1 e its underlying mechanisms, we subjected 13
Sprague Dawley adult rats to unilateral 14 psi blast exp
2 e rats to determine whether outbred strains,
Sprague Dawley and Long-Evans, and/or the inbred WAG/Rij
3 Male
Sprague-Dawley and Fisher 344 rats, VWR or sedentary for
4 radykinin, and collagenase were performed in
Sprague-Dawley and Long-Evans rats.
5 Timed-pregnant
Sprague-Dawley dams underwent bilateral uterine artery l
6 formed in streptozotocin-induced and control
Sprague-Dawley female rats with DM (type 1 [t1DM]) using
7 conducted on 56 eyes of 28 healthy new born
Sprague Dawley male albino rat.
8 aluate short-term and long-term SRM in adult
Sprague-Dawley male rats (n = 38).
9 fed through an intragastric feeding tube on
Sprague-Dawley male rats after 18 h fasting.
10 We sought to examine whether exposure of
Sprague-Dawley male rats for two weeks to different shap
11 al rats without and after VA supplementation.
Sprague-Dawley neonatal rats (n = 104) were nursed by mo
12 In auditory sensory hair cells of rats (
Sprague Dawley)
of either sex, PIP2 localizes within ste
13 oltage oscillations at 100 Hz in dissociated
Sprague Dawley rat hippocampal neurons in single trial r
14 ding on receptor movement and positioning in
Sprague Dawley rat hippocampal neurons.
15 t that acutely increasing O-GlcNAcylation in
Sprague Dawley rat hippocampal slices induces an NMDA re
16 In the current study, changes in male
Sprague Dawley rat liver caused by dietary treatment wit
17 We report here that in
Sprague Dawley rat, the MOP receptor-selective agonist D
18 For the in vivo effect, we employed a
Sprague-Dawley rat mandible defect model utilizing 1 mic
19 paminergic neurons in the SNpc of Wistar vs.
Sprague-Dawley rat strains.
20 Sprague Dawley rats (24, female) were randomly assigned
21 cordings of phrenic nerve activity in female
Sprague Dawley rats (3-4 months) revealed a direct corre
22 Male
Sprague Dawley rats (350-450 g) were chronically implant
23 Maxillary second molars were extracted in
Sprague Dawley rats (n = 30), and either bisphosphonate
24 Male
Sprague Dawley rats (n = 32) received a four-boost serie
25 Metabolic changes in fed and fasted
Sprague Dawley rats (n = 36) were studied at 9.4 T after
26 Seven week old
Sprague Dawley rats (n=18 male, n=18 female) received da
27 Young
Sprague Dawley rats (PND 21) were assigned to environmen
28 s were administered in an i.v. bolus to male
Sprague Dawley rats after starting a s.c. infusion of ME
29 d by anti-OPH IgG and cytokines formation in
Sprague Dawley rats and Balb/c mice, respectively.
30 sensitization to cocaine was established in
Sprague Dawley rats and was measured by locomotion and b
31 PH was induced in male
Sprague Dawley rats by monocrotaline, hypoxia, or bleomy
32 The present study in
Sprague Dawley rats examined the possibility that the or
33 prelimbic region of the mPFC of adult, male,
Sprague Dawley rats impaired the acquisition and reconso
34 ion in awake and spontaneously behaving male
Sprague Dawley rats interacting with a female, I tested
35 Sprague Dawley rats received a spinal cord transection a
36 ion brain injury or sham surgery, adult male
Sprague Dawley rats received vehicle or rolipram (0.03 m
37 that spinal nerve ligation (SNL, L5) in male
Sprague Dawley rats resulted in behavioral allodynia, wh
38 we show that in conscious, unrestrained male
Sprague Dawley rats the infusion of insulin into the thi
39 ressure and heart rate were recorded in male
Sprague Dawley rats throughout this study.
