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1     In 90% of cases, the indication for DMEK was FED.
2               During the pulse, rats (n = 5) were fed (13)C6-labeled lysine ("heavy") feed for 23 day
3 BPS) affect the placenta, C57BL6J mouse dams were fed 200 mug/kg body weight BPA or BPS daily for 2 w
4 ld-type and Nlrp3 knockout (Nlrp3(-/-)) mice were fed 3,5-diethoxycarbonyl-1,4-dihydrocollidine (DDC;
5         Mice underwent bile duct ligation or were fed 3,5-diethoxycarbonyl-1,4-dihydrocollidine to in
6                                         Mice were fed 5-diethoxycarbonyl-1,4-dihydrocollidine (DDC) o
7  (89.8% Anopheles gambiae sensu lato), 88.3% were fed, 51.9% had a human blood meal, and 9.2% were sp
8  weeks or (d) 9 weeks (n = 8 per group); (e) were fed 6 weeks of CDAHFD and switched to standard chow
9 report that when female Ppp1r15a mutant mice are fed a high fat diet they gain less weight than wild
10       Reduced wheel running occurs when mice are fed a high-fat diet but is normalized when mice cons
11 pose tissue to reduce obesity even when mice are fed a high-fat diet.
12 pensable for whole-body metabolism when mice are fed a low-fat diet.
13                Young germ-free mice that had been fed a Bangladeshi diet were colonized with bacteria
14 s, was significantly increased when rats had been fed a high-salt diet for 7 days (n = 6 or 9, p < 0.
15 f wild animals with captive animals that had been fed a standard captive or improved diet reveals str
16 ased hepatic inflammation and fibrosis after being fed a high-fat, -cholesterol, and -fructose (HFCF)
17                                 If an animal is fed a soft diet from the time of weaning, then this b
18                Male and female C57BL/6J mice were fed a 2.6% alcohol or isocaloric diet for 3 wk prio
19                                   Mosquitoes were fed a blood meal supplemented with [1,2-(13)C2]gluc
20                   At weaning, male offspring were fed a C diet.
21      Streptozotocin-treated male Wistar rats were fed a cholesterol-supplemented diet and gavaged dai
22                                   Thus, mice were fed a choline-deficient-amino-acid-defined (CDAA) d
23                          C57BL/6 female mice were fed a chow (21%) or high-fat (60%) diet and further
24 cw mice (a model of BE, called L2-IL1B mice) were fed a chow (control) or high-fat diet (HFD) or were
25                                C57BL6/J mice were fed a chow diet or a fast-food diet (FFD) with or w
26 ce with the full-length Il6 gene (controls), were fed a chow or a high-fat diet; some mice were given
27                             HCR and LCR rats were fed a chow or HFD for 3 days and received a single
28  (LDL-R-/-) and C57BL/6J wild type (WT) mice were fed a chow or WD for 8 weeks.
29                                     Minipigs were fed a complete meal with either cubed F&V (apple, p
30 nction and fetal growth, female C57Bl6J mice were fed a control (CD) or a high fat/high sucrose (HF/H
31 , heterozygous ERalpha knockout (WT/KO) dams were fed a control breeder chow diet (25% fat) or a semi
32                        Female C57BL/6 J mice were fed a control diet (CON) or a high-fat diet (HFD) w
33 e blubber, whereas their eight male siblings were fed a control diet containing pig fat as the main f
34                                         Mice were fed a control diet or a diet supplemented with the
35 nd l-histidine decarboxylase (Hdc(-/-)) mice were fed a control diet or an HFD coupled with a high fr
36                                  Female mice were fed a control or HFHS diet from day (D) 1 of pregna
37                                Adult females were fed a control or WSD prior to and during pregnancy
38 ochrome p450 7A1 knockout (Cyp7A1(-/-)) mice were fed a control, cholestyramine-containing, or bile a
39                                         Mice were fed a conventional or a methionine- and choline-def
40 eghorn (WLH) and Rhode Island Red (RIR) hens were fed a corn-soybean-based diet enriched with flaxsee
41                     A separate group of mice were fed a diet containing fructo-oligosaccharides, with
42 nimals were implanted with zeranol and three were fed a diet containing zearalenone.
