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Four hundred and twenty fingerlings were randomly distributed into seven different experimental groups in triplicates following completely randomised design (CRD).
The samples of three types of radar emitters are distributed into seven clusters.
The solutions obtained were distributed into seven cuvettes, and the prepared solutions were stirred and maintained for different periods of time, respectively [1, 3, 6, 18, 36, 48 and 72 h (a‒g)].
The questionnaire consists of 24 items equally distributed into seven subscales.
Twenty-eight rats were randomly distributed into seven groups (n = 4).
The remaining Arabidopsis PDIs with ER retention signals and 15 soybean orthologs were distributed into seven distinct eggNOG v4.0-generated groups that were significantly conserved (Additional file 1).
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Four hundred eighty fingerlings were distributed into eight experimental groups.
Ninety-four female blue fox cubs were distributed into two groups with either handling or no handling.
Nine eight-month-old, clinically healthy buffalo calves were used and distributed into three groups.
Tumor-bearing animals were distributed into four groups: BT474 treated and control, HR6 treated and control.
Forty-eight ICR mice were randomly distributed into six groups with 8 mice in each group.
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