40 ced by 2,4,6-trinitrobenzenesulfonic acid in
Sprague Dawley rats to identify inflammation-induced cha
41 cordings in an in vitro slice preparation of
Sprague Dawley rats to investigate the effects of physio
42 we used activity-guided optogenetics in male
Sprague Dawley rats to silence IL pyramidal neurons opti
43 udal extent of the ventrolateral medulla, in
Sprague Dawley rats treated with hydralazine or saline.
44 Sprague Dawley rats were allowed free access to a palata
45 Seventy
Sprague Dawley rats were divided into control, experimen
46 inistering and 36 cocaine-administering male
Sprague Dawley rats were employed).
47 Male
Sprague Dawley rats were exposed to repeated hypoxia or
48 For this,
Sprague Dawley rats were given access either to 1 hour (
49 Following acquisition, male and female
Sprague Dawley rats were given either short access (thre
50 Male
Sprague Dawley rats were given GABAergic lesions of the
51 Male
Sprague Dawley rats were implanted with a cannula in the
52 Young, adult male
Sprague Dawley rats were implanted with bilateral dorsal
53 Male
Sprague Dawley rats were infused with angiotensin II (An
54 Male
Sprague Dawley rats were initially conditioned for morph
55 Forty mature female
Sprague Dawley rats were subjected to ligature-induced e
56 RMTg in punished reward seeking, adult male
Sprague Dawley rats were tested in several cost-benefit
57 Male adult
Sprague Dawley rats were trained on a water maze spatial
58 lth in two generations of offspring, GC-eGFP
Sprague Dawley rats were weaned onto HFD (45% fat) or Co
59 vical ganglion (SCG) neurons from adult male
Sprague Dawley rats with or without added NGF and compar
60 ibrillary acidic protein promoter in 62 male
Sprague Dawley rats, 4 dominant-negative soluble N-ethyl
61 ein 1) is administered at the spinal cord of
Sprague Dawley rats, priming is detected at the peripher
62 We studied, in male
Sprague Dawley rats, the role of the cognate hyaluronan
63 ng 40 seconds on the right cornea of 36 male
Sprague Dawley rats, under general anesthesia.
64 Using male
Sprague Dawley rats, we examined if PACAP (.25-1.0 micro
65 Here, after research involving
Sprague Dawley rats, we reported that spinal nerve ligat
66 learning and retention compared with outbred
Sprague Dawley rats, whereas bLRs show reduced extinctio
67 vector and to knock down VAN GLP-1Rs in male
Sprague Dawley rats.
68 ular, and imaging approaches in adult female
Sprague Dawley rats.
69 ive taste memory on taste preference in male
Sprague Dawley rats.
70 endritic release of CCK in the brain in male
Sprague Dawley rats.
71 e post-retrieval extinction paradigm in male
Sprague Dawley rats.
72 al ischemia-reperfusion injury (IRI) in male
Sprague Dawley rats.
73 tegmental area (VTA) of adolescent mice and
Sprague Dawley rats.
74 enates and cultured hippocampal neurons from
Sprague Dawley rats.
75 One hundred sixteen male
Sprague Dawley rats.
76 Twenty-seven healthy
Sprague Dawley rats.
77 learned helplessness (cNLH); and (3) control
Sprague Dawley rats.
78 seeking, an animal model of relapse, in male
Sprague Dawley rats.
79 rotid artery occlusion (BCCAO) in adult male
Sprague Dawley rats.
80 capable, uncontrollable tail shocks (ISs) in
Sprague Dawley rats.
81 uced seizures in urethane anesthetized, male
Sprague Dawley rats.
