ライフサイエンスコーパス: IVR

1 otein exocytosis was enhanced by ivermectin (IVR).

2 n the beta-tubulin internal variable region (IVR).

3 h" (BACK) domain, and an intervening region (IVR).

4 future studies of context conditioning using iVR.

5 system, even above the threshold for facile IVR.

6 intramolecular motions and thus inefficient IVR.

7 ual acuity measures compared with studies of IVR 0.5 mg PRN and dexamethasone 0.7 mg implants based o

8 d visual acuity (BCVA) with IVT-AFL 2q8 over IVR 0.5 mg PRN by 4.67 letters [95% credible interval (C

9 s in safety outcomes between IVT-AFL 2q8 and IVR 0.5 mg PRN or dexamethasone 0.7 mg implants.

10 IVT-AFL 2q8 versus intravitreal ranibizumab (IVR) 0.5 mg as needed (PRN) (10 studies) and IVT-AFL 2q8

11 edistribution (IVR) and the relation between IVR and molecular structure.

12 hH4v is on LG IVR and the hH2A-hH2B pair is located immediately right

13 molecular vibrational energy redistribution (IVR) and the relation between IVR and molecular structur

14 al views, and SR was measured during IVR (SR(IVR)) and early LV filling (SR(E)).

15 PRP compared with IVR as primary treatment for PDR is less expensive over

16 ervations support further advancement of TDF IVRs as well as the concept that extended duration drug

17 The elastomeric IVR body (matrix) was produced by hot melt extrusion of

18 solid hydrophilic core, embedded within the IVR by compression, contained the small molecule ZA and

19 Global SR(IVR) by 2-dimensional speckle tracking is strongly depen

20 E/SR(IVR) can predict LV filling pressures with reasonable ac

21 However, there is growing evidence that IVR competes with the reaction timescales, resulting in

22 The MZCL IVR contains four active pharmaceutical ingredients (API

23 ent-reported severity score stiffness on the IVR diary.

24 s recorded on an interactive voice response (IVR) diary (scale of 1 = minimal to 9 = worst ever exper

25 However, whether the effective IVR dimensionality can vary with time and whether the me

26 The BACK/IVR domains of ARA3 also are sufficient to modify AHR si

27 nslocator/simple-minded) domain and the BACK/IVR domains of ARA3 mediate the AHR-ARA3 interaction.

28 sotropic and anomalous nature of the quantum IVR dynamics and show that multiple power law scalings d

29 ng a measure of the nature and extent of the IVR dynamics.

30 molecular vibrational energy redistribution (IVR) effects.

31 Conversely, during IVR, flow was initially directed toward the apex and the

32 rate proof-of-concept of a novel core-matrix IVR for sustained and simultaneous delivery of diverse m

33 ove useful for the continuing development of IVRs for HIV prevention or other women's health indicati

34 polyether urethane (HPEU) intravaginal ring (IVR) for sustained delivery of the anti-HIV agent tenofo

35 y intramolecular vibrational redistribution (IVR) from the pumped rotational mode to all others.

36 hanges in this repeated challenge model, TDF IVRs generated reproducible and protective drug levels.

37 SR(IVR) had a strong correlation with time constant of LV p

38 Although a few IVRs have entered the clinical pipeline, 100% efficacy i

39 Cost utility for PRP would be 85% lower than IVR in the facility setting and 90% lower than IVR in th

40 R in the facility setting and 90% lower than IVR in the nonfacility setting.

41 transition state theory, which suggests that IVR in this reaction can be studied by conventional KIEs

42 f intramolecular vibrational redistribution (IVR) in p-benzyne is too slow to prevent this.

43 etime, the cost differential between PRP and IVR increases, and IVR therapy may exceed the typical ac

44 molecular vibrational energy redistribution (IVR) is at the heart of chemical reaction dynamics.

45 molecular vibrational energy redistribution (IVR) is indicated through the extensive local perturbati

46 IVRs loaded with 21% TFV (w/w) released greater than 2mg

47 Intravaginal rings (IVRs) may improve efficacy by providing long-term sustai

48 pH 4.2 for 30 or 90 days, during which times IVR mechanical properties and swelling kinetics were mon

49 contraction (IVC) and isovolumic relaxation (IVR) might represent a transient feature of myocardial w

50 PRP treatment of $14 219 to $24 005 and with IVR of $138 852 to $164 360.

51 TFV-HPEU IVRs of varying sizes and drug loadings were fabricated

52 ime constant of LV pressure decay during the IVR period (tau) (r=-0.83, P<0.001), whereas SR(E) was s

53 R ratio during the isovolumetric relaxation (IVR) period can be used to estimate LV filling pressures

54 stical rate theories, assuming instantaneous IVR, predict exponential decay of the population with th

55 The fact that the IVR process produces isomerization is deduced through a

56 n and echocardiographic imaging, mitral E/SR(IVR) ratio had the best correlation with mean wedge pres

57 Secondary end points included IVR-reported changes in pain, weakness, and tiredness; c

58 eas nonaxonemal beta-tubulins vary widely in IVR sequences.

59 e 3 apical views, and SR was measured during IVR (SR(IVR)) and early LV filling (SR(E)).

60 At baseline, 18 of 28 animals had negative IVR(SR) (i.e., PSS) in at least one segment.

61 During coronary artery occlusion, IVR(SR) became negative and larger in magnitude than S(S

62 ring systole (S(SR)), isovolumic relaxation (IVR(SR)), and rapid filling (E(SR)) phases in both ische

63 The IVR(SR)/S(SR) and epsilon(ps) best differentiated ischem

64 Here we describe a reservoir IVR technology that delivers the tenofovir prodrug tenof

65 Fortunately, immersive Virtual Reality (iVR) technology has improved appreciably and affords a r

66 ered from intravaginal rings, we designed an IVR that contains a drug matrix encapsulated in the core

67 cribe a novel core-matrix intravaginal ring (IVR), the MZCL IVR, which effectively delivered the MZC

68 ferential between PRP and IVR increases, and IVR therapy may exceed the typical accepted limit of cos

69 All TDF IVR-treated macaques (n = 6) remained seronegative and s

70 When IVR was the primary treatment, the 2-year cost in the fa

71 E/SR(IVR) was most useful in patients with ratio of E to mitr

72 Mechanical properties of IVRs were similar to NuvaRing, although the matrix elast

73 nvariant glycine 56 and a strongly conserved IVR, whereas nonaxonemal beta-tubulins vary widely in IV

74 drug matrix encapsulated in the core of the IVR whereby the mechanism of drug release is uncoupled f

75 Deuteration increases the rate of IVR, which decreases the fraction of recrossing and incr

76 ore-matrix intravaginal ring (IVR), the MZCL IVR, which effectively delivered the MZC combination mic

77 text have come from the state space model of IVR, which predicts power law behavior for the rates wit

78 was released by diffusion via a pore on the IVR while the MIV-150/LNG diffused from the matrix conti