ライフサイエンスコーパス: low-turnover

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1 s, possibly contributing to their relatively low turnover.

2 crophages, are long-lived cells, and exhibit low turnover.

3 play a role in the maintenance of a state of low turnover and sustained expansion of the CD4 T cell p

4 vivo is limited in most organ systems by the low turnover and/or the asynchronous nature of cell cycl

5 Bone histology revealed low turnover bone disease in 50% of the patients at base

6 e may have additional fracture risks such as low turnover bone disease.

7 centrations may influence the development of low-turnover bone disease and coronary artery calcificat

8 Compared with normal or low turnover, bone with high turnover had material and n

9 The Ecad-lo subset contained more low-turnover cells, correlating with resistance to the c

10 ared with high or normal turnover, bone with low turnover had microstructural abnormalities such as l

11 ed with the repressive Polycomb-Group showed low turnover in ESCs.

12 e populations exhibit a long life span and a low turnover in the steady state.

13 gether, these results provide evidence for a low-turnover, mesenchymal-like sub-population in SCCs wi

14 H4K20 was methylated in low-turnover nucleosomes in euchromatic regions, notably

15 Both forms of the enzyme had a low turnover number at Vmax (0.23 to 0.68 C5/min/enzyme)

16 RNA-dependent ATPase activity, albeit with a low turnover number.

17 (-1)), combine to yield the overall observed low turnover number.

18 These homogeneous systems exhibited low turnover numbers (TONs).

19 Our results indicate that low turnover numbers may be a general feature of I-CLiPs

20 they often feature high catalyst loading and low turnover numbers relative to non-oxidative cross-cou

21 results indicate that a lack of deletion and low turnover of repetitive DNA are major contributors to

22 Superimposing CKD resulted in a low turnover osteodystrophy, whereas VC worsened and hyp

23 phy characterized by osteitis fibrosa, and a low-turnover osteodystrophy characterized initially by o

24 lastic function in an adult mouse leading to low-turnover osteopenia and suggest that Runx2-I and II

25 ver relative to Amazonia, where unexpectedly low turnover over great distances suggests that populati

26 lization in the absence of copper, to form a low-turnover phosphoenzyme intermediate, with a conforma

27 genes, particularly when deletion occurs in low turnover populations.

28 y for ligated tRNA (K(m,RNA), 0.35 nM) and a low turnover rate (k(cat), 0.3 min(-1)).

29 states: an autoinhibited basal state with a low turnover rate and a low H(+)/ATP coupling ratio and

30 rbon-fixing enzyme Rubisco, which exhibits a low turnover rate and can react with O2 instead of CO2 ,

31 E552A/S1173A had extremely low turnover rate for ATPase, while E552A/S528A showed z

32 Low turnover rate of this monoamine neurotransmitter is

33 In addition, our results revealed a low turnover rate of transcription and pre-mRNA splicing

34 function in skeletal muscle, a tissue with a low turnover rate, has never been investigated.

35 e N-terminal domain of ZntA, compared to its low turnover rate, indicates that this step is not rate

36 ssors and this protein displays a relatively low turnover rate.

37 roduct dissociation, thus accounting for its low turnover rate.

38 Mature hemidesmosomes, once present, have a low turnover rate.

39 But relatively low turnover rates (particularly towards non-natural sub

40 th substrates, lysozyme exhibited processive low turnover rates of 20-50 s(-1) and rapid (200-400 s(-

41 nsp2 species were relatively stable and had low turnover rates.

42 For low-turnover rates, increasing the number of drugs will

43 3' product was consistent with the extremely low turnover under steady-state conditions as 3' product

44 ontrast to QSOX, Erv2p shows a comparatively low turnover with a range of small thiol substrates, wit

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