82 We tested male
Sprague-Dawley rats (12 months old) with permanent middl
83 tering HUP-A i.p. or intrathecally to female
Sprague-Dawley rats (200-235 g body weight) after modera
84 Male
Sprague-Dawley rats (200-250 g) and male C3H/HeN wild-ty
85 Sprague-Dawley rats (3 mo old) that received HNGF6A requ
86 Male
Sprague-Dawley rats (3-6 months) were administered eithe
87 Pregnant
Sprague-Dawley rats (5-month-old) were exposed to high d
88 ted 4 different hemorrhage models using male
Sprague-Dawley rats (6 rats/model), aged 10 to 14 weeks
89 Sprague-Dawley rats (6-8 weeks old) were injected with f
90 Two groups of
Sprague-Dawley rats (n = 15 for group 1; n = 10 for grou
91 Sprague-Dawley rats (n = 32) were subjected to sham or v
92 ut function from the (18)F-FDG PET images in
Sprague-Dawley rats (n = 4) and C57BL/6 mice (n = 5), us
93 Male
Sprague-Dawley rats (n = 45; age, 12 weeks) were inocula
94 Sprague-Dawley rats (n = 7) underwent ferric chloride ap
95 Male
Sprague-Dawley rats (n=31) were anesthetized and treated
96 ction, and colon mucosal environment in male
Sprague-Dawley rats (n=8/group).
97 xperiments were conducted using anesthetized
Sprague-Dawley rats 3 weeks after treatment with either
98 In male
Sprague-Dawley rats 6-OHDA (n = 12) or vehicle (n = 10)
99 Tregs, we studied selected groups of newborn
Sprague-Dawley rats according to feeding plan: dam+/-LR1
100 ed Geniposide-induced hepatic injury in male
Sprague-Dawley rats after 3-day intragastric administrat
101 We conducted a 9-month study in
Sprague-Dawley rats after 45 minutes of bilateral renal
102 to a pharmacokinetic study performed on male
Sprague-Dawley rats after administration of a single dos
103 Thirty-two healthy male
Sprague-Dawley rats and 47 human adults underwent threat
104 We also performed experiments with male
Sprague-Dawley rats and CPEB-deficient mice (C57BL6 or m
105 ehaviorally sensitive, low alcohol-consuming
Sprague-Dawley rats and DBA/2 mice and behaviorally inse
106 using microdosing of the unlabeled ligand in
Sprague-Dawley rats and in wild-type and KOR knockout mi
107 is and/or beta-AR levels in diabetic hearts,
Sprague-Dawley rats and miR-133a transgenic (miR-133aTg)
108 rom freshly excised lung, obtained from both
Sprague-Dawley rats and New Zealand White rabbits.
109 Adult male
Sprague-Dawley rats and pulmonary epithelial cells.
110 Normal
Sprague-Dawley rats as well as RH or streptozotocin (STZ
111 g to AKAPs in the nucleus accumbens shell of
Sprague-Dawley rats attenuates reinstatement induced by
112 PAH was induced in male
Sprague-Dawley rats by administering monocrotaline.
113 8)F- AMC20: was evaluated in brain slices of
Sprague-Dawley rats by in vitro autoradiography and in l
114 TPase (RhoAV14) in the AH outflow pathway in
Sprague-Dawley rats by using lentiviral vector-based gen
115 tic dysfunction and hypertension in pregnant
Sprague-Dawley rats challenged with lipopolysaccharide (
116 Male
Sprague-Dawley rats consumed caffeine (0.3 g/l) or water
117 ed behaviors occurred in both Long-Evans and
Sprague-Dawley rats despite the fact that the 6-week HFD
118 Studies were performed on adult, male,
Sprague-Dawley rats exposed to either short-term (ST; 10
119 iver, and fat were collected from adult male
Sprague-Dawley rats exposed to increasing doses of the P
120 selectively bred Crl:OP[CD] rats and outbred
Sprague-Dawley rats fed an HE diet showing high levels o
121 ingivalis lipopolysaccharide injection in 64
Sprague-Dawley rats for 7 to 21 days.
122 on the medial surface of the kidney in five
Sprague-Dawley rats for MR imaging at 11.7 T.
123 tumor-bearing aged, female, retired breeder
Sprague-Dawley rats for PET imaging.