43 Wild-type (WT) and TRPC5 knock-out (KO) mice were fed a diet supplemented with 0.5% cholic acid (CA)
44          Ileal cannulated pigs (50+/-1.9 kg) were fed a fibre-free diet for seven days (n=14) followe
45 either medication alone, four groups of rats were fed a fixed amount of a normal calcium and phosphor
46    Female Mthfd1S(+/+) and Mthfd1S(+/-) mice were fed a folic acid-supplemented diet (FASD) (5-fold h
47                                         Mice were fed a HCFD for 12 months.
48                               Female SD rats were fed a HFD for 8 weeks to induce obesity and, then,
49                          With this aim, rats were fed a high fat diet with 5% sucrose in the drinking
50 ntly greater in VP neurons from animals that were fed a high salt diet compared with controls.
51 ) low density lipoprotein receptor(-/-) mice were fed a high-cholesterol diet to investigate the func
52 centrations were lower in TRPC1 KO mice that were fed a high-fat (HF) (45% fat) diet and exercised as
53 ale strains of Collaborative Cross (CC) mice were fed a high-fat and high-sucrose (HF/HS) diet or a c
54                                         Mice were fed a high-fat diet (HFD) for 12 weeks before food
55 p40(-/-)), and p35IL-12(-/-) (p35(-/-)) mice were fed a high-fat diet (HFD) for 12 weeks.
56   ACE2 null (ACE2KO) and wild-type (WT) mice were fed a high-fat diet (HFD) or a control diet and stu
57                                         They were fed a high-fat diet (HFD) or regular chow for 4 wee
58                                    When mice were fed a high-fat diet (HFD), we found that fatty live
59 pha-AF1-deficient ovariectomized female mice were fed a high-fat diet and concomitantly administered
60 p130, the signal transducer protein of IL-6, were fed a high-fat diet for 12 weeks.
61          For in vivo studies, ApoE(-/-) mice were fed a high-fat diet for 12 weeks.
62                                      Animals were fed a high-fat diet for 8 weeks and then sensitized
63              Apoe(-/-) Malat1(-/-) mice that were fed a high-fat diet showed increased plaque size an
64                                         Mice were fed a high-fat diet to induce obesity and to study
65                               ApoE(-/-) mice were fed a high-fat diet, exposed to low-dose (60)Co gam
66                 When mice with CrAT deletion were fed a high-fat diet, kidney disease was more severe
67                                    When mice were fed a high-fat diet, this hepatic phenotype, as wel
68 however, this did not occur when Ad-FLD mice were fed a high-fat diet.
69 SK3 (gsk3(KI)) and wild-type mice (gsk3(WT)) were fed a high-fat diet.
70 h1 deficient antisense transgenic (NAS) mice were fed a high-fat diet.
71 ne (Il11ra1(-/-)) mice and Il11ra1(+/+) mice were fed a high-fat methionine- and choline-deficient di
72  and D374Y-PCSK9 transgenic Yucatan minipigs were fed a high-fat, high-cholesterol diet to induce ath
73 s apolipoprotein E knockout mice (ApoE(-/-)) were fed a high-fat-diet (HFD) for up to four-months pri
74          We found that when chimeric animals were fed a high-fat-diet, animals with low levels of chi
75                     Dahl salt-sensitive rats were fed a high-salt diet (8% NaCl) from 7 weeks of age
76                     Dahl salt-sensitive rats were fed a high-salt diet (8% NaCl) from 7 weeks of age
77             In Dahl salt-sensitive rats that were fed a high-salt diet, a model for hypertension-indu
78               In this model, new born calves were fed a highly processed, starch-rich diet starting f
79                        Aralar-deficient mice were fed a KD to investigate its therapeutic potential e
80 k (Trigonella foenum-graecum), C57BL/6J mice were fed a low- or high-fat diet for 16 weeks with or wi
81              In the present study, male mice were fed a low-fat diet (LFD, 10% kcal), HFD (45% kcal),
82 g Src(Y529F)-transduced regeneration tissues were fed a low-fat diet or a high-fat diet and treated w
83                                         Mice were fed a low-fat or Western diet for 12 weeks followed
84 infection was significantly lower when flies were fed a low-P high-C diet, revealing that flies shift
85              However, when Zdhhc7 (-/-) mice were fed a low-salt diet, they developed hyponatremia an
86                          In this study, rats were fed a meat based diet to compare the possible genot
87 -)), which limits mitochondrial lipid entry, were fed a moderate fat (25%) diet, and samples were sub
