ライフサイエンスコーパス: Fischer

1 Fischer (F344) rats resembled Lewis rats in being simila

2 Fischer 344 rat hepatocytes were transplanted into synge

3 Fischer 344 rat recipients of Lewis allografts were trea

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

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

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

7 Fischer 344 rats with intracerebral HSV-tk transduced RG

8 Fischer 344 x Brown Norway rats received fractionated wh

9 Fischer and Lewis rat strains often serve as animal vuln

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

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

12 Fischer indolization followed by RCM delivers the cis is

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

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

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

16 Fischer's exact test was used for survival.

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

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

19 Fischer-Tropsch catalysis performed under industrially r

20 Fischer-Tropsch synthesis is a process for flexible prod

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

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

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

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

25 adenocarcinoma nodules were implanted in 250 Fischer rats.

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

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

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

29 A Fischer indolization step carried out on a tricyclic ket

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

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

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

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

34 about Alzheimer, only little is known about Fischer.

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

36 Adult Fischer 344 rats were anesthetized and injected with BMP

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

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

39 EG), or both, were transplanted in the adult Fischer rat thoracic (T9) spinal cord 1 week after a mod

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

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

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

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

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

45 l and replacement were tested in middle-aged Fischer-344 rats using different memory tasks.

46 + 2] cycloaddition reaction between alkynyl Fischer carbene complexes and tropothione leads to the r

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

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

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

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

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

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

53 Since Lewis and Fischer rats have opposite susceptibility to experimenta

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

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

56 tribution studies in normal Fischer rats and Fischer rats implanted intracranially with 9L gliosarcom

57 vivo microdialysis in urethane-anesthetized Fischer 344 rats.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 how different reactivity than the equivalent Fischer carbene complexes.

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

84 was implanted subcutaneously into 107 female Fischer 344 rats.

85 were implanted subcutaneously in 132 female Fischer rats.

86 own within the mammary fat pads of 19 female Fischer rats.

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

88 sel changes were examined in 28 adult female Fischer 344 rats at 1, 3, 7, 14, 28, and 60 days after a

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

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 rcinoma (1.1-1.4 cm) was implanted in female Fischer rats.

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

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

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

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

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

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

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

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

105 pe did not affect the AUC or sensitivity for Fischer digital images, it did affect specificity (P =.0

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

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

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

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

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

111 the postmitochondrial fraction prepared from Fischer 344 rat liver.

112 nitric oxide mediated effect, in tissue from Fischer 344 rats at different ages (4, 13, and 23 mo) to

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 fferentiated (RHF < 1%) histology growing in Fischer X Copenhagen rats.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

149 The interrupted Fischer indole synthesis of arylhydrazines and biocataly

150 disclosed benzannulation approach involving Fischer carbene complexes and alkynes.

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

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

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

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

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

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

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

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

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

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

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

162 regulates ENaC in two epithelial cell lines (Fischer rat thyroid and H441); small interfering RNA (si

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 rats showed a significantly attenuated HPA axis

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

168 26-month-old calorie-restricted (26CR) male Fischer 344 rats (CR = 40% restriction compared with ad

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

170 e, purified from liver cytosol of adult male Fischer 344 rats, catalyzes transfer of a methyl group f

171 Aged male Fischer 344 rats were given apple (5 mg dry weight), spi

172 nd 26-month-old calorie-restricted (CR) male Fischer 344 rats (CR = 40% restricted compared to ad lib

173 adenovirally transduced into MSCs from male Fischer rats.

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

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

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

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

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

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

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

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

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

183 g (3-month-old) and aged (25-month-old) male Fischer 344 rats the expression of 96 cytokines, chemoki

184 (6 months old) and old (24 months old) male Fischer 344 rats.

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

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

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

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

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

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

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

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

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

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

195 Treatment of molybdenum Fischer carbene complexes with 6-methylene-7-octen-1-yne

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

197 and spatial learning in aged (24-26 months) Fischer 344 rats.

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

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

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

201 ed chronic inflammation in Lewis but neither Fischer nor Buffalo rats, indicating a differential gene

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

203 Cardiomyocytes from male neonatal Fischer 344 rats (1 to 2 days, 3 to 5x10(6)) or medium w

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

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

206 Tissue distribution studies in normal Fischer rats and Fischer rats implanted intracranially w

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

208 The coupling of Fischer carbene complexes with 3-alkynyl-2-heteroaromati

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

210 ce to a recent study of the deprotonation of Fischer carbene complexes are discussed.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

225 Proteins from adult, middle age, and old Fischer 344 Brown Norway rats were compared.

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

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

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

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

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

231 by comparing NPY expression in sham operated Fischer Control and anorectic TB rats.

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

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

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

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

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

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

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

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

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

241 -1 activation and cytolysis of LT-sensitive (Fischer and Brown-Norway) rat macrophages.

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

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

244 r CO molecule and the generation of a stable Fischer carbene.

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

246 Subsequent Fischer indole synthesis with hydrazine 5 then provided

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

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

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

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

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

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

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

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

255 The Fischer-Tropsch process, or the catalytic hydrogenation

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

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

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

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

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

261 3 h for metalloimine formation, 15 h for the Fischer indole reaction and 2 h for isolation and purifi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

290 We transplanted Fischer 344 rat hepatocytes into syngeneic dipeptidyl pe

291 ngraftment of transplanted cells, we treated Fischer 344 (F344) rats lacking dipeptidyl peptidase IV

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 Using Fischer 344 rats, we demonstrate that vaccination with r

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 the digital images, which were acquired with Fischer, General Electric, and Lorad digital mammography

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