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1 We subjected male and female rats to 0 (Sed; n = 8 males

2 To isolate the effects of these forces, we subjected intact cartilage explants to 1-24 h of cont

3 We subjected 8- to -10-week-old male C57BL/6 and ob/ob m

4 ermine if and how the cost could be reduced, we subjected plasmid-containing bacteria to 1100 generat

5 usion model and an intraventricular balloon, we subjected hearts to 20 minutes of ischemia followed b

6 andomized, counterbalanced crossover design, we subjected participants to 3 weeks of chronic sleep re

7 To exclude low-abundance infections, we subjected 514 of these samples to 454 sequencing, tar

8 Here, we subjected C57BL/6 mice to 6 h of sleep deprivation us

9 ted Langendorff perfused rabbit heart model, we subjected hearts to 8 hours of hypothermic ischemia w

10 Here, we subject this unusual structural feature to a direct t

11 lay of hyperexcitability and dietary stress, we subjected AAA and KO mice to a high-fat diet.

12 yze the behavioral effects of CN deficiency, we subjected CN mutant mice to a comprehensive behaviora

13 is causally related to neointimal formation, we subjected mice lacking Mac-1 to a novel form of mecha

14 We subjected neonatal rats to a series of 25 brief fluro

15 onal residues involved in 3-PGA interaction, we subjected P52L LS DNA to a second round of mutagenesi

16 origin of these inter-individual variations, we subjected rats to a differential auditory fear condit

17 ics at a scale relevant for these organisms, we subjected soil microcosms to a heat disturbance and f

18 Here, we subjected the complete system to a high throughput sc

19 We subjected the selected mutants to a series of seconda

20 he development of chronic tissue remodeling, we subjected these graft recipients to a battery of hist

21 We subjected insulinoma (INS-1) cells to adenoviral expr

22 expand our understanding of Inc function(s), we subjected putative C. trachomatis Incs to affinity pu

23 We subjected Escherichia coli to an antibiotic to obtain

24 nse to decreased parathyroid hormone levels, we subjected osteocytes to an in vitro unloading environ

25 To further understand the L1 loop, we subjected this region to both alanine- and arginine-s

26 Th17 phenotype in acute glomerulonephritis, we subjected nephritic mice to CD3-specific Ab treatment

27 We subjected rats to cervical level 1 (C1) lesions and c

28 produce a rapid and extensive demethylation, we subjected mouse ES cells to chemically defined hypome

29 ure overload-induced myocardial hypertrophy, we subjected transgenic mice lacking gp91phox to chronic

30 he CI hypothesis with Frederiksen's opinion, we subjected 34 relevant papers to CI analysis.

31 We subjected HD5 to comprehensive alanine scanning mutag

32 system approximating the in vivo situation, we subjected mouse hippocampal slice preparations to con

33 We subject the alga Chlamydomonas reinhardtii to conditi

34 In the present studies, we subjected cultured rat mesangial cells to continuous

35 Next, we subjected transfected GT1-1 cells to continuous monit

36 We subjected adult mice to controlled cortical impact (C

37 To test this idea, we subjected one group of rats to cortical contusion inj

38 sis for the RNA-binding specificity of RRMs, we subjected 330 aligned RRM sequences to covariance ana

39 macologically reduce FoxM1 activity in HCCs, we subjected these HCC-bearing mice to daily injections

40 We subjected PBMC of normal adults to density fractionat

41 A homeostasis remains to be defined in vivo We subjected Stra6-knockout mice to diets sufficient and

42 Here we subject this collective guidance hypothesis to direct

43 Here we subject RAG1, covalently cross-linked to DNA substrat

44 We subjected rats to either partial midcervical or compl

45 In this study, we subjected snake venom to enzymatic hydrolysis to iden

46 When we subjected healthy volunteers to external elastic load

47 Using specialized apparatus, we subjected single kinesin molecules to forces in diffe

48 In parallel to genomic analysis, we subjected the samples to gas chromatography analysis

49 To probe the mechanism, we subjected isolated cardiac mitochondria to gradual Ca

50 Finally, we subjected animals with preexisting hypertrophy to HDA

51 O metabolites could modulate cytoprotection, we subjected CS-eNOS-Tg mice to hepatic ischemia-reperfu

52 We subjected F344 rats to hepatic RT and partial hepatec

53 ntilator-induced lung injury (VILI) in vivo, we subjected 12 anesthetized, paralyzed rabbits to high

54 nt in protection against reperfusion injury, we subjected the flies to hypoxia, followed by recovery

55 was inactivated in these murine MTC samples, we subjected tumor tissue to immunohistochemical stainin

56 in both neural and glioblastoma stem cells, we subjected both cell types to in-vitro differentiation