88                            Adult female mice were fed a normal chow (NC) or a high fat diet (HFD) for
89             Three groups of six animals each were fed a normal diet alone or a treatment of 50 or 100
90                                         Pigs were fed a normocholesterolemic (NC) or hypercholesterol
91                                  Female mice were fed a standard (C) or high fat (HF) diet before mat
92                                     All mice were fed a standard chow diet.
93          Fancd2 (-/-) and wildtype (WT) mice were fed a standard diet (SD), a diet enriched in fat, c
94                                         Mice were fed a standard diet, a high fat diet, or these diet
95             Eight-week-old male C57BL/6 mice were fed a standard laboratory diet (SLD) or a HFD for 1
96 cing diet (Treated) and the rest of the four were fed a standard starter diet (Control).
97                                  C57BL6 mice were fed a WD, which activated Na/K-ATPase signaling in
98                                         Mice were fed a well-defined high fat diet, with (HFD/ATI) or
99                                 C57BL/6 mice were fed a Western diet (WD) (35% kcal from fat enriched
100                            C57BL/6 male mice were fed a Western diet (WD) +/-75 mg PDX twice daily by
101     Apolipoprotein (apo)E(-/-) mice (n = 20) were fed a Western diet (WD) to induce CAVD.
102                               LDLR(-/-) mice were fed a Western diet for 12 weeks, then administered
103 Ldlr (-/-) double knockout (DKO) mice, which were fed a Western diet for 16 weeks.
104                           Sham-operated mice were fed ad libitum or food restricted to match their bo
105 ed a less twig-like posture than larvae that were fed ad libitum.
106                                     Patients were fed after a median of 2 days (1-4 days).
107                                     All mice were fed AIN-76A rodent diet, and mice in the Inoculatio
108  hairless and immunocompetent mice (n = 180) were fed AIN-93G or AIN-93G + 10% tangerine or red tomat
109                             A second reactor was fed ammonium sulfate to mimic breakdown products of
110 m surgery and thereafter either continued to be fed an SPI diet or control diet for 1 or 3 wk.
111 e receptor 4 (TLR4; TLR4( KO) ), and animals were fed an HFD or treated with lipopolysaccharide (LPS)
112 ith CD8 and L-selectin antibody-treated mice were fed an HFD, and hepatocellular injury was assessed
113                   Weanling C57BL/6 male mice were fed an iron-deficient (4 ppm) or iron-adequate (35
114 Captive American kestrels (Falco sparverius) were fed an isotopically characterized diet and patterns
115                Mice lacking JNK1 (JNK1(-/-)) were fed an obesogenic high-fat diet (HFD) for a long pe
116  intuitive explanation: needy chicks want to be fed and parents want to feed them.
117                           Half of the corals were fed Artemia sp. brine shrimp in a separate feeding
118 orella thermoacetica The acetic acid product is fed as a substrate to a second bioreactor, where it i
119            The resulting decision signal may be fed back to visual cortex.
120                         This signal may have been fed back from brain regions involved in decision pr
121                      The error in the output is fed back through fixed random connections with a nega
122 that this sensitivity first arises in V2 and is fed back to modulate activity in V1.SIGNIFICANCE STAT
123  about efficacy of the early immune response is fed back to the immune signaling network, modulating
124 e random "seed" rhythms; their reproductions were fed back as the stimulus and over time became domin
125 an of nematodes increased by 28% after worms were fed BB68, and this extension of lifespan was comple
126  MODULEN IBD(R) powder, while remaining rats were fed breeding chow.
127 d to standard chow for 3 weeks (n = 12); (f) were fed CDAHFD for 9 weeks with daily treatment of elaf
128                             When the Tg mice were fed chow containing IC3, plasma prolactin concentra
129 ific ILK-deficient (ILK(lox/lox)HSAcre) mice were fed chow or a high-fat (HF) diet for 16 weeks.
