ライフサイエンスコーパス: be entered into

1 idated SNPs with minor allele frequency > 5% are entered into a high-throughput pipeline for genotypi

2 lidated SNPs with minor allele frequency >5% are entered into a high-throughput pipeline for genotypi

3 nst cancer cells and its low toxicity it has been entered into a number of clinical trials.

4 Detailed patient information was entered into a computerized database, and 36 discree

5 Information from each study was entered into a database.

6 ensus Conference criteria, from these trials was entered into a formal meta-analysis.

7 regional metabolic glucose response to m-CPP was entered into a group (impulsive aggressive, control)

8 re performed, and each significant parameter was entered into a multivariate logistic regression anal

9 iotherapy with curative intent before PET/CT was entered into a prospective database.

10 either deceleration time or WMSI or LV mass was entered into a regression equation to predict follow

11 Clinical response was entered into a survival analysis, and Cox regression

12 for residual positive or negative symptoms, were entered into a 10-week double-blind, parallel-group

13 Eighty-six people with schizophrenia were entered into a 12-week double-blind, placebo-contro

14 on and passive viewing conditions, and these were entered into a between-group random effects analysi

15 Data were entered into a centralized database.

16 e urban hospital with a new diagnosis of HCC were entered into a clinical database.

17 uantity as well as implant size and position were entered into a computer database.

18 Cell locations were entered into a computer imaging system.

19 Patients' details were entered into a computerised database at the time of

20 Clinical data from these patients were entered into a computerized data base for storage,

21 y-one variables for each patient (series II) were entered into a computerized database and analyzed (

22 Pathologic data from these patients were entered into a computerized database for storage, r

23 Clinical data from these patients were entered into a computerized database for storage, r

24 nts treated by TTE by one author (1989-1999) were entered into a computerized database.

25 after consensus development, financial data were entered into a costing protocol to determine which

26 This score and other variables were entered into a Cox model to explore the independent

27 All data were entered into a database.

28 lure Assessment, and the Severe Sepsis Score were entered into a database.

29 Demographics and in-hospital outcomes were entered into a database; subsequent outcomes and mo

30 ation (75 patients) or flutter (16 patients) were entered into a double-blind, randomized multicenter

31 -two patients with infrainguinal vein grafts were entered into a graft surveillance program for > or

32 ics, comorbidities, and socioeconomic status were entered into a hierarchical generalized linear mixe

33 uggesting an acute coronary syndrome and who were entered into a large national registry.

34 tween race and cardiovascular risk variables were entered into a logistic regression model for CAC th

35 All 10 risk factors were entered into a logistic regression model to determi

36 Sociodemographic and stress variables were entered into a logistic-regression analysis to find

37 However, when all the SNPs were entered into a logit model, only the effect of APOE

38 ariables known to be associated with outcome were entered into a multiple logistic regression analysi

39 Variables found to be significant were entered into a multiple logistic regression model t

40 y identified using single regressor analysis were entered into a multiple logistic regression model.

41 Bivariate predictors of death were entered into a multiple logistic regression model.

42 However, when these were entered into a multiple regression analyses that co

43 Data were entered into a multivariable analysis controlling f

44 statistical threshold in univariate analysis were entered into a multivariable Cox proportional hazar

45 x, race/ethnicity, and Injury Severity Score were entered into a multivariable logistic regression mo

46 exploratory univariate P<0.2) with rejection were entered into a multivariable logistic regression mo

47 ificant risk factors on univariable analysis were entered into a multivariable logistic regression mo

48 ted with RHF (exploratory univariate P<0.10) were entered into a multivariable logistic regression mo

49 ical conditions and obstetric complications, were entered into a multivariable logistic regression mo

50 ant in univariate analysis at the 0.05 level were entered into a multivariate competing risk regressi

51 teristics of 2,136 randomized STICH patients were entered into a multivariate equation created using

52 icant association in the univariate analysis were entered into a multivariate logistic regression mod

53 d access to general practice services; these were entered into a negative binomial regression model w

54 Forty-five subjects with adult periodontitis were entered into a parallel design, single-blind study

55 for each gene; empirically significant genes were entered into a pathway analysis.

56 Thirty-four children were entered into a pilot trial of calcineurin inhibitor

57 School subjects were entered into a principal components analysis and pr

58 in the last 10 years at the authors' center were entered into a prognostic survival model to predict

59 hese and other clinically relevant variables were entered into a propensity model that reflected like

60 All patient data were entered into a prospective clinical data management

61 e 30, 2002 with RFA for hepatic malignancies were entered into a prospective database.

