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1 dependent on morphologic examination of bone marrow aspirates.
2 tokeratin assay in preoperatively taken bone marrow aspirates.
3 nalyze peripheral-blood lymphocytes and bone marrow aspirates.
4 a and fused with myeloma cells obtained from marrow aspirates.
5  lymphoma cells mixed with normal human bone marrow aspirates.
6 t cells that can be easily derived from bone marrow aspirates.
7 s been applied to the in vitro study of bone marrow aspirates.
8 as tested on four human and four canine bone marrow aspirates.
9 rred by 21-28 months in a second iliac crest marrow aspirate 1 year after the first aspirate in the D
10 R1 (n = 183) or CR2 (n = 70) who had pre-HCT marrow aspirates analyzed by 10-color flow cytometry.
11 t rigorous staging as defined by both a bone marrow aspirate and biopsy and an imaging study (a compu
12                                         Bone marrow aspirate and biopsy and bone scan are unnecessary
13                                            A marrow aspirate and biopsy revealed normal trilineage he
14                                         Bone marrow aspirate and biopsy specimens were studied, and p
15 ents had less than 10% total plasma cells on marrow aspirate and biopsy.
16           Sensitivity was comparable between marrow aspirate and biopsy.
17                                       A bone marrow aspirate and peripheral blood were obtained for m
18  therefore, peripheral blood smears and bone marrow aspirates and biopsies from 87 patients (143 tota
19                       Unilateral iliac crest marrow aspirates and biopsies were performed on all pati
20  leukemia cells mixed with normal human bone marrow aspirates and can also identify cancer cells clos
21 e of lymphoblasts from day 7 and day 14 bone marrow aspirates and more prolonged asparaginase activit
22 d cellular immune assays of iliac crest bone marrow aspirates and peripheral blood have begun to be c
23                                         Bone marrow aspirates and peripheral blood were obtained betw
24    Primary human MSC were cultured from bone marrow aspirates and then passaged at least three times
25  isolated from white adipose tissue and bone marrow aspirates and were s.c. implanted into immunodefi
26      Our data demonstrate that serum, urine, marrow aspirate, and myeloblast 2-HG levels are signific
27 croscopy by 10-fold in samples of fresh bone marrow aspirate approximating minimal residual disease.
28                            We collected bone marrow aspirates, archival bone marrow samples, and bloo
29 w measurements of recipient iliac crest bone marrow aspirates as in previous studies on peripheral bl
30            Among the seven centers, all used marrow aspirates as the starting material, but no two ce
31 c flow cytometry (MFC) was performed on bone marrow aspirates before HCT.
32            Peripheral-blood (PB) and/or bone marrow aspirate (BM) samples were obtained from 28 patie
33   In primary myeloma cells derived from bone marrow aspirates, CD46-ADC induced apoptosis and cell de
34                   Moreover, iliac crest bone marrow aspirates contained an average of thirteen times
35 nd mesenchymal cells derived from human bone marrow aspirates express the cell-bound form of fractalk
36 ral blood mononuclear cells (PBMCs) and bone marrow aspirates for regulatory T cells (Tregs) (e.g., C
37 bulin FISH done on cytospin slides from bone marrow aspirates for t(11;14), t(4;14), and -17(p13.1) (
38 ng, to identify mutations in samples of bone marrow aspirate from 439 patients with myelodysplastic s
39 rom a mean +/- SD of 23.4 +/- 5.9 mL of bone marrow aspirate from all patients.