130 L10(-/-), CXCR3(-/-) and wild type (WT) mice were fed chow or high saturated fat, fructose, and chole
131                               C57Bl/6 J mice were fed chow or the GAN diet rich in saturated fat (40%
132                           C57BL/6-Ly5.1 mice were fed chronic plus binge ethanol to create a model of
133                                   F0 females were fed control diet (CD; 10%kcal from fat) or HFD (60%
134                             Pregnant baboons were fed control or maternal nutrient restricted (MNR) d
135 rse effects of high fat diets, C57BL/6J mice were fed control/low fat (CD) or high fat (HFD) diets ea
136                          Female C57BL/6 mice were fed cuprizone for 3 weeks, followed by a period of
137 intestinal system, male and female zebrafish were fed DEHP (3 ppm) daily for two months.
138  the contractile reserve, a group of animals were fed dichloroacetate, an activator of pyruvate oxida
139     Eight weeks after AOM treatment, animals were fed diets containing Rosuvastatin and difluromethyl
140                                         Mice were fed diets lacking prebiotic fiber with or without a
141                                         Hens were fed diets supplemented (2.8% wt:wt) with corn oil (
142 ave been demonstrated to adapt when the host is fed different ingredients.
143                 On either diet, participants were fed each of 3 sodium levels (50, 100, and 150 mmol/
144 of 576 (19 days old) Cobb 500 broiler chicks were fed eight finisher diets consisting of 4 control (C
145 e, the male and female Sik2(S587A) mice that were fed either a chow or high-fat diet showed similar w
146                           Female Wistar rats were fed either a control (C) or cafeteria diet (O) for
147                          C57BL/6 female mice were fed either a control diet (10% energy from fat) or
148                                C57BL6/J mice were fed either a control diet, a diet containing cholin
149 an APOE3 and APOE4 targeted replacement mice were fed either a control high-fat diet (HFD) or an HFD
150                             Male C57BL6 mice were fed either a control normal protein diet (NPD; 18%
151                    To determine, female mice were fed either a control or HFD during lactation.
152                           C57BL/6 mouse dams were fed either a corn oil-based HF or control diet duri
153  and two females, whereas the remaining pups were fed either a high- or low-fat diet until PND105, wh
154                             Male Wistar rats were fed either a high-fat diet (HFD; 35% fat) or a stan
155                          Female C57BL/6 mice were fed either a high-fat, high-carbohydrate (Western-s
156                          Male C57BL/6 J mice were fed either a low-fat (10% kcal) or one of three hig
157                                         Mice were fed either a normal diet or high-fat diet (HFD, 60
158  care committee, 60 male Sprague-Dawley rats were fed either a standard chow for 4 weeks or a methion
159 ) pups from wild-type (WT) or TLR2(-/-) dams were fed either by their biologic dam or a dam of the al
160                                    EFAD mice were fed either control (10% fat, 7% sugar) or WD (45% f
161                       Interventions: Infants were fed either donor milk or formula for 90 days or to
162                           Male C57BL/6J mice were fed either low-fat or high-fat diet to induce obesi
163 -old female ECMR knockout and wild-type mice were fed either mouse chow or WD for 16 weeks.
164                             BALB/c male mice were fed either standard chow diet or Western-type diet
165 le-body deletion of perilipin-2 (Plin2-null) were fed either Western or control diets for 30 weeks.
166  a Lieber-DeCarli liquid diet, in which they were fed ethanol for 8 weeks, as a model of ALD, or a co
167                         Female C57BL6/J mice were fed ethanol or pair-fed control diets and treated o
168  After first administration of TNBS, 10 rats were fed exclusively MODULEN IBD(R) powder, while remain
169                     Eight patients could not be fed (fasting group).
170 ess only 1 copy of human REG3A transgene but were fed feces from control mice (not expressing hREG3A)
171  deoxycholic acid and an increase after they were fed fenofibrate.