62 ic bypass since the inception of the program were entered into a prospective database.

63 Forty adults aged 28 to 73 years were entered into a prospective trial of imatinib for th

64 Patients with hepatic malignancies were entered into a prospective, nonrandomized trial.

65 ts with DSM-IV obsessive-compulsive disorder were entered into a prospective, open-label treatment tr

66 r period, patients with 60-<70% ACS with CCO were entered into a protocol of clinical examination and

67 Subjects with COPD exacerbations were entered into a randomized biomarker-directed double

68 rimary care patients with current depression were entered into a randomized controlled trial.

69 ' human patients at ~12 months after injury) were entered into a randomized double-blinded clinical t

70 sual interstitial pneumonia (idiopathic UIP) were entered into a randomized prospective treatment tri

71 Between 1992 and 1994, 836 patients were entered into a randomized study (489 in Rochester,

72 ntenance proton pump inhibitor (PPI) therapy were entered into a randomized, single-blind, prospectiv

73 om all stenoses had an FFR of more than 0.80 were entered into a registry and received the best avail

74 Their transcription profiles were entered into a relational database, EyeSAGE, includ

75 luding testability and estimated refractions were entered into a Research Electronic Data Capture dat

76 tive cerebral injury was scored, and results were entered into a sequential analysis, which allows fo

77 ctors collected within 24 hours of admission were entered into a step-wise backward elimination logis

78 than 0.2 or that were thought to be relevant were entered into a stepdown Cox proportional hazard reg

79 rom univariate analyses differing at P < .20 were entered into a stepwise logistic regression model t

80 5 weeks and maternal sensitivity at 29 weeks were entered into a weighted linear regression as predic

81 led information regarding each adverse event was entered into an online form.

82 ex, diabetes, and present cigarette smoking) were entered into an analysis of covariance model, follo

83 d procedures and abstracted locally; results were entered into an ASCO-maintained database and analyz

84 Patients from 5 institutions undergoing SILC were entered into an IRB approved database from November

85 Seventy-two were entered into an observational study with convention

86 Sixteen adults with chronic ITP were entered into an open-label, single-arm cohort dose-

87 eurocognitive measures found to be heritable were entered into analyses designed to determine which t

88 athology in living patients so that they can be entered into appropriate etiology-directed clinical t

89 Several GPR119 agonists have been entered into clinical studies, but many have failed

90 Sixty-four of these patients had been entered into clinical trials using growth factors b

91 As a result, countless chemicals were entered into commercial use without toxicological i

92 The data were entered into epi data statistical software version

93 Data were entered into EpiData version 3.1 and analyzed by St

94 dence for each day of the first year of life were entered into hazards models as time-dependent covar

95 r hypoxia-associated obstetric complications was entered into logistic regression models, along with

96 ong with cerebrospinal fluid (CSF) proteins, were entered into logistic regression models (dependent

97 and without cirrhosis in univariate analysis were entered into logistic regression models, and the pe

98 PH were performed, and significant variables were entered into multiple linear regression models.

99 mptom levels at post-treatment and follow-up were entered into multiple regression analyses that cont

100 All significant variables (p < 0.05) were entered into multivariate analysis.

101 Transcripts were entered into NVivo.

102 The time-integrated activities were entered into OLINDA/EXM 1.1 to derive the dose with

103 Before randomization, patients were entered into one of two cohorts on the basis of cli

104 not sought out) to estimate Cohen's d, which was entered into random effects models (REM) to compare

105 Performance on these tasks were entered into regression models.

106 who received placebo in stage 1 of the study were entered into stage 2; 210 participants completed st

107 come, level of education, and home ownership were entered into stepwise logistic or stepwise multiple

108 s then will allow susceptible individuals to be entered into surveillance and/or chemoprevention stud

109 inical and paraclinical features of patients are entered into the algorithm, and a patient's total sc

110 diagnostic measurements for each individual are entered into the model, producing accurate predictio

111 graphics, diagnoses, treatment, and outcomes are entered into the Project IMPACT database by staff at

112 he re-engineered RCSB's site for the PDB can be entered into the PISCES server by a single click, com

113 ined from all patients whose records were to be entered into the research database.

114 sure that only those likely to benefit would be entered into the study.

115 ve undergone transplantation since 1994 have been entered into the relational database.

