ライフサイエンスコーパス: couplet

1 es that cut through the Ries seismite-ejecta couplet.

2 from one cell to the other cell of an HepG2 couplet.

3 airs complementary to the face-to-face codon couplets.

4 duced cholestasis in isolated rat hepatocyte couplets.

5 or on fluid secretion in isolated hepatocyte couplets.

6 icular bile secretion in isolated hepatocyte couplets.

7 mbers of PVCs (202 +/- 655 vs. 116 +/- 435), couplets (1.9 +/- 5 vs. 1.2 +/- 10), and NSVT runs (0.4

8 tions (66+/-117 versus 18+/-20, P=0.055) and couplets (3.2+/-6 versus 0.2+/-0.21, P=0.031) decreased.

9 DE than those without DE (PVCs: 89% vs. 72%; couplets: 40% vs. 17%; NSVT: 28% vs. 4%; p < 0.0001 to 0

10 ding 21 (12%) with >/=500 PVCs, 74 (42%) had couplets, 67 (37%) had supraventricular tachycardia (SVT

11 plet at the B0-position that overlaps with a couplet 790 cm-1 higher in energy, which we assigned to

12 and without PVCs (8.2% vs. 9.1%; p = 0.93), couplets (8.5% vs. 8.4%; p = 0.99), or NSVT (8.3% vs. 8.

13 o-microscopic studies of isolated hepatocyte couplets and isolated bile duct segments show that this

14 were performed using isolated rat hepatocyte couplets and pancreatic acini, plus SkHep1 cells as nonp

15 0.03), with higher prevalence of ventricular couplets and triplets (33 vs. 8%, p = 0.02).

16 CRDS had no arrhythmias, 1 had a monomorphic couplet, and 2 could not undergo EST (deceased).

17 ing isolated perfused rat livers, hepatocyte couplets, and isolated bile duct units (IBDU) from rat l

18 imentologically, including creating mud-sand couplets, and lead to single thread, active meandering c

19 Premature ventricular contractions (PVCs), couplets, and nonsustained ventricular tachycardia (NSVT

20 stained ventricular tachycardia, ventricular couplets, and premature ventricular contractions showed

21 premature ventricular beats; 2, bigeminy; 3, couplets; and 4, nonsustained ventricular tachycardia).

22 ier molecule (guest) confirmed that their CD couplets arise from the preferred porphyrin helicity of

23 201-202 nm and the near-UV negative exciton couplet around 230-240 nm.

24 bstituted resorcin[4]arenes, the ECD exciton couplet at longer wavelength depends on the chirality in

25 the ferri-state displays a nearly symmetric couplet at the B0-position that overlaps with a couplet

26 es displayed symmetric negative and positive couplets at 190 and 210 nm, which are interpreted as ind

27 VCD intensity becomes weaker and the amide I couplet becomes more conservative, while the amide II VC

28 lls, IL-9(+) cells, and mast cell-eosinophil couplets before and after treatment.

29 Mast cells and eosinophils were found in couplets before therapy, and these were significantly de

30 The experimentally obtained positive exciton couplet by CD and FDCD of the bis-TPPcin derivative of g

31 steric size of substituents, the observed CD couplet can be applied for straightforward assignment of

32 e model in single family rooms with complete couplet-care for the mother-newborn dyad during maternit

33 in this study using isolated rat hepatocyte couplets, causes a reduction of the accumulation of (flu

34 oism (CD) spectrum and gave a characteristic couplet composed of a positive maximum Cotton effect at

35 report on a sequence of rhythmic sedimentary couplets comprising the Paleocene/Eocene Marlboro Clay (

36 Immunofluorescence of hepatocyte couplets confirmed the intracellular/canalicular localiz

37 brane fractions isolated from rat hepatocyte couplets contain lipid microdomains ("rafts") enriched i

38 3.5 per thousand delta(13)C decrease over 13 couplets defining the CIE onset, which requires a large,

39 nic center of the substrate, the sign of the couplet determines the absolute configuration at this ce

