ライフサイエンスコーパス: Fischer

1 Fischer 344 rat hepatocytes were transplanted into synge

2 Fischer 344 rat recipients of Lewis allografts were trea

3 Fischer 344 rats that are maintained on an ad libitum di

4 Fischer 344 rats were treated according to the RS-based

5 Fischer 344 rats were treated with 2 doses (30 mg/kg bod

6 Fischer 344 x Brown Norway rats received fractionated wh

7 Fischer and Lewis rat strains often serve as animal vuln

8 Fischer et al. make two challenges to our paper's conclu

9 Fischer et al. recently constructed a mouse in which the

10 Fischer indolization followed by RCM delivers the cis is

11 Fischer rat thyroid cells expressing CFTR and a halide-s

12 Fischer rats were divided into: MCA tumor bearing fed ch

13 Fischer rats with one-week-old myocardial infarcts were

14 Fischer's exact test was used for survival.

15 Fischer-344 (F-344 Rat) or Dark Agouti (DA Rat) donor an

16 Fischer-Brown Norway rats at 10 months of age were hindl

17 Fischer-Tropsch catalysis performed under industrially r

18 Fischer-Tropsch synthesis is a process for flexible prod

19 Fischer-Tropsch type (FTT) synthesis has long been propo

20 "Fischer-Tropsch" type coupling of non-native C(1) substr

21 n of self-dimerization of alkoxychromium(0) (Fischer) carbene complexes resulted in the selection of

22 hs old; n=10) and aged (20 months old; n=10) Fischer rats underwent cardiac micro-CT imaging as well

23 Among 20 Fischer rats with implanted FN13762 tumors in the liver,

24 th 95% confidence intervals of 0.003%-0.56% (Fischer exact test).

25 SI ionization of alkenyl and alkynyl group 6 Fischer carbene complexes.

26 ed on conventional military jet fuel (JP-8), Fischer-Tropsch synthetic jet fuel (FT), and a 50/50 ble

27 A Fischer indolization step carried out on a tricyclic ket

28 A Fischer's exact probability test revealed that more grou

29 amolecular cyclopentannulation reaction of a Fischer aminocarbene complex provided the key step and o

30 ng the OLETF-derived, CCK1R-null gene onto a Fischer 344 genetic background, we have been able to gen

31 ed by 6pi(*), 6theta(*), and 6rho(*) using a Fischer phase diagram.

32 about Alzheimer, only little is known about Fischer.

33 these data point to a strongly pi-accepting Fischer-type carbyne ligand that confers stability to a

34 Adult Fischer 344 rats were anesthetized and injected with BMP

35 Protein depletion was induced in adult Fischer (F344) male rats by the ad libitum provision of

36 ected into either the BLA or the DS of adult Fischer 344 rats, and shock-elicited fear and shuttle bo

37 Microarray analysis of HD-treated adult Fischer 344 rats identified 128 altered sperm mRNA trans

38 Now, more than 120 years after Fischer's first synthesis of (D)-glucose (1890), we are

39 exes of juvenile, adolescent, adult and aged Fischer 344 rats.

40 ET-1 system in arteries from young and aged Fischer-344 rats.

41 In aged Fischer 344 (F344) rats, noradrenergic (NA) nerve densit

42 + 2] cycloaddition reaction between alkynyl Fischer carbene complexes and tropothione leads to the r

43 Many biologically and Fischer-Tropsch synthesized fuels contain branched alkan

44 ing IRI in both Lewis-to-Lewis isografts and Fischer-to-Lewis allografts.

