The fistula was identified, double ligated and divided.
While four markers identified double polymorphic loci, the other 334 markers generated single polymorphic loci.
Double immunofluorescent staining of α-SMA+/Ki67+ cells identified double-positive cells (proliferative smooth muscle cells) in the IMZ and LBZ.
Double immunofluorescent staining of RECA-1+/Ki67+ cells identified double-positive cells (proliferative endothelial cells) in the IMZ and LBZ.
Nineteen, three, and one markers identified doubled, tripled, and quadrupled polymorphic loci, respectively, while 1,156 markers generated single polymorphic loci.
In the electron-dense cytosol cell, we identified double-membrane vacuoles, as shown in detail in Figure 7d.
The risks close to the identified double peaks suggest a hazard that is often double that of the mean hazard for the particular treatment group over time.
The exact measurement site on the artery was determined in the B-mode, in a region free of plaque with a clearly identified double-line pattern.
To generate double mutants with the strong ethylene-resistant mutant ein2-1 (Alonso et al. 1999), we crossed ein2-1 to ibr5-1, tir1-1, axr1-3, and aux1-7 and identified double mutants using PCR-based polymorphic markers.
When mice heterozygous for Fancd2 and Msh2 were interbred and embryos were harvested between 13 and 14 days of gestation, we identified double-mutant embryos, which upon visual inspection resembled wild-type embryos.
Genome- and network-based classification was largely consistent with accepted viral taxonomy and suggested that (i) 264 new viral genera were identified (doubling known genera) and (ii) cross-taxon genomic recombination is limited.