40 The magnitude of a CD exciton couplet (due to the two Trp residues) and the chemical s

41 Immunofluorescence staining on hepatocyte couplets for both caveolin-1 and cholera toxin B showed

42 The sign of the CD couplet has also been found to be inverted when the ster

43 The fludarabine and cyclophosphamide couplet has become the backbone of the chronic lymphocyt

44 These couplets have corresponding delta(18)O cycles that imply

45 nhanced vibrational circular dichroism (VCD) couplet in the amide I' band region that is nearly 2 ord

46 within the clusters consisted of a synaptic couplet in which two processes synapsed with each other

47 ng bulk sample and a decoupling of the Hf-Nd couplets in the clay formation during the weathering pro

48 as quenched antennas, give intense excitonic couplets in the electronic circular dichroism spectra wh

49 lls, IL-9(+) cells, and mast cell-eosinophil couplets in the esophageal epithelium after anti-IL-5 th

50 ed rat liver (IPRL), isolated rat hepatocyte couplets (IRHC), and WIF-B cells to study the cellular l

51 In bisignated ECD spectra, the sign of the couplet is determined not only by the handedness of chir

52 For the ferro-state, the couplet is greatly reduced, but still detectable.

53 The dynamically induced exciton couplet is observed when the biphenyl chromophores are p

54 d using isolated perfused livers, hepatocyte couplets, isolated bile duct units, and cholangiocytes f

55 This cross-couplet kinetic linkage and the stiffening function of t

56 The diagonal-couplet lateral sequence gait was accomplished by rotati

57 s waterfalls with a salamander-like diagonal-couplets lateral sequence gait and has evolved a robust

58 G-cells and the ECL cells are coupled by the couplet molecules gastrin and histamine and by a prior a

59 The sign of the exciton couplets observed for inductor-reporter systems might be

60 ivity of retCPr 2a and the observed negative couplet of 11,12-dihydro-Rh7.

61 tion of the previously published negative CD couplet of 11,12-dihydrorhodopsin also leads to a chromo

62 or gliotoxin requires a seemingly extraneous couplet of condensation (C) and thiolation (T) domains i

63 hypothesis, we perform the same analyses on couplets of G. ruber (W) specimens with attributes inter

64 understood as a superposition of asymmetric couplets of split Q0 and Qv-states.

65 premature ventricular contractions with >/=1 couplet or (2) sustained or nonsustained ventricular tac

66 In vivo truncation of GliP to remove the CT couplet or just the T domain abrogated production of gli

67 ntricular bigeminy or trigeminy, ventricular couplets or triplets, ventricular tachycardia, ventricul

68 either nonsustained ventricular tachycardia, couplets, or premature ventricular contractions, the ext

69 directional VT and borderline if polymorphic couplets, premature ventricular contractions, or nonsust

70 data, to evaluate whether the limestone/marl couplets reflect an original cyclic signal.

71 lysis of the B-band profile reveals that the couplet reflects a B-band splitting of 350 cm (-1), whic

72 fungal DKPs terminate with similar CT domain couplets, suggesting a conserved strategy for DKP biosyn

73 e correlated with the sign of the CD exciton couplet that establishes the absolute configuration at t

74 t cytochrome c (pH 7.0) exhibit a pronounced couplet that is maintained below 343 K, before protein u

75 Upon exposure of couplets to a choleretic stimulus (i.e. dibutyryl cAMP),

76 In addition, exposure of couplets to dibutyryl cAMP caused an increase in canalic

77 estimates suggest lateral sequence diagonal couplet walks, in which the footfalls of the diagonal li

78 ed to the chiral center, the signs of the CD couplets were opposite to those predicted on the basis o

79 hemistry and chiroptical properties for this couplet, while its application at shorter wavelengths is

80 All three models predict Soret exciton couplets with signs in agreement with experiment.

81 forming a unique continental seismite-ejecta couplet within a distance of up to 180 km from the crate

82 pted by glycine residues and glycine-alanine couplets within MiSp1-like as well as repeats of the hep