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 Spontaneously-Hypertensive-Heart-Fail
4 Timed-pregnant
Sprague-Dawley dams underwent bilateral uterine artery l
5 formed in streptozotocin-induced and control
Sprague-Dawley female rats with DM (type 1 [t1DM]) using
6 conducted on 56 eyes of 28 healthy new born
Sprague Dawley male albino rat.
7 Here, we characterized, in freely behaving
Sprague Dawley male rats, the MD neural activity around
8 nyl and diluted Ensure((R)) reinforcement in
Sprague-Dawley male and female rats.
9 aluate short-term and long-term SRM in adult
Sprague-Dawley male rats (n = 38).
10 Adolescent
Sprague-Dawley male rats (PD30-43) were given 10 intermi
11 Colitis was induced in 20 five-week-old
Sprague-Dawley male rats by weekly rectal injections of
12 We sought to examine whether exposure of
Sprague-Dawley male rats for two weeks to different shap
13 al rats without and after VA supplementation.
Sprague-Dawley neonatal rats (n = 104) were nursed by mo
14 In auditory sensory hair cells of rats (
Sprague Dawley)
of either sex, PIP2 localizes within ste
15 zed NOD-scid IL2Rgamma(null) (NSG) mouse and
Sprague-Dawley-
Rag2(tm2hera) Il2rgamma(tm1hera) (SRG) ra
16 oltage oscillations at 100 Hz in dissociated
Sprague Dawley rat hippocampal neurons in single trial r
17 ding on receptor movement and positioning in
Sprague Dawley rat hippocampal neurons.
18 In the current study, changes in male
Sprague Dawley rat liver caused by dietary treatment wit
19 Using a male
Sprague Dawley rat model of PNS-CNS injury, we show that
20 Sprague Dawley rat pups underwent 14 days of postnatal m
21 We report here that in
Sprague Dawley rat, the MOP receptor-selective agonist D
22 Female
Sprague-Dawley rat bladders were partially obstructed (P
23 The RHV
Sprague-Dawley rat challenge model enables comparative t
24 ution data and blood clearance kinetics from
Sprague-Dawley rat data.
25 apping was performed in Langendorff-perfused
Sprague-Dawley rat hearts (n=18), where novel algorithms
26 Langendorff-perfused adult
Sprague-Dawley rat hearts were subjected to acute region
27 paminergic neurons in the SNpc of Wistar vs.
Sprague-Dawley rat strains.
28 Sprague Dawley rats (2 months old) were commercially acq
29 Male
Sprague Dawley rats (2-mo-old) were untreated (Con) or g
30 cordings of phrenic nerve activity in female
Sprague Dawley rats (3-4 months) revealed a direct corre
31 Male
Sprague Dawley rats (350-450 g) were chronically implant
32 Male
Sprague Dawley rats (N = 125) were trained to self-admin
33 Metabolic changes in fed and fasted
Sprague Dawley rats (n = 36) were studied at 9.4 T after
34 Male
Sprague Dawley rats (n = 62) were trained to self-admini
35 Female
Sprague Dawley rats (N = 64) were evaluated for skilled
36 s were administered in an i.v. bolus to male
Sprague Dawley rats after starting a s.c. infusion of ME
37 d by anti-OPH IgG and cytokines formation in
Sprague Dawley rats and Balb/c mice, respectively.
38 s cocaine self-administration in 10-week-old
Sprague Dawley rats and C57BL/6 mice.
39 We injected streptozotocin in male
Sprague Dawley rats and treated them with a neutralizing
40 sensitization to cocaine was established in
Sprague Dawley rats and was measured by locomotion and b
41 omics data were collected from the livers of
Sprague Dawley rats at 4 or 14 days of being subjected t
42 Diabetes was surgically induced in male
Sprague Dawley rats by 90% pancreatectomy (Px).
