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The diabetic mice were distributed into two groups (n = 23 per group).
In contrast, EGFP− (Fig 5E) and EGFPhi (Fig. 5F) cells from MMTV-Wnt1 mice were distributed in both CD24/CD49f subpopulations.
Paneth cells in the Cre+Cdh1fl/fl mice were distributed all over the crypts and villi and the number of Paneth cells at the bottom of the crypts appeared reduced (Fig. 5C and D).
Twenty-four days later, diabetic mice were distributed into experimental groups according to if they received or not insulin and/or one or two doses of healthy donor-derived MSCs.
Seventy mice were distributed into 7 groups of 10.
C57BL/6 male mice were distributed into four groups (n = 6).
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In brief, 200 μL of plasma from mice was distributed in a 96-well plate, and 10 μL of crude venom containing different concentrations (0.312, 0.625, 1.25, 2.5, 5, and 10 μg) of proteins was added.
Nevertheless, the data suggest a model where recognition of M. tb in these mice is distributed among many low and high frequency clones, sharing characteristic amino acid triples or quadruplets.
With the threshold of allowing maximum 2 mismatches for RNA-seq mapping, this would mean little cross-species mappable reads if the differences between coding regions of human and mouse were distributed evenly.
The tissue powder from each mouse was distributed into four 2-ml Nunc cryotubes on dry ice and then stored in two liquid-nitrogen freezers.
The olive mouse is distributed along Chile and Argentinean Patagonia, from 18ºS to 55ºS latitude [ 4], extending for over 1000 km latitudinally, and encompassing a great variety of environments: coastal deserts in the north, Mediterranean scrubs in central Chile, Valdivian and Magallanic forests through the south of Chile and Argentina and Patagonian steppe towards the Atlantic coast.
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