ライフサイエンスコーパス: be turned over

1 equires transport to the vacuole in order to be turned over.

2 s a pathway by which TCR-activated NF-kappaB is turned over.

3 nt of the number of substrate molecules that are turned over.

4 that of the other pair, with excess subunits being turned over.

5 e dynamic structures and that their channels are turned over actively, suggesting that regulated traf

6 This indicates that episomal cDNAs are turned over by degradation rather than through death

7 nd rpL37, fail to assemble, and preribosomes are turned over by Rat1.

8 ndicate that tens of molecules of casein can be turned over by the ClpAP complex before significant d

9 ful because the probe was too deactivated to be turned over by the enzyme.

10 unstimulated cells, both subtypes appear to be turned over by the same mechanism.

11 Our results also suggest that ERManI is turned over by an active autophagic process.

12 isomal Pex15, exaggerated by overexpression, is turned over by Msp1.

13 yers, cleaving only one-sixth of the PG that is turned over by the lytic transglycosylases.

14 LO1 protein is associated with ubiquitin and is turned over by the proteasome.

15 idence that the fluorescent substrate analog is turned over by the toxin in either glucosyltransferas

16 When the presynaptic glutamate pool was turned over by synaptic activity, inhibiting the pre

17 ommon perception that carotenoids are simply being turned over during wheat grain development after t

18 10% of the photoreceptor outer segment (OS) is turned over each day, requiring large amounts of lipi

19 The chimeric reporter protein is turned over every cell cycle and hence its histochemi

20 tro culture system in which infected T cells are turned over frequently to provide a model system tha

21 s organization lies at the heart of how OMPs are turned over in the membrane.

22 how rapidly individual R1 and R2 insertions are turned over in the rDNA locus by these processes, we

23 yeast Saccharomyces cerevisiae, LDs can also be turned over in vacuoles/lysosomes by a process that m

24 It is known that Tip60 is turned over in cells by the ubiquitin-proteasome syst

25 otein, a negative regulator of GA signaling, is turned over in GA-treated cells in the presence and a

26 One target of GSK-3beta is cyclin D, which is turned over in response to this phosphorylation.

27 In mammalian cells, significantly more RNA is turned over in the nucleus than in the cytoplasm.

28 otein stability analysis suggested that FlaA was turned over in the flaB mutant.

29 and covalently closed circular DNA (cccDNA) were turned over independently of cell division.

30 he only known mechanism whereby mitochondria are turned over is through macroautophagy.

31 and that transcripts from both types of gene are turned over quickly.

32 is not controlled; instead, the L transcript is turned over rapidly late in infection.

33 ion assays demonstrated that the LHY protein is turned over rapidly through the proteasome pathway.

34 In addition, COX-2 protein is turned over rapidly.

35 activity but loses membrane localization and is turned over rapidly.

36 In vivo, FtsZ is turned over slower in a clpX deletion mutant compared

37 The compounds studied were turned over slowly or not at all by acetylcholinest

38 that the entire staircase stereocilia bundle was turned over synchronously.

39 s ER degradation, suggesting that ER protein is turned over through the ubiquitin-proteasome pathway.

40 ues that lack a second hydroxyl group cannot be turned over to products, although they can bind to th

41 promote the reductive cleavage of SAM, 6-CP is turned over to 6-deoxyadenosylpterin (6-dAP), presuma

42 cture of HPP but added bulky terminal groups were turned over to give products analogous to those fro

43 terning or whether developmental transcripts are turned over via specific pathways.

44 gene, we found that ductal epithelial cells are turned over with a half time of approximately 1month

45 ch that diverse aryl and alkyl phosphoesters are turned over with similar catalytic efficiency.

46 the two proteins is not known, but both can be turned over with AhpF from Salmonella typhimurium or,

47 The dehalogenation reactions could be turned over with catalytic amounts of photosensitizer

48 BACE was also found to be quite stable, being turned over with a t(12) of approximately 16 h.

49 MoFe protein (alpha-70(Ala)/alpha-195(Gln)) is turned over with hydrazine as substrate, the FeMo-cof

50 he order of 24,000 tons, of which two-thirds were turned over within 1 week.