43 cephalographic data gathered from adult male
Sprague Dawley rats during the aforementioned experiment
44 /-), and Tlr2(-/-)/Tlr4(-/-) mice as well as
Sprague Dawley rats for all in vitro studies.
45 Pharmacokinetic studies in male
Sprague Dawley rats highlighted a good exposure after or
46 prelimbic region of the mPFC of adult, male,
Sprague Dawley rats impaired the acquisition and reconso
47 We provided
Sprague Dawley rats of renal calcium oxalate stones with
48 ic reduced uterine perfusion pressure (RUPP)
Sprague Dawley rats on gestational days (GD) 14, 16, and
49 Sprague Dawley rats received a lethal dose of AFB(1) (0.
50 Sprague Dawley rats received a spinal cord transection a
51 GLP1R signaling within the alBST, adult male
Sprague Dawley rats received bilateral alBST-targeted in
52 n maxillary molars was examined in 40 female
Sprague Dawley rats received zoledronic acid (7.5 ug/kg)
53 Male
Sprague Dawley rats self-administered cocaine during dai
54 we show that in conscious, unrestrained male
Sprague Dawley rats the infusion of insulin into the thi
55 ressure and heart rate were recorded in male
Sprague Dawley rats throughout this study.
56 this, we used fasted or 4 hour postprandial
Sprague Dawley rats to analyze ENaC expression and activ
57 ced by 2,4,6-trinitrobenzenesulfonic acid in
Sprague Dawley rats to identify inflammation-induced cha
58 we used activity-guided optogenetics in male
Sprague Dawley rats to silence IL pyramidal neurons opti
59 udal extent of the ventrolateral medulla, in
Sprague Dawley rats treated with hydralazine or saline.
60 tations of CeA 5-HT signaling in adult, male
Sprague Dawley rats using an established model of alcoho
61 Sprague Dawley rats were allowed free access to a palata
62 Seventy
Sprague Dawley rats were divided into control, experimen
63 inistering and 36 cocaine-administering male
Sprague Dawley rats were employed).
64 Male
Sprague Dawley rats were exposed to BOP frontally and la
65 For this,
Sprague Dawley rats were given access either to 1 hour (
66 Following acquisition, male and female
Sprague Dawley rats were given either short access (thre
67 Male
Sprague Dawley rats were implanted with a cannula in the
68 Young, adult male
Sprague Dawley rats were implanted with bilateral dorsal
69 Male
Sprague Dawley rats were infused with angiotensin II (An
70 Male
Sprague Dawley rats were injected with PBS or G-CSF duri
71 Thoracic aorta rings from
Sprague Dawley rats were mounted in isolated tissue bath
72 Male
Sprague Dawley rats were socially housed and underwent l
73 Forty mature female
Sprague Dawley rats were subjected to ligature-induced e
74 RMTg in punished reward seeking, adult male
Sprague Dawley rats were tested in several cost-benefit
75 Male adult
Sprague Dawley rats were trained on a water maze spatial
76 lth in two generations of offspring, GC-eGFP
Sprague Dawley rats were weaned onto HFD (45% fat) or Co
77 In
Sprague Dawley rats with Cre-mediated expression of the
78 nt improvement in the cardiac output in male
Sprague Dawley rats with no significant changes in eithe
79 ibrillary acidic protein promoter in 62 male
Sprague Dawley rats, 4 dominant-negative soluble N-ethyl
80 ein 1) is administered at the spinal cord of
Sprague Dawley rats, priming is detected at the peripher
81 We studied, in male
Sprague Dawley rats, the role of the cognate hyaluronan
82 ng 40 seconds on the right cornea of 36 male
Sprague Dawley rats, under general anesthesia.
83 Using in vivo electrophysiology in male
Sprague Dawley rats, we demonstrate that intra-vHipp THC
84 Using male
Sprague Dawley rats, we examined if PACAP (.25-1.0 micro
85 Here, after research involving
Sprague Dawley rats, we reported that spinal nerve ligat
86 learning and retention compared with outbred
Sprague Dawley rats, whereas bLRs show reduced extinctio
87 and stress-response signaling genes in male
Sprague Dawley rats.
