ライフサイエンスコーパス: intrarectally

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1 ould also be effectively delivered orally or intrarectally.

2 d the other half were exposed to SIV(mac251) intrarectally.

3 s SIVmac239, prevents infection by SIVsmE660 intrarectally.

4 mAbs) to rhesus macaques and challenged them intrarectally 24 h later with either of two different R5

5 gnificantly earlier than macaques challenged intrarectally and well past the initial resolution of vi

6 ast vaccination, the animals were challenged intrarectally at weekly intervals with a titrated dose o

7 ed rhesus macaques were either uninfected or intrarectally challenged with SIV, with a subset receivi

8 in significant proportions, animals infected intrarectally had predominantly E11S-type sequences.

9 Animals were inoculated intrarectally (i.r.) or intravenously (i.v.) with stocks

10 with SIVmac239Delta nef and challenged them intrarectally (i.r.) with repeated low doses of the path

11 a major reservoir for virus replication, in intrarectally immunized animals than in subcutaneously i

12 ements, and patterns of coreceptor switch in intrarectally infected animals were thus remarkably cons

13 rliest published example of CD8-TL escape in intrarectally infected macaques.

14 l lines and human cancer cells were injected intrarectally into nonobese diabetic/SCID mice.

15 and four adult AGMs as well as two PTMs were intrarectally (IR) exposed, while two additional adult f

16 Twenty-nine rhesus macaques were challenged intrarectally or intravenously with either a single dose

17 pe and SIV(SM) Pbj deltaVpx intravenously or intrarectally, the deltaVpx mutant was at a strong compe

18 ed to mimic the RV144 trial and exposed them intrarectally to a dose of the simian immunodeficiency v

19 /gp120, or gp120 alone, and all were exposed intrarectally to SIV(mac251) at one of three doses.

20 Vaccinated macaques were challenged intrarectally with 50 50% animal infectious doses of SHI

21 e infected, 12 male macaques were inoculated intrarectally with amounts of SHIV(SF162P3) (10 median t

22 These animals were challenged intrarectally with pathogenic molecularly cloned SIVmac2

23 he CTL specificity, we immunized BALB/c mice intrarectally with recombinant MVA 89.6.

24 n coreceptor preference in macaques infected intrarectally with SHIV(SF162P3N).

25 dian and Chinese origin were next inoculated intrarectally with SHIV-1157ipd3N4; this virus replicate

26 ed and naive control monkeys were challenged intrarectally with SIV strain DeltaB670 (SIV/DeltaB670),

27 ) and Mamu-A*01(-) macaques, were challenged intrarectally with SIVmac239.

28 naive, Mamu-A*01(+) controls were challenged intrarectally with SIVmac239.

29 oculated pigtailed macaques intravenously or intrarectally with the molecularly cloned, macrophage tr

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