45 wo emerging naval biofuels (camelina-JP5 and Fischer-Tropsch-F76) and their potential to exacerbate c

46 Lewis (LEW) and Fischer 344 (F344) rat strains have been reported to dif

47 Inbred Lewis (LEW) and Fischer 344 (F344) rats are differentially sensitive to

48 Lewis and Fischer 344 (F344) rats differ in responses to cocaine a

49 Since Lewis and Fischer rats have opposite susceptibility to experimenta

50 Water-deprived Lewis and Fischer rats were given 5 min access to 0.15% saccharin

51 Dark Agouti, Brown Norway, and Fischer 344 kidneys were transplanted to Lewis rats to i

52 rogenation mechanisms: methanol reaction and Fischer-Tropsch based carbon dioxide hydrogenation.

53 We used Wilcoxon rank sum and Fischer exact tests to compare patients who died versus

54 vivo microdialysis in urethane-anesthetized Fischer 344 rats.

55 alysts of the type used in reactions such as Fischer-Tropsch synthesis is highly debated.

56 In cobalt-based Fischer-Tropsch synthesis (FTS), the size of Co nanopart

57 Cobalt-based Fischer-Tropsch systems are widely used to convert synth

58 uctose ((18)F-FBPA-Fr) in F98 glioma-bearing Fischer 344 rats by means of intravenous injection of (1

59 ensitivity, or specificity was found between Fischer, Fuji, and GE soft-copy digital and screen-film

60 lophanes by a Grignard reaction, followed by Fischer indolization and ring-closing metathesis (RCM) a

61 vers the cis isomer, whereas RCM followed by Fischer indolization gives the trans isomer.

62 everse water-gas shift reaction, followed by Fischer-Tropsch synthesis, and iron is a well-known cand

63 e been attributed to abiogenic production by Fischer-Tropsch type (FTT) reactions, although clear evi

64 The mechanism originally proposed by Fischer and Tropsch for carbon monoxide (CO) hydrogenati

65 The report by Fischer and colleagues in this issue of Neuron describes

66 hey can be easily prepared on large scale by Fischer glycosylation and stored indefinitely before che

67 pine blister rust (Cronartium ribicola J.C. Fischer ex Raben.).

68 An acid-catalyzed Fischer indolization is a central step in its synthesis.

69 , for example, the heterogeneously catalyzed Fischer-Tropsch process.

70 mation by examining some of the most complex Fischer indolization substrates to date.

71 tilization of a Japp-Klingemann condensation/Fischer cyclization to prepare cycloalkyl[b]indolones, (

72 xual receptivity in adult, regularly cycling Fischer rats.

73 ltra-low sulfur/low-aromatic content diesel, Fischer-Tropsch synthetic diesel, and conventional diese

74 The present article discusses Fischer's work on dementia in the context of his life an

75 tidyl peptidase IV (DPPIV) positive (DPPIV+) Fischer donor rats into the spleen of partially hepatect

76 ally hepatectomized, DPPIV negative (DPPIV-) Fischer host rats exposed to retrorsine.

77 emisorbed CO (CO*) and its activation during Fischer-Tropsch synthesis (FTS).

78 of chemical sintering of supported Co during Fischer-Tropsch synthesis.

79 catalysts, we have studied the CO/H2 (i.e., Fischer-Tropsch synthesis) and CO2/H2 reactions.

80 ergies that result may enable more efficient Fischer-Tropsch conversions and extraction of CO from in

81 Eighteen Fischer 344 rats received radiation doses of 0, 10, or 2

82 By 1892, when Emil Fischer succeeded Hofmann, the DChG was the world's larg

83 o new selective cascade processes for enynyl Fischer carbene complexes 1 are described in their react

84 how different reactivity than the equivalent Fischer carbene complexes.

85 tion was performed in (DPPIV)-deficient F344-Fischer rats.

86 was implanted subcutaneously into 107 female Fischer 344 rats.

87 ors (1.3-1.5 cm) were implanted in 48 female Fischer rats.

88 We compared aged male and female Fischer 344 rats (21.5 months at testing) without stress

89 n image of 41 four-month-old male and female Fischer 344 rats.

90 e-a dose that induced CPP in male and female Fischer rats.