88 ular, and imaging approaches in adult female
Sprague Dawley rats.
89 rotid artery occlusion (BCCAO) in adult male
Sprague Dawley rats.
90 capable, uncontrollable tail shocks (ISs) in
Sprague Dawley rats.
91 uced seizures in urethane anesthetized, male
Sprague Dawley rats.
92 vector and to knock down VAN GLP-1Rs in male
Sprague Dawley rats.
93 ive taste memory on taste preference in male
Sprague Dawley rats.
94 endritic release of CCK in the brain in male
Sprague Dawley rats.
95 gy in the basolateral amygdala (BLA) in male
Sprague Dawley rats.
96 pmental age and exposure to NEC stressors in
Sprague Dawley rats.
97 ion of OVLT neurons, was used in adult, male
Sprague Dawley rats.
98 he nucleus accumbens shell (AcbSh) in female
Sprague Dawley rats.
99 6 intracranial glioma tumor model in 37 male
Sprague Dawley rats.
100 ting to create a conditional GR knockdown in
Sprague Dawley rats.
101 Anesthetized, ventilated
Sprague-Dawley rats (280 +/- 30 g) and Vietnamese minipi
102 Using
Sprague-Dawley rats (350-450 g; n = 61) and the recently
103 Materials and Methods Seventy male
Sprague-Dawley rats (4 weeks old) received intraperitone
104 Pregnant
Sprague-Dawley rats (5-month-old) were exposed to high d
105 ted 4 different hemorrhage models using male
Sprague-Dawley rats (6 rats/model), aged 10 to 14 weeks
106 rtery ligation surgery was performed in male
Sprague-Dawley rats (n = 13) followed by dual MEMRI and
107 For four weeks, healthy
Sprague-Dawley rats (n = 30) were fed one of three diets
108 Sprague-Dawley rats (n = 32) were subjected to sham or v
109 Male
Sprague-Dawley rats (n = 45; age, 12 weeks) were inocula
110 Sprague-Dawley rats (n = 7) underwent ferric chloride ap
111 Male
Sprague-Dawley rats (n=31) were anesthetized and treated
112 ction, and colon mucosal environment in male
Sprague-Dawley rats (n=8/group).
113 Primary tenocytes from Achilles tendon of
Sprague-Dawley rats 1 week after collagenase injection w
114 We fed male
Sprague-Dawley rats a control diet, MCD diet, or betaine
115 heart compared to a control group (pregnant
Sprague-Dawley rats administered vehicle).
116 ed Geniposide-induced hepatic injury in male
Sprague-Dawley rats after 3-day intragastric administrat
117 We conducted a 9-month study in
Sprague-Dawley rats after 45 minutes of bilateral renal
118 Thirty-two healthy male
Sprague-Dawley rats and 47 human adults underwent threat
119 Blood-brain-barrier studies in
Sprague-Dawley rats and CD-1 mice indicated that the maj
120 We also performed experiments with male
Sprague-Dawley rats and CPEB-deficient mice (C57BL6 or m
121 is and/or beta-AR levels in diabetic hearts,
Sprague-Dawley rats and miR-133a transgenic (miR-133aTg)
122 rom freshly excised lung, obtained from both
Sprague-Dawley rats and New Zealand White rabbits.
123 Adult male
Sprague-Dawley rats and pulmonary epithelial cells.
