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1 not to receive daily intramuscular doses of recombinant human growth hormone (0.15 mg rhGH/kg/day).
2 nts were randomly assigned to receive either recombinant human growth hormone, 0.1 mg/kg of body weig
3 sequence coverage of a therapeutic protein, recombinant human growth hormone, and in detection of si
4 tween protein molecules within aggregates of recombinant human growth hormone are responsible for the
12 minimum, administration of anabolic agents, recombinant human growth hormone, insulin, oxandrolone,
15 he characterization of disulfide linkages of recombinant human growth hormone (Nutropin), a therapeut
16 nt of metabolic bone disease, and the use of recombinant human growth hormone provide some hope for c
20 s the current evidence concerning the use of recombinant human growth hormone (rhGH) as a potential t
22 level I trauma center who were treated with recombinant human growth hormone (rhGH) for > or =7 days
23 pared and shown to promote the absorption of recombinant human growth hormone (rhGH) from the gastroi
26 l reference method for the quantification of recombinant human growth hormone (rhGH) in serum has bee
30 sively burned children during treatment with recombinant human growth hormone (rhGH), and to ascertai
35 ren with JRA and growth retardation received recombinant human growth hormone (rHuGH) for 1 year.
38 is important to recognize that the impact of recombinant human growth hormone therapy on adult height
40 kbar to suspensions containing aggregates of recombinant human growth hormone (up to 8.7 mg/ml) and 0
41 types of insoluble, non-native aggregates of recombinant human growth hormone were formed by agitatio
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