91 Adult, regularly cycling female Fischer rats were injected daily with 10 mg/kg fluoxetin

92 durance training were investigated in female Fischer 344 rats (n = 42; seven groups of six rats) aged

93 ral history of pneumonic tularemia in female Fischer 344 rats after nose-only inhalational exposure t

94 to the wall of the abdominal aorta in female Fischer rats (n=22 in each group).

95 cal displacement SCI was performed in female Fischer rats, and behavior was assessed for 8 weeks.

96 n address this problem, we inoculated female Fischer 344 (F344), Lewis (LEW), Sprague-Dawley (SD), an

97 tus in young (6 mon) and old (24 mon) female Fischer-344 rats.

98 This study randomized 30 nonanemic, female Fischer 344 rats into three treatment arms to examine th

99 For in vivo studies, female Fischer-344 rats after permanent coronary artery ligatio

100 MATERIALS AND Five Fischer 344 rats that weighed 200-425 g were prepared fo

101 AUC differences of 0.09, 0.08, and 0.06 for Fischer, Fuji, and GE, respectively.

102 copy digital and screen-film mammography for Fischer, Fuji, and GE digital mammography equipment.

103 boronic acid as a phase-transfer reagent for Fischer glycosidations in low-polarity organic solvents

104 ith XylNC (Xyl = 2,6-dimethylphenyl) to form Fischer carbene complexes [PhBP(Ph)3]Ru(H) horizontal li

105 In Experiment 1, four Fischer and four Lewis rats earned their daily food rati

106 We welcome the correspondence from Fischer and colleagues regarding our recent paper on voc

107 Kidneys from Fischer-344 rats were transplanted into Lewis rats as li

108 witch extensor digitorum longus muscles from Fischer(344) x Brown Norway (FBN) rats (n = 8 per group)

109 the postmitochondrial fraction prepared from Fischer 344 rat liver.

110 ted in athymic mice bearing s.c. tumors from Fischer rat embryo fibroblasts transfected with erbB2.

111 nyl carbon atom to give boryl-functionalized Fischer carbene complexes Fe(CO)4{C(OLi(THF)3)B(NDippCH)

112 formed studies in animals, including healthy Fischer 344 rats or rats treated with carbon tetrachlori

113 In the stress-hyperresponsive Fischer strain, P1-14 pups were isolated for 4 h/day (ea

114 yl ether leads to formation of an iridium(I) Fischer carbene complex, (PNP)Ir C(H)OtBu, by double C-H

115 Copper(I) and silver(I) Fischer carbenes are synthesized in the gas phase.

116 R3230 mammary adenocarcinomas in Fischer rats were treated with either RF ablation (n = 4

117 uld cause the glomerulosclerosis of aging in Fischer 344 rats at ages 2, 6, 17, and 24 mo was evaluat

118 KS-WNK1 and the epithelial Na(+) channel in Fischer rat thyroid epithelial cells also stimulates Na(

119 Moreover, TSA increased ENaC current in Fischer rat thyroid and kidney collecting duct epithelia

120 ryonic kidney 293 cells but had no effect in Fischer rat thyroid epithelia.

121 ASK-3 channels were transiently expressed in Fischer rat thyroid cells, and their function was studie

122 conducted on TASK-3 transiently expressed in Fischer rat thyroid epithelial monolayers; channel funct

123 CO(2) is converted into hydrocarbon fuels in Fischer-Tropsch synthesis via the water gas shift reacti

124 hypoxia in R3230Ac and FSA tumors growing in Fischer 344 rats.

125 car of a 1-week-old myocardial infarction in Fischer rats.

126 luorometric measurements of iodide influx in Fischer rat thyroid cells expressing DeltaF508-CFTR show

127 train an epigenetic age (DNAmAge) measure in Fischer 344 CDF (F344) rats.

128 tetrachloride-induced liver injury model in Fischer 344 rats.

129 The effects of monocrotaline in Fischer 344 rats were examined by tissue morphology, ser

130 ng the reactivity of cobalt nanoparticles in Fischer-Tropsch synthesis.

