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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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