ライフサイエンスコーパス: Kf

1 Kf exo(+) removed dA, dG, and T opposite M(1)dG and N(2)

2 Kf was invariant with orthostasis.

3 Kf was negatively associated with a measure of glycemia

4 Kf(-) incorporated purines opposite the R isomer with gr

5 N leukocytes, and sigma alb (0.74 +/- 0.05); Kf was not different.

6 enow fragment lacking proofreading activity, Kf (exo-), than deoxythymidine glycol triphosphate (dTgT

7 n and thromboxane release, but sigma alb and Kf were not altered.

8 For equivalent EC clearance, Ppa, and Kf as in normoxic EC, postbacteremic H/R increased TNF-a

9 ly occurred opposite dC and was catalyzed by Kf(-) with equal efficiencies.

10 d form of 8-oxoA direct insertion of dTMP by Kf exo-.

11 MP and dGMP insertion opposite the lesion by Kf exo- with transient inhibition of primer extension oc

12 Internal mismatches were recognized by Kf exo+ resulting in the excision of the correct base pa

13 n and replication beyond the adduct sites by Kf was reduced compared to unadducted controls.

14 s efficiently and selectively synthesized by Kf within the context of natural DNA.

15 Calculated Kf rose because filtration increased even though the hyd

16 With BP, calculated Kf rose from 0.26 +/- 0.09 at baseline to 0.50 +/- 0.20

17 n produces little or no change in calculated Kf.

18 With TD, calculated Kf rose from 0.28 +/- 0.13 at baseline to 0.43 +/- 0.19

19 le change in Pnf, suggesting that calculated Kf also rises.

20 ired muscle microvascular exchange capacity (Kf), independently of visceral fat mass.

21 assessed microvascular filtration capacity (Kf), which is the linear relationship between filtration

22 iance, and capillary filtration coefficient (Kf) permit analysis of preservation solutions or modific

23 Changes in the filtration coefficient (Kf) were evaluated at 180 min when cytokine mRNA levels

24 The capillary filtration coefficient (Kf), a sensitive measure of changes in microvascular per

25 nd the microvascular filtration coefficient (Kf).

26 0.05) and decreased filtration coefficient (Kf, 0.05 +/- 0.01 versus 0.11 +/- 0.03 g.min-1.mm Hg-1.1

27 urement of capillary filtration coefficient (Kf,c), a sensitive index of lung microvascular permeabil

28 he whole-kidney ultrafiltration coefficient (Kf) by the single-nephron ultrafiltration coefficient (S

29 the glomerular ultrafiltration coefficient (Kf), which also increased early and then remained consta

30 extension experiments using Escherichia coli Kf exo(-) DNA polymerase were carried out under "standin

31 w fragment of DNA polymerase I from E. coli (Kf) and found to be recognized to varying degrees.

32 support, maintaining the ability to compute Kf.

33 Lung liquid conductance (Kf) is calculated as the quotient of lung lymph flow div

34 ligand (citrate) complex formation constant (Kf).

35 Formation constants (Kf) proved the formation of stable inclusion complexes.

36 erences, increased compliance, and decreased Kf values as compared to both EC and UW.

37 did not incorporate a method for determining Kf.

38 extension catalyzed by Klenow fragment exo- (Kf exo-), calf thymus DNA polymerase alpha (pol alpha) o

39 Finally, Kf (g . min-1 . cm H2O-1 . 100 g-1) increased the most i

40 found for the high-fidelity Klenow fragment (Kf) of Escherichia coli DNA Pol I.

41 that the filtration surface area (and hence, Kf) increased in proportion to renocortical volume after

42 w fragment of Escherichia coli polymerase I (Kf exo+).

43 ith the Klenow fragment of DNA polymerase I (Kf).

44 at protein depletion causes little change in Kf, leaving open the question of how lung lymph flow can

45 to 5 mL.kg tidal volume had no elevation in Kf,c at any time point regardless of respiratory frequen

46 requency of 80 had significant elevations in Kf,c at all times after baseline compared with lungs exp

47 ss, and M:I explained 38% of the variance in Kf (in a linear regression model with Kf as the outcome

48 ant factor for lung hemorrhage and increased Kf (two-way analysis of variance; p < .05).

49 posite template CEdG when either the Klenow (Kf(-)) or Thermus aquaticus (Taq) polymerases were used.

50 -P in the presence of ADP would follow kobsd=Kf+Kr+9.2 x 10(2) s-1.

51 d storage, lungs stored in Celsior had lower Kf values than those stored in EC, indicating decreased

52 nd orthotopic transplant models, maintaining Kf determination, a sensitive indicator of reperfusion i

53 To address this, we measured Kf in sheep following two kinds of protein depletion: ba

54 selection of capping agents on the basis of Kf and demonstrates the correlation between sizes and sp

55 s included in the circuit for measurement of Kf.

56 ered flow at 35 degrees tilt, the product of Kf and Pv, was approximately twice that of control (0.41

57 The pre-tilt value of Kf did not change after the imposition of the passive ti

58 Supine Kf was not significantly increased in the forearm in pat

59 ide incorporation experiments indicated that Kf exo(-) incorporates all four nucleotides opposite M(1

60 The Kf(-) polymerase preferentially incorporated dGTP, where

61 Furthermore, the Kf,c at 90 mins was significantly higher than permeabili

62 attributed exclusively to an increase in the Kf.

63 e pO2 of the pulmonary effluent blood or the Kf; analyzed to determine whether the sequence of reperf

64 This is in marked contrast to Kf, which showed a rigid size preference, varying by 110

65 The data establish that, unlike Kf, Dpo4 has very low steric selectivity and that steric

66 M:I was associated with Kf independently of visceral fat mass (B coefficient 3.1

67 adducts when replication was conducted with Kf exo(+).

68 In contrast, with Kf exo(-), primers extended past M(1)dG contained T oppo

69 nce in Kf (in a linear regression model with Kf as the outcome [R2 = 0.38, P = 0.005]).

70 ect insertion of T during DNA synthesis with Kf exo-.