Sentence examples for pups were analyzed from inspiring English sources

Heterozygous Cdk2ap1+/− mice were mated with K14-Cdk2ap1 mice and pups were analyzed by PCR based genotyping on tail biopsies.

Subventricular zone NSPs isolated from newborn mouse pups were analyzed for proliferation, self-renewal, and differentiation, shortly after irradiation.

To examine the formation of glial-vascular units by newly born dentate cells, Gli1-Cre ERt2 mice were injected with TM at E17.5 and pups were analyzed at P2.

Pups were analyzed for the presence of the Cre transgenic construct by PCR amplification of tail DNA using 5′-CTCTGGTGTAGCTGATGATC-3′ as forward primer and 5′-TAATCGCCATCTTCCAGCAG-3′ as reverse primer.

The treated pups were analyzed after 6 weeks (n = 3 5), 10 weeks (n = 4 6), and 6 months (n = 3 5 for histology and Western blots, n = 5 11 for magnetic resonance imaging [MRI]) of continued postnatal treatment.

Tail DNA from the agouti pups was analyzed by Southern blot analysis using 5' and 3' probes to identify Muc16 heterozygous mutants.

The weight of mouse pups was analyzed by descriptive statistics and t test (Statistica software, StatSoft, Inc., Tulsa, OK, USA).

RNA from WT and Ptbp2-NestinKO E18 pups was analyzed on Affymetrix MJAY arrays (see 'Materials and methods').

Wild type (WT) and HT7KO female littermates were mated to WT sires and their ability to bear litters and sustain pups was analyzed.

Myography data from male and female pups was analyzed separately to determine whether sex differences existed for contraction and relaxation data.

(a) Recombinant purified GST-BirA* (R118G, BioID) and GST-PafA (PUP-IT) were analyzed with coomassie stain.