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1 2.83 +/- 0.27 (SEM) pmol/10 minutes per 6-mm trephine.
2 lated from the peripheral region with a 3 mm trephine.
3 -), and MyD88(-/-) mice were abraded using a trephine and epithelial brush and were exposed to heat-
5 meter epithelial defects were created with a trephine and mechanical scraping in the center of human
6 m the center of the optic disc, using a 2-mm trephine and were processed for transmission electron mi
12 harvested from the calvarium of rats with a trephine bur (3-mm internal diameter) and placed on the
13 ling, final measurements were performed, and trephine core biopsies were obtained for histomorphometr
14 Prior to implant placement, a 2.7 x 6.0 mm trephine core was obtained and preserved in formalin for
15 All sites were reentered at 4 months, and a trephine core was obtained for histologic analysis befor
17 We determined whether coverage of a 3 mm trephine defect in a mouse skull with a collagen scaffol
19 ptic nerve head and peripapillary sclera was trephined from each scleral shell and cut into 4-microm
20 7 mm diameter fenestrations were made with a trephine in the mid-root of both maxillary canines in ea
31 sual acuity, formula used for calculation of trephine size, size of the trephine used, and duration o
32 rhesus monkeys were dissected with circular trephines so that the innermost disc, centered on the fo
34 y evaluated clinical records and bone marrow trephine specimens of 183 patients with thrombocytosis-1
36 perfusion fixation at 10 mm Hg, the ONH was trephined, the specimen embedded in a paraffin block, an
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