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1 many epidemiologic studies preserve only the buffy coat.
2 lasma (PRP), platelet-poor plasma (PPP), and buffy coat.
3  was positively correlated with detection in buffy coats.
4 nohistochemical analysis of peripheral blood buffy coats.
5 was confirmed in human B cells isolated from buffy coats.
6  less than 3 hours, and produce an ultrapure buffy coat (96.6% white blood cell yield, 0.0059% red bl
7                                              Buffy coat analysis for WZhet was positive in 16 of 27 (
8 infection showed high diagnostic accuracy in buffy coat and bone marrow, ranging from 93.1 to 96.9%.
9  female donors and genomic DNA from maternal buffy coat and placenta samples.
10   Our results show that 8oxoG levels in both buffy coat and plasma were significantly associated with
11                                       Frozen buffy coat and residual blood cells each yielded only ha
12 ever, could be detected in DNA isolated from buffy coats and bone marrow by PCR as early as 1 to 2 we
13 aving MNGIE, determination of TP activity in buffy coats and thymidine levels in plasma are diagnosti
14 were PCR positive by testing of whole blood, buffy coat, and bone marrow aspirates, respectively.
15 ike virus in 83%, 75%, and 87% of the serum, buffy coat, and ear notch samples, respectively, while t
16 I calves) were generated and sampled (serum, buffy coat, and ear notches) on the day of birth (DOB) a
17 t amounts of all-cell-pellet (ACP) fraction, buffy coat, and residual blood cells from fresh blood (n
18 re isolated from 27 non-selected blood donor buffy coats, and ILCs were sorted by FACS.
19 peripheral blood mononuclear cell (PBMC) and buffy coat (BC) samples from three independent cohorts o
20                    If one wishes to separate buffy coat before freezing, one should also save the res
21 idney cell cultures both with urine and with buffy coat blood cells resulted in a cytopathic response
22 ancer cells from the undiluted and untreated buffy coat blood samples.
23 nd total NK cell concentrations in undiluted buffy coat blood samples.
24               Genomic DNA was extracted from buffy coat blood using a phenol/chloroform method.
25 agnosis is made by detection of the virus by buffy-coat blood culture or by polymerase chain reaction
26 Not only does ACP yield twice as much DNA as buffy coat but it is easier to process, and its yield is
27              Neutrophils were separated from buffy coats by the double dextran gradient method.
28 ils (polymorphonuclear leukocytes, PMNL) and buffy coat cells (polymorphonuclear leukocytes/periphera
29 plenocytes, thymocytes, lymph node cells, or buffy coat cells can prolong skin allograft survival in
30  and TaqI polymorphisms were determined from buffy coat cells following polymerase chain reaction (PC
31 the presence of male fetal microchimerism in buffy coat cells from women with a prior history of brea
32               Genomic DNA was extracted from buffy coat cells isolated from peripheral blood samples,
33 alysis of variants from nasal secretions and buffy coat cells lacked extensive positive selection; ho
34 plenocytes, thymocytes, lymph node cells, or buffy coat cells led to prolonged skin allograft surviva
35                                              Buffy coat cells were added to ISE6 tick cell cultures a
36                                              Buffy coat cells were added to produce concentrations of
37 tial viruses isolated from nasal secretions, buffy coat cells, and semen of seven experimentally infe
38 ) concentration of 477 +/- 128 nM, excluding buffy coat cells.
39 CN, measured in an easily accessible tissue (buffy coat/circulating leukocytes), can improve risk cla
40           Mitochondrial DNA-CN measured from buffy coat/circulating leukocytes.
41 itis despite prolonged antiviral therapy had buffy coat CMV isolates that were resistant to both ganc
42 V PCR, 84 and 20 were also analyzed by blood buffy coat culture and anti-CMV antibody IgM assays, res
43 ssays, although the specificity of the blood buffy coat culture is as good as that of the CMV PCR, wh
44                                              Buffy coat DNA analysis showed that 75-85% were EBV DNA-
45                               Methylation of buffy coat DNA at exam 3 was measured using the Illumina
46   PCR was carried out for HTLV-1 provirus on buffy-coat DNAs.
47 he child in July and August were negative by buffy-coat examination and hemoculture but positive by P
48 34(+) marrow graft (Arm A) versus a standard buffy coat fraction (Arm B).
