly in vitro (t (1/2) = 1- 4.8 days).

43 Intragenic LD decays rapidly in conifers; thus SNPs showing genetic as

44 ive, as expected for a high-spin ferryl, and decays rapidly in fluid solution at cryogenic temperatur

45 s, and show that correlation among CpG sites decays rapidly, making predictions solely based on neigh

46 s, the main metabolic organ of decapods that decays rapidly post-mortem.

47 However, post-mortem DNA decay rapidly reduces the number and quality of survivin

48 trations in the absence of heparin, activity decayed rapidly (t1/2 = 1-4 min at 37 degrees C) to an i

49 ted wild-type, human GM-CSF (hGM-AUUUA) mRNA decayed rapidly (t1/2 = 9 min), while a mutated version

50 ment, with a peak of expression at 3 h, that decayed rapidly thereafter.

51 Because the L and M1 states decay rapidly, they can be present only if they are in e

52 hly stable but upon imidazole addition, they decay rapidly to pMHC monomers, allowing flow-cytometric

53 -state component in hippocampal neurons, but decayed rapidly to baseline in dorsal root ganglion (DRG

54 ted large, rapidly rising initial peaks that decayed rapidly to smaller, steady-state levels.

55 to compound I and, upon H2O2 exhaustion, it decayed rapidly to the ferric form.

56 his pulse, a very large outward current that decayed rapidly to the previous activating current basel

57 50 generations for the beetle, the cline had decayed rapidly to yield rather uniform frequencies of m

58 activated initiation complex is unstable and decays rapidly to an inactive state in the presence of t

59 +) (compound 0) accumulates within 5 mus and decays rapidly to CYP101Fe(3+), with a k440 nm of 9.6 x

60 However, the active photoproduct decays rapidly to opsin and free all-trans-retinal.

61 As singlet oxygen decays rapidly to triplet oxygen, the bubbles leave behi

62 behavior of capacitor, the response current decays rapidly to zero, making the determination of the

63 We determine that the NI decays rapidly under optimal turnover conditions, and th

64 te that monoterpene and sesquiterpene levels decayed rapidly upon ozone exposure, while oxygen-contai

65 le cavity mode, their dipoles will align and decay rapidly via a superradiant burst.

66 of the A-side bacteriopheophytin, H(A)) can decay rapidly via recombination through the neighboring

67 ted VA.+ formed by oxidation of VA by Ce(IV) decayed rapidly with a first-order mechanism in air- or

68 N antibodies, however, decayed rapidly with a half-life of 60 days (95% confide

69 ort-term temporally-volatile component, that decays rapidly with a time constant of just 15 to 20 s a

70 ranscranial magnetic stimulation (TMS) pulse decays rapidly with distance.

71 orthern European populations, disequilibrium decays rapidly with physical distance, which is consiste

72 Total HIV-1 DNA decays rapidly with suppression of virus replication in

73 thalamus, sensory-evoked activity in cortex decayed rapidly, with a time constant of 10 ms, which is

74 IPSCs in these cells decayed rapidly, with a weighted time constant tau(Decay

75 This intermediate then decays rapidly, with k = 743 s-1, and this rate constant

76 on of the 2nd EPSP (655 +/- 380% at 5-20 ms) decayed rapidly, within 50-60 ms.

77 High susceptibility to adhesion decays rapidly, within 30-60 min.