116 d 1.6 million cardiac surgical patients have been entered into the VA and STS databases, respectively

117 ysis is limited data quality, with cases not being entered into the database, cases not reporting exp

118 equence through our annotation system before being entered into the database.

119 The development of pneumonia after being entered into the study was also significantly dela

120 ogous clusters per genome for the 17 strains was entered into the finite-supragenome model, which pre

121 When BMI was entered into the HDL cholesterol-ATFM regression mod

122 is significant effect remained when latitude was entered into the model as a predictor.

123 Each group of variables was entered into the model sequentially to assess the ef

124 When health literacy was entered into the model, the hazard ratio for age cha

125 Their demographic and clinical information was entered into the REDCap (Research Electronic Data Ca

126 ial visit for the validation cohort patients were entered into the algorithm, the predicted survival

127 Baseline scores on these outcomes were entered into the analyses as covariates.

128 Following the matching process, 258 lesions were entered into the analysis.

129 Data were entered into the central database, cleaned, and ana

130 ast 180 days of prior health plan enrollment were entered into the cohorts between January 1, 1998, a

131 ed automatically when the questionnaire data were entered into the computer program.

132 A total of 3809 patients were entered into the database.

133 Data were entered into the medical record and a prospective r

134 hole body, and the resulting residence times were entered into the MIRDOSE3 program.

135 sive costs from Shanghai and Yunnan province were entered into the model in order to estimate the eff

136 Over 2.3 million patients were entered into the National Trauma Data Bank.

137 d based on these genes, the results of which were entered into the pathotyping model to yield a predi

138 Twenty-one and 23 patients were entered into the PAV and PSV groups, respectively,

139 litation between 1998 and 2004, and all data were entered into the Preventive Cardiology Information

140 severe symptomatic emphysema without bullae were entered into the protocol (39 staple, 33 laser).

141 ble, palpable, or unknown metastatic lesions were entered into the protocol.

142 Approximately 10% more such cases were entered into the Registry in winter or spring than

143 extracted by two reviewers, and outcome data were entered into the Review Manager software package.

144 Twenty-three patients were entered into the second stage of accrual.

145 units (ICUs), and those with sepsis in ICUs were entered into the SSC database.

146 g a calcium channel blocker since transplant were entered into the study (86 in Manchester, 78 in Bel

147 Thirty-five patients were entered into the study after the attending physicia

148 One hundred low risk patients were entered into the study and randomized either to an

149 Patients older than 18 years of age were entered into the study if they presented with previ

150 ith unilateral treatment-naive exudative AMD were entered into the study over 6 months.

151 Thirty patients were entered into the study, for a total of 46 measureme

152 An initial 30 donors were entered into the study.

153 abony and/or molar Class II furcation defect were entered into the study.

154 healthy young Landrace Yorkshire white pigs were entered into the study.

155 h or without a history of a suicide attempt, were entered into the study.

156 Twelve patients were entered into the study.

157 patients with baseline hematocrit 25 to 35% were entered into the study.

158 ng) between September 1989 and November 1997 were entered into the study.

159 g FNAB of lung masses over a 28-month period were entered into the study.

160 atients whose conventional treatments failed were entered into the study.

161 Forty-five patients were entered into the study.

162 014, and June 10, 2015, 68 eligible patients were entered into the study.

163 Forty-eight patients were entered into the study; 22 (46%) with and 26 (54%)

164 or equivocal after 1 dose of measles vaccine were entered into the trial and reimmunized.

165 Of those, 3350 with a low ABI (< or = 0.95) were entered into the trial, which was powered to detect

166 e-matched live donor (18) kidney transplants were entered into the trial.

167 Participants' zip codes were entered into the United States Food Access Research

168 list of acceptable and unacceptable antigens were entered into the UNOS computer for each patient lis

169 pendence not seeking treatment or abstinence were entered into this crossover, double-blind trial.

170 recurrent or advanced endometrial carcinoma were entered into this Gynecologic Oncology Group (GOG)

171 therapy-naive patients with metastatic NSCLC were entered into this phase I dose-escalation and pharm

172 including apoB and year 25 (Y25) CAC score, were entered into this study.

173 ma center between January 2004 and June 2006 were entered into this study.

174 atic hypertrophic obstructive cardiomyopathy were entered into this trial after baseline studies cons

175 hese aggressive features after biopsy should be entered into treatment intensification trials.

176 Strains originated from patients who had been entered into two phase 3 randomized clinical trials