ライフサイエンスコーパス: reload

1 ion of the alternative pathway at 6 hours of reloading.

2 urred in nontreated animals after 6 hours of reloading.

3 ay was activated during the first 2 hours of reloading.

4 cating that SERCA function was important for reloading.

5 the need for hospitalization for dofetilide reloading.

6 iffering by over 60-fold in rates of vesicle reloading.

7 ned replication forks and mediate replisomal reloading.

8 es from vesicles undergoing neurotransmitter reloading.

9 emia-reperfusion, and hindlimb unloading and reloading.

10 proteins PriA, PriB, and DnaT for replisome reloading.

11 d in control animals between days 2 and 4 of reloading.

12 macrophages were reduced by 86% at 4 days of reloading.

13 PCI and randomly assigned to receive aspirin reload (325 mg orally, n=46) or no reload (control group

14 o make subsequent cracks form elsewhere upon reloading after healing.

15 ble 17% higher muscle fibre size compared to reloading alone, and myofibrillar protein synthesis, but

16 18% with massage during regrowth compared to reloading alone, and this was accompanied by elevated my

17 er PCI, 61% of patients allocated to aspirin reload and only 32% of patients allocated to control gro

18 ady-state transmission revealed that vesicle reloading and release at individual release sites is sig

19 reagents to a well containing the sample by reloading and slipping the well containing the reagent.

20 RISC reloading and subsequent induction of detectable cleavag

21 andling functions (Ca(2+) release and Ca(2+) reloading) and that any potential interference between C

22 Calcium sparks, SR Ca(2+) reloading, and caffeine-evoked Ca(2+) release amplitude

23 mg group; p = 0.019) and in the atorvastatin reload arm (18.4% vs. 35.0% in the no statin reload grou

24 le, can be induced upon muscle unloading and reloading, associates with myofibrils and is able to ubi

25 from the helix and a weak ability of EXOI to reload at the RPA-bound gap in the product, as well as M

26 n was required in 30 of 102 patients (29.4%) reloaded at a previously tolerated dose and in 11 of 30

27 e reloading for atrial arrhythmias, 102 were reloaded at a previously tolerated dose, 30 with a highe

28 d to be at higher risk for TdP than patients reloaded at a prior tolerated dose.

29 They also show that while vesicle reloading at AZs is not diffusion-limited at the onset o

30 reloading period did not differ at 2 days of reloading between anti-F4/80-treated mice and mice that

31 of the normal Brd4 levels, were defective in reloading Brd4 onto chromosomes.

32 of fibres with membrane lesions at 4 days of reloading, but this membrane repair did not occur in mac

33 stributed and may have a general function to reload Ca(2+) into sarcoplasmic reticulum as well as spe

34 Sufficiently rapid reloading capable of sustaining a large array, however,

35 in film thickness and no obvious changes in reloading capacity or release profiles.

36 Principal component analysis of recycled and reloaded casings resulted in classification of the penul

37 duced associations between CD4 and CCR5, and reloading cholesterol restored the associations in live

38 lcium responses were effectively restored by reloading cholesterol.

39 By contrast, a fast reloading class recovers within tens of milliseconds and

40 A slow reloading class requires seconds to recover and contribu

41 4.8-fold) and macrophages (11.3-fold) during reloading, compared to mice that experienced unloading o

42 muscle fiber diameter (10%), after 7 days of reloading, compared with PBS-injected soleus muscles.

43 e aspirin reload (325 mg orally, n=46) or no reload (control group, n=45) >/=1 hour before elective P

44 Reloading could be partially inhibited by 10 microM CPA,

45 er prolonged load that causes a delay in the reload curve which ultimately catches up with the origin

46 escribed as time-dependent forces (unloading/reloading cycles) acting on the Earth.