49                     vCJD appendix and blood (Buffy coat fraction) were negative for PrP(Sc) at this l
50 et engraftment compared to women who receive buffy coat fractions of marrow.
51  We measured levels of EBV DNA in saliva and buffy coats from 233 asymptomatic Ugandan children with
52                      EBV DNA was detected in buffy coats from 86% of the children (median [IQR] level
53                                              Buffy coats from blood donors were examined for inflamma
54  with virus readily detectable in saliva and buffy coats from persons without apparent symptoms in Af
55                                              Buffy coat inoculation and a shorter interval between sa
56 d-derived platelets (platelet-rich plasma or buffy coat intermediate steps) result in differing degre
57   The quantity of HSPCs was 0.15 +/- 0.1% of buffy coat leukocytes.
58 re thymidine phosphorylase deficiency in the buffy coat (<10% of normal activity), we reviewed their
59 50) showed excellent agreement with those of buffy coat microscopy.
60                                  Analysis of buffy coat mRNA levels showed the same correlations.
61                This assay can detect SPPV in buffy coats, nasal swabs, oral swabs, scabs, and skin le
62 nuclear cells/lymphocytes were isolated from buffy coats obtained from blood center, and activated wi
63   Human primary monocytes were isolated from buffy coats obtained from healthy individuals.
64 probe and nuclear proteins isolated from the buffy coat of blood obtained at the beginning of the pro
65  Peripheral blood mononuclear cells from the buffy coat of patients with early acute lung injury (n=4
66         We profiled DNAm from the cord blood buffy coat of singletons using the MethylationEPIC BeadC
67 +)) were enumerated and characterized in the buffy coats of fresh peripheral blood samples from 15 co
68  blood-based measurements of 8oxoG from both buffy coat PBMCs and plasma to determine associations wi
69      We tested for MAP by PCR and culture in buffy coat preparations from 28 individuals with Crohn's
70 sis of the African trypanosomiases in simple buffy coat preparations of human blood.
71   We show here that neutrophils within human buffy coat preparations stimulated with a mixture of int
72    Primary human NK cells were isolated from buffy coats, primed with a cytokine cocktail and used fo
73  in diabetic ketoacidosis was confirmed with buffy coat quantitative real-time polymerase chain react
74 samples being taken include baseline plasma, buffy coat, red blood cells, serum, blood clot from seru
75 d as measure of antigen concentration in the buffy coat sample.
76  of extraneous protein to plasma, serum, and Buffy coat samples and may interfere with biomarker dete
77   We analyzed 617 plasma, 701 serum, and 657 buffy coat samples from a 7-year longitudinal multi-omic
78 examined sequences amplified from saliva and buffy coat samples from the same subjects, to investigat
79 5.0% of serum samples, whereas only 37.1% of buffy coat samples were free of contamination by hemoglo
80 ho provided sufficient clinical information, buffy coat samples, and adequate consent for genotyping
81 quencing of patients' tumor and normal blood buffy coat samples, with a subset of these CH alteration
82 ently and at higher levels in saliva than in buffy-coat samples and in children than in mothers.
83   We used immunohistochemical examination of buffy-coat smears to enumerate circulating endothelial c
84 ied blood, buccal cells, cultured cells, and buffy coats specimens, generating large amounts of DNA f
85                 PCR for CMV was performed on buffy-coat specimens every week for 15 weeks and at mont
86 ase chain reaction (PCR) were performed upon buffy-coat specimens weekly for 12 to 16 wk.
87 A was detected more frequently in saliva and buffy coats than was human herpesvirus 8 DNA.
88 reated with monoclonal antibodies (ZMapp), a buffy coat transfusion from an Ebola survivor, and the b
89                                 A subsequent buffy coat virus isolate was resistant to all three drug
90                             Genomic DNA from buffy coat was genotyped for BDNF Val66Met.
91                        MAP DNA in uncultured buffy coats was identified by PCR in 13 (46%) individual
92 al cells were removed surgically, and blood (buffy coat) was analyzed.
93        Human mononuclear cells isolated from buffy coat were seeded on collagen type 1 matrix and out
94 als showed that conjunctival swabs and blood buffy coat were the samples of choice for epidemiologica
95                             TP activities in buffy coats were reduced drastically in all 27 MNGIE pat
96 cancer cells within a complex sample matrix (buffy coat) while simultaneously quantifying cell concen
97 ges of the European method of manufacture of buffy coat whole-blood-derived platelet concentrate have