124 Male
Sprague-Dawley rats had an intracaudate injection of aut
125 Sprague-Dawley rats in four parallel groups (N=9 per gro
126 Adult male
Sprague-Dawley rats INTERVENTIONS: Anesthetized rats wer
127 We assigned 25 male
Sprague-Dawley rats into four groups: intraosseous lipid
128 is issue, we transduced primary neurons from
Sprague-Dawley rats or APP(-/-) mice (B6.129S7-App(tm1Db
129 analyzed hepatic transcriptional dynamics in
Sprague-Dawley rats over a period of 24 hours to assess
130 To test this hypothesis, 6-week-old
Sprague-Dawley rats received a neurotoxic dose of capsai
131 Male
Sprague-Dawley rats received bilateral infusions of a Cr
132 Seventy-two
Sprague-Dawley rats received daily 0, 10 (low-dose [LD])
133 Nine immunocompetent
Sprague-Dawley rats received intravenous injection of fe
134 Male
Sprague-Dawley rats received multiple intracutaneous inj
135 In two separate experiments, male
Sprague-Dawley rats received nicotine injections (0.4 mg
136 To test this hypothesis, adult male
Sprague-Dawley rats received sham surgery or moderate pa
137 This study used male
Sprague-Dawley rats responding under a progressive ratio
138 le burst of high-intensity exercise) in male
Sprague-Dawley rats restores the defective hypoglycemia
139 Male
Sprague-Dawley rats subjected to myocardial infarction (
140 nction compared with reconsolidation in male
Sprague-Dawley rats that had been trained to self-admini
141 study in chronically catheterized awake male
Sprague-Dawley rats that received an acute VMH microinje
142 A controlled laboratory study of 3y male
Sprague-Dawley rats that were randomized to 4 groups of
143 he pharmacokinetic studies were performed in
Sprague-Dawley rats to assess the feasibility of transde
144 ime course study was performed exposing male
Sprague-Dawley rats to CB11 via nose-only inhalation wit
145 Esophagojejunostomy was performed on
Sprague-Dawley rats to induce carcinogenesis, and LY3023
146 After exposing
Sprague-Dawley rats to intra-aortic porcine pancreatic e
147 Preliminary in vivo recording in
Sprague-Dawley rats to monitor GluA in the cortex during
148 We trained male
Sprague-Dawley rats to self-administer methamphetamine (
149 ways and their postsynaptic targets in adult
Sprague-Dawley rats to understand how these striatal cir
150 anastomosis rat and sham-operated, pair-fed
Sprague-Dawley rats treated with ammonia-lowering therap
151 next generation sequencing of the livers of
Sprague-Dawley rats treated with TAA at three doses (4.5
152 Sprague-Dawley rats under isoflurane anesthesia were exp
153 Fifteen
Sprague-Dawley rats underwent 2D phase-contrast MR imagi
154 Separate groups of intact male
Sprague-Dawley rats underwent a single episode of social
155 Sprague-Dawley rats underwent bilateral subdiaphragmatic
156 Pregnant
Sprague-Dawley rats underwent bilateral uterine artery l
157 To address this issue, male
Sprague-Dawley rats underwent cocaine self-administratio
158 Male
Sprague-Dawley rats underwent complete spinal cord trans
159 Adult male
Sprague-Dawley rats underwent diaphragm electromyography
160 Seven-day-old
Sprague-Dawley rats underwent left carotid ligation foll
161 Therefore, to address this question, male
Sprague-Dawley rats underwent surgeries for implantation
162 Adult male
Sprague-Dawley rats underwent UNx (n = 6) or sham (n = 6
163 n, the extent of covalent protein binding in
Sprague-Dawley rats upon exposure to 8:2 FTOH and the 6:
164 s after the initial ischemic injury, in male
Sprague-Dawley rats via intraspinal injections of chondr
165 The common peroneal nerve of
Sprague-Dawley rats was transected and repaired immediat
166 Sprague-Dawley rats weighing approximately 400 g receive
167 illation was electrically induced in 30 male
Sprague-Dawley rats weighing between 450 and 550 g.
