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1 nses to CO(2) in experimental animals (adult laboratory rats).
2 f pluripotency and cell reprogramming in the laboratory rat.
3 h data from the hamster, Nile grass rat, and laboratory rat.
4 at (Arvicanthis niloticus) and the nocturnal laboratory rat.
5 e of tissues and developmental stages of the laboratory rat.
6 ces and of the RT1.Ba gene of six strains of laboratory rat.
7 in the human eye, can now be applied to the laboratory rat.
8 ral pattern of female sexual behavior in the laboratory rat.
9 ility, are also prevalent in healthy outbred laboratory rats.
10 cells, and induced pluripotent stem cells of laboratory rats.
11 l as full woodrat microbial communities into laboratory rats.
12 to myocardial lipidosis and heart lesions in laboratory rats.
13 expression are seen in grass rats but not in laboratory rats.
14 cortical area) compared with closely related laboratory rats.
15 ave been obtained from wild-derived mice and laboratory rats.
16 e-xylazine is a commonly used anesthetic for laboratory rats.
17 e day in both forms of grass rats but not in laboratory rats.
18 g brain and behavioral changes in humans and laboratory rats.
19 e genome assembly for Rattus norvegicus, the laboratory rat, a widely used experimental animal model
20 The mild hypothermia seen in homeothermic laboratory rats after NPY injected ICV is exaggerated, o
21 oimmune thyroiditis can be induced in normal laboratory rats after thymectomy and split dose gamma-ir
23 Material balance calculations using both laboratory rates and field product concentrations demons
25 ecause its Animal Welfare Act (AWA) excludes laboratory rats and mice (RM), government veterinarians
26 Here we show in experimental animal models (laboratory rats and mice) that the neuronal activity-dep
28 conclusion that logically extends to outbred laboratory rats and possibly to those that have been inb
29 viding evidence that the spatial behavior of laboratory rats (and the associated HD network) is insen
30 arboxamide (SB-277011-A) was administered to laboratory rats, and the following measures were assesse
31 In conclusion, PhIP-induced lymphomas in the laboratory rat appears to be a very useful model to anal
36 ckling' induces positive affective states in laboratory rats as evidenced by the production of 50-kHz
37 hronic seizures from medication, we used the laboratory rat, because an epileptic condition can be in
38 er, our controlled interventional study with laboratory rats bred for low and high intrinsic fitness
42 tense maladaptive attractions are created in laboratory rats by pairing optogenetic channelrhodopsin
43 peated injections of cocaine and morphine in laboratory rats cause a variety of molecular neuroadapta
46 justified, the advanced domestication of the laboratory rat does suggest that resuming studies of wil
47 dating" study has not been performed for the laboratory rat, even though it is the species of choice
49 t genetic effects in four cohorts of outbred laboratory rats exposed to distinct but controlled envir
50 SCN of both groups of grass rats, as well as laboratory rats, Fos was elevated during the light compa
52 sychiatric illnesses, most studies involving laboratory rats have focused on males while females have
53 ergic projections reach the SCN of nocturnal laboratory rats, however, nothing is known about these p
55 dy that chronic naltrexone administration in laboratory rats increases the cytolytic activity of NK c
57 f O. formigenes in regulating hyperoxaluria, laboratory rats known to be noncolonized were colonized
58 ics, however, are routinely found in outbred laboratory rats, leading to debate on whether SWD/immobi
59 ver oocysts from rat feces suggests that the laboratory rat may be a convenient substitute for rumina
61 centres and a national clinical neurogenetic laboratory; rates of discovery were comparable, making s
62 tory and informatics platform related to the laboratory rat, one of the most important model organism
65 ssibility, we designed a series of tests for laboratory rats, paralleling human regulatory focus rese
66 ver, these events are also common in outbred laboratory rats, raising concerns about whether SWD/immo
70 sion quantitative trait locus mapping in the laboratory rat (Rattus norvegicus) to gain a broad persp
72 ere, we explore chemical signaling by female laboratory rats (Rattus norvegicus) to test i) whether f
75 wever, rodent hepacivirus (RHV) infection in laboratory rats recapitulates the lifelong chronic hepat
76 ateral preoptic area (VLPO) of the nocturnal laboratory rat receives direct input from the retina and
78 pared to the night, at a time when nocturnal laboratory rats show superior retention; acquisition of
79 Studies conducted in experimental animals (laboratory rats) show that astrocytes respond to acute d
82 timulation of the SCN between grass rats and laboratory rats that may reflect a rewiring of neural pr
86 rhage (PH) on prerandomization imaging (core laboratory rating) using adjusted risk differences betwe
89 igate the cause of unexplained deaths in his laboratory rats, which he hypothesized were due to an "u