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1 ician could participate as a local physician-principal investigator.
2 by trained researchers and confirmed by the principal investigator.
3 lands, or analysed data were shared with the principal investigator.
4 ore the age of 51, the average age of an NIH principal investigator.
5 nd regimen received had been provided by the principal investigator.
6 ross 10 708 trials, 3151 (29.2%) had a woman principal investigator.
7 ines, and inconsistencies were resolved by a principal investigator.
8 inistry of Science and Innovation with CS as principal investigator.
9 ic training and professional profiles of the principal investigators.
10 n oncologists; 37%, women; and 83%, research principal investigators.
11 cal trial ($110,869) and multimode ($59,916) principal investigators.
12 ry 1985 through March 1996 and by queries of principal investigators.
13 n binge diaries and reviewed weekly with the principal investigators.
14 ailed to all potential participants by local principal investigators.
15 most prevalent career outcome was Academia: Principal Investigator (636/2284=27.8% of alumni), follo
16 Science Foundation's recent mandate that all Principal Investigators address the broader impacts of t
18 l, basic, or social science faculty who were principal investigators), amount of annual income receiv
19 of Population Health, University of Oxford, Principal Investigator and Chief Executive, UK Biobank,
20 n day 1 of each treatment cycle (28 days) by principal investigator and coinvestigators at the site.
21 are described, and a survey was sent to the principal investigator and primary clinical coordinator
24 were judged unrelated to treatment by local principal investigators and confirmed by the data safety
25 ts from an NCI-sponsored meeting with MBCCOP principal investigators and data from a follow-up survey
28 easing numbers of new agents, fewer domestic principal investigators, and more companies off-shoring
29 tes of the early studies, the names of their principal investigators, and references to a single defi
30 or leadership, academic positions, or acting principal investigators, as well as actively involved in
34 moriam of Professor Anderson de Sa Pinheiro, principal investigator at the Laboratory of Molecular Bi
35 grants awarded to first-time male and female principal investigators at top research institutions, in
37 dation (NSF) Biological Sciences Directorate principal investigators (BIO PIs), nearly 90% indicated
39 lusively conducted basic science research as principal investigators compared with translational rese
41 nd nine other publications coauthored by the principal investigator contain at least one major untrue
42 ty among research teams, particularly, study principal investigators, could address this inequity is
43 active vs comparator group assignments) and principal investigators/data analysts (to group assignme
45 linical trials found that those with a woman principal investigator enrolled a higher proportion of w
47 dividual participant data requested from the principal investigator for each eligible trial, adjustin
49 n for the Study of Diabetes (EASD) journals; principal investigators for ADA, JDRF, and National Inst
53 dary analyses found that trials with a woman principal investigator had a higher proportion of women
56 Trial registration number: ISRCTN17005348, principal investigator: Ilze Maldupa, registration date:
57 in the context of the author's experience as principal investigator in a large, randomized trial on c
59 centre directors, global oncology leads, and principal investigators in 36 US states and the District
62 n the context of the authors' experiences as principal investigators in the phase I/II and/or phase I
63 nior investigators into independently funded principal investigators is comparable to other mentoring
64 new laboratory members, everyone, including principal investigators, is encouraged to use a set of p
65 ants between 1964 and 2004 stratified by the principal investigators' major degrees (MD, PhD, or MD a
73 vidual participant data were provided by the principal investigators of the respective trials and col
76 participated in our study reported becoming principal investigators on industry clinical trials prim
77 ician scientists are less likely to serve as principal investigators on mid- and later careers awards
79 emic, private-sector physicians who serve as principal investigators on US clinical trials sponsored
81 y while 45% (n = 40) required them only from principal investigators or those conducting research.
82 ical researchers (OR, 1.6; 95% CI, 1.1-2.3), principal investigators (OR, 4.3; 95% CI, 2.8-7.0), facu
83 llocation, but allocation was concealed from principal investigators, participants and their guardian
85 lacking industry sponsorship (for which the principal investigator pays the translation costs) than
86 b of a research-intensive faculty member and principal investigator (PI) as both unattainable and und
87 ose who were awarded grants with more than 1 principal investigator (PI) by querying the internal dat
88 ical Pharmacology/Micromedex), or study site principal investigator (PI) opinion-among patients recei
89 enges facing a new independent group leader, principal investigator (PI) or university lecturer are f
92 viewers to know the identity of a proposal's principal investigator (PI), which opens the possibility
96 In this article, we present advice to both principal investigators (PIs) and postdocs for successfu
97 stered electronic survey and focus groups of principal investigators (PIs) and project coordinators (
100 ealth in the US by African-American or Black Principal Investigators (PIs) are less likely to be fund
101 less of their previous funding success, many principal investigators (PIs) encounter a funding gap in
102 udy included a national cohort of NIH-funded principal investigators (PIs) from the NIH Information f
106 bmitted by African American or Black ('AAB') Principal Investigators ('PIs') skewed toward a small nu
112 d mRNA vaccine biotechnology-on the basis of principal investigator, project title, and abstract.
113 Blood Institute-supported publications each principal investigator published in the 5 years before g
115 first draft was written in April 1996 by the principal investigator (S.G.P.) after the consensus grou
116 the role of these authors rather than of the principal investigator(s) as in the previous policy.
118 (ie, R01-equivalent) grant and being a super principal investigator (SPI) with $750 000 or more in to
119 esearch project grants, referred to as super principal investigators (SPIs), by gender, race, and eth
122 located to placebo; none were judged by site principal investigators to be related to study medicatio
123 for extensive response and redrafting by the principal investigator until all members were satisfied.
124 ial UNIP assessment were not gathered by the principal investigator until all other study procedures
125 n enrollment of women in trials with a woman principal investigator was 54.1% (95% CI, 53.0%-55.1%) c
126 95% CI, 46.3%-47.5%) for trials in which the principal investigator was a man (absolute adjusted diff
127 r, the corresponding ethics committee or the principal investigator was contacted for clarification.
128 m for interns, host/employer, and supervisor/principal investigator were assessed using a mixed-metho
130 TICIPANTS: Big Ten COVID-19 Cardiac Registry principal investigators were surveyed for aggregate obse
133 total dollar amount of R01 grants awarded to principal investigators with only an MD degree trended d
134 Sites selected for participation were led by principal investigators with research experience, who we