1 iting oxygen loading, synthetic reject water
was fed (
0.75 g-N/L .
2 During the pulse, rats (n = 5)
were fed (
13)C6-labeled lysine ("heavy") feed for 23 day
3 ld-type and Nlrp3 knockout (Nlrp3(-/-)) mice
were fed 3,5-diethoxycarbonyl-1,4-dihydrocollidine (DDC;
4 The rats in the experimental group
were fed 30 mg/kg CsA daily for 4 weeks, whereas the con
5 Mice
were fed 5 or 10 mg/kg of an inhibitor of glycosphingoli
6 pose tissue to reduce obesity even when mice
are fed a high-fat diet.
7 weight gain is due to hypophagia after mice
are fed a highly palatable diet rich in fats and sugar b
8 s severely diminished in obese mice that had
been fed a high-fat/sucrose diet, and this effect could
9 s, was significantly increased when rats had
been fed a high-salt diet for 7 days (n = 6 or 9, p < 0.
10 After
being fed a high-fat diet (HFD) for 2 weeks, rats were f
11 One group
was fed a basal diet as a control and the diets of the o
12 ch subject underwent a 24-hour fast and then
was fed a fixed-calorie meal.
13 ng diet-induced obesity (DIO), in which they
were fed a "Western" diet.
14 Mosquitoes
were fed a blood meal supplemented with [1,2-(13)C2]gluc
15 At weaning, male offspring
were fed a C diet.
16 Streptozotocin-treated male Wistar rats
were fed a cholesterol-supplemented diet and gavaged dai
17 Thus, mice
were fed a choline-deficient-amino-acid-defined (CDAA) d
18 pring, 6-week-old C57BL/6 virgin female mice
were fed a chow (21%) or high-fat (60%) diet and divided
19 C57BL/6 female mice
were fed a chow (21%) or high-fat (60%) diet and further
20 -);Gsk3a(+/-), and Ldlr(-/-);Gsk3a(-/-) mice
were fed a chow diet or a high-fat diet for 10 weeks and
21 ce with the full-length Il6 gene (controls),
were fed a chow or a high-fat diet; some mice were given
22 HCR and LCR rats
were fed a chow or HFD for 3 days and received a single
23 ) and heterozygous knockout mice (sod2(+/-))
were fed a chow or high-fat (HF) diet, which accelerates
24 Fish reared at 21-22 degrees C (range)
were fed a commercial diet at 3% body mass d(-1) (non-sa
25 Minipigs
were fed a complete meal with either cubed F&V (apple, p
26 Rats
were fed a control (C) or experimental diet containing 3
27 nction and fetal growth, female C57Bl6J mice
were fed a control (CD) or a high fat/high sucrose (HF/H
28 , heterozygous ERalpha knockout (WT/KO) dams
were fed a control breeder chow diet (25% fat) or a semi
29 Female C57BL/6 J mice
were fed a control diet (CON) or a high-fat diet (HFD) w
30 e blubber, whereas their eight male siblings
were fed a control diet containing pig fat as the main f
31 Mice
were fed a control diet or a diet supplemented with the
32 nd l-histidine decarboxylase (Hdc(-/-)) mice
were fed a control diet or an HFD coupled with a high fr
33 Female mice
were fed a control or HFHS diet from day (D) 1 of pregna
34 Mice
were fed a control or high-fat diet (60% kcal) for 12 we
35 ochrome p450 7A1 knockout (Cyp7A1(-/-)) mice
were fed a control, cholestyramine-containing, or bile a
36 young (4 mo) and old (22-24 mo) C57BL/6 mice
were fed a diet containing 30-PPM (control) or 500-PPM (
37 F-344 rats or C57BL/6 mice
were fed a diet containing T3 for 2-7 days.
38 nimals were implanted with zeranol and three
were fed a diet containing zearalenone.
39 than 100 unique inbred mouse strains, which
were fed a diet rich in fat and carbohydrates.
