コーパス検索結果 (left1)
通し番号をクリックするとPubMedの該当ページを表示します
1 MACS is associated with cardiovascular morbidity, frailt
2 MACS is diagnosed (based on an abnormal overnight dexame
3 MACS was localized to 6q21 between D6S266 (LOD > 3.0) an
7 nd magnetic-activated cell sorting (FACS and MACS, respectively), to more specialized approaches base
8 .62]; aPRs for use of >=3 antihypertensives: MACS-2, 1.31 [CI, 1.02 to 1.68], and CS, 2.22 [CI, 1.62
9 idual data from Swedish (BAMSE), Australian (MACS), Dutch (PIAMA), Canadian (CAPPS and SAGE), and Ger
10 -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
13 report multiband observations of the cluster MACS J1149+2223 that have revealed (with high probabilit
17 sampled directly from a suspension culture, MACS bypasses the need for sample preparation, and there
20 nally, we provide instructions for extending MACS using an external growth chamber (1 d) and for how
23 of linked and neighboring polymorphisms for MACS and MLP should permit similar genetic studies in ot
24 d more likely to require insulin therapy for MACS-2 (aPR, 1.89 [CI, 1.01 to 3.52]) and CS (aPR, 3.06
25 ribe the two sources of line broadening from MACS, sample temperature gradient and anisotropic magnet
26 tudied 1123 men (589 HIV+ and 534 HIV-) from MACS (Multicenter AIDS Cohort Study), using the ZioXT am
27 ronegative (HEPS; n = 90) Caucasian men from MACS more frequently carried heterozygous G*2 (Delta32)
29 4 kb of promoter from the human MARCKS gene (MACS), with an epitope tag sequence inserted at the carb
31 ninfected individuals in both the pre-HAART (MACS only) and HAART eras; and adjusted Cox proportional
32 ident respiratory infections both pre-HAART (MACS, odds ratio [adjusted-OR], 2.4; 95% confidence inte
33 % had NFAT (n = 649; 64.1% women), 34.6% had MACS-1 (n = 451; 67.2% women), 10.7% had MACS-2 (n = 140
34 had MACS-1 (n = 451; 67.2% women), 10.7% had MACS-2 (n = 140; 73.6% women), and 5.0% had CS (n = 65;
36 igh-resolution magic-angle coil spinning (HR-MACS) resonator that improves the spectral resolution.
37 igh-resolution magic-angle coil spinning (HR-MACS), a simple conversion of a standard HR-MAS probe to
38 d prevalence ratios [aPRs] for hypertension: MACS-2, 1.15 [95% CI, 1.04 to 1.27], and CS, 1.37 [CI, 1
40 ructive pulmonary disease was more common in MACS HIV-infected vs. HIV-uninfected participants pre-HA
42 and severity of hypertension were higher in MACS-2 and CS than NFAT (adjusted prevalence ratios [aPR
43 V-negative individuals (8.7 years younger in MACS (P < 0.01) and 7.6 years younger in WIHS (P < 0.01)
44 death compared to those without infections (MACS adjusted-HR, 1.5; 95%CI, 1.3-1.7; p<0.001; WIHS adj
48 Broadly consistent findings in the larger MACS Caucasian SCs and the smaller groups of MACS Africa
50 mor [NFAT]; 50 to 138 nmol/L, possible MACS [MACS-1]; >138 nmol/L and absence of typical clinical Cus
51 ltitarget magnetic activated cell sorter (MT-MACS), which makes use of microfluidics technology to ac
55 ing substantial optimization, the ability of MACS to isolate increased cell numbers in less time than
56 a lack of specific biomarkers diagnostic of MACS-related health outcomes and a paucity of clinical t
57 MACS Caucasian SCs and the smaller groups of MACS African-American SCs and the DCG and SFMHS Caucasia
62 e in glucocorticoid excretion from NFAT over MACS-1 and MACS-2 to CS, whereas androgen excretion decr
64 nal tumor [NFAT]; 50 to 138 nmol/L, possible MACS [MACS-1]; >138 nmol/L and absence of typical clinic
67 m for microfluidics-assisted cell screening (MACS) that overcomes this trade-off by temporarily immob
70 antibody and Magnetic Activated Cell Sorter (MACS) technique, we successfully purified Thy-1 positive
73 lood by magnetically activated cell sorting (MACS) and sheep erythrocyte rosetting methods, and the q
75 protocol of magnetic-activated cell sorting (MACS) to separate them effectively both as viable and bi
76 nction with magnetic activated cell sorting (MACS), followed with a flow cytometric cell sorting (FAC
77 on, such as magnetic activated cell sorting (MACS), only allow the binary separation of target cells
78 at combines magnetic activated cell sorting (MACS)-based screening of yeast surface display (YSD) lib
84 e microchannelled alkylated chitosan sponge (MACS) exhibits the capacity for water and blood absorpti
85 tal Corticosteroids for Preterm Birth Study (MACS) was an international randomized clinical trial tha
86 rg-Munster Affective Disorders Cohort Study (MACS) and completed the Life Events Questionnaire (LEQ)
87 combined the Multicenter AIDS Cohort Study (MACS) and the Women's Interagency HIV Study (WIHS) into
88 (HIV) in the Multicenter AIDS Cohort Study (MACS) and Women's Interagency HIV Study (WIHS) from 1984
90 ants from the Multicenter AIDS Cohort Study (MACS) of homosexual and bisexual men enrolled in 1984-19
92 d HIV) in the Multicenter AIDS Cohort Study (MACS) were stimulated with peptide pools spanning 19 CMV
93 ters from the Multicenter AIDS Cohort Study (MACS) who were selected to reflect the full spectrum of
94 launch of the Multicenter AIDS Cohort Study (MACS), a cohort study of homosexual men in 4 US cities,
95 nually by the Multicenter AIDS Cohort Study (MACS), a four-center prospective cohort study of acquire
96 ut HIV in the Multicenter AIDS Cohort Study (MACS), a longstanding study of the natural and treated h
97 er FOR 2107 Affective Disorder Cohort Study (MACS), collected between September 2014 and November 201
98 ipants in the Multicenter AIDS Cohort Study (MACS), the District of Columbia Gay (DCG) Study, and the
99 ed within the Multicenter AIDS Cohort Study (MACS), using serum samples obtained 2 years prior to dia
100 nfection, the Multicenter AIDS Cohort Study (MACS), was established; 10 years later, the Women's Inte
101 Utilizing the Multicenter AIDS Cohort Study (MACS), we retrospectively examined the early HIV-1-speci
109 ples from the Multicenter AIDS Cohort Study (MACS; samples were collected in heparin-containing tubes
110 tivation can lead to MC activation syndrome (MACS), which is observed in patients with long COVID.
113 e tested the novel MLP1 polymorphism and the MACS flanking markers in a series of 43 Caucasian simple
115 sponge, CELOX(TM), and CELOX(TM)-gauze, the MACS provides higher pro-coagulant and hemostatic capaci
121 7) or CH-C (n = 343) at study entry into the MACS were prospectively followed to death, last follow-u
124 entrations in archived plasma samples of the MACS was confirmed by the similarity of CD4(+)-cell coun
128 ently, the spectral resolution acquired with MACS is not efficient for detailed characterization of s
133 escents with CP (N = 14; Age = 15.7 4 years; MACS I-III; GMFCS I-IV) and neurotypical (NT) adolescent