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1 implants in a large animal model (Goettingen minipigs).
2 anti-B5 immune response in both mice and the minipig.
3 extracted mandibular premolar teeth in three minipigs.
4 ther young domestic pigs or adult Goettingen minipigs.
5 erated in a 28-day safety study in Gottingen minipigs.
6 8 implants were placed into sockets in three minipigs.
7 erior descending coronary artery (LAD) of 41 minipigs.
8 in all plasma samples isolated from four NIH minipigs.
9 h period when dosed intramuscular to dogs or minipigs.
10 created fossa ovalis ASD was attempted in 15 minipigs.
11 ar antigen (PCNA) in livers from ethanol-fed minipigs.
12 ncreas gland and pancreatic duct ligation in minipigs.
18 2) derivatives were evaluated in dogs and in minipigs, at a dose of 5mg-eq. nalmefene/kg and plasma n
19 ress this, we studied eight adult Goettingen minipigs before and after an approximately 60% reduction
21 se, was necessary to prevent inflammation in minipigs (effective dexamethasone dose was 100mug delive
34 Finally, in a randomized efficacy study, 14 minipigs received allogeneic cardiospheres (1.3 x 10(6))
36 ed absorption compared with oral Taxotere in minipigs, resulting in relative bioavailability and Cmax
37 LV apex at 120 bpm for 1 year (7 age-matched minipigs served as controls with spontaneous heart rates
41 fter ingestion of four dairy matrices by six minipigs: unheated or heated skim milk and corresponding
42 ncentrations can be achieved in both dog and minipig using nalmefene prodrugs and that the pharmacoki
47 was observed from day 7 post-implantation in minipigs, whereas in rats this did not occur until day 1
48 , PTCA was performed in hypercholesterolemic minipigs whose left anterior descending (LAD) coronary a
49 Whereas oral administration in mice or the minipig with collard-derived insoluble pB5 did not gener
50 transplantation was performed in 10 Yucatan minipigs with coronary arteries from farm pigs as donors
51 ternal elastic lamina in a carotid artery of minipigs with hypercholesterolemia induced by feeding th
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