40 Notably, Pstpip2(cmo) mice that
were fed a diet rich in fat and cholesterol maintained a
41 Wild-type (WT) and TRPC5 knock-out (KO) mice
were fed a diet supplemented with 0.5% cholic acid (CA)
42 Ileal cannulated pigs (50+/-1.9 kg)
were fed a fibre-free diet for seven days (n=14) followe
43 Rats
were fed a fixed amount of a normal calcium (1.2%) diet
44 In vivo, adult C57BL/6J male mice
were fed a folate-free diet for 4 weeks to induce hHcys,
45 Female Mthfd1S(+/+) and Mthfd1S(+/-) mice
were fed a folic acid-supplemented diet (FASD) (5-fold h
46 Pregnant nonobese diabetic (NOD) mice
were fed a GF or standard diet until all pups were weane
47 Mice
were fed a HCFD for 12 months.
48 Sprague-Dawley rats
were fed a HFD (45% fat) or a matched control diet (10%
49 Swiss mice
were fed a HFD (59% kcal from fat) or standard chow (9%
50 Male mice
were fed a HFD (60% calories from fat) or regular diets
51 when mice with chronically circadian rhythms
were fed a HFD, there was a significant proteoglycan (PG
52 With this aim, rats
were fed a high fat diet with 5% sucrose in the drinking
53 ntly greater in VP neurons from animals that
were fed a high salt diet compared with controls.
54 ) low density lipoprotein receptor(-/-) mice
were fed a high-cholesterol diet to investigate the func
55 Pre-pubertal female pigs, age 35 d,
were fed a high-energy diet (HED; n = 12), containing 15
56 centrations were lower in TRPC1 KO mice that
were fed a high-fat (HF) (45% fat) diet and exercised as
57 Mice
were fed a high-fat (HF) or low-fat (LF) diet plus a cof
58 To test this hypothesis, C57BL/6J mice
were fed a high-fat diet (HFD) containing 1% Concord gra
59 lpha mice and nontransgenic (NT) littermates
were fed a high-fat diet (HFD) for 10 weeks, followed by
60 p40(-/-)), and p35IL-12(-/-) (p35(-/-)) mice
were fed a high-fat diet (HFD) for 12 weeks.
61 Lean or obese mice
were fed a high-fat diet (HFD) for five days and switche
62 ACE2 null (ACE2KO) and wild-type (WT) mice
were fed a high-fat diet (HFD) or a control diet and stu
63 t (KO) and wild-type (WT) mice (as controls)
were fed a high-fat diet (HFD), and metabolic studies we
64 pha-AF1-deficient ovariectomized female mice
were fed a high-fat diet and concomitantly administered
65 p130, the signal transducer protein of IL-6,
were fed a high-fat diet for 12 weeks.
66 Mice
were fed a high-fat diet to initiate obesity and T2D.
67 Four groups of mice
were fed a high-fat diet with 20% casein (control group)
68 ctly mediates rosiglitazone-induced CH, mice
were fed a high-fat diet with rosiglitazone, and cardiac
69 However, when females
were fed a high-fat diet, diet-induced obesity (DIO) wil
70 ApoE(-/-) mice
were fed a high-fat diet, exposed to low-dose (60)Co gam
71 When mice
were fed a high-fat diet, this hepatic phenotype, as wel
72 SK3 (gsk3(KI)) and wild-type mice (gsk3(WT))
were fed a high-fat diet.
73 h1 deficient antisense transgenic (NAS) mice
were fed a high-fat diet.
74 n an apolipoprotein e (apoe(-/-)) background
were fed a high-fat diet.
75 stress induced by Pdx-1 loss, Pdx1(+/-) mice
were fed a high-fat diet.
76 however, this did not occur when Ad-FLD mice
were fed a high-fat diet.
77 n the current study, 4-week-old C57Bl/6 mice
were fed a high-fat/high-fructose Western diet (WD) or a
78 he same populations, where African Americans
were fed a high-fibre, low-fat African-style diet and ru
79 Dahl salt-sensitive rats
were fed a high-salt diet (8% NaCl) from 7 weeks of age
80 In Dahl salt-sensitive rats that
were fed a high-salt diet, a model for hypertension-indu
81 of human and mouse Th17 cells and mice that
were fed a high-sodium diet were described to develop mo
82 k (Trigonella foenum-graecum), C57BL/6J mice
were fed a low- or high-fat diet for 16 weeks with or wi
83 Both groups
were fed a low-calorie diet for 3 weeks after surgery.
