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Bone marrow samples were collected from the lesion site (P) and the iliac crest (IC) of 7 patients affected by CPT and type 1 neurofibromatosis (NF1+) and 6 patients affected by CPT without NF1 (NF1−).
Long bone marrow samples were collected, dried, and the % marrow fat calculated by this method.
Bone marrow samples were collected at week 4 and 5 after reconstitution, at which time mature T cells were not detected in the periphery and there were no signs of immunopathology in the crt−/− FLC.
After 2 hours, blood and bone marrow samples were collected.
Bone marrow samples were collected at diagnosis and before treatment.
Repeat bone marrow samples were collected, which showed macrophage inclusions consistent with hemolysis.
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Blood and bone marrow sample was collected in heparinized tubes.
Bone marrow (BM) samples were collected from 4 healthy subjects and 7 MDS patients, seen at the Hematology and Hemotherapy Center, University of Campinas.
Leukaemic bone-marrow (BM) samples were collected from 14 patients with BCP-ALL aged less than 1 14 years (median, 6 years) either at the time of diagnosis (nine patients) or at relapse (five patients).
Necropsies were performed on all euthanized carrion crows; heart, liver, spleen, kidney, bone marrow, and brain samples were collected.
Animals were sacrificed, bone marrow and blood samples were collected and subjected to series of genotoxicity assay such as micronucleus, chromosome aberration and single cell gel electrophoresis (SCGE) assay respectively.
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