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1                                              MACS was localized to 6q21 between D6S266 (LOD > 3.0) an
2                                    Among 341 MACS Caucasian SCs with 6- to 12-month human immunodefic
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
6 yzed CCR2-V64I using subjects in the Chicago MACS.
7 report multiband observations of the cluster MACS J1149+2223 that have revealed (with high probabilit
8 dren enrolled in the Melbourne Atopy Cohort (MACS) Study, a high-risk birth cohort study.
9  sampled directly from a suspension culture, MACS bypasses the need for sample preparation, and there
10 ommon in HIV-infected participants in either MACS or WIHS participants.
11 nally, we provide instructions for extending MACS using an external growth chamber (1 d) and for how
12 e- and magnetic-activated cell sorting (FACS/MACS).
13                                     Finally, MACS can be used to impart mechanical pressure for asses
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)
17                                 Furthermore, MACS facilitates the visualization of individual cytopla
18 4 kb of promoter from the human MARCKS gene (MACS), with an epitope tag sequence inserted at the carb
19 er 433 bp to the promoter of the human gene, MACS, which encodes the MLP homologue MARCKS.
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
22      We demonstrate with the high quality HR-MACS NMR spectra of micronematodes and tissue biopsy, an
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
28 automation software is provided to integrate MACS control with image acquisition.
29 ho were 18 years or older were enrolled into MACS.
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
32                               We used the MT-MACS device to purify 2 types of target cells, which had
33                                 Similar to O-MACS and Gstm2 had zonally restricted expression pattern
34 , Capza1, Bin3, Tom1, Acl6, and similar to O-MACS.
35 MACS Caucasian SCs and the smaller groups of MACS African-American SCs and the DCG and SFMHS Caucasia
36                             The operation of MACS is described, and automation software is provided t
37 enocytes ex vivo depleted of CD25+ cells, or MACS-isolated CD4+ CD25+ Treg.
38  specific and expensive labels (e.g. FACS or MACS).
39                           Among HIV-positive MACS participants, the proportion of deaths unrelated to
40 m for microfluidics-assisted cell screening (MACS) that overcomes this trade-off by temporarily immob
41      A combination of magnetic cell sorting (MACS) and fluorescent in situ hybridization (FISH) techn
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
45 (EpCAM) via magnetic-activated cell sorting (MACS).
46  (FACS) and magnetic-activated cell sorting (MACS).
47 ll sorting (FACS) and magnetic cell sorting (MACS).
48               The magic-angle coil spinning (MACS) resonator allows a simple approach for nanoliter n
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
51 axis from the Multicenter AIDS Cohort Study (MACS) during 1989-1993.
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
58 groups in the Multicenter AIDS Cohort Study (MACS).
59 tients in the Multicenter AIDS Cohort Study (MACS).
60 ponent of the Multicenter AIDS Cohort Study (MACS).
61 teer from the Multicenter AIDS Cohort Study (MACS).
62 ples from the Multicenter AIDS Cohort Study (MACS; samples were collected in heparin-containing tubes
63                                          The MACS cohort continues to be followed actively 3 decades
64                                          The MACS enrolled participants through a range of community
65 e tested the novel MLP1 polymorphism and the MACS flanking markers in a series of 43 Caucasian simple
66 say-adjusted HIV-1 RNA concentrations in the MACS and BCDTP.
67 a redshift z = 0.54 elliptical galaxy in the MACS J1149.6+2223 cluster.
68  50% compared with previous donations in the MACS.
69 7) or CH-C (n = 343) at study entry into the MACS were prospectively followed to death, last follow-u
70 -handling components and the creation of the MACS microfluidics chip.
71 entrations in archived plasma samples of the MACS was confirmed by the similarity of CD4(+)-cell coun
72                               In contrast to MACS, the MLP and Mlp promoters contain a TATA box appro
73 OVA-sensitized BALB/c mice were sorted using MACS and FACS for phenotype analysis.
74 ently, the spectral resolution acquired with MACS is not efficient for detailed characterization of s

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