84 dysfunction (liver or muscle) when 79 humans
were fed a low-choline diet.
85 g Src(Y529F)-transduced regeneration tissues
were fed a low-fat diet or a high-fat diet and treated w
86 Mice
were fed a low-fat or Western diet for 12 weeks followed
87 Female severe combined immunodeficient mice
were fed a low-fat/no-cholesterol diet and then randomiz
88 lawian donors into young germ-free mice that
were fed a Malawian diet revealed that immature microbio
89 In this study, rats
were fed a meat based diet to compare the possible genot
90 Three groups of six animals each
were fed a normal diet alone or a treatment of 50 or 100
91 Seven groups, with eight rats each,
were fed a normal diet for 4 weeks, and were force-fed d
92 Pigs
were fed a normocholesterolemic (NC) or hypercholesterol
93 Juvenile fish
were fed a preoogenesis MeHg diet for 28 days, after whi
94 To this end, mice
were fed a purified control or heme diet (0.5 mumol/g he
95 Female mice
were fed a standard (C) or high fat (HF) diet before mat
96 he 26-wk-old apolipoprotein E-deficient mice
were fed a standard chow diet and treated either with IL
97 mice on a C57BL/6 background (n = 3-5/group)
were fed a standard chow diet and water ad libitum.
98 All mice
were fed a standard chow diet.
99 Doxycycline-treated mice
were fed a standard commercial diet for 18 weeks and the
100 Eight-week-old male C57BL/6 mice
were fed a standard laboratory diet (SLD) or a HFD for 1
101 Mice
were fed a standard, iron-balanced chow diet or an iron-
102 C57BL/6 mice
were fed a Western diet (WD) (35% kcal from fat enriched
103 C57BL/6 male mice
were fed a Western diet (WD) +/-75 mg PDX twice daily by
104 Apolipoprotein E-deficient (apoE(-/-)) mice
were fed a Western diet (WD) for 3, 6, and 9 mo (n = 108
105 Apolipoprotein (apo)E(-/-) mice (n = 20)
were fed a Western diet (WD) to induce CAVD.
106 LDLR(-/-) mice
were fed a Western diet for 12 weeks, then administered
107 Ldlr (-/-) double knockout (DKO) mice, which
were fed a Western diet for 16 weeks.
108 L-sIDOL mice
were fed a Western diet for 20 or 30 weeks and then anal
109 LDLr(-/-) mice
were fed a Western-type diet for 10 wk, after which they
110 Ldlr(-/-) mice and Csf2(-/-)Ldlr(-/-) mice
were fed a Western-type diet for 12 weeks, and then para
111 Thirty apolipoprotein E-deficient mice
were fed a western-type diet.
112 NHPs
were fed a WSD (36% fat) supplemented with 0.37% resvera
113 ppressed dark-onset food intake in rats that
were fed ad libitum, whereas central infusion of a GLP-1
114 Patients
were fed after a median of 2 days (1-4 days).
115 All mice
were fed AIN-76A rodent diet, and mice in the Inoculatio
116 hairless and immunocompetent mice (n = 180)
were fed AIN-93G or AIN-93G + 10% tangerine or red tomat
117 A second reactor
was fed ammonium sulfate to mimic breakdown products of
118 fants <2 mo of age were randomly assigned to
be fed an MFGM-supplemented, low-energy, low-protein exp
119 m surgery and thereafter either continued to
be fed an SPI diet or control diet for 1 or 3 wk.
120 Subsequently, she
was fed an elemental diet with enteral tube feeding, and
121 All mice then
were fed an atherogenic diet for 16 weeks.
122 han control mice, regardless of whether they
were fed an HFD or a standard diet.