172 e drinking water (HFS) for 7 months and then were fed for 1 month with HFS + 5% nopal (HFS + N).
173 ricted feeding (TRF) paradigm in which flies were fed for 12 h during the day counteracts obesity-ind
174               Male C57Bl6 mice ( 5 week old) were fed for 3 weeks prior to infection and continuing d
175 diapause-destined female post-adult eclosion were fed for 7 days with 10% glucose containing 1% D-[(1
176                                     All rats were fed for 8 weeks.
177 l consequences of this common practice, mice were fed for more than 3 months with a low, medium or hi
178  a high (HD) or low (LD) expression of fads2 were fed for three months during the spawning season wit
179                                  Infants who are fed formula with varying concentrations of iron gene
180 ducted where exclusively formula-fed infants were fed formula containing either lactose or CSS-based
181 gher levels result in prediction errors that are fed forward from lower levels, to update the current
182 de useful representations of the information being fed forward from primary visual cortex to extrastr
183 ghly fit double-mutant 'jackpot' clones that are fed from exponentially growing single mutants, a pro
184  ATI-containing diet compared with mice that were fed gluten-free and thus ATI-free diet.
185   In the second protocol, sensitized animals were fed HEWP for 28 days.
186                                         Mice were fed high-fat (HF) diet and orally given arctigenin
187                                     DIO mice were fed high-fat diet (HFD) for 12 weeks and then treat
188                 Three inbred ILSXISS strains were fed high-fat or chow diets and subjected to metabol
189 st associations between 1) never versus ever being fed human milk and atopic dermatitis in childhood
190 ted evidence suggests that never versus ever being fed human milk is associated with higher blood pre
191  evidence suggests that 1) never versus ever being fed human milk is associated with higher risk of c
192 -control evidence suggests never versus ever being fed human milk is associated with higher risk of c
193 a, and 2) among children and adolescents who were fed human milk as infants, shorter versus longer du
194                  Wild type Swiss albino mice were fed i-Extract, and hippocampal cells from naive mic
195  different sizes (1500, 3000, and 7000 bees) were fed imidacloprid (0, 10, 20, 50, and 100 ppb) in sy
196                                  Each forage was fed in fresh or dried state for 3 weeks.
197 y group to a control group in which patients were fed in a traditional way (traditional feeding).Most
198 ch as age, tumor size and histological type) are fed into a support vector machine (SVM) to generate
199 ction and (iii) the obtained feature vectors are fed into XGBoost to predict protein submitochondrial
200 w resultant fitted values and parameters can be fed into empirical models to map disturbance causal a
201 l magnetic space groups, we generate data to be fed into the algorithm of MTQC to determine the topol
202 n described by a histogram of gradients that is fed into a Multi-Label Learning with Label-Specific F
203 ly-driven RS Flip-Flop, one of whose outputs is fed into an INHIBIT gate.
204 ase of 7962 bioactive molecules within foods was fed into the model, which predicted 110 cancer-beati
205 found significant in the univariate analysis were fed into a multivariate regression model and models
206 found significant in the univariate analysis were fed into a multivariate regression model, and model
207                                   These data were fed into a physiologically informed model of tissue
208                     Male Sprague-Dawley rats were fed isocaloric amounts of an EtOH-containing (Liebe
209                                Pregnant mice were fed low dose fluoride (LF(-)) or high dose fluoride
210 d when L. vannamei (Pacific whiteleg shrimp) were fed mealworm biomass grown with PS containing HBCD.
211                             When the Tg mice were fed normal chow (NC), plasma prolactin concentratio
212 d control mice with normal senescence (n=15) were fed normal chow or a high-fat, high-salt diet (WD).