57 fications relevant in myocardial infarction, we subjected isolated myocardial complex II to in vitro

58 We subjected mice lacking SUR1 subunits to in vivo myoca

59 Finally, we subjected this library to in vitro selection and obta

60 We subjected this library to increasing concentrations o

61 We subjected the bacteriophage phi6 to intensified genet

62 To investigate the role of antigen, we subjected mice with disrupted microbiota to intranasa

63 In addition, we subjected our libraries to lactic and inorganic acids

64 We subjected vesicles to large deformations in the acous

65 he potential role of MPO in atherosclerosis, we subjected LDL receptor-deficient mice to lethal irrad

66 ilepsy result in similar structural changes, we subjected rat pups to lithium-pilocarpine-induced sta

67 We subjected maize (Zea mays L.) to low water potentials

68 d resolve individual molecular mass species, we subjected purified calsequestrin to mass spectrometry

69 To define the nature of this response, we subjected Dictyostelium discoideum cells to measurabl

70 We subjected neonatal rat ventricular myocytes to mechan

71 he role of CycD2 and its downstream targets, we subjected CycD2-null mice to mechanical stress.

72 thods and Results-- To test this hypothesis, we subjected isolated, perfused rat hearts to mechanical

73 volatile organic compounds (VOCs) analysis, we subjected the plant to mechanical damage and monitore

74 To test this, we subjected the PAD4(-/-) mice to mild and severe polym

75 Here, we subjected thrombocytopenic mice to models of dermatit

76 y of antimycobacterials and drug candidates, we subjected Nos2 (-/-) mice with TB to monotherapy befo

77 carries out its role in coat morphogenesis, we subjected its gene to mutagenesis and studied the eff

78 Here, we subjected PACAP-deficient mice to myelin oligodendroc

79 We subjected a subset of samples to next-generation RNA

80 o understand drivers of plant stoichiometry, we subjected four herbaceous legume species to nine leve

81 We subjected F0 mice to odor fear conditioning before co

82 distinguish between these two possibilities, we subjected owls to optical conditions that differed in

83 To test this hypothesis directly, we subjected Cav-1(-/-) mice to ovariectomy and estrogen

84 Methods and Results- We subjected 24 pigs to overstretch coronary artery inju

85 We subjected young mice to pilocarpine-induced SE for 2

86 ess temporal variation of olfactory stimuli, we subjected flies to precisely defined odor concentrati

87 ve regions of functional importance in CheZ, we subjected cheZ to random mutagenesis and isolated 107

88 We subjected five repeats of GTF3 to random oligonucleot

89 n various steps of CPE action, in this study we subjected the cloned cpe gene to random mutagenesis i

90 ious Cys-scanning analysis of permease XanQ, we subjected YgfU to rationally designed site-directed m

91 Here we subjected the 9A2 deoxyribozyme to re-selection for i

92 the kidney from ischemia-reperfusion injury, we subjected hif1a(+/-) and hif2a(+/-) mice to renal isc

93 ischemic changes that tumor tissues undergo, we subjected harvested xenograft tumors to room temperat

94 To determine mechanisms of adaptation, we subjected the model poxvirus vaccinia to serial propa

95 50-180 microm) at speeds approaching 10 m/s, we subject the protein to shear rates dv(z)/dr as large

96 Third, we subject the T2DM RBCs to shear flow and probe the eff

97 Third, we subjected the RBC to shear flow and investigated the

98 To identify such mutations, we subjected PYR1 to site-saturation mutagenesis at 39 h

99 the molecular basis of this delayed injury, we subjected rats to spinal cord injury and identified g

100 Subsequently, we subjected deletion mutants to suboptimal temperatures

101 irectly demonstrate this function for miR-7, we subjected the networks to temperature fluctuation and

102 Here, we subject As(V)-coprecipitated schwertmannite to therma

103 We subjected rats after myocardial infarction to three p

104 To further examine this phenomenon, we subjected rats to three brief pulses of several DA-re

105 erstanding the genetic determinants of Ref1, we subjected Ref1-positive TE671 cells to three sequenti

106 d in the adult ventricle during hypertrophy, we subjected animals to transverse aortic constriction (

107 In this study, we subjected AL-uPA mice to two-thirds partial hepatecto

108 We subjected rat pups to unilateral carotid cauterizatio

109 assess the generalizability of our findings, we subjected the hypomorphs to unilateral ureteral obstr

110 amin D receptor (VDR) in renal fibrogenesis, we subjected VDR-null mice to unilateral ureteral obstru

111 We subjected cells to various manipulations and show tha

112 To address this question, we subjected neurons genetically lacking NR3A to various

113 We subjected these strains to whole-genome sequencing an