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The Multiple Myeloma Research Consortium has funded the collection of 1,900 patients' bone marrow samples that are being studied by the mit-Harvard Broad Institute, a genetic research center.
To address the possibility that the cellular heterogeneity present in MDS bone marrow samples could limit the use of unfractionated cells for DNA based genomic studies, we used the SNP resequencing data to determine whether we could detect clonality in MDS bone marrow samples that had less than 5 percent myeloblasts.
These cells are generated from bone marrow samples that are serially passaged and cultured on plastic.
The bone marrow samples that were taken for diagnostic purposes, with a blast load of ⩾90% and the CD7 positivity of ⩾90%, were included in the study.
The blood and bone marrow samples that had been treated in culture with fludarabine (∼10 cells) were initially incubated for 15 min with anti-CD19 PerCP and anti-CD5 APC-conjugated monoclonal antibody (MoAb) (DAKO, Denmark) at room temperature.
For this purpose, the osteogenic potential of the complete BMC population (called MSC postamplification) was compared with bone marrow samples that have been depleted from all CD34+ and CD133+ cells (called depleted MSCs).
Similar(52)
Similar to the bone marrow sampling that doctors do with leukemia patients, we would like to re-sample cancerous brain tumours to gaining a better understanding on glioblastoma evolution with Temozolomide (the chemotherapeutic drug) as well as identifying genetic drivers within a patient's tumour.
Transcriptional profiles were measured from bone marrow aspirate samples that were taken seven times over the course of three months after infection.
This finding suggests that the amount of memory NK cells might be extremely low in blood or bone marrow samples, or that CD45RO may not be a marker of memory NK cells.
Finally, bone marrow samples demonstrated that expression of CB2 receptor is much lower in osteoporotic patients than in healthy donors.
In order to confirm these results in HL-60 cells, we used primary leukemic blasts from AML patient marrows (AML-M3 and AML-M2 samples) that were treated with 6-BT (10 μM) for 24, 48 or 72 hours.
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