123 ith CD8 and L-selectin antibody-treated mice
were fed an HFD, and hepatocellular injury was assessed
124 ison with the oral doses obtained when flies
were fed an IMI-sucrose mixture revealed that the inhale
125 Weanling C57BL/6 male mice
were fed an iron-deficient (4 ppm) or iron-adequate (35
126 Rats
were fed an iron-deficient diet (IDD, 7 mg/kg) and inves
127 Captive American kestrels (Falco sparverius)
were fed an isotopically characterized diet and patterns
128 Mice lacking JNK1 (JNK1(-/-))
were fed an obesogenic high-fat diet (HFD) for a long pe
129 Analytes
are fed and retained in 500 nL droplets, which are conce
130 intuitive explanation: needy chicks want to
be fed and parents want to feed them.
131 orella thermoacetica The acetic acid product
is fed as a substrate to a second bioreactor, where it i
132 When acetate
was fed as the rate-limiting substrate, the SCMFC acted
133 The resulting decision signal may
be fed back to visual cortex.
134 This signal may have
been fed back from brain regions involved in decision pr
135 The error in the output
is fed back through fixed random connections with a nega
136 about efficacy of the early immune response
is fed back to the immune signaling network, modulating
137 e random "seed" rhythms; their reproductions
were fed back as the stimulus and over time became domin
138 an of nematodes increased by 28% after worms
were fed BB68, and this extension of lifespan was comple
139 ndeed, when human-like Neu5Gc-deficient mice
were fed bioavailable Neu5Gc and challenged with anti-Ne
140 TIM-1
was fed blueberry juice (BBJ) or blueberry polyphenol-en
141 Cynomolgus monkeys
were fed brain of (eleven) cows with bovine spongiform e
142 andomized dietary intervention, 6 volunteers
were fed breakfast doses of 0, 1, 2, 4, or 6 egg yolks.
143 arc, suggesting that these spreading centres
are fed by melting along upwelling zones from the west,
144 mall-scale, point-source eruptive events can
be fed by multiple melt bodies rather than from a single
145 ing a critical need of the primary tumour to
be fed by the vasculature.
146 outflow channel sources are too high to have
been fed by south polar basal melting.
147 Our observations suggest that the lake
was fed by surface meltwater flowing down a nearby mouli
148 In both cases, the CHs
were fed by high-flow vessels and the ensuing massive bl
149 e obtained from facilities housing pigs that
were fed chlortetracyline, tylosin or bacitracin and wer
150 thionine gamma-lyase was decreased when mice
were fed cholic acid but increased when they were placed
151 ween iron loading and high TGs, Fischer rats
were fed chow containing 1% carbonyl iron.
152 e the contribution of FXa and thrombin, mice
were fed chow containing either rivaroxaban or dabigatra
153 When the Tg mice
were fed chow containing IC3, plasma prolactin concentra
154 ation was even more pronounced when the mice
were fed chow diet.
155 ific ILK-deficient (ILK(lox/lox)HSAcre) mice
were fed chow or a high-fat (HF) diet for 16 weeks.
156 L10(-/-), CXCR3(-/-) and wild type (WT) mice
were fed chow or high saturated fat, fructose, and chole
157 C57BL/6-Ly5.1 mice
were fed chronic plus binge ethanol to create a model of
158 were individually stalled and, for 56 days,
were fed concentrates with 60% barley (n = 8 lambs), or
159 Pregnant baboons
were fed control (ad libitum, n=11) or an MNR diet (70%
160 Rats
were fed control or HFD (14% or 60% kilocalories from fa
161 fed a high-fat diet (HFD) for 2 weeks, rats
were fed CSEE (100, 200 or 300 mg/kg) once daily for 8 w
162 Female C57BL/6 mice
were fed cuprizone for 3 weeks, followed by a period of
163 Diabetic rats
were fed daily with human lactobacilli engineered to sec
164 Fish
were fed diets containing different n-6/n-3 fatty acid r
165 For 5-6 mo, middle-aged F344 rats
were fed diets containing low, medium (typical amount),
166 Eight weeks after AOM treatment, animals
were fed diets containing Rosuvastatin and difluromethyl
167 Hens
were fed diets supplemented (2.8% wt:wt) with corn oil (
168 nsgenic mice, and the double-transgenic mice
were fed doxycycline.