47 The reloading defect observed in Brd4+/- cells coincided wit

48 associate with moving EEs and that "off- and reloading" distributes the protein translation machinery

49 ough no TdP occurred in patients admitted to reload dofetilide at the same dose as previously tolerat

50 ing from clopidogrel to ticagrelor without a reloading dose is feasible, and it does not hinder plate

51 e onset of release, diffusion limits vesicle reloading during sustained high-frequency signalling.

52 ent from ambulatory controls after 4 days of reloading, during which time plantaris mass also returne

53 At plate margins, tectonic motions quickly reload earthquake ruptures, making the location of recen

54 The RISC pathway is also capable of being reloaded even in the absence of new protein synthesis.

55 all major criteria necessary for loading and reloading extensive two-dimensional arrays, as will be r

56 by immunohistochemistry after 24 h of muscle reloading following 10 days of unloading.

57 ied loading by using a mouse model of muscle reloading following a period of unloading.

58 METHODS AND Patients admitted for dofetilide reloading for atrial arrhythmias were retrospectively re

59 Of 138 patients admitted for dofetilide reloading for atrial arrhythmias, 102 were reloaded at a

60 nvolving SSB may coordinate replication fork reloading from start to finish.

61 ntly increased after PCI only in the aspirin reload group (P=0.0005).

62 farction frame count more evident in aspirin reload group (P=0.0023).

63 0447) from PCI in control but not in aspirin reload group.

64 .31; P=0.0413) in control but not in aspirin reload group.

65 reload arm (18.4% vs. 35.0% in the no statin reload group; p = 0.031).

66 No TdP occurred in the same dose reloading group, but TdP occurred in 2 patients admitted

67 lomycin, as did loss of the replication fork reloading helicases rep and priA.

68 Continuous operation was demonstrated by reloading hydrogen at regular intervals to maintain the

69 tive for recycling cohesin so that it can be reloaded in interphase for both non-mitotic and mitotic

70 flux, either for microdomain signaling or to reload internal Ca(2+) stores in the endoplasmic reticul

71 f trained personnel, the risks of dofetilide reloading justifying repeat hospitalization have not bee

72 phage numbers in soleus muscles at 2 days of reloading, macrophages were reduced by 86% at 4 days of

73 Prior to the onset of reloading, mice received a series of intraperitoneal inj

74 This suggests, within a "fire and reload" model of exocytosis, that the ribbon translocate

75 However, membrane damage in the reloaded muscles of transgenic mice did not differ from

76 sgenic mice showed 51 % fewer neutrophils in reloaded muscles than those of non-transgenic mice, but

77 efore intervention and either a atorvastatin reload (n = 76; 80 mg + 40 mg initiating 12 h before the

78 ting 12 h before the procedure) or no statin reload (n = 80).

79 ve phoshorylation was required to accelerate reloading of an intracellular calcium compartment before

80 p, which could be reversibly sealed to allow reloading of cells and reuse of the chip, was shown by m

81 fertilization and by removal and subsequent reloading of CENP-A during oogenic meiotic prophase.

82 XCR3 via IL-16/CD4, which was restored after reloading of cholesterol, indicating a requirement for i

83 esult from its capacity to mediate efficient reloading of DnaB helicase onto rolling circle replicati

84 act to ensure that efficient PriA-catalysed reloading of DnaB occurs only onto the lagging strand te

85 ns elicited by IP3 uncaging, indicating that reloading of endoplasmic reticulum stores via plasma mem

86 cells are in S-phase, presumably to prevent reloading of pre-replication complexes once S-phase has

87 Reloading of purified TTase into the TTase(-/-) cells re

88 modifying the Ras:SOS complex to prevent the reloading of Ras with GTP.

89 is maintained at each release site by rapid reloading of release-ready vesicles from an unusually la

90 of 0.2-0.5 during the startup phase or after reloading of the log wood burner.