168 The alterations in
Sprague-Dawley rats were accompanied by an increase in a
169 es of medial prefrontal cortex (mPFC) of six
Sprague-Dawley rats were acquired with a transmission el
170 Sprague-Dawley rats were administered a combination of a
171 lt (4-6 months) and aged (20-24 months) male
Sprague-Dawley rats were anesthetized with isoflurane, p
172 Forty 5-week-old male
Sprague-Dawley rats were assigned to two study groups af
173 Male neonatal
Sprague-Dawley rats were briefly exposed to 0.1 to 5,000
174 Female
Sprague-Dawley rats were concurrently exposed to vapor-p
175 Sprague-Dawley rats were distributed into three groups,
176 Male
Sprague-Dawley rats were divided into 3 groups, an ethan
177 Eighty-five adult
Sprague-Dawley rats were divided into 3 groups: control,
178 Thirty-two
Sprague-Dawley rats were divided into 4 groups based on
179 Sprague-Dawley rats were divided into experimental (E),
180 Using a validated ischemic wound model,
Sprague-Dawley rats were divided into four groups for da
181 Twenty-four male
Sprague-Dawley rats were divided into three groups (cont
182 Ten-week old female
Sprague-Dawley rats were divided into three groups (n =
183 Male
Sprague-Dawley rats were dosed orally with 3 mg/kg of on
184 Sprague-Dawley rats were exposed (parental, F1, and F2 g
185 Male
Sprague-Dawley rats were exposed nose-only to citrate-bu
186 Sprague-Dawley rats were fed a HFD (45% fat) or a matche
187 Male
Sprague-Dawley rats were fed either a HFD or low-fat die
188 institutional animal care committee, 60 male
Sprague-Dawley rats were fed either a standard chow for
189 Male
Sprague-Dawley rats were fed isocaloric amounts of an Et
190 Adult, male
Sprague-Dawley rats were given either lipopolysaccharide
191 Sprague-Dawley rats were given feed containing dioxin-li
192 Adult male
Sprague-Dawley rats were implanted with electrodes targe
193 Sprague-Dawley rats were intraperitoneally given dimethy
194 In vivo small-animal PET studies in
Sprague-Dawley rats were performed at baseline and after
195 Sprague-Dawley rats were presented randomly with mild st
196 Male
Sprague-Dawley rats were pretreated with octreotide or o
197 Twenty-four
Sprague-Dawley rats were randomized into controls, mild,
198 Thus, adult
Sprague-Dawley rats were randomized into four groups: 1)
199 Male
Sprague-Dawley rats were randomized into two groups and
200 Forty
Sprague-Dawley rats were randomized to cecal ligation an
201 One week after MI, adult male
Sprague-Dawley rats were randomized to treatment for 4 w
202 Fifty-six
Sprague-Dawley rats were randomly assigned to two groups
203 One hundred and twelve male
Sprague-Dawley rats were randomly divided into 4 groups:
204 Forty
Sprague-Dawley rats were randomly divided into four grou
205 Male adult
Sprague-Dawley rats were rendered insulin-resistant by f
206 BMSCs isolated from femur and tibia of
Sprague-Dawley rats were seeded onto 3 types of titanium
207 Eight groups (n=6) of normal
Sprague-Dawley rats were studied: four groups received t
208 Sprague-Dawley rats were subjected to cold-water swim st
209 Male
Sprague-Dawley rats were subjected to middle cerebral ar
210 Seven-day-old
Sprague-Dawley rats were subjected to TBI using the cont
211 Male
Sprague-Dawley rats were trained on an auditory fear con
212 To study cognitive performance, male
Sprague-Dawley rats were trained on an object-discrimina
213 Groups of male and female adult
Sprague-Dawley rats were trained on either the standard
214 Eight male
Sprague-Dawley rats were trained to discriminate 10.0 mg
215 Male
Sprague-Dawley rats were treated with CsA (n = 8, 20 mg/
216 Sprague-Dawley rats were treated with four injections of
217 Sprague-Dawley rats were untreated (control), laparatomi
218 Thirty-six
Sprague-Dawley rats were used (n = 6/group/time point).