131 ed by a single systemic injection of 3-NP in Fischer 344 rats.

132 onally distinct corticospinal populations in Fischer 344 rats from postnatal day 18 through 75 using

133 why pyridylhydrazines are poorly reactive in Fischer indolization reactions, in addition to the origi

134 onger to develop than previously reported in Fischer female rats.

135 a series of passive immunization studies in Fischer 344 (F344) rats.

136 cleaved HK (HKa) was faster in Lewis than in Fischer or Buffalo rat plasma.

137 with more pronounced effect in Lewis than in Fischer rats.

138 The inbred Fischer 344 rat is being evaluated for testing novel vac

139 Water increases Fischer-Tropsch synthesis (FTS) rates on Ru through H-sh

140 s compared with an existing metabolic index, Fischer's BCAA/AAA molar ratio, as well as indexes gener

141 based catalysts have been used in industrial Fischer-Tropsch synthesis for decades, little is known a

142 electrons and protons, while the industrial Fischer-Tropsch process uses dihydrogen as a combined so

143 inserted with the Neusidl Corneal Inserter (Fischer Surgical Inc).

144 Intact Fischer 344 rats (>20 months) were implanted with Silast

145 on showed a commodity-by-strain interaction: Fischer rats defended consumption with greater vigor whe

146 The approach features an interrupted Fischer indolization to construct the pyrrolidinoindolin

147 scaffold as well as a late-stage interrupted Fischer indolization to install the furoindoline and con

148 The interrupted Fischer indole synthesis of arylhydrazines and biocataly

149 disclosed benzannulation approach involving Fischer carbene complexes and alkynes.

150 In this issue, Fischer et al. offer compelling evidence that a monoclon

151 pounds which react with iodine, causing Karl Fischer titration (KFT) to give inaccurate, typically hi

152 ntified with the oven based coulometric Karl Fischer (KF) technique.

153 terials that are normally the domain of Karl Fischer titration, such as edible oils, mineral oils, bi

154 ures by using the kinetic parameters of Karl Fischer water titration (KFT).

155 Moisture sorption studies, Karl Fischer titration, and differential scanning calorimetry

156 The Karl Fischer method was combined with an automated NIR imagin

157 ic ionic liquids, where the widely used Karl Fischer titration method suffering from an esterificatio

158 ial least-squares (PLS) regression with Karl Fischer titration being used as a reference method.

159 lubility limitations, as is common with Karl Fischer titrations.

160 embly of the [3.3.1]-azabicyclic core, a key Fischer indolization reaction to forge the natural produ

161 hind leg of Nembutal-anesthetized (50 mg/kg) Fischer 344 rats.

162 by a model of human shift-work and jet-lag, Fischer (344) rats were exposed to either a standard 12:

163 Male Fischer 344 rats (6, 12 and 24 months old) underwent 7 m

164 Male Fischer 344 rats (young: 3 months; aged: 24 months) were

165 Male Fischer 344 young (4 month old) and aged (20-22 month ol

166 Male Fischer-344 rats were treated s.c. with 0.25 mg/kg b.w.

167 26-month-old calorie-restricted (26CR) male Fischer 344 rats (CR = 40% restriction compared with ad

168 To test this, we exposed adult male Fischer 344 rats to low doses of model testicular toxica

169 adenovirally transduced into MSCs from male Fischer rats.

170 SkMs from male Fischer-344 rats (rSkMs) were PC for 30 minutes with 200

171 d intact and young gonadectomized (GDX) male Fischer 344 rats were anaesthetized, neuromuscularly blo

172 The present study, in male Fischer Brown Norway rats, seeks to determine the locati

173 Age-matched male Fischer 344 rats underwent a 30-minute coronary occlusio

174 lated from young (6 mo) and old (24 mo) male Fischer-344 rats.

