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Cells were allocated into groups, treated with RNAs purified from plasma of juvenile diabetics, adult type 1 diabetic patients, control healthy children, healthy adult persons, nucleic acids and polynucleotide standards (RNA, polyC, PolyA, PolyIC, and CpG).
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Nonetheless the within-site correlation was not as dramatic for LINE-1 methylation as was seen for XCI skewing and thus some variability at these repeated sequences must be acquired after cells are allocated into the primary villi.
Cells were allocated to ex vivo flow cytometry, cell culture or RT-PCR.
All physiologically identified cells were allocated their respective laminar locations.
Cases were allocated into diploid (⩾90% of cells forming a single peak between 1,6c and 2,4c), tetraploid (a minimum of 10% of cells forming a peak between 3,6c and 4,4c) or aneuploid (>10% of cells outside diploid and tetraploid ranges).
Two weeks after tumor cell challenge, when the tumor volume reached approximately 100 mm, mice were allocated into two groups for therapy.
Studies were allocated into three groups.
Participants were allocated into 17 dyads.
Design: forty rabbits were allocated into five equal groups.
Pigs were allocated into intravenous saline and LPS group, respectively.
Patients were allocated into two groups.
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