219 Sprague-Dawley rats were used for cardiomyocyte isolatio
220 Male
Sprague-Dawley rats were used to assess dosimetry, antag
221 BALB/cJ mice and
Sprague-Dawley rats were used to evaluate the effects du
222 Thirty-six
Sprague-Dawley rats were used.
223 ds were generated on the dorsal skin of male
Sprague-Dawley rats with a 10-mm sterile punch.
224 ) into the dorsal medial NTS (dmNTS) of male
Sprague-Dawley rats with coronary artery ligation-induce
225 Four male
Sprague-Dawley rats with different blood glucose concent
226 ation in sympathetic neurons from adult male
Sprague-Dawley rats with electrophysiological and optica
227 Adult male
Sprague-Dawley rats with hyperglycemia were divided into
228 t maternal inflammation (modeled by pregnant
Sprague-Dawley rats with lipopolysaccharides (LPS) chall
229 ry-olfactory artery (ACA/OA) bifurcations in
Sprague-Dawley rats with or without ECFCs transfusion.
230 In this study, intrarectal inoculations of
Sprague-Dawley rats with predatory bacteria were perform
231 IUGR (bilateral uterine artery ligation) in
Sprague-Dawley rats with sham controls was used.
232 cemic (10-15 mg/dL) clamps were performed in
Sprague-Dawley rats with simultaneous electrocardiogram
233 odium azide, 37 degrees C) and in vivo (male
Sprague-Dawley rats).
234 After gingival resection in 120
Sprague-Dawley rats, 2 microg rhTSG-6 in 5-microL phosph
235 Sprague-Dawley rats, SU5416/hypoxia-treated
Sprague-Dawley rats, and SU5416/hypoxia-treated C57BL/6
236 Male
Sprague-Dawley rats, Balb/c mice, and C57Bl6/J mice.
237 Sprague-Dawley rats, implanted for EEG/EMG recording, we
238 We isolated EGCs from male
Sprague-Dawley rats, intestinal resections of 6 patients
239 neurons from the glabrous skin of adult male
Sprague-Dawley rats, NCX activity, as assessed with fura
240 C57Bl/6J mice; juvenile
Sprague-Dawley rats, primary human neutrophils.
241 ted and high-fat, high-carbohydrate diet-fed
Sprague-Dawley rats, respectively, using intravenous adm
242 PH was studied in monocrotaline-treated
Sprague-Dawley rats, SU5416/hypoxia-treated Sprague-Dawl
243 l function for both strains; however, in the
Sprague-Dawley rats, VWR exacerbated falls in GFR and RP
244 In
Sprague-Dawley rats, VWR reduced eNOS and EC SOD, but in
245 Using female
Sprague-Dawley rats, we carried out two rounds of experi
246 In male
Sprague-Dawley rats, we performed bile diversions from t
247 In adult
Sprague-Dawley rats, we used intracranial self-stimulati
248 C450Y CCT4 was identified in a stock of
Sprague-Dawley rats, whereas H147R CCT5 was found in a h
249 frying under vacuum (9.9kPa), after feeding
Sprague-Dawley rats, while also understanding its relati
250 cision in the anterior edentulous maxilla of
Sprague-Dawley rats.
251 One dose of amphetamine was injected into
Sprague-Dawley rats.
252 d high CNS permeability in C57Bl/6s mice and
Sprague-Dawley rats.
253 e superior colliculus and globus pallidus of
Sprague-Dawley rats.
254 owing its intravenous administration to male
Sprague-Dawley rats.
255 growth, and phenotype of OMECs cultured from
Sprague-Dawley rats.
256 both autistic-like behavior and epilepsy in
Sprague-Dawley rats.
257 nds were created on the palatal mucosa of 54
Sprague-Dawley rats.