175 ng (5-8 months) and aged (22-24 months) male Fischer 344 rats were exposed to environmental enrichmen

176 ng (5-8 months) and aged (22-24 months) male Fischer 344 rats.

177 Three- and 22-month-old male Fischer 344 rats were assigned to young sedentary, young

178 Young and old male Fischer 344 rats were divided into young sedentary (YS),

179 Three-month-old and 18-month-old male Fischer 344 rats were randomly assigned to receive 1.8%

180 (6 months old) and old (24 months old) male Fischer 344 rats.

181 In this study, male Fischer 344 rats received striatal 6-OHDA lesions follow

182 ater maze performance in aged and young male Fischer 344 rats.

183 Male, Fischer 344 rats, 12 months of age, were fed an ethanol

184 mammography systems from four manufacturers (Fischer, Fuji, GE, and Hologic) were used.

185 Loss of N(2) generates a metastable Fischer carbene, which subsequently undergoes Wolff rear

186 volving a nitrile and an epoxide, a modified Fischer indole protocol, a late-stage oxidative lactoniz

187 he resultant amine to an epoxide; a modified Fischer indolization; an oxidative lactonization of a di

188 aterials, i.e., Rh-based, Mo-based, modified Fischer-Tropsch and modified methanol synthesis catalyst

189 nts (K(ATRP)) were determined using modified Fischer's equations for the persistent radical effect.

190 llenges associated with developing molecular Fischer-Tropsch catalysts is the design of systems that

191 iddle-aged (14 months), and aged (24 months) Fischer-344 rats of both sexes.

192 d (15-17 months) and five old (25-29 months) Fischer 344 x Brown Norway male rats were perfused, and

193 Aged (24 months) and adult (6 months) Fischer 344 rats were treated with AcCN (300 mg/kg i.p.

194 In a recent report in Nature, Fischer et al. show that the ability to learn and rememb

195 Cardiomyocytes from neonatal Fischer rats (both sexes) or medium were injected into t

196 In this issue of Neuron, Fischer and Ullsperger demonstrate that EEG signatures o

197 Lewis isografts and normal Fischer-344 kidneys served as controls.

198 ses were investigated by using Brown Norway, Fischer 344, Lewis and WKY, genetically and behaviorally

199 in good yields by selenative demetalation of Fischer aminocarbene complexes.

200 el, glomerular histopathological findings of Fischer-344 kidneys transplanted into Lewis rats have ne

201 Two groups of Fischer 344 rats (6-month-old [young group] and 26-month

202 of monoclonal antibodies by immunization of Fischer rats with enzymatically dispersed nonparenchymal

203 as higher alkanes and oxygenates by means of Fischer-Tropsch synthesis.

204 studies, drawing links to the mechanisms of Fischer-Tropsch and methanol syntheses.

205 putamen (CPu) and nucleus accumbens (NAc) of Fischer rats.

206 ct with ketenes generated from photolysis of Fischer chromium carbene complexes to generate either be

207 This work furthers the potential of Fischer-type ruthenium alkylidenes in polymerization str

208 Fos protein levels in the caudate/putamen of Fischer rats.

209 The benzannulation reaction of Fischer carbene complexes is investigated under conditio

210 has not been seen before in the reaction of Fischer carbene complexes with alkynes.

211 es were prepared via the thermal reaction of Fischer carbene complexes with triisopropylsilyl- or ter

212 the degree of bond formation in reactions of Fischer carbene complexes as well as reactions of other

213 erization as a strategy for the synthesis of Fischer carbene-containing polymers.

214 Additionally, an interrupted variant of Fischer azaindolization methodology is disclosed, which

215 bilaterally, into the lateral ventricles of Fischer albino male rats (1 nmol/2 microl/side).

216 f producing: MD from conventional crude oil; Fischer-Tropsch MD from natural gas and coal; fermentati

217 ochondria, and microsomes from young and old Fischer 344 rats.

