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1 ich was overcome by crossing them to outbred ICR mice.
2 inhibition of capsaicin-induced flinching in ICR mice.
3 munoreactivity (irBC) in the hypothalamus of ICR mice.
4 cells, and lack of neurovirulence in newborn ICR mice.
5  benzo[a]pyrene-evoked forestomach tumors in ICR mice.
6 ague-Dawley rats and antinociception in male ICR mice.
7 ect the gastric mucosa of wild-type, outbred ICR mice.
8 xidative stress and hepatic fibrosis in male ICR mice.
9 liver short hairpin (shRNA) genes to healthy ICR mice.
10 for inbred (BALB/c and C57BL/6) and outbred (ICR) mice.
11                         Subjects were female ICR mice 8-10 weeks old.
12 cal determinants for neuroinvasion of normal ICR mice by SPYF virus were also in the E protein, seque
13 utrition (TPN) to genetically normal, immune ICR mice by the i.v. route results in loss of nasal anti
14 or RVV-X (the venom factor X-activator) into ICR mice did not significantly deplete the plasma fibrin
15 lecule MIF antagonist, CPSI-1306, to outbred ICR mice following induction of NIDDM significantly lowe
16         miRNAs were extracted from hearts of ICR mice following IPC.
17 A/H-F/V was transplanted subcutaneously into ICR mice for up to 4 weeks to assess its in vivo effect
18 assess the following conditions in male CD-1/ICR mice: group size (1, 2, or 3), age at grouping (5 or
19 , were not neurovirulent in 3- to 4-week-old ICR mice inoculated by the intracerebral route, and were
20    Corneal clarity in young adult Swiss (HSD:ICR) mice is restored after Pseudomonas aeruginosa infec
21 micro-MRI scanner in 8-to-10-week-old female ICR mice (n = 28) before and after surgically induced bl
22       Experiment 1: Intravenously cannulated ICR mice received chow, PN, or PN + BBS injections for 5
23 s of estren's action on male-orchidectomized ICR mice revealed estren's AR agonist actions on the lev
24 equences of viruses recovered from brains of ICR mice succumbing to encephalitis with the parental SP
25                                  However, in ICR mice, the anatomic extent of colonization was more l
26                           Here, we subjected ICR mice to mTBI and examined the bone response in the s
27 -treated primary pancreatic islet cells from ICR mice to unravel the protective mechanism of berberin
28                                              ICR mice treated with CP 55,940 (2 mg/kg) twice a day fo
29 e next introduced into the livers of outbred ICR mice via hydrodynamic tail vein injection.
30                               Eight-week-old ICR mice were administered 20 microL/CCl(4) kg dissolved
31                          RESEARCH DESIGN AND ICR mice were food restricted by 50% from gestational da
32                            Groups of outbred ICR mice were given one or two doses of recombinant plas
33           Groups of 3- to 5-week-old, female ICR mice were immunized intranasally with three doses of
34  transthoracic echocardiography (TTE), adult ICR mice were injected i.p. with vehicle (10% DMSO) or t
35                                         Male ICR mice were pretreated with neurogranin antisense or m
36                                         Male ICR mice were randomized to 1 of 4 treatments: saline, s
37                       Prenatal and postnatal ICR mice were treated with FdU to ascertain the regimen
38                          Adult male out-bred ICR mice were treated with p38 activator, anisomycin (0.
39                                   Adult male ICR mice were treated with saline or sildenafil (0.7 mg/
40 67) controlled by the keratin 14 promoter in ICR mice were used to determine the effects of OA on AP-
41            H isolates did not infect newborn ICR mice, whereas 1 of the 2 C isolates tested did.
42  (51)MnCl2 was intravenously administered to ICR mice which were scanned by dynamic and static PET, f