ライフサイエンスコーパス: a shift of @3 from @2 to

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1 n 11 and 12 days in vitro (DIV) resulting in a shift of the EC50 from 10.7 to 2.4 uM.

2 dramatic enhancement of ANS fluorescence and a shift of the emission maximum from 520 to 482 nm.

3 of EPSP or the (6R)-6-fluoro analogue causes a shift of the fluorescence from 520 to 495 nm.

4 60%-40% relative-spreading probability, with a shift of the maximum from 103 down to 50 Gy, and about

5 The change of pH from 6.5 to 2 causes a shift of the absorption maximum from 568 to 600 nm (ac

6 on of the electron confinement energy caused a shift of the emission band from 510 to 665 nm with unu

7 recovery of activity is also accompanied by a shift of the pK(a) from 9.29 to 7.46 (close, and withi

8 SII(-Mn, +Fe) samples blocked in D(2)O shows a shift of the pK(app) from 6.1 to 7.6, and an increase

9 This has been accompanied by a shift of focus from enzymology to a search for substra

10 of unlabeled PAL1 with PAL2-GFP resulted in a shift of fluorescence localization from endomembranes

11 Exposure to METH resulted in a shift of occludin localization from plasma membranes t

12 ption of the plus-end motor kinesin I causes a shift of dynein from posterior to anterior.

13 ity of states modulation manifests itself as a shift of states from above to below the superconductin

14 Interestingly, a shift of CD11c(+) cells from CD86(low) to CD86(high) i

15 istant cell line EL-4, but rather, there was a shift of Ras from membrane to cytosol, as expected for

16 activating mechanisms in Dcp2 also result in a shift of the substrate specificity from bacterial to e

17 ovision of energy to eukaryotic cells, makes a shift of paradigm from gonadal histology to energy met

18 Impeding FGF signaling results in a shift of ectodermal markers from neural to epidermal.

19 bitory postsynaptic currents, and ultimately a shift of GABA-elicited responses from inhibitory to ex

20 petites within two to four generations after a shift of the culture from glucose to galactose medium.

21 without routine imaging and, more generally, a shift of focus from relapse detection to improved surv

22 (i) inhibited protein synthesis, (ii) caused a shift of mRNA from heavy to light polysomes, (iii) inh

23 rong gene expression dynamics in response to a shift of cells from high carbon to low levels of inorg

24 the voltage-dependent anion channels causing a shift of calcium from the ER to mitochondrial compartm

25 arbon and nitrogen isotope tracers reflected a shift of the gull diet from aquatic to more terrestria

26 quitin protein levels, which correlated with a shift of ubiquitin mRNAs from larger polysomes to non-

27 of cell wall changes was performed following a shift of the mutants from permissive to nonpermissive

28 s on granule cell dendrites, consistent with a shift of the gamma2 subunit from synaptic to perisynap

29 A shift of cells from restrictive to permissive temperat

30 lacenta from a non-placental ancestor causes a shift of maternal investment from pre- to post-fertili

31 Further, we observed a shift of BMP receptors from early to recycling endosom

32 23 alternative splicing specifically promote a shift of expression from STAT3alpha to STAT3beta.

33 eas coexpression of NBR1 and CIB resulted in a shift of CIB protein expression from the nucleus to th

34 expression of alpha 3- and beta 1-integrins, a shift of beta 1-integrins from the cytoplasm to the pl

35 se data suggest that CD40L treatment induces a shift of Ku from the cytoplasm to the cell surface, an

36 cycle, or in vitro by cell lysis, results in a shift of Nup2p from the nucleoplasm to the cytoplasmic

37 and the dorsal attention network indicating a shift of resources from the visual to the auditory dom

38 tribution of the Vps10 protein, resulting in a shift of Vps10p from the Golgi to the vacuolar membran

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