213 WDF) to induce steatohepatitis; control mice were fed normal chow.
214              Many infants and young children are fed nutritional milk formulas.
215    The extinction of species that feed on or are fed on by many others (i.e. 'hubs') has traditionall
216            Laboratory-reared Anopheles dirus were fed on blood from 119 Pf-infected Cambodian adults,
217                                        Ticks were fed on bovine blood containing 10-fold dilutions of
218 nfected and uninfected I. scapularis females were fed on naive mice for 1, 3, and 6 hours, and Illumi
219                                  BALB/c mice were fed once with high doses of nCyp c 1 or mCyp c 1, b
220                                Rats (n = 48) were fed one of four sausages; a pork sausage enriched w
221                           Newly emerged bees were fed one of the following treatments for 15 and 30 d
222  weeks, healthy Sprague-Dawley rats (n = 30) were fed one of three diets: inulin-fortified pork sausa
223                                    Some mice were fed or given intraperitoneal injections of S100A8 o
224 n infect individuals by the oral route, mice were fed phosphate-buffered saline or 10(6)M. canettii m
225 ment where caterpillars from two populations were fed plant tissue from two hosts.
226 ew slowly and even paled; however, once they were fed (RAS-B modified to RAS+B), their pigmentation i
227 argc1a(f/f) Alb-cre(+/0) mice, respectively) were fed regular chow (control) or a high-fat diet suppl
228                                    Offspring were fed regular chow throughout their life and tested f
229                                         Rats were fed respective diets for 8 months, during which ene
230   At 12 months, 32.6% of infants (42 of 129) were fed rice snacks.
231                                    Male rats were fed semi-synthetic diets for 1 wk that differed onl
232                                         Rats were fed six protein diets for 14 days, including casein
233                                     Patients were fed so they would fall asleep and placed in the sca
234 adjustment for confounders, term infants who were fed solids in addition to breast milk at 4 mo postp
235 cantly influenced by diet, 2-day old piglets were fed soy or milk formula (n = 6/group/gender) until
236     Male wild-type (WT) and Cyp2e1-null mice were fed standard chow or FF for 2, 12, and 24 weeks.
237                     Male Sprague-Dawley rats were fed standard rat chow containing normal (0.25%) and
238 on of collagen were normalized even when EPA was fed, supporting that the deleterious effects of EPA-
239                                 After having been fed the HFCF diet, WT mice displayed up-regulated p
240 ies were more reactive and less settled when being fed the HS diet compared to the HF diet.
241                                 Four of them were fed the acidosis-inducing diet (Treated) and the re
242                              ob/ob-NASH mice were fed the AMLN diet high in trans-fat, fructose and c
243   Male leptin-deficient Lep(ob)/Lep(ob) mice were fed the Amylin liver NASH (AMLN) diet for 16 weeks
244 hibition can reverse NAFLD progression, mice were fed the FFD for 5 months, with or without canertini
245                                      Animals were fed the following diets for 6 weeks: control (AIN-9
246 in the transition of steatosis to NASH, mice were fed the HFCF diet for 4 weeks, followed by Shp dele
247     Isolated, perfused hearts from rats that were fed the ketone diet had greater free energy availab
248                   Apolipoprotein E(-/-) mice were fed the Paigen diet (1.25% cholesterol, 0.5% cholic
249                         After PN21 offspring were fed the same control diet until adulthood.
250        Chicks from both maternal diet groups were fed the same diet after hatch.
251      The Apulo-Calabrese and crossbreed pigs were fed the same diet and slaughtered at 135 and 155 kg
252                                 Control mice were fed the same diets but not exposed to UV.
253  proteins and lipids) in preterm infants who were fed their mothers' own milk either raw or pasteuriz
254 colonization when individual germ-free flies were fed their own natural commensals (including the pro
255                            However, when I3C was fed, these indicators of NO production became signif
256            For indirect xenodiagnosis, flies were fed through a membrane on the patient's blood.
257                        The obtained features are fed to a hybrid Random Under-Sampling-Boosting algor
258 all forward and reverse elementary reactions are fed to a microkinetic model giving excellent agreeme
259 ding speech sound features; this information is fed to auditory cortices, most likely facilitating sp
260                                    This diet was fed to aging C57BL/6J (B6) mice to identify phenotyp
261 otonin, a substrate for melatonin synthesis, was fed to purified chloroplasts, they produced melatoni
262                   Undiluted hydrolyzed urine was fed to the caustic-generating cathode compartment fo
263 asive cyprinids (common carp, Prussian carp) were fed to captive mallards.