91 ycling, a process that involves the repeated reloading of the polymerase on the same transcription un

92 of blocked forks in vivo is due to continual reloading of the replication apparatus at the site of th

93 st be reactivated through origin-independent reloading of the replication machinery (replisome) to en

94 replisome activity creates a requirement for reloading of the replication machinery, a potentially mu

95 s the first step of DNA replication restart, reloading of the replicative DnaB helicase onto an aband

96 Serotonin reloading of Tph1(-/-) mice reversed this phenotype, res

97 Reloading of TTase protein into the TTase(-/-) cells was

98 Specifically, slowed reloading of vesicle release sites leads to augmented sy

99 rast, at a G2/M nocodazole arrest, Cdc6 will reload onto chromatin if and only if its CDK sites have

100 ring late G1 or S, it will not substantially reload onto chromatin no matter whether its CDK sites ar

101 Yet, when nocodazole was withdrawn, Brd4 was reloaded onto chromosomes, and cells proceeded to comple

102 The repaired cofactor is then reloaded onto IcmF in a GTPase-gated step.

103 ytic activity, explaining how cohesin can be reloaded onto telophase chromatin in the absence of secu

104 n of EGTA, and fresh ProtA-CaM can be easily reloaded onto the column.

105 ase catalyzes the initial steps of replisome reloading onto repaired DNA replication forks in bacteri

106 Muscle membrane lysis during the reloading period did not differ at 2 days of reloading b

107 lication restart mechanisms that function to reload replisomes onto abandoned DNA replication forks.

108 oad the sarcoplasmic reticulum, but complete reloading required increases in [Ca2+]c (as measured wit

109 Complete reloading required large increases in the fura-2 signal.

110 x but lose Pol epsilon, and that Pol epsilon reloading requires ATM and ATR.

111 t show any increase in ubiquitination at the reloading stage, suggesting that calpain 3 is necessary

112 muscles of non-transgenic mice experiencing reloading than in ambulatory controls.

113 experimental model of hindlimb unloading and reloading that has been shown to induce sarcomere remode

114 loys the original fork, avoiding the need to reload the replication apparatus, then the blocked repli

115 rt initiator in Escherichia coli and acts to reload the replicative helicase DnaB back onto the chrom

116 semble, the restart primosome is required to reload the replicative helicase so that chromosomal repl

117 pm (as measured with aequorin) can partially reload the sarcoplasmic reticulum, but complete reloadin

118 d remodeling abandoned replication forks and reloading the replicative helicase.

119 The beetle reloads the glands at a rate of 126 microg of formic aci

120 g from the hindlimbs for 10 days followed by reloading through normal ambulation.

121 he hindlimbs of mice for 10 days followed by reloading through normal ambulation.

122 Reloading treated cells with cholesterol but not 4-chole

123 Replisomes must be reloaded under these circumstances to avoid incomplete r

124 changes to shoulder muscles and responses to reloading upon landing were rapid.

125 The incidence of TdP in dofetilide reloading was compared with patients admitted for dofeti

126 ted to hindlimb muscle unloading followed by reloading, which causes muscle inflammation and membrane

127 itinated proteins was observed during muscle reloading, which is presumably necessary to remove atrop

128 h a 600-mg clopidogrel load and a short-term reload with high-dose atorvastatin protects against earl

129 he sarcoplasmic reticulum could be partially reloaded with Ca2+ by manipulations that increased the a

130 elanin synthesis, tyrosinase is subsequently reloaded with copper within specialized organelles calle

131 th local anesthesia and be easily removed or reloaded with fresh islets.

132 n along with the epoxidation reactivity once reloaded with manganese.

133 Patients admitted for reloading with a higher dose tended to be at higher risk

134 fter Sec14p has ejected bound ligand, and is reloading with another phospholipid molecule.

135 te polypeptides in ATP-tunable bursts before reloading with nucleotide.

136 cate HLA-DR molecules to early endosomes for reloading with peptides prior to recycling to the cell s

137 oad and a short-term, high-dose atorvastatin reload would improve outcomes in clopidogrel-naive, stat