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1 MACS was localized to 6q21 between D6S266 (LOD > 3.0) an
3 nd magnetic-activated cell sorting (FACS and MACS, respectively), to more specialized approaches base
4 idual data from Swedish (BAMSE), Australian (MACS), Dutch (PIAMA), Canadian (CAPPS and SAGE), and Ger
5 -2.7; p<0.001) and after HAART availability (MACS, adjusted-OR, 1.5; 95%CI 1.3-1.7; p<0.001; WIHS adj
7 report multiband observations of the cluster MACS J1149+2223 that have revealed (with high probabilit
9 sampled directly from a suspension culture, MACS bypasses the need for sample preparation, and there
11 nally, we provide instructions for extending MACS using an external growth chamber (1 d) and for how
14 of linked and neighboring polymorphisms for MACS and MLP should permit similar genetic studies in ot
15 ribe the two sources of line broadening from MACS, sample temperature gradient and anisotropic magnet
16 ronegative (HEPS; n = 90) Caucasian men from MACS more frequently carried heterozygous G*2 (Delta32)
18 4 kb of promoter from the human MARCKS gene (MACS), with an epitope tag sequence inserted at the carb
20 ninfected individuals in both the pre-HAART (MACS only) and HAART eras; and adjusted Cox proportional
21 ident respiratory infections both pre-HAART (MACS, odds ratio [adjusted-OR], 2.4; 95% confidence inte
23 igh-resolution magic-angle coil spinning (HR-MACS) resonator that improves the spectral resolution.
24 igh-resolution magic-angle coil spinning (HR-MACS), a simple conversion of a standard HR-MAS probe to
25 ructive pulmonary disease was more common in MACS HIV-infected vs. HIV-uninfected participants pre-HA
26 V-negative individuals (8.7 years younger in MACS (P < 0.01) and 7.6 years younger in WIHS (P < 0.01)
27 death compared to those without infections (MACS adjusted-HR, 1.5; 95%CI, 1.3-1.7; p<0.001; WIHS adj
30 Broadly consistent findings in the larger MACS Caucasian SCs and the smaller groups of MACS Africa
31 ltitarget magnetic activated cell sorter (MT-MACS), which makes use of microfluidics technology to ac
35 MACS Caucasian SCs and the smaller groups of MACS African-American SCs and the DCG and SFMHS Caucasia
40 m for microfluidics-assisted cell screening (MACS) that overcomes this trade-off by temporarily immob
42 lood by magnetically activated cell sorting (MACS) and sheep erythrocyte rosetting methods, and the q
43 nction with magnetic activated cell sorting (MACS), followed with a flow cytometric cell sorting (FAC
44 on, such as magnetic activated cell sorting (MACS), only allow the binary separation of target cells
49 tal Corticosteroids for Preterm Birth Study (MACS) was an international randomized clinical trial tha
50 (HIV) in the Multicenter AIDS Cohort Study (MACS) and Women's Interagency HIV Study (WIHS) from 1984
52 ants from the Multicenter AIDS Cohort Study (MACS) of homosexual and bisexual men enrolled in 1984-19
53 ters from the Multicenter AIDS Cohort Study (MACS) who were selected to reflect the full spectrum of
54 launch of the Multicenter AIDS Cohort Study (MACS), a cohort study of homosexual men in 4 US cities,
55 nually by the Multicenter AIDS Cohort Study (MACS), a four-center prospective cohort study of acquire
56 ipants in the Multicenter AIDS Cohort Study (MACS), the District of Columbia Gay (DCG) Study, and the
57 Utilizing the Multicenter AIDS Cohort Study (MACS), we retrospectively examined the early HIV-1-speci
62 ples from the Multicenter AIDS Cohort Study (MACS; samples were collected in heparin-containing tubes
65 e tested the novel MLP1 polymorphism and the MACS flanking markers in a series of 43 Caucasian simple
69 7) or CH-C (n = 343) at study entry into the MACS were prospectively followed to death, last follow-u
71 entrations in archived plasma samples of the MACS was confirmed by the similarity of CD4(+)-cell coun
74 ently, the spectral resolution acquired with MACS is not efficient for detailed characterization of s
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