1 andard deviations (RSD) between the cycles for human plasma
samples were 0.84-6.6%.
2 Sums of 4HAAs concentrations for different grilled meat
samples were 2.75-6.17 ng g(-1).
3 The sensitivities in female vaginal swabs and urine
samples were 96.6% (95% confidence interval [CI], 88.5 to 99.
4 Saliva and serum
samples were also collected.
5 Samples were analyzed by histology, immunohistochemistry, wes
6 e kinds (Indica and Japonica) plus thirty adulterated flour
samples were analyzed by ICP OES.
7 Drinking water
samples were analyzed for F(-), and the results obtained by o
8 Spot urine
samples were analyzed for IPM3 using ultrahigh-performance li
9 The
samples were analyzed using 16S rRNA-gene sequencing (MiSeq-I
10 565 plant-based food
samples were analyzed using UHPLC-HRMS and advanced data anal
11 Microbial
samples were analyzed with 16S amplicon sequencing to identif
12 rticipants' race/ethnicity, and half of the remaining study
samples were at least 90% white; however, 20% of the studies
13 rbonated products was offset by the CO(2) mineralised (i.e.
samples were '
carbon negative', even when 10% w/w CEM 1 was u
14 Twenty-nine honey
samples were collected and evaluated by principal component a
15 Blood
samples were collected for 96 h after dosing.
16 a daily basis during a 20-day experimental period and blood
samples were collected for hemogram determination and periphe
17 Blood and urine
samples were collected for up to 4 h after injection to asses
18 One hundred
samples were collected from 10 periodontitis patients and sev
19 Colostrum and early lactation milk
samples were collected from 285 mothers enrolled in a high-al
20 Samples were collected from 550 participants (298 cases and 2
21 After a full periodontal clinical assessment, GCF
samples were collected from healthy (n = 5) and diseased (n =
22 Air
samples were collected from multiple locations in the school,
23 Fingerstick whole-blood
samples were collected from participants in an observational
24 Air and surface
samples were collected from seven clinical areas, occupied by
25 Skin biopsy specimens and blood
samples were collected on days 0, 4, 14, 42, and 84 and proce
26 Environmental
samples were collected pre- and post-application to identify
27 Donor serum
samples were evaluated by indirect immunofluorescence antibod
28 The undertaken plant
samples were found to have good amounts of total phenolic, to
29 Stored water
samples were frequently contaminated with E. coli (69%), and
30 A total of 160 random
samples were gathered from private dairy farms in Damietta Pr
31 there is a lack of spatial resolution as either the tissue
samples were homogenized or specific proteins were selected f
32 GCF
samples were investigated by means of fluorescent in situ hyb
33 ies of laser molten zone, in this paper, the AISI4140 steel
samples were melted by laser with different parameters.
34 Overall, 636 (22%)
samples were norovirus-positive, of which 567 (89%) were GII.
35 Clinical data and biological
samples were obtained at admission, days 3 to 5, and days 7 t
36 Samples were obtained before and after (median=82 days) left
37 Skin and blood
samples were obtained from 61 patients with AD (20 with mild
38 s, provider-collected cervical samples, and cervical biopsy
samples were obtained from all enrolled women.
39 Corneal
samples were obtained from human donors with and without diab
40 Maternal blood, saliva, and cervicovaginal wash (CVW)
samples were obtained.
41 Correlative studies on blood and tumor
samples were performed to investigate potential biomarkers of
42 The meat
samples were periodically analysed for microbial count, chemi
43 this prospective study, a total of 226 stool and 178 plasma
samples were received from patients referred to colonoscopy u
44 Simultaneous arterial and jugular venous bulb blood gas
samples were recorded prospectively.
45 Random
samples were selected from the lists of the California Board
46 Follow-up
samples were studied to evaluate within-patient clustering st
47 Samples were subsequently transferred to a custom-built slit-
48 NAAT-positive stool
samples were tested by an ultrasensitive toxin assay (clinica
49 Serum
samples were used to measure the levels of tumor necrosis fac
50 ingredients) along with the anthocyanin profiles (on cooked
samples) were negative correlated with HI.