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2 the effective dose to 0.0149 mSv/MBq (0.0551 rem/mCi) or 0.0171 mSv/MBq (0.0634 rem/mCi), respectivel
5 ive dose equivalent was 0.018 mSv/MBq (0.065 rem/mCi), and the effective dose was 0.016 mSv/MBq (0.05
15 dose was the kidneys at 0.066 mSv/MBq (0.24 rem/mCi), followed by the heart wall at 0.048 mSv/MBq (0
16 iding model) and uptake in the spleen (0.250 rem/mCi +/- 0.168 [0.068 mSv/MBq +/- 0.046]) and large i
18 to an estimated effective dose of 3 mSv (0.3 rem) and an estimated dose to the target organ or tissue
19 ective dose for women would be 3.1 mSv (0.31 rem), with a liver dose of 17.1 mSv (1.7 rem); the effec
20 primary clearance through the kidneys (0.360 rem/mCi +/- 0.185 [0.098 mSv/MBq +/- 0.050]) and bladder
23 due to balloon rupture was estimated to be 5 rem/50 mCi treatment activity and compared favorably wit
27 n effective dose equivalent of 5.9 mSv (0.59 rem) and a lung dose of 21.8 mGy (2.18 rad) in young, he
29 bladder wall (ca. 180 +/- 30 mSv/MBq or 0.7 rem/mCi with a 2.4 h void interval) suggests that multip
30 .31 rem), with a liver dose of 17.1 mSv (1.7 rem); the effective dose for men would be 2.6 mSv (0.26
32 0.098 mSv/MBq +/- 0.050]) and bladder (0.862 rem/mCi +/- 0.436 [0.233 mSv/MBq +/- 0.118], voiding mod
33 ix WWTPs range from 1.5 to 13.4 gCH(4)/kgCOD(rem), higher than those observed in previous studies usi
34 tion corresponding to an intron of the viral rem accessory gene, suggesting its derivation from splic
35 sponding to the processed mRNA for the viral rem gene; such Mtvs likely derive from spliced viral mRN
36 MTV-infected cells or cells transfected with rem or env cDNAs express SP, which is the active compone