ライフサイエンスコーパス: be reversed to

1 The decline in neurogenesis in aged mice was reversed to 50% of young control levels by running.

2 However this positive emergent effect was reversed to a negative multi-predator effect in whea

3 emia (PML)-defined structure in iPSCs, which was reversed to a regular sphere upon differentiation.

4 rom low toward high density, and this effect was reversed to a similar extent by restoring sterols wi

5 ed on neuronal activity suggests that it can be reversed to achieve perceptual constancy across speed

6 repression is sequence-dependent, because it is reversed to activation when P2 is substituted by the

7 eir segregation into daughter cells but must be reversed to allow for postmitotic functions.

8 of precursor fates, but how this repression is reversed to allow cell differentiation is unknown.

9 iments showing that inactive APE/Ref-1 could be reversed to an active DNA repair protein with phospha

10 affected, while the stimulatory effect of F was reversed to an inhibitory effect.

11 whether the neurodegenerative processes can be reversed to any extent after a successful eradication

12 atch repair (62.3-93.1 mL/m(2); P=0.028) but was reversed to baseline values after hTPV implantation

13 longest normothermic no-flow time that could be reversed to complete cerebral recovery.

14 The dilation at 10(-12) M ET-1 was reversed to constriction 4 days following hematoma a

15 paB in cardiac tissue of rats with cirrhosis were reversed to control levels (P < 0.05).

16 stimulated membrane hyperpolarization, which was reversed to depolarization within 35 to 160 seconds.

17 Also, vasoconstrictions to A23187 were reversed to dilations (-18.7+/-2.2 versus 18.8+/-1.

18 y fast if the polarity of the electric field is reversed to drive the analyte back and forth past the

19 alleles of FRI confer late flowering, which is reversed to earliness by vernalization.

20 hway is suppressed, and this inhibition must be reversed to engender tissue effects; however, the mec

21 the effect of strychnine on GABAergic IPSCs was reversed to facilitation, indicating a tonic glycine

22 ated intermediates formed during folding can be reversed to give active species.

23 ha selectivity observed with C-mannosylation was reversed to high beta selectivity if the C-5 alkoxya

24 Severe hypophosphatemia of Hyp mice was reversed to hyperphosphatemia in Hyp/klotho(-/-) dou

25 of a proteolytic site, and whether it could be reversed to immunodominance by engraftment of a novel

26 of the CVLM with glutamate (500 pmol, 50 nl) were reversed to increases in the presence of RVLM GABA(

27 This facilitation was reversed to initial levels following a 10-min agonis

28 he three distances, the donor/acceptor pairs were reversed to minimize uncertainty in the distance me

29 peractivity observed under visible light can be reversed to nativelike conditions upon exposure to UV

30 cells, Na-glutamine co-transport stimulation was reversed to normal levels by ketotifen.

31 These effects were reversed to normal by either the absence epilepsy d

32 th the catalytically inactive mutant of AMSH were reversed to normal.

33 scimol caused an inhibition of sIPSCs, which was reversed to potentiation by the GABA(B) receptor ant

34 LTD, but in adults (6 months), the phenotype is reversed to promote LTD and reduce LTP, compared to a

35 mechanisms by which cardiac hypertrophy may be reversed to reduce this risk have not been fully dete

36 If desired, cross-links can be reversed to release the target after capture.

37 The flow in the production zone is reversed to release the particles for collection and

38 However, whether this modification is reversed to repress the expression of p53 target gene

39 maging sessions with two subjects, the rules were reversed to require a button press whenever an obje

40 involves substantial ion movements that must be reversed to restore homeostasis.

41 involves substantial ion movements that must be reversed to restore homeostasis.

42 privation-induced synaptic modifications can be reversed to restore normal visual function.

43 ect responses and decreased errors when cues were reversed to reward spatial cues.

44 ssions revealed that this facilitation could be reversed to suppression if stimulus pairs with the sa

45 -helix, or an alpha-helical coiled-coil, can be reversed to test the effect of the helix dipole in co

46 cardiac TG content in double transgenic mice is reversed to that of wild-type mice.

47 Compound 2 can be reversed to the original material upon reabsorption o

48 ere seeded at low density, but its targeting was reversed to the basolateral membrane under the influ

49 namic cardiac function of the knockout mouse was reversed to the same extent by reinsertion of either

50 roduct, indicating that the cis-syn dimer is being reversed to TT by UVC light.

51 During spore germination, SP is reversed to two intact thymines in situ by the DNA re

52 mutant ameloblasts, the phenotypes of which were reversed to undifferentiated epithelium.

53 of CD4(+) T cells in the gut mucosa that can be reversed to various degrees with antiretroviral thera

54 In contrast, NOC/oFQ-induced vasodilation was reversed to vasoconstriction in H+I+R animals and in

55 c analysis showed that the BAC-excised virus was reversed to wild-type RRV.