Sentence examples for bone wafer from inspiring English sources
We examined this possibility with the bone wafer assay.
Direct measurements during surgery and bone wafer measurements do not reveal the true shape, provide rotational references, or maintain coordinate axes [ 10, 25].
In contrast to MHCII+CD16- cells that generated very few TRAP+ cells on the bone wafer (data not shown), both MHCII+CD16int and MHCII+CD16+ cells were able to develop into mature OC- b)).
We would like to thank Mike Strong and Dr. Peter Keng for their help in sterile cell sorting, and Dr. Ruolin Guo and Dr. Lianping Xing for their help in bone wafer resorption assay and bone pit erosion quantification.
Figure 7(c - d) shows the c - dshowsing bone erosions on the same bone wafers.
KAM and MT helped with micro-CT scanning on bone wafers.
Splenocytes were seeded at 1.75 × 10 cells/well on sterile 4 mm × 4 mm bovine femoral cortical bone wafers.
These cells took on the morphology of osteoclasts, expressed mRNA for osteoclast-related genes and excavated pits on bone wafers.
On day 14, bone wafers were TRAP-stained for OC quantification, followed by toluidine blue staining for visualization of erosion pits on the bone surface.
Sorted cells were cultured alone or with bone wafers in the presence of receptor activator of nuclear factor kappa-B ligand (RANKL) and macrophage colony-stimulating factor (M-CSF).
MHCII+ cells isolated from three PsA patients were sterile sorted into CD16-, CD16int, and CD16+ populations and cultured together with bone wafers in the presence of RANKL and M-CSF.