264                                        Diets were fed to juvenile LMB (initial weight, 25.87 +/- 0.08
265 ty) and alfalfa hay (AH, high-quality) diets were fed to lactating cows to explore how forage quality
266                                 All patients were fed via these catheters using a standardized feedin
267 or wild-type control littermate) bone marrow were fed western diet for 8 weeks with or without anti-C
268         C57BL/6 wild-type and Tlr4(-/-) mice were fed wheat- or ATI-containing diets or a wheat-free
269                        Mass-reared predators are fed with factitious prey mites such as Tyrophagus pu
270                                   When worms are fed with two neutrally competing, fluorescently labe
271  less emphasized that female broodstock must be fed with live feeds such as polychaetes for this prac
272 gevity was observed in adult aphids that had been fed with dsMpNa(v) solution at the nymphal stage.
273 ody weight of the WT and Cld-1 Tg mice after being fed with 2.5% DSS were measured every day until da
274 ed-culture microbial electrolysis cell (MEC) is fed with a fermentable substrate, such as glucose, a
275 s in a membrane-aerated biofilm reactor that was fed with methane and ammonium.
276                              When the device was fed with transdermal extracts, containing only 30 mu
277      From the stool sample of five mice that were fed with (15)N hydrolysate from Ralstonia eutropha,
278 on alcohol exposure model, adult female rats were fed with 6.7% alcohol in their diet for 4 weeks, we
279 re subjected to bile duct ligation (BDL) and were fed with a 0.1% DDC (3,5-diethoxycarbonyl-1,4-dihyd
280                                    Some mice were fed with a cholestyramine-containing diet for 7 day
281 -)) MALAT1-deficient (Malat1(-/-)) mice that were fed with a high-fat diet and by studying the regula
282                           Male C57BL/6J mice were fed with a high-fat diet for 16 weeks.
283                       Female C57BL/6JRJ mice were fed with a short-term HFD or chow diet (CD) for 12
284 ells from gliadin-immunized C57BL/6 mice and were fed with an AIN-76A-based diet containing wheat glu
285     Six to eight week-old male C57BL/6J mice were fed with either a high-cholesterol atherogenic diet
286                    Male Wistar rats (n = 24) were fed with either a normal diet (n = 8) or a HFD (n =
287               Wild-type and nSIRT1OE Tg mice were fed with either control diet (6.2% fat) or a HFD (3
288                                Rats (n = 32) were fed with either normal diet (ND) or HFD for 20 week
289                     Finally, when these mice were fed with ethanol, the presentation of hepatic megam
290                             Male Wistar rats were fed with HFD for 12 weeks, and were randomly divide
291                                C57BL/6J mice were fed with HFD or standard diet (SD) for 1, 2, or 8 w
292 deficient diet for 12 weeks and C57BL/6 NTac were fed with HFMCD for 10 weeks or WDF for 16 weeks.
293 er wild type (WT) or miR-146a deficient (KO) were fed with high (60% kcal) fat diet (HFD) for 16 week
294 ST Tg), the endogenous inhibitor of calpains were fed with high (60% kcal) fat diet for 16 weeks.
295            Dahl salt-sensitive (Dahl-S) rats were fed with high salt diet with or without 0.1% caffei
296                              When rice calli were fed with increasing levels of 1-pyrroline, 2AP leve
297                                   db/db mice were fed with methionine- and choline-deficient diet for
298            Six-month-old WT and APP/PS1 mice were fed with standard mouse chow or OLT1177-enriched ch
299 diapausing counterparts after adult eclosion were fed with three different carbohydrate sources for 7
300 l/fl)LysM(cre) and ApoE(-/-)LKB1(fl/fl) mice were fed with western diet for 16 weeks.

 
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