40 ositivity for MMc was demonstrated in a bone marrow aspirate from an SSc patient in whom peripheral b
41                             We obtained bone marrow aspirates from 11 patients on ART who had undetec
42 , cytokine mRNA levels were measured in bone marrow aspirates from 27 naturally infected dogs from Br
43  (ISH) for IL-1beta was performed using bone marrow aspirates from 51 MM, 7 smoldering MM, 21 MGUS, a
44     Despite the peripheral neutropenia, bone marrow aspirates from affected individuals contain abund
45 icroscopic levels of leukaemic cells in bone-marrow aspirates from children with acute lymphoblastic
46 tency, these transcripts are present in bone marrow aspirates from naturally infected, healthy seropo
47 ocedure, the extent of demethylation in bone marrow aspirates from patients with leukemia receiving d
48                                         Bone marrow aspirates from the patient showed <0.1% CD19(+) B
49          Repeated analyses of blood and bone marrow aspirates gave no indication of hematopoietic dis
50  In the DBMC group, chimerism in iliac crest marrow aspirates has increased 3-fold in yearly sequenti
51 er for magnetic separation of CTPs from bone marrow aspirates in a canine model.
52 color multiparametric flow cytometry on bone marrow aspirates in all patients.
53                                         Bone marrow aspirates in two patients had markedly decreased
54       Potential admixture of blood with bone marrow aspirate limits our ability to determine the orig
55 tion of transplantable tissues in which bone marrow aspirates may serve as an accessible source of au
56                                         Bone marrow aspirates (n = 629) were collected at the end of
57                              Ten normal bone marrow aspirates (NBM) were first analyzed using an eryt
58                                     One bone marrow aspirate obtained before treatment, one whole blo
59 id cells subsequently detected in sequential marrow aspirates obtained from 2 primary NOD/SCID-IL2Rga
60 CD70 in the CD10(+)/CD19(+) fraction of bone marrow aspirates obtained from relapsed compared with no
61                 MSCs were prepared from bone marrow aspirates obtained from the iliac crest or from t
62 ells isolated by CD138 sorting from the bone marrow aspirates of 6 patients.
63  levels of serglycin are present in the bone marrow aspirates of at least 30% of newly diagnosed MM p
64 ected by a rapid immunological assay in bone-marrow aspirates of children with ALL.
65 ropagation and function of MSCs derived from marrow aspirates of CLL patients in vitro.
66 ygen on the growth and function of MSCs from marrow aspirates of CLL patients.
67           Moreover, cells isolated from bone marrow aspirates of patients in different stages of CML
68 20) that can typically be obtained from bone marrow aspirates of prostate-cancer patients.
69 cies of mature B cells were observed in bone marrow aspirates of these individuals compared with HIV-
70 an mesenchymal stem cells were isolated from marrow aspirates of volunteer donors.
71 f hematopoietic stem cells from a human bone marrow aspirate possessing only 4000 total cells.
72 ce of platelet-rich plasma derived from bone marrow aspirate (PRP-BMA) on the healing of periodontal
73 testing of whole blood, buffy coat, and bone marrow aspirates, respectively.
74 etails of the individual cases reviewed bone marrow aspirate slides to determine plasmablastic classi
75                               Blood and bone marrow aspirate testosterone concentrations declined to
76 n >/= 10% was correlated with increased bone marrow aspirate testosterone.
77  uncomplicated typhoid and satisfactory bone marrow aspirates, the number of serovar Typhi CFU in bon
78 ssion of testosterone in both blood and bone marrow aspirate to less than picograms-per-milliliter le
79 tained from peripheral blood or through bone marrow aspirates, together with recent advances in cance
80                                 A small bone marrow aspirate was taken from the iliac crest of health
81 tes, the number of serovar Typhi CFU in bone marrow aspirates was a median value of 9 (interquartile
82 utologous granulocytic progenitors from bone marrow aspirate were performed in two patients with unex
83                                         Bone marrow aspirates were analyzed for their neutrophil diff
84                                         Bone-marrow aspirates were collected after induction therapy
85              Results of studies in bilateral marrow aspirates were highly concordant.
86                               Blood and bone marrow aspirates were obtained from 4 patients (2 unrela
87                                         Bone marrow aspirates were performed at baseline for explorat
88                                         Bone marrow aspirates were stained with the pancytokeratin ma
89                                         Bone marrow aspirates were subject to a negative-selection pr
90 rations of PDGF-AA and PDGF-BB found in bone marrow aspirates, which were detected by ELISA, do not a
91                                       A bone-marrow aspirate with biopsy was performed, yielding the

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