169 On either diet, participants
were fed each of 3 sodium levels (50, 100, and 150 mmol/
170 After surgery, animals
were fed either a chow (standard) diet or a high-fat die
171 le (HSP72Tg) and control wild-type (WT) mice
were fed either a chow or high-fat diet (HFD).
172 Thirty-one twin-bearing sheep
were fed either a control (n=15) or low-protein diet (n=
173 C57BL/6 female mice
were fed either a control diet (10% energy from fat) or
174 G) and their nontransgenic counterparts (NT)
were fed either a control diet (CD) or a high-fat diet (
175 C57BL6/J mice
were fed either a control diet, a diet containing cholin
176 an APOE3 and APOE4 targeted replacement mice
were fed either a control high-fat diet (HFD) or an HFD
177 To determine, female mice
were fed either a control or HFD during lactation.
178 Male Sprague-Dawley rats
were fed either a HFD or low-fat diet (LFD) for 4 weeks.
179 Male C57BL/6 J mice
were fed either a low-fat (10% kcal) or one of three hig
180 of C57/B6 a/a females, which are nonagouti,
were fed either a phytoestrogen-free control diet or one
181 care committee, 60 male Sprague-Dawley rats
were fed either a standard chow for 4 weeks or a methion
182 Weaned C57BL/6 mice
were fed either a vitamin D-sufficient or vitamin D-defi
183 Adult zebrafish
were fed either control food (1.3 mug Se/g, dry mass or
184 Pregnant Wistar rats
were fed either control or protein-restricted diets thro
185 y, while subjects in the intervention groups
were fed either custom-made lipid- and protein-rich nutr
186 Interventions: Infants
were fed either donor milk or formula for 90 days or to
187 n the sensory quality of salmon fillets that
were fed either FO or 100% CO diets.
188 Pups
were fed either HF or chow diets after weaning.
189 -old female ECMR knockout and wild-type mice
were fed either mouse chow or WD for 16 weeks.
190 ild-type (C57BL/6J) littermates when animals
were fed either normal or sodium-deficient diets.
191 rexpressing OPN in hepatocytes (Opn(HEP) Tg)
were fed either the control or the ethanol Lieber-DeCarl
192 trol (WT) mice were divided into groups that
were fed either the Lieber DeCarli diet containing 5% al
193 le-body deletion of perilipin-2 (Plin2-null)
were fed either Western or control diets for 30 weeks.
194 a Lieber-DeCarli liquid diet, in which they
were fed ethanol for 8 weeks, as a model of ALD, or a co
195 Female C57BL6/J mice
were fed ethanol or pair-fed control diets and treated o
196 Eight patients could not
be fed (
fasting group).
197 ess only 1 copy of human REG3A transgene but
were fed feces from control mice (not expressing hREG3A)
198 deoxycholic acid and an increase after they
were fed fenofibrate.
199 mly divided into 2 groups (n = 65 each) that
were fed folate-deficient (FD) or standard diets for 8 w
200 Louis, MO)
was fed for 3 weeks to induce liver fibrosis.
201 e drinking water (HFS) for 7 months and then
were fed for 1 month with HFS + 5% nopal (HFS + N).
202 Male C57Bl6 mice ( 5 week old)
were fed for 3 weeks prior to infection and continuing d
203 Rats
were fed for 5weeks with control diet (0.15mug Se/g feed
204 All rats
were fed for 8 weeks.
205 Groups of 8 male sheep
were fed for a 10% increase or 10% decrease in body mass
206 Infants who
are fed formula with varying concentrations of iron gene
207 ducted where exclusively formula-fed infants
were fed formula containing either lactose or CSS-based
208 gher levels result in prediction errors that
are fed forward from lower levels, to update the current
209 de useful representations of the information
being fed forward from primary visual cortex to extrastr
210 address that question, groups of BALB/c mice
were fed high (10%) or low (2%) fiber diets and infected
211 Cows
were fed high-concentrate low-forage (HCLF) or high-fora
212 Thirty-day-old, female mdr2(-/-) mice
were fed high-fat chow containing 0.006% SC-435, a minim
213 Three inbred ILSXISS strains
were fed high-fat or chow diets and subjected to metabol
214 different sizes (1500, 3000, and 7000 bees)
were fed imidacloprid (0, 10, 20, 50, and 100 ppb) in sy
215 Recipient lab rats
were fed increasing concentrations of tannic acid, and w
216 sed for sucrose feeding after the mosquitoes
were fed infected blood.