124 avioral sex differences had been reported in
Sprague-Dawley rats and repeated some of the above measu
125 cardial left ventricular free walls of adult
Sprague-Dawley rats and then treated with collagenase to
126 Normal
Sprague-Dawley rats as well as RH or streptozotocin (STZ
127 In
Sprague-Dawley rats at 10 mg/kg, compared to o(LA)(8)-PT
128 A patients post-resuscitation, and from male
Sprague-Dawley rats at baseline and after 20 min CA foll
129 g to AKAPs in the nucleus accumbens shell of
Sprague-Dawley rats attenuates reinstatement induced by
130 Renal failure was induced in
Sprague-Dawley rats by a high adenine diet supplemented
131 AAAs were generated in
Sprague-Dawley rats by exposing the infrarenal, intralum
132 8)F- AMC20: was evaluated in brain slices of
Sprague-Dawley rats by in vitro autoradiography and in l
133 TPase (RhoAV14) in the AH outflow pathway in
Sprague-Dawley rats by using lentiviral vector-based gen
134 tic dysfunction and hypertension in pregnant
Sprague-Dawley rats challenged with lipopolysaccharide (
135 Male
Sprague-Dawley rats consumed caffeine (0.3 g/l) or water
136 ed behaviors occurred in both Long-Evans and
Sprague-Dawley rats despite the fact that the 6-week HFD
137 Studies were performed on adult, male,
Sprague-Dawley rats exposed to either short-term (ST; 10
138 B) and examined the pharmacokinetics (PK) in
Sprague-Dawley rats for 3 months in comparison to CAB.
139 tumor-bearing aged, female, retired breeder
Sprague-Dawley rats for PET imaging.
140 Forty-eight male and female
Sprague-Dawley rats had lumbar IVD puncture or sham surg
141 To examine this, we profiled cohorts of
Sprague-Dawley rats in a test of motivation to consume s
142 Male
Sprague-Dawley rats received bilateral infusions of a Cr
143 Seventy-two
Sprague-Dawley rats received daily 0, 10 (low-dose [LD])
144 Nine immunocompetent
Sprague-Dawley rats received intravenous injection of fe
145 Male
Sprague-Dawley rats received monocrotaline (MCT; 60 mg/k
146 Male
Sprague-Dawley rats received multiple intracutaneous inj
147 To test this hypothesis, adult male
Sprague-Dawley rats received sham surgery or moderate pa
148 This study used male
Sprague-Dawley rats responding under a progressive ratio
149 le burst of high-intensity exercise) in male
Sprague-Dawley rats restores the defective hypoglycemia
150 In vivo experiments in anaesthetized
Sprague-Dawley rats showed that pregnant animals (gestat
151 aintained intravenous self-administration in
Sprague-Dawley rats similar to cocaine.
152 Male
Sprague-Dawley rats subjected to myocardial infarction (
153 nction compared with reconsolidation in male
Sprague-Dawley rats that had been trained to self-admini
154 A controlled laboratory study of 3y male
Sprague-Dawley rats that were randomized to 4 groups of
155 Esophagojejunostomy was performed on
Sprague-Dawley rats to induce carcinogenesis, and LY3023
156 After exposing
Sprague-Dawley rats to intra-aortic porcine pancreatic e
157 We trained male
Sprague-Dawley rats to self-administer methamphetamine (
158 ype 1 diabetes (T1D) was established in male
Sprague-Dawley rats to study the efficacy and safety of
159 ntal protocols were performed in nondiabetic
Sprague-Dawley rats to test the SNS with 1) adrenal deme
160 Using adult male
Sprague-Dawley rats trained to self-administer intraveno
161 In
Sprague-Dawley rats treated orally with DEP from birth t
162 anastomosis rat and sham-operated, pair-fed
Sprague-Dawley rats treated with ammonia-lowering therap
163 Materials and Methods The cerebral cortex in
Sprague-Dawley rats treated with gadopentetate dimeglumi
164 next generation sequencing of the livers of
Sprague-Dawley rats treated with TAA at three doses (4.5
165 Fifteen
Sprague-Dawley rats underwent 2D phase-contrast MR imagi
