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1 on, a group of immature rats each received a silastic capsule (1.57 mm i.d., 3.18 mm o.d., 1.5 cm lon
4 ized and implanted for 6 weeks with either a Silastic capsule containing testosterone or an empty cap
5 weeks later, subcutaneously implanted with a silastic capsule containing vehicle or 17beta-estradiol.
6 tes were implanted subcutaneously with empty silastic capsules (BSIL) or silastic capsules containing
7 gonadectomized Sternopygus with either empty SILASTIC capsules (control), one capsule filled with est
9 ere implanted with blank or 17beta-estradiol Silastic capsules concurrently with the last three SERM
10 s and treated from the time of grafting with Silastic capsules containing 25 mg of testosterone plus
11 gen stimulation via s.c. implantation of two silastic capsules containing 40 mg testosterone each; (b
12 re gonadectomized (GDX'd) and implanted with Silastic capsules containing dihydrotestosterone propion
13 ariectomized 7 days prior to implantation of silastic capsules containing either vehicle (cholesterol
15 wley males were castrated and implanted with SILASTIC capsules containing testosterone (T) or nothing
16 Rats were orchidectomized and implanted with silastic capsules designed to produce physiological leve
17 omized rats received empty or steroid-filled Silastic capsules for 2 weeks according to one of the fo
19 rats administered T, DHT, or 3alpha-diol via Silastic capsules or intrahippocampal infusions had grea
20 ysiological levels of estrogen, delivered in Silastic capsules, improved response accuracy without af
25 ced in the animals by placing a nonocclusive silastic collar around the left common carotid artery.
27 took was to use replica molding to construct silastic devices to consistently deposit oriented, elong
28 n male mouse fetuses (released by a maternal Silastic estradiol implant) induced a 40% increase in th
31 strone by a continuous-release, subcutaneous Silastic implant, or they received an empty Silastic imp
33 d rats that were given chronic estradiol via Silastic implants resulting in serum estradiol concentra
34 ups of OVX mice bearing A+ cells received E2 Silastic implants to clamp plasma levels at 5, 7, 10, an
35 e-aged (13 months old) Brown Norway rats via Silastic implants to suppress endogenous Leydig cell tes
36 re determined relative to morpholine using a Silastic membrane to deliver NO. at a rate of approximat
37 tricular myocytes cultured on laminin-coated silastic membranes were stretched cyclically (1 Hz) at l
38 entiation, astrocytes cultured on deformable SILASTIC membranes were subjected to rapid, reversible s
41 Fatty infiltration causing changes in the silastic poppet of the Model 1000 series Starr-Edwards a
43 us occlusion plethysmography with mercury-in-Silastic strain gauges with drugs infused locally at the
45 imals were subcutaneously implanted with one Silastic TP capsule, with the other half sham implanted.
46 imals were subcutaneously implanted with one Silastic TP capsule, with the remainder sham implanted.
47 thelial cells cultured in compliant or stiff silastic tubes were pulse perfused by arterial pressure/
48 er 344 rats (>20 months) were implanted with Silastic tubing containing testosterone (T), T plus an a
49 mpared to gonadectomized rats implanted with Silastic tubing containing testosterone (T), T plus an a
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