217 w resultant fitted values and parameters can
be fed into empirical models to map disturbance causal a
218 The organized terms may
be fed into formal ontologies to boost their coverage.
219 n described by a histogram of gradients that
is fed into a Multi-Label Learning with Label-Specific F
220 uptake of nitrate, this major macronutrient
is fed into the vasculature for long-distance transport.
221 citrate coated AgNPs as well as Ag as AgNO3
were fed into sequencing batch reactors (SBRs) inoculate
222 Male Sprague-Dawley rats
were fed isocaloric amounts of an EtOH-containing (Liebe
223 Mice
were fed low-fibre, or that supplemented with soluble fi
224 -28 days) were assigned into four groups and
were fed milk and milk fortified with calcium, vitamin D
225 daily for 4 weeks, whereas the control rats
were fed mineral oil.
226 When the Tg mice
were fed normal chow (NC), plasma prolactin concentratio
227 d control mice with normal senescence (n=15)
were fed normal chow or a high-fat, high-salt diet (WD).
228 )(-/-), and C57BL/6 (wild-type control) mice
were fed normal or Western diets for 3 weeks and were th
229 Many infants and young children
are fed nutritional milk formulas.
230 The extinction of species that feed on or
are fed on by many others (i.e. 'hubs') has traditionall
231 In addition, a group of mosquitoes
was fed on R. felis-infected BALB/c mice.
232 Ixodes scapularis larvae
were fed on EMLA-infected mice, and after molting, infec
233 Newly emerged bees
were fed one of the following treatments for 15 and 30 d
234 n infect individuals by the oral route, mice
were fed phosphate-buffered saline or 10(6)M. canettii m
235 ment where caterpillars from two populations
were fed plant tissue from two hosts.
236 Smad3(-/-) mice
were fed purified diet with either maintenance (1 IU vit
237 Mice
were fed R848 to determine its effects on migration of D
238 argc1a(f/f) Alb-cre(+/0) mice, respectively)
were fed regular chow (control) or a high-fat diet suppl
239 poprotein E(-/-) mice (12 weeks of age; n=6)
were fed regular chow or a Western diet (1.25% cholester
240 Feeds for livestock and farmed fish that
are fed rely largely on the same crops, although the fra
241 At 12 months, 32.6% of infants (42 of 129)
were fed rice snacks.
242 Male rats
were fed semi-synthetic diets for 1 wk that differed onl
243 Rats
were fed six protein diets for 14 days, including casein
244 adjustment for confounders, term infants who
were fed solids in addition to breast milk at 4 mo postp
245 cantly influenced by diet, 2-day old piglets
were fed soy or milk formula (n = 6/group/gender) until
246 Male wild-type (WT) and Cyp2e1-null mice
were fed standard chow or FF for 2, 12, and 24 weeks.
247 Thereafter, offspring
were fed standard rodent chow.
248 eaning of offspring; post weaning, offspring
were fed the control diet.
249 Animals
were fed the following diets for 6 weeks: control (AIN-9
250 Isolated, perfused hearts from rats that
were fed the ketone diet had greater free energy availab
251 Apolipoprotein E(-/-) mice
were fed the Paigen diet (1.25% cholesterol, 0.5% cholic
252 Chicks from both maternal diet groups
were fed the same diet after hatch.
253 Control mice
were fed the same diets but not exposed to UV.
254 lt male American kestrels (Falco sparverius)
were fed the same dose (22 ng OPFR/g kestrel/d) daily (2
255 proteins and lipids) in preterm infants who
were fed their mothers' own milk either raw or pasteuriz
256 colonization when individual germ-free flies
were fed their own natural commensals (including the pro
257 However, when I3C
was fed,
these indicators of NO production became signif
258 We randomly assigned patients who could
be fed through either the parenteral or the enteral rout
259 Test meals
were fed through an intragastric feeding tube on Sprague
260 all forward and reverse elementary reactions
are fed to a microkinetic model giving excellent agreeme
261 ents, including turning, the spinal activity
is fed to a mechanical model of lamprey swimming.