218 Forty-one, eight month old Fischer 344 male rats were treated with either the AIN (

219 ed the amygdala in 4-, 12-, and 24-month-old Fischer 344 rats following perfusion with 4% paraformald

220 ontal cortex of 3-, 9-, and >/= 23-month-old Fischer 344 rats.

221 Female, 18-month-old, Fischer F344 rats were divided into an aged group, aged

222 Four-week-old, Fischer-Brown Norway F1-generation male rats were given

223 The original Fischer's equations could be used only for low conversio

224 In the same year, Oskar Fischer reported neuritic plaques in 12 cases of senile

225 The main ones are reduction, oxidation, Fischer-Tropsch, C-H activation, CO(2) transformation, a

226 striatum of LID-resistant Lewis or LID-prone Fischer-344 (F344) male rats.

227 Forty-two rats (Fischer CDF) were treated with 10 cN of force for 5 diff

228 Relative to Lewis rats, Fischer rats exhibit greater avoidance of a saccharin cu

229 ron transfer results in one-electron-reduced Fischer-type nitrene radicals (N(*)Ns(-)) that are inter

230 in cell engraftment and liver repopulation, Fischer 344 rat hepatocytes were transplanted into synge

231 n the susceptible (Lewis; LEW) or resistant (Fischer 344; F344) rats that have identical MHC class II

232 or after transplantation in a low-responder Fischer 344-to-Lewis rat kidney-transplantation model.

233 on the deprotonation of some cyclic rhenium Fischer-type carbene complexes where the reaction that l

234 Three strains [Sprague-Dawley (SD), Fischer 344 (F344), and Brown-Norway (BN)] of male rats

235 rease in Ca-ATPase activity in the senescent Fischer 344 rat heart relative to that of young adult he

236 -1 activation and cytolysis of LT-sensitive (Fischer and Brown-Norway) rat macrophages.

237 nalized self-assembled monolayer and in situ Fischer esterification, a simple and reversible chemical

238 cal variables were compared using chi-square/Fischer's exact test.

239 e issues are reflected using as a case study Fischer-Tropsch diesel derived from boreal forest biomas

240 Subsequent Fischer indole synthesis with hydrazine 5 then provided

241 completely protected the highly susceptible Fischer F344 rats from lethal toxin.

242 disease progression and death in susceptible Fischer rats and BALB/c mice challenged with LT.

243 disease progression and death in susceptible Fischer rats and increased survival in BALB/c mice after

244 border zone of subacute infarcted syngeneic Fischer rat hearts and compared with medium-injected con

245 induced complete remission in the syngeneic Fischer F344 rat model of aggressive NK-LGL leukemia.

246 induced complete remission in the syngeneic Fischer rat model of NK-cell leukemia.

247 Students t-test, Fischer exact test, and multivariable regression analyse

248 sociation between iron loading and high TGs, Fischer rats were fed chow containing 1% carbonyl iron.

249 The authors previously demonstrated that Fischer 344 (F344) and Lewis inbred rats differ in acqui

250 The Fischer-Tropsch process, or the catalytic hydrogenation

251 The Fischer-Tropsch synthesis of lower olefins (FTO) is an a

252 meruli are prone to failure, we analyzed the Fischer 344 rat model of aging under ad libitum-fed (rap

253 Here, inspired by the Fischer indole synthesis, we report an iridium-catalysed

254 duced suppression of saccharin intake by the Fischer rats is not likely mediated by differences in se

255 ce for the rs7848647 SNP was assessed by the Fischer's exact test.

256 3 h for metalloimine formation, 15 h for the Fischer indole reaction and 2 h for isolation and purifi

257 ylhydrazones, the starting materials for the Fischer indole reaction.

258 the AUC, sensitivity, or specificity for the Fischer, General Electric, or Lorad digital images.

259 esis of dimethyl ether, methanol and for the Fischer-Tropsch process using established catalysts.