166 Pregnant
Sprague-Dawley rats underwent bilateral uterine artery l
167 To address this issue, male
Sprague-Dawley rats underwent cocaine self-administratio
168 Male
Sprague-Dawley rats underwent complete spinal cord trans
169 Adult male
Sprague-Dawley rats underwent diaphragm electromyography
170 To investigate this issue, male
Sprague-Dawley rats underwent inhibitory avoidance train
171 To address this, male and female
Sprague-Dawley rats underwent spatial or cued-response B
172 Therefore, to address this question, male
Sprague-Dawley rats underwent surgeries for implantation
173 Sprague-Dawley rats underwent surgery to induce volume o
174 Adult male
Sprague-Dawley rats underwent UNx (n = 6) or sham (n = 6
175 sk/reward decision-making in male and female
Sprague-Dawley rats using a probabilistic discounting ta
176 chotic drug administration on SV2A levels in
Sprague-Dawley rats using western blotting, [(3)H]UCB-J
177 Induction of diabetes in
Sprague-Dawley rats via a single dose of STZ (70 mg/kg)
178 s after the initial ischemic injury, in male
Sprague-Dawley rats via intraspinal injections of chondr
179 The common peroneal nerve of
Sprague-Dawley rats was transected and repaired immediat
180 Sprague-Dawley rats weighing approximately 400 g receive
181 es of medial prefrontal cortex (mPFC) of six
Sprague-Dawley rats were acquired with a transmission el
182 Sprague-Dawley rats were administered a combination of a
183 Forty 5-week-old male
Sprague-Dawley rats were assigned to two study groups af
184 Male neonatal
Sprague-Dawley rats were briefly exposed to 0.1 to 5,000
185 Female
Sprague-Dawley rats were concurrently exposed to vapor-p
186 Sprague-Dawley rats were distributed into three groups,
187 Male
Sprague-Dawley rats were divided into 3 groups, an ethan
188 Eighty-five adult
Sprague-Dawley rats were divided into 3 groups: control,
189 Thirty-two
Sprague-Dawley rats were divided into 4 groups based on
190 Here, adult
Sprague-Dawley rats were divided into acute and chronic
191 Sprague-Dawley rats were divided into experimental (E),
192 Twenty-three
Sprague-Dawley rats were divided into three experimental
193 Eighteen male
Sprague-Dawley rats were divided into three groups (6 ra
194 Twenty-four male
Sprague-Dawley rats were divided into three groups (cont
195 Ten-week old female
Sprague-Dawley rats were divided into three groups (n =
196 Sprague-Dawley rats were divided into three treatment gr
197 Male
Sprague-Dawley rats were dosed orally with 3 mg/kg of on
198 Male,
Sprague-Dawley rats were employed in this study.
199 Sprague-Dawley rats were exposed (parental, F1, and F2 g
200 Female
Sprague-Dawley rats were exposed either to SAM or filter
201 Male
Sprague-Dawley rats were exposed nose-only to citrate-bu
202 Sprague-Dawley rats were exposed to 5 doses of BPA [0, 2
203 Sprague-Dawley rats were exposed to BPA, vehicle, or pos
204 Adult, male
Sprague-Dawley rats were exposed to nicotine (0.2 or 0.4
205 The maxillary first molars of 30 male
Sprague-Dawley rats were extracted, and after healing, b
206 The maxillary right first molars of
Sprague-Dawley rats were extracted, and gelatin scaffold
207 Sprague-Dawley rats were fed a HFD (45% fat) or a matche
208 Male
Sprague-Dawley rats were fed either a HFD or low-fat die
209 institutional animal care committee, 60 male
Sprague-Dawley rats were fed either a standard chow for
210 Male
Sprague-Dawley rats were fed isocaloric amounts of an Et
211 Male
Sprague-Dawley rats were fed standard rat chow containin
212 ugh) were created in mandibular angles of 24
Sprague-Dawley rats were filled with DBBM Control, DBBM
213 Adult, male
Sprague-Dawley rats were given either lipopolysaccharide
214 Male
Sprague-Dawley rats were injected with streptozotocin (3
215 Papillary muscles from male
Sprague-Dawley rats were mounted onto an organ bath perf
216 In vivo small-animal PET studies in
Sprague-Dawley rats were performed at baseline and after
217 Male
Sprague-Dawley rats were pretreated with octreotide or o
218 teen days prior to treatment with MDMA, male
Sprague-Dawley rats were provided water or water treated
219 Twenty-four
Sprague-Dawley rats were randomized into controls, mild,
220 Thus, adult
Sprague-Dawley rats were randomized into four groups: 1)
221 Male
Sprague-Dawley rats were randomized into two groups and
222 Forty
Sprague-Dawley rats were randomized to cecal ligation an
223 One week after MI, adult male
Sprague-Dawley rats were randomized to treatment for 4 w
224 Here, 24 male
Sprague-Dawley rats were randomly divided into four grou
225 Forty
Sprague-Dawley rats were randomly divided into four grou
226 Twenty-four male
Sprague-Dawley rats were randomly divided into three gro
227 Male adult
Sprague-Dawley rats were rendered insulin-resistant by f
228 BMSCs isolated from femur and tibia of
Sprague-Dawley rats were seeded onto 3 types of titanium
229 155 male
Sprague-Dawley rats were subjected to a combination of f
230 To study cognitive performance, male
Sprague-Dawley rats were trained on an object-discrimina
231 Male
Sprague-Dawley rats were trained to nose-poke for discre
232 Male,
Sprague-Dawley rats were trained to self-administer coca
233 Male
Sprague-Dawley rats were treated with CsA (n = 8, 20 mg/
234 Thirty-six
Sprague-Dawley rats were used (n = 6/group/time point).
235 Sprague-Dawley rats were used for cardiomyocyte isolatio
236 Sprague-Dawley rats were used in asphyxial cardiac arres
237 Male
Sprague-Dawley rats were used to assess dosimetry, antag
238 uite of in vitro transactivation assays, and
Sprague-Dawley rats were used to assess maternal, fetal,
239 BALB/cJ mice and
Sprague-Dawley rats were used to evaluate the effects du
240 ds were generated on the dorsal skin of male
Sprague-Dawley rats with a 10-mm sterile punch.
241 ) into the dorsal medial NTS (dmNTS) of male
Sprague-Dawley rats with coronary artery ligation-induce
242 Four male
Sprague-Dawley rats with different blood glucose concent
243 ation in sympathetic neurons from adult male
Sprague-Dawley rats with electrophysiological and optica
244 Male
Sprague-Dawley rats with jugular-vein catheterization we
245 t maternal inflammation (modeled by pregnant
Sprague-Dawley rats with lipopolysaccharides (LPS) chall
246 ry-olfactory artery (ACA/OA) bifurcations in
Sprague-Dawley rats with or without ECFCs transfusion.
247 In this study, intrarectal inoculations of
Sprague-Dawley rats with predatory bacteria were perform
248 al preoptic nucleus (VLPO) is lesioned (male
Sprague-Dawley rats).
249 ns, 12 rhesus monkeys, 20 Yorkshire pigs, 20
Sprague-Dawley rats, 10 New Zealand White rabbits and 14
250 After gingival resection in 120
Sprague-Dawley rats, 2 microg rhTSG-6 in 5-microL phosph
251 Sprague-Dawley rats, SU5416/hypoxia-treated
Sprague-Dawley rats, and SU5416/hypoxia-treated C57BL/6
252 Sprague-Dawley rats, implanted for EEG/EMG recording, we
253 We isolated EGCs from male
Sprague-Dawley rats, intestinal resections of 6 patients
254 S5B from RHV (ChAd-NS) was used to vaccinate
Sprague-Dawley rats, resulting in high levels of cluster
255 PH was studied in monocrotaline-treated
Sprague-Dawley rats, SU5416/hypoxia-treated Sprague-Dawl
256 Using female
Sprague-Dawley rats, we carried out two rounds of experi
257 In male
Sprague-Dawley rats, we performed bile diversions from t
258 We investigated, in male
Sprague-Dawley rats, whether BLA activity enables prelim
259 frying under vacuum (9.9kPa), after feeding
Sprague-Dawley rats, while also understanding its relati
260 growth, and phenotype of OMECs cultured from
Sprague-Dawley rats.
261 of this study was to test this hypothesis in
Sprague-Dawley rats.
262 vivo in DMBA induced mammary tumor in female
Sprague-Dawley rats.
263 Male
Sprague-Dawley rats.
264 ed liver samples was examined using eighteen
Sprague-Dawley rats.
265 cardium 1 week after ischemia-reperfusion in
Sprague-Dawley rats.
266 olliphor P 407 gels (KP 407) intranasally in
Sprague-Dawley rats.
267 bicin were conducted in male BALB/c mice and
Sprague-Dawley rats.
268 adult-born hippocampal neurons in adult male
Sprague-Dawley rats.
269 cision in the anterior edentulous maxilla of
Sprague-Dawley rats.
270 One dose of amphetamine was injected into
Sprague-Dawley rats.
271 d high CNS permeability in C57Bl/6s mice and
Sprague-Dawley rats.
272 e superior colliculus and globus pallidus of
Sprague-Dawley rats.
273 owing its intravenous administration to male
Sprague-Dawley rats.
274 both autistic-like behavior and epilepsy in
Sprague-Dawley rats.
275 nds were created on the palatal mucosa of 54
Sprague-Dawley rats.
276 entration and AQP2 protein in the kidneys of
Sprague-Dawley rats.
277 y, with greater effects in BN versus control
Sprague-Dawley rats.
278 T ) were recorded in 28 conscious adult male
Sprague-Dawley rats.
279 signaling and hedonic expression in 21 male
Sprague-Dawley rats.
280 in O/W emulsions after oral gastric feeding
Sprague-Dawley rats.
281 AL did not affect CO2 sensitivity in control
Sprague-Dawley rats.
282 es and brought forward for testing in female
Sprague-Dawley rats.
283 % in both humans without diabetes and normal
Sprague-Dawley rats.
284 -maze spatial reversal learning task in male
Sprague-Dawley rats.
285 low-twitch soleus (SOL) muscles derived from
Sprague-Dawley rats?
286 of P. gingivalis to produce ISAR and FGR in
Sprague Dawley (
SD) and Wistar (WIS) rats.
287 bular functions in anesthetized non-diabetic
Sprague Dawley (
SD) rats and 5/6 nephrectomized (Nx) SD
288 We knocked out Rag1, Rag2, and Il2rg in
Sprague Dawley (
SD) rats by clustered regularly interspa
289 pendence and social isolation in non-anxious
Sprague Dawley (
SD) rats, and a depression model, Wistar
290 dian of Foot-Shaoyang (GMFS) in healthy male
Sprague Dawley (
SD) rats.
291 glucose metabolism on adult female and male
Sprague Dawley (
SD) rats.
292 opathological conditions: C57BL/6 J mice and
Sprague Dawley (
SD) rats.
293 ned the distribution of T-2 toxin and DON in
Sprague-Dawley (
SD) rats after a single dose exposure.
294 To generate HFrEF,
Sprague-Dawley (
SD) rats underwent permanent left anteri
295 mean arterial pressure (MAP) in young female
Sprague-Dawley (
SD) rats, however, the underlying mechan
296 trophysiological and behavioral responses in
Sprague-Dawley (
SD) rats.
297 Three strains [
Sprague-Dawley (
SD), Fischer 344 (F344), and Brown-Norwa
298 isted of Zucker lean (ZL; n = 13) and normal
Sprague-Dawley (
SprD; n = 30) rats.
299 percent body fat) in the Long-Evans, but not
Sprague-Dawley,
strains.
300 Male rats (
Sprague-Dawley)
with histologically confirmed neurotoxin