262 This diet
was fed to aging C57BL/6J (B6) mice to identify phenotyp
263 y (BSE)-contaminated meat and bone meal that
was fed to cattle and precipitated the BSE epidemic in t
264 otonin, a substrate for melatonin synthesis,
was fed to purified chloroplasts, they produced melatoni
265 rolled by the amount of RR-S-Ac3 ManNAz that
was fed to target tumor cells.
266 Undiluted hydrolyzed urine
was fed to the caustic-generating cathode compartment fo
267 Thermally oxidized vegetable ghee
was fed to the rabbits for 14 days with specific doses o
268 a known inhibitor of dopamine in Drosophila,
was fed to workers similarly reduced their locomotory ac
269 ty) and alfalfa hay (AH, high-quality) diets
were fed to lactating cows to explore how forage quality
270 ld higher than recommended) and control diet
were fed to male Mthfr(+/+) and Mthfr(+/-) mice for 6 mo
271 d, crickets were analyzed for Ce content or
were fed to wolf spiders (family Lycosidae).
272 ansmission in nature, where vertebrate hosts
are fed upon by both infected and uninfected mosquitoes
273 Mice
were fed vitamin D-deficient or -sufficient chow for 6 w
274 or wild-type control littermate) bone marrow
were fed western diet for 8 weeks with or without anti-C
275 Mass-reared predators
are fed with factitious prey mites such as Tyrophagus pu
276 based on association networks analyses that
are fed with long-term measurements of microbial and env
277 When worms
are fed with two neutrally competing, fluorescently labe
278 ed-culture microbial electrolysis cell (MEC)
is fed with a fermentable substrate, such as glucose, a
279 As a result, each nucleus
is fed with more monomers and grows faster in the presen
280 When the device
was fed with transdermal extracts, containing only 30 mu
281 on alcohol exposure model, adult female rats
were fed with 6.7% alcohol in their diet for 4 weeks, we
282 Some mice
were fed with a cholestyramine-containing diet for 7 day
283 Thus, in the present study, rats
were fed with a high-fat diet to induce inflammation and
284 Animals
were fed with a methionine-choline-deficient (MCD) diet.
285 Gravid female rats
were fed with a resveratrol-enriched diet during gestati
286 Thirty-two lambs
were fed with barley straw supplemented by a concentrate
287 eek-old CSE gene knockout and wild-type mice
were fed with either a control chow or atherogenic paige
288 Six to eight week-old male C57BL/6J mice
were fed with either a high-cholesterol atherogenic diet
289 Male Wistar rats (n = 24)
were fed with either a normal diet (n = 8) or a HFD (n =
290 mary malarial vectors in sub-Saharan Africa,
were fed with either blood meal infected with R. felis o
291 Male Wistar rats
were fed with HFD for 12 weeks, and were randomly divide
292 ST Tg), the endogenous inhibitor of calpains
were fed with high (60% kcal) fat diet for 16 weeks.
293 Dahl salt-sensitive (Dahl-S) rats
were fed with high salt diet with or without 0.1% caffei
294 When rice calli
were fed with increasing levels of 1-pyrroline, 2AP leve
295 mesh mesocosms for up to 16 days where they
were fed with indigenous contaminated zooplankton.
296 with poly(I:C) to label mature hepatocytes,
were fed with the DDC diet, we found LacZ(+)Sox9(+) cell
297 ent VO-based diets; after a period, all sole
were fed with the FO diet.
298 diapausing counterparts after adult eclosion
were fed with three different carbohydrate sources for 7
299 In this study, the newly mated queens
were fed with water containing 0.01 or 0.25 mug/ml imida
300 l/fl)LysM(cre) and ApoE(-/-)LKB1(fl/fl) mice
were fed with western diet for 16 weeks.