260 dependence of cobalt (Co) catalysts for the Fischer-Tropsch reaction was studied with colloidally pr

261 the occurrence of hysteresis effects in the Fischer-Tropsch reaction over potassium promoted Co/MnO(

262 rocess of ammonia synthesis and later in the Fischer-Tropsch reaction.

263 ve function as measured by water maze in the Fischer/Brown Norway (FBN) rat, comparing 24 h of sleep

264 nt of a high-resolution 3-D MRI atlas of the Fischer 344 adult rat brain.

265 Finally, trapping of the Fischer carbene by various functional groups attached th

266 he success of our approach is the use of the Fischer indolization reaction to introduce the C7 quater

267 no, lxyo, ribo, or xylo by inspection of the Fischer projection formulas permits prediction of confor

268 n efficient regioselective iodination of the Fischer-Borsche ring has been achieved using molecular i

269 lycosidic bond following the dictates of the Fischer-Ingold persistent radical effect.

270 Despite the long history of the Fischer-Tropsch reaction, carbon monoxide has proven rem

271 as a rare model of the initial stages of the Fischer-Tropsch synthesis.

272 In a new variation on the Fischer indole synthesis, readily available haloarenes a

273 ors and prolonged drug access by testing the Fischer (F344), Lewis (LEW), and Wistar rat strains in a

274 and computational studies pertaining to the Fischer azaindolization reaction are reported.

275 ifold of vast significance: it underlies the Fischer-Tropsch process, Mizoroki-Heck reaction, Ziegler

276 aphy system than for lesions imaged with the Fischer (P = .0070) and Fuji (P = .0070) devices.

277 Combining this approach with the Fischer indole reaction produces indoles in an efficient

278 u-SBz)MoCp* ( S 4 MeBz), consistent with the Fischer-Ingold persistent radical effect.

279 ial magnesium compounds hold for use in the "Fischer-Tropsch-like" transformation of CO/H2 mixtures t

280 technique with a commercial LQIT, the Thermo Fischer Scientific LTQ mass spectrometer.

281 Herein, we highlight the ability of these Fischer-type carbenes to participate in cascade alternat

282 n model vesicles using 1-3 SCAs, even though Fischer-Tropsch-type synthesis under hydrothermal condit

283 of the reactions of thiolate ions with three Fischer-type [aryloxy(phenyl)carbene]pentacarbonyl chrom

284 oups) have been efficiently prepared through Fischer indolization and subsequent diastereoselective r

285 t in Wistar rats (allogeneic) as compared to Fischer rats (syngeneic).

286 itrogenase mechanism and the relationship to Fischer-Tropsch production of hydrocarbons from CO are d

287 ced avoidance of a saccharin cue relative to Fischer 344 rats; while reward-preferring mice that over

288 uction of the Co at temperatures relevant to Fischer-Tropsch synthesis and CO2 methanation.

289 ansplantation of MSC derived from transgenic Fischer alkaline phosphatase (AP) rats, in combination w

290 We generated transgenic Fischer 344 rats that express a dominant negative AA-4E-

291 We transplanted Fischer 344 rat hepatocytes into syngeneic dipeptidyl pe

292 Under Fischer the Society promoted international collaboration

293 The C-C coupling from CO2 indicates a unique Fischer-Tropsch-like reaction with an atypical carbonace

294 es the reaction of an alpha,beta-unsaturated Fischer carbene complex of chromium with a propargyl eth

295 Our system, which uses Fischer's lock-and-key principle, employs colloidal sphe

296 e, this is the first MRI atlas created using Fischer 344 rats and will thus provide an appropriate ne

297 wed by naphtha and diesel fuel synthesis via Fischer-Tropsch (FT).

298 ponses but high TNF-alpha levels in Lewis vs Fischer inbred rats.

299 ized pipeline was a Bayesian classifier with Fischer Score feature selection, achieving an external v

300 est; false-negative rates were compared with Fischer exact test.