258 entration and AQP2 protein in the kidneys of
Sprague-Dawley rats.
259 y, with greater effects in BN versus control
Sprague-Dawley rats.
260 T ) were recorded in 28 conscious adult male
Sprague-Dawley rats.
261 signaling and hedonic expression in 21 male
Sprague-Dawley rats.
262 in O/W emulsions after oral gastric feeding
Sprague-Dawley rats.
263 AL did not affect CO2 sensitivity in control
Sprague-Dawley rats.
264 enovirus-mediated overexpression of sFlt1 in
Sprague-Dawley rats.
265 was induced by cortical contusion injury in
Sprague-Dawley rats.
266 ar changes were seen after 6 weeks of VWR in
Sprague-Dawley rats.
267 of this study was to test this hypothesis in
Sprague-Dawley rats.
268 Lewis rats but were significantly altered in
Sprague-Dawley rats.
269 lorinated, and provided as drinking water to
Sprague-Dawley rats.
270 Agents were administered in diets to female
Sprague-Dawley rats.
271 GDER was induced in 6- to 8-week-old male
Sprague-Dawley rats.
272 m DORA-22, an analog of the DORA MK-6096, in
Sprague-Dawley rats.
273 y sustained testosterone suppression in male
Sprague-Dawley rats.
274 al day 5 (P5), 14 (P14), and adults (P72) in
Sprague-Dawley rats.
275 atial memory for a well-learned task in male
Sprague-Dawley rats.
276 behaviors and drug consumption compared with
Sprague-Dawley rats.
277 vivo in DMBA induced mammary tumor in female
Sprague-Dawley rats.
278 Male
Sprague-Dawley rats.
279 ed liver samples was examined using eighteen
Sprague-Dawley rats.
280 cardium 1 week after ischemia-reperfusion in
Sprague-Dawley rats.
281 olliphor P 407 gels (KP 407) intranasally in
Sprague-Dawley rats.
282 bicin were conducted in male BALB/c mice and
Sprague-Dawley rats.
283 adult-born hippocampal neurons in adult male
Sprague-Dawley rats.
284 ous pancreatic lesions in three rat strains (
Sprague-Dawley [
S-D] rats, Zucker diabetic fatty [ZDF] r
285 petence by injection into Dark Agouti (DA) X
Sprague Dawley (
SD) blastocysts.
286 bular functions in anesthetized non-diabetic
Sprague Dawley (
SD) rats and 5/6 nephrectomized (Nx) SD
287 120 male
Sprague Dawley (
SD) rats were treated with lithium chlor
288 pendence and social isolation in non-anxious
Sprague Dawley (
SD) rats, and a depression model, Wistar
289 dian of Foot-Shaoyang (GMFS) in healthy male
Sprague Dawley (
SD) rats.
290 l aspiration (OPA), and three labs evaluated
Sprague-Dawley (
SD) or Fisher 344 (F344) rats following
291 ned the distribution of T-2 toxin and DON in
Sprague-Dawley (
SD) rats after a single dose exposure.
292 Wistar and
Sprague-Dawley (
SD) rats received 1 of 3 diets: control
293 Compared with
Sprague-Dawley (
SD) rats, Brown-Norway (BN) rats exhibit
294 mean arterial pressure (MAP) in young female
Sprague-Dawley (
SD) rats, however, the underlying mechan
295 trophysiological and behavioral responses in
Sprague-Dawley (
SD) rats.
296 slices of three other rat strains, including
Sprague-Dawley (
SD), were unaffected.
297 Normal [
Sprague-Dawley (
SD)] and metabolic syndrome [James C. Ru
298 Here we demonstrate that the female
Sprague-Dawley SDN-POA volume increased from weaning to
299 isted of Zucker lean (ZL; n = 13) and normal
Sprague-Dawley (
SprD; n = 30) rats.
300 percent body fat) in the Long-Evans